| geneid | 255488 |
|---|---|
| ensemblid | ENSG00000137393.10 |
| hgncid | 21578 |
| symbol | RNF144B |
| name | ring finger protein 144B |
| refseq_nuc | NM_182757.4 |
| refseq_prot | NP_877434.2 |
| ensembl_nuc | ENST00000259939.4 |
| ensembl_prot | ENSP00000259939.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 18387350 |
| end | 18468870 |
| strand | + |
| ver | v1.2 |
| region | chr6:18387350-18468870 |
| region5000 | chr6:18382350-18473870 |
| regionname0 | RNF144B_chr6_18387350_18468870 |
| regionname5000 | RNF144B_chr6_18382350_18473870 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 303 | 384 | 90 | 82 | 150 | 18 | 42 | 113 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0002 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0003 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 912 | 380 | 90 | 81 | 149 | 16 | 42 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| c0002 | 0/0 | 912 | 2 | 0 | 0 | 0 | 2 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| c0003 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| c0004 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| c0005 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| c0006 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4126 | 31 | 0 | 2 | 28 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0002 | 0/0 | 4125 | 23 | 1 | 4 | 16 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0003 | 0/0 | 4122 | 17 | 0 | 0 | 16 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0004 | 0/0 | 4126 | 15 | 0 | 0 | 12 | 1 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0005 | 0/0 | 4122 | 15 | 1 | 6 | 6 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0006 | 0/0 | 4121 | 14 | 2 | 2 | 8 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0007 | 0/0 | 4117 | 13 | 1 | 7 | 1 | 3 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0008 | 0/0 | 4122 | 11 | 1 | 1 | 9 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0009 | 0/0 | 4120 | 10 | 2 | 0 | 7 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0010 | 0/0 | 4120 | 10 | 2 | 5 | 0 | 3 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0011 | 0/0 | 4125 | 9 | 1 | 8 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0012 | 0/0 | 4122 | 8 | 3 | 1 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0013 | 0/0 | 4125 | 8 | 4 | 0 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0014 | 0/0 | 4126 | 7 | 0 | 1 | 3 | 0 | 3 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0015 | 0/0 | 4122 | 7 | 0 | 3 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0016 | 0/0 | 4122 | 7 | 2 | 4 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0017 | 0/0 | 4121 | 6 | 3 | 1 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0018 | 0/0 | 4116 | 5 | 0 | 0 | 1 | 0 | 4 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0019 | 0/0 | 4125 | 5 | 2 | 2 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0020 | 0/0 | 4124 | 5 | 4 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0021 | 0/0 | 4124 | 5 | 4 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0022 | 0/0 | 4122 | 5 | 0 | 3 | 0 | 2 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0023 | 0/0 | 4127 | 5 | 0 | 0 | 5 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0024 | 0/0 | 4119 | 4 | 3 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0025 | 0/0 | 4120 | 4 | 0 | 1 | 3 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0026 | 0/0 | 4121 | 4 | 0 | 2 | 0 | 1 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0027 | 0/1 | 4125 | 4 | 0 | 2 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0028 | 0/0 | 4124 | 4 | 4 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0029 | 0/0 | 4126 | 4 | 0 | 3 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0030 | 0/0 | 4125 | 4 | 2 | 1 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0031 | 0/0 | 4126 | 4 | 0 | 0 | 4 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0032 | 0/0 | 4123 | 4 | 0 | 1 | 3 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0033 | 0/0 | 4119 | 3 | 3 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0034 | 0/0 | 4121 | 3 | 0 | 0 | 2 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0035 | 0/0 | 4117 | 3 | 0 | 0 | 1 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0036 | 0/0 | 4123 | 3 | 0 | 1 | 1 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0037 | 0/0 | 4121 | 3 | 0 | 1 | 1 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0038 | 0/0 | 4125 | 3 | 3 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0039 | 0/0 | 4122 | 3 | 2 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0040 | 1/0 | 4121 | 3 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0041 | 0/0 | 4125 | 3 | 1 | 1 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0042 | 0/0 | 4125 | 3 | 0 | 1 | 0 | 1 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0043 | 0/0 | 4122 | 2 | 0 | 0 | 0 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0044 | 0/0 | 4119 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0045 | 0/0 | 4117 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0046 | 0/0 | 4122 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0047 | 0/0 | 4126 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0048 | 0/0 | 4125 | 2 | 1 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0049 | 0/0 | 4122 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0050 | 0/0 | 4126 | 2 | 1 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0051 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0052 | 0/0 | 4125 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0053 | 0/0 | 4122 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0054 | 0/0 | 4126 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0055 | 0/0 | 4126 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0056 | 0/0 | 4122 | 2 | 0 | 1 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0057 | 0/0 | 4120 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0058 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0059 | 0/0 | 4126 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0060 | 0/0 | 4122 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0061 | 0/0 | 4122 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0062 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0063 | 0/0 | 4120 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0064 | 0/0 | 4119 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0065 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0066 | 0/0 | 4120 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0067 | 0/0 | 4121 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0068 | 0/0 | 4121 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0069 | 0/0 | 4121 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0070 | 0/0 | 4120 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0071 | 0/0 | 4114 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0072 | 0/0 | 4118 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0073 | 0/0 | 4122 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0074 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0075 | 0/0 | 4126 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0076 | 0/0 | 4126 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0077 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0078 | 0/0 | 4126 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0079 | 0/0 | 4122 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0080 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0081 | 0/0 | 4124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0082 | 0/0 | 4124 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0083 | 0/0 | 4124 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0084 | 0/0 | 4121 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0085 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0086 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0087 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0088 | 0/0 | 4126 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0089 | 0/0 | 4122 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0090 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0091 | 0/0 | 4124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0092 | 0/0 | 4124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0093 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0094 | 0/0 | 4127 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0095 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0096 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0097 | 0/0 | 4119 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0098 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0099 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0100 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0101 | 0/0 | 4124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0102 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0103 | 0/0 | 4124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0104 | 0/0 | 4124 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0105 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0106 | 0/0 | 4123 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| t0107 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0370 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 912 | 380 | 90 | 81 | 149 | 16 | 42 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0002 | 0/0 | 912 | 2 | 0 | 0 | 0 | 2 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0003 | 0/0 | 912 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0005 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0002c0004 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0003c0006 | 0/0 | 912 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5037 | 31 | 0 | 2 | 28 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0002 | 0/0 | 5036 | 23 | 1 | 4 | 16 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0003 | 0/0 | 5033 | 17 | 0 | 0 | 16 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0004 | 0/0 | 5037 | 15 | 0 | 0 | 12 | 1 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0005 | 0/0 | 5033 | 15 | 1 | 6 | 6 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0006 | 0/0 | 5032 | 14 | 2 | 2 | 8 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0007 | 0/0 | 5028 | 13 | 1 | 7 | 1 | 3 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0008 | 0/0 | 5033 | 11 | 1 | 1 | 9 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0009 | 0/0 | 5031 | 9 | 2 | 0 | 6 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0010 | 0/0 | 5031 | 10 | 2 | 5 | 0 | 3 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0011 | 0/0 | 5036 | 9 | 1 | 8 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0012 | 0/0 | 5033 | 8 | 3 | 1 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0013 | 0/0 | 5036 | 8 | 4 | 0 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0014 | 0/0 | 5037 | 7 | 0 | 1 | 3 | 0 | 3 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0015 | 0/0 | 5033 | 7 | 0 | 3 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0016 | 0/0 | 5033 | 7 | 2 | 4 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0017 | 0/0 | 5032 | 6 | 3 | 1 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0018 | 0/0 | 5027 | 5 | 0 | 0 | 1 | 0 | 4 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0019 | 0/0 | 5036 | 5 | 2 | 2 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0020 | 0/0 | 5035 | 5 | 4 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0021 | 0/0 | 5035 | 5 | 4 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0022 | 0/0 | 5033 | 3 | 0 | 3 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0023 | 0/0 | 5038 | 5 | 0 | 0 | 5 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0024 | 0/0 | 5030 | 4 | 3 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0025 | 0/0 | 5031 | 3 | 0 | 0 | 3 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0026 | 0/0 | 5032 | 4 | 0 | 2 | 0 | 1 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0027 | 0/1 | 5036 | 4 | 0 | 2 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0028 | 0/0 | 5035 | 4 | 4 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0029 | 0/0 | 5037 | 4 | 0 | 3 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0030 | 0/0 | 5036 | 4 | 2 | 1 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0031 | 0/0 | 5037 | 4 | 0 | 0 | 4 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0032 | 0/0 | 5034 | 4 | 0 | 1 | 3 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0033 | 0/0 | 5030 | 3 | 3 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0034 | 0/0 | 5032 | 3 | 0 | 0 | 2 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0035 | 0/0 | 5028 | 3 | 0 | 0 | 1 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0036 | 0/0 | 5034 | 3 | 0 | 1 | 1 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0037 | 0/0 | 5032 | 3 | 0 | 1 | 1 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0038 | 0/0 | 5036 | 3 | 3 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0039 | 0/0 | 5033 | 3 | 2 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0040 | 1/0 | 5032 | 3 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0041 | 0/0 | 5036 | 3 | 1 | 1 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0042 | 0/0 | 5036 | 3 | 0 | 1 | 0 | 1 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0043 | 0/0 | 5033 | 2 | 0 | 0 | 0 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0044 | 0/0 | 5030 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0045 | 0/0 | 5028 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0046 | 0/0 | 5033 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0047 | 0/0 | 5037 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0048 | 0/0 | 5036 | 2 | 1 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0049 | 0/0 | 5033 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0050 | 0/0 | 5037 | 2 | 1 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0051 | 0/0 | 5036 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0052 | 0/0 | 5036 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0053 | 0/0 | 5033 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0054 | 0/0 | 5037 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0055 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0056 | 0/0 | 5033 | 2 | 0 | 1 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0057 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0058 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0059 | 0/0 | 5037 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0060 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0061 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0062 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0063 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0064 | 0/0 | 5030 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0065 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0066 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0067 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0068 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0069 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0070 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0071 | 0/0 | 5025 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0072 | 0/0 | 5029 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0073 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0074 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0075 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0076 | 0/0 | 5037 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0077 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0079 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0080 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0081 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0082 | 0/0 | 5035 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0083 | 0/0 | 5035 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0084 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0085 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0086 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0087 | 0/0 | 5036 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0088 | 0/0 | 5037 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0089 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0090 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0091 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0092 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0093 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0094 | 0/0 | 5038 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0095 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0096 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0097 | 0/0 | 5030 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0098 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0099 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0100 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0101 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0102 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0103 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0104 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0105 | 0/0 | 5036 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0106 | 0/0 | 5034 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0001t0107 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0002t0022 | 0/0 | 5033 | 2 | 0 | 0 | 0 | 2 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0003t0025 | 0/0 | 5031 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0001c0005t0009 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0002c0004t0078 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| a0003c0006t0055 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | copy fasta | chr6 | 18382350 | 18473870 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0019g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0019g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0019g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0019g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0022g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0022g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0022g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0024g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0024g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0024g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0024g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0025g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0025g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0025g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0026g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0026g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0026g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0026g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0027g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0027g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0027g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0027g0370 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0028g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0028g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0028g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0028g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0029g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0029g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0029g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0029g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0030g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0030g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0030g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0030g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0031g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0031g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0031g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0031g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0032g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0032g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0032g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0032g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0033g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0033g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0033g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0034g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0034g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0034g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0035g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0035g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0035g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0036g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0036g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0036g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0037g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0037g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0037g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0038g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0038g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0038g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0039g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0039g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0039g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0040g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0040g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0040g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0041g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0041g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0041g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0042g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0042g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0042g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0043g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0043g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0044g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0044g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0045g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0045g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0046g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0046g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0047g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0047g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0048g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0048g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0049g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0049g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0050g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0050g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0051g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0052g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0052g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0053g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0053g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0054g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0054g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0055g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0056g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0056g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0057g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0058g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0059g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0060g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0061g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0062g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0063g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0064g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0065g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0066g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0067g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0068g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0069g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0070g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0071g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0072g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0073g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0074g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0075g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0076g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0077g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0079g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0080g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0081g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0082g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0083g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0084g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0085g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0086g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0087g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0088g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0089g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0090g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0091g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0092g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0093g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0094g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0095g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0096g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0097g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0098g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0099g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0100g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0101g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0102g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0103g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0104g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0105g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0106g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0107g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0002t0022g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0002t0022g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0003t0025g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0005t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0002c0004t0078g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0003c0006t0055g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0235 | EUR | GBR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0318 | EUR | GBR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00140 | hp1 | a0001 | c0001 | t0084 | g0107 | EUR | GBR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00140 | hp2 | a0001 | c0001 | t0071 | g0299 | EUR | GBR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0233 | EUR | FIN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0243 | EUR | FIN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00323 | hp1 | a0001 | c0001 | t0042 | g0071 | EUR | FIN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00323 | hp2 | a0001 | c0001 | t0029 | g0118 | EUR | FIN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00423 | hp1 | a0001 | c0001 | t0053 | g0205 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0327 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00438 | hp1 | a0001 | c0001 | t0089 | g0182 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00438 | hp2 | a0001 | c0001 | t0023 | g0042 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0367 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00609 | hp2 | a0001 | c0001 | t0034 | g0231 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00621 | hp2 | a0001 | c0001 | t0015 | g0347 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0274 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00639 | hp2 | a0001 | c0001 | t0056 | g0044 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00642 | hp1 | a0001 | c0001 | t0017 | g0088 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0362 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00733 | hp1 | a0001 | c0001 | t0022 | g0159 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0241 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00735 | hp1 | a0001 | c0001 | t0059 | g0142 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00735 | hp2 | a0001 | c0001 | t0076 | g0371 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0244 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00738 | hp2 | a0001 | c0001 | t0039 | g0173 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00741 | hp1 | a0001 | c0001 | t0012 | g0189 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00741 | hp2 | a0001 | c0001 | t0094 | g0209 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0257 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01069 | hp2 | a0001 | c0001 | t0015 | g0374 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01070 | hp1 | a0001 | c0001 | t0016 | g0073 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01070 | hp2 | a0001 | c0001 | t0022 | g0218 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01071 | hp1 | a0001 | c0001 | t0016 | g0046 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0007 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0352 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0128 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01081 | hp1 | a0001 | c0001 | t0037 | g0136 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01099 | hp1 | a0001 | c0001 | t0022 | g0158 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0236 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0298 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01106 | hp2 | a0001 | c0001 | t0015 | g0137 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01109 | hp1 | a0001 | c0001 | t0016 | g0076 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01109 | hp2 | a0001 | c0001 | t0021 | g0196 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01167 | hp1 | a0001 | c0001 | t0029 | g0121 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01167 | hp2 | a0001 | c0001 | t0024 | g0296 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01168 | hp1 | a0001 | c0001 | t0046 | g0124 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01168 | hp2 | a0001 | c0001 | t0087 | g0119 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01169 | hp1 | a0001 | c0001 | t0046 | g0125 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01169 | hp2 | a0001 | c0001 | t0029 | g0117 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0238 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01175 | hp2 | a0001 | c0001 | t0029 | g0112 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01192 | hp1 | a0001 | c0001 | t0105 | g0063 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01243 | hp1 | a0001 | c0001 | t0027 | g0305 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01243 | hp2 | a0001 | c0001 | t0030 | g0162 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01255 | hp1 | a0001 | c0001 | t0032 | g0207 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01255 | hp2 | a0001 | c0001 | t0041 | g0031 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0279 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01256 | hp2 | a0001 | c0001 | t0019 | g0004 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01257 | hp1 | a0001 | c0001 | t0052 | g0151 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01257 | hp2 | a0001 | c0001 | t0042 | g0090 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01258 | hp1 | a0001 | c0001 | t0019 | g0004 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01258 | hp2 | a0001 | c0001 | t0052 | g0150 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01261 | hp1 | a0001 | c0001 | t0016 | g0048 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01358 | hp1 | a0001 | c0001 | t0026 | g0263 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01361 | hp1 | a0001 | c0001 | t0014 | g0322 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01361 | hp2 | a0001 | c0001 | t0083 | g0123 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01433 | hp1 | a0001 | c0001 | t0106 | g0045 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01433 | hp2 | a0001 | c0001 | t0027 | g0364 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0323 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01496 | hp2 | a0001 | c0001 | t0020 | g0120 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01515 | hp1 | a0001 | c0002 | t0022 | g0180 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01515 | hp2 | a0001 | c0001 | t0082 | g0102 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0234 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01516 | hp2 | a0001 | c0001 | t0041 | g0051 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0242 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01517 | hp2 | a0001 | c0002 | t0022 | g0194 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01884 | hp1 | a0001 | c0001 | t0050 | g0214 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0295 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01891 | hp1 | a0001 | c0001 | t0062 | g0294 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01891 | hp2 | a0001 | c0001 | t0030 | g0197 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0306 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01928 | hp2 | a0001 | c0001 | t0073 | g0373 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0312 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01934 | hp2 | a0001 | c0003 | t0025 | g0249 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0246 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0325 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01975 | hp2 | a0001 | c0001 | t0026 | g0282 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01981 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01993 | hp1 | a0001 | c0001 | t0011 | g0324 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01993 | hp2 | a0001 | c0001 | t0060 | g0147 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02004 | hp1 | a0001 | c0001 | t0011 | g0375 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0155 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02055 | hp1 | a0001 | c0001 | t0058 | g0227 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02055 | hp2 | a0001 | c0001 | t0080 | g0099 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02056 | hp1 | a0001 | c0001 | t0012 | g0175 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02071 | hp1 | a0002 | c0004 | t0078 | g0317 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02074 | hp1 | a0001 | c0001 | t0079 | g0361 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0078 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0187 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02132 | hp1 | a0001 | c0001 | t0053 | g0204 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0185 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02145 | hp2 | a0001 | c0001 | t0033 | g0286 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02148 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0315 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0369 | EAS | CDX | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02155 | hp2 | a0001 | c0005 | t0009 | g0248 | EAS | CDX | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02165 | hp2 | a0001 | c0001 | t0017 | g0029 | EAS | CDX | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02257 | hp1 | a0001 | c0001 | t0017 | g0003 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0007 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02258 | hp1 | a0001 | c0001 | t0020 | g0127 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02258 | hp2 | a0001 | c0001 | t0028 | g0100 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0310 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02280 | hp1 | a0001 | c0001 | t0103 | g0093 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0082 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0232 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02293 | hp2 | a0001 | c0001 | t0036 | g0301 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0372 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0240 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02451 | hp1 | a0001 | c0001 | t0044 | g0268 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0094 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02523 | hp1 | a0001 | c0001 | t0015 | g0348 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02572 | hp1 | a0001 | c0001 | t0047 | g0106 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02572 | hp2 | a0001 | c0001 | t0049 | g0144 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02602 | hp1 | a0001 | c0001 | t0014 | g0135 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0239 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02615 | hp1 | a0001 | c0001 | t0101 | g0018 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02615 | hp2 | a0001 | c0001 | t0024 | g0290 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0183 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02622 | hp2 | a0001 | c0001 | t0030 | g0213 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02630 | hp1 | a0001 | c0001 | t0020 | g0113 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02630 | hp2 | a0001 | c0001 | t0041 | g0033 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02683 | hp1 | a0001 | c0001 | t0013 | g0091 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02683 | hp2 | a0001 | c0001 | t0048 | g0103 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02717 | hp1 | a0001 | c0001 | t0028 | g0105 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0087 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02723 | hp1 | a0001 | c0001 | t0104 | g0024 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02723 | hp2 | a0001 | c0001 | t0070 | g0226 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02735 | hp1 | a0001 | c0001 | t0077 | g0304 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02735 | hp2 | a0001 | c0001 | t0030 | g0201 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0314 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02738 | hp2 | a0001 | c0001 | t0042 | g0089 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0049 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02809 | hp2 | a0001 | c0001 | t0067 | g0273 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02818 | hp1 | a0001 | c0001 | t0085 | g0114 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02818 | hp2 | a0001 | c0001 | t0066 | g0285 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02886 | hp1 | a0001 | c0001 | t0107 | g0019 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02886 | hp2 | a0001 | c0001 | t0028 | g0097 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02896 | hp1 | a0001 | c0001 | t0039 | g0149 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02896 | hp2 | a0001 | c0001 | t0044 | g0265 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02897 | hp1 | a0001 | c0001 | t0038 | g0098 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02897 | hp2 | a0001 | c0001 | t0039 | g0146 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0228 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0219 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02965 | hp1 | a0001 | c0001 | t0092 | g0179 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0148 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02970 | hp1 | a0001 | c0001 | t0100 | g0017 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02970 | hp2 | a0001 | c0001 | t0021 | g0198 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02976 | hp1 | a0001 | c0001 | t0020 | g0005 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02976 | hp2 | a0001 | c0001 | t0038 | g0101 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03017 | hp1 | a0001 | c0001 | t0034 | g0272 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03017 | hp2 | a0001 | c0001 | t0014 | g0357 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0359 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03041 | hp2 | a0001 | c0001 | t0038 | g0143 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0172 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03098 | hp2 | a0001 | c0001 | t0096 | g0202 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03130 | hp1 | a0001 | c0001 | t0033 | g0287 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03130 | hp2 | a0001 | c0001 | t0099 | g0084 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03139 | hp1 | a0001 | c0001 | t0019 | g0145 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03139 | hp2 | a0001 | c0001 | t0028 | g0134 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03195 | hp1 | a0001 | c0001 | t0021 | g0195 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03195 | hp2 | a0001 | c0001 | t0040 | g0109 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0126 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03209 | hp2 | a0001 | c0001 | t0054 | g0086 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03225 | hp1 | a0001 | c0001 | t0057 | g0229 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03225 | hp2 | a0001 | c0001 | t0024 | g0291 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03239 | hp1 | a0001 | c0001 | t0015 | g0138 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03239 | hp2 | a0001 | c0001 | t0026 | g0264 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03453 | hp1 | a0001 | c0001 | t0040 | g0110 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03453 | hp2 | a0001 | c0001 | t0091 | g0215 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0363 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0003 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0250 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03491 | hp1 | a0001 | c0001 | t0043 | g0140 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03491 | hp2 | a0001 | c0001 | t0018 | g0269 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03492 | hp2 | a0001 | c0001 | t0043 | g0141 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0014 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03516 | hp2 | a0001 | c0001 | t0021 | g0177 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03540 | hp1 | a0001 | c0001 | t0054 | g0013 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03540 | hp2 | a0001 | c0001 | t0102 | g0081 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03579 | hp1 | a0001 | c0001 | t0098 | g0206 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03654 | hp1 | a0001 | c0001 | t0061 | g0115 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03654 | hp2 | a0001 | c0001 | t0019 | g0104 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03669 | hp1 | a0001 | c0001 | t0068 | g0281 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0283 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03704 | hp2 | a0001 | c0001 | t0018 | g0271 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0157 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03710 | hp2 | a0001 | c0001 | t0035 | g0270 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03834 | hp1 | a0001 | c0001 | t0027 | g0129 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0300 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0131 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0156 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04115 | hp1 | a0001 | c0001 | t0035 | g0267 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04115 | hp2 | a0001 | c0001 | t0012 | g0199 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04184 | hp1 | a0001 | c0001 | t0064 | g0376 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04184 | hp2 | a0001 | c0001 | t0036 | g0337 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04199 | hp1 | a0001 | c0001 | t0037 | g0334 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0186 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04204 | hp1 | a0001 | c0001 | t0056 | g0056 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04204 | hp2 | a0001 | c0001 | t0074 | g0139 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04228 | hp1 | a0001 | c0001 | t0018 | g0256 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0188 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0292 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18747 | hp2 | a0001 | c0001 | t0008 | g0077 | EAS | CHB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18906 | hp1 | a0001 | c0001 | t0063 | g0293 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18906 | hp2 | a0001 | c0001 | t0093 | g0178 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18939 | hp1 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18939 | hp2 | a0001 | c0001 | t0009 | g0252 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18941 | hp1 | a0001 | c0001 | t0055 | g0075 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18941 | hp2 | a0001 | c0001 | t0009 | g0253 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18944 | hp2 | a0001 | c0001 | t0045 | g0258 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18945 | hp2 | a0001 | c0001 | t0025 | g0280 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18948 | hp1 | a0001 | c0001 | t0023 | g0064 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18948 | hp2 | a0001 | c0001 | t0025 | g0278 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0344 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18949 | hp2 | a0001 | c0001 | t0097 | g0224 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18951 | hp1 | a0001 | c0001 | t0016 | g0066 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0328 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18956 | hp1 | a0001 | c0001 | t0014 | g0307 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18956 | hp2 | a0001 | c0001 | t0023 | g0020 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18959 | hp2 | a0003 | c0006 | t0055 | g0067 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0360 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18962 | hp2 | a0001 | c0001 | t0031 | g0210 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18964 | hp2 | a0001 | c0001 | t0013 | g0036 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18965 | hp1 | a0001 | c0001 | t0032 | g0200 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18969 | hp1 | a0001 | c0001 | t0012 | g0011 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18971 | hp2 | a0001 | c0001 | t0018 | g0261 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18972 | hp1 | a0001 | c0001 | t0037 | g0339 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0343 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18981 | hp1 | a0001 | c0001 | t0032 | g0193 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0342 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18982 | hp2 | a0001 | c0001 | t0009 | g0230 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18984 | hp1 | a0001 | c0001 | t0015 | g0335 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0072 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18985 | hp2 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18986 | hp1 | a0001 | c0001 | t0013 | g0027 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18989 | hp2 | a0001 | c0001 | t0025 | g0276 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18991 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18994 | hp2 | a0001 | c0001 | t0014 | g0356 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18995 | hp2 | a0001 | c0001 | t0045 | g0259 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19000 | hp1 | a0001 | c0001 | t0036 | g0336 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19000 | hp2 | a0001 | c0001 | t0034 | g0247 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19004 | hp2 | a0001 | c0001 | t0095 | g0225 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19009 | hp1 | a0001 | c0001 | t0013 | g0026 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19011 | hp1 | a0001 | c0001 | t0075 | g0326 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0092 | AFR | LWK | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19043 | hp2 | a0001 | c0001 | t0051 | g0006 | AFR | LWK | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0358 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19056 | hp1 | a0001 | c0001 | t0031 | g0211 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19057 | hp2 | a0001 | c0001 | t0009 | g0255 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19058 | hp2 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19060 | hp1 | a0001 | c0001 | t0032 | g0165 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19060 | hp2 | a0001 | c0001 | t0031 | g0160 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19064 | hp1 | a0001 | c0001 | t0035 | g0260 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0368 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19076 | hp2 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19079 | hp1 | a0001 | c0001 | t0031 | g0167 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19080 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0366 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19081 | hp2 | a0001 | c0001 | t0009 | g0254 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19082 | hp2 | a0001 | c0001 | t0023 | g0061 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19083 | hp2 | a0001 | c0001 | t0069 | g0277 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19084 | hp1 | a0001 | c0001 | t0023 | g0025 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0365 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0341 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19088 | hp1 | a0001 | c0001 | t0017 | g0065 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0251 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0288 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19240 | hp2 | a0001 | c0001 | t0065 | g0289 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20129 | hp1 | a0001 | c0001 | t0047 | g0132 | AFR | ASW | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0245 | AFR | ASW | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20752 | hp1 | a0001 | c0001 | t0026 | g0262 | EUR | TSI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20752 | hp2 | a0001 | c0001 | t0088 | g0111 | EUR | TSI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20805 | hp1 | a0001 | c0001 | t0010 | g0237 | EUR | TSI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20805 | hp2 | a0001 | c0001 | t0050 | g0161 | EUR | TSI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20905 | hp1 | a0001 | c0001 | t0072 | g0275 | SAS | GIH | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20905 | hp2 | a0001 | c0001 | t0014 | g0316 | SAS | GIH | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01123 | hp2 | a0001 | c0001 | t0011 | g0321 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02109 | hp1 | a0001 | c0001 | t0033 | g0284 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02109 | hp2 | a0001 | c0001 | t0049 | g0116 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02559 | hp1 | a0001 | c0001 | t0090 | g0174 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02559 | hp2 | a0001 | c0001 | t0081 | g0122 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG06807 | hp1 | a0001 | c0001 | t0051 | g0006 | AFR | USA | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0085 | AFR | USA | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20300 | hp1 | a0001 | c0001 | t0086 | g0005 | AFR | USA | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0001 | AFR | USA | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA21309 | hp1 | a0001 | c0001 | t0048 | g0096 | AFR | LWK | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0083 | AFR | LWK | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0027 | g0370 | REF | REF | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0040 | g0108 | REF | REF | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:18399610
|
C | T | 1 | a0003 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.76C>T | p.Pro26Ser | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/8 | 393/5032 | 76/912 | 26/303 | chr6 | 18399610 | ||
| chr6:18459713
|
A | G | 1 | a0002 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.643A>G | p.Lys215Glu | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/8 | 960/5032 | 643/912 | 215/303 | chr6 | 18459713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:18399606
|
G | A | 1 | a0001c0002 | 2 | HG01515.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.72G>A | p.Pro24Pro | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/8 | 389/5032 | 72/912 | 24/303 | chr6 | 18399606 | ||
| chr6:18459670
|
C | A | 1 | a0001c0003 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.600C>A | p.Ile200Ile | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/8 | 917/5032 | 600/912 | 200/303 | chr6 | 18459670 | ||
| chr6:18459688
|
C | T | 1 | a0001c0005 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.618C>T | p.Cys206Cys | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/8 | 935/5032 | 618/912 | 206/303 | chr6 | 18459688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:18387446
|
T | C | 2 | a0001c0001t0057a0001c0001t0058 | 2 | HG02055.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-221T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 12089 | chr6 | 18387446 | |||||
| chr6:18387452
|
T | C | 3 | a0001c0001t0043a0001c0001t0059a0001c0001t0060 | 4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-215T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 12083 | chr6 | 18387452 | |||||
| chr6:18387461
|
A | G | 21 | a0001c0001t0001a0001c0001t0008a0001c0001t0013others(18): Show | 89 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
5_prime_UTR_variant | MODIFIER | c.-206A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 12074 | chr6 | 18387461 | |||||
| chr6:18387521
|
G | A | 1 | a0001c0001t0061 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-146G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 12014 | chr6 | 18387521 | |||||
| chr6:18387537
|
CTCCTG | C | 27 | a0001c0001t0007a0001c0001t0009a0001c0001t0010others(24): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
5_prime_UTR_variant | MODIFIER | c.-126_-122delTGTCC | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 11990 | INFO_REALIGN_3_PRIME | chr6 | 18387537 | ||||
| chr6:18387584
|
A | C | 23 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(20): Show | 79 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-83A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 11951 | chr6 | 18387584 | |||||
| chr6:18387600
|
C | T | 1 | a0001c0001t0045 | 2 | NA18944.hp2 NA18995.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-67C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | chr6 | 18387600 | ||||||
| chr6:18399519
|
T | C | 65 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(62): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
5_prime_UTR_variant | MODIFIER | c.-16T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/8 | 16 | chr6 | 18399519 | |||||
| chr6:18465450
|
G | A | 2 | a0001c0001t0089a0001c0001t0090 | 2 | HG00438.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*383G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 383 | chr6 | 18465450 | |||||
| chr6:18465479
|
G | A | 106 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(103): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*412G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 412 | chr6 | 18465479 | |||||
| chr6:18465636
|
G | A | 9 | a0001c0001t0024a0001c0001t0028a0001c0001t0062others(6): Show | 15 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*569G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 569 | chr6 | 18465636 | |||||
| chr6:18465727
|
G | C | 1 | a0001c0001t0073 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 660 | chr6 | 18465727 | |||||
| chr6:18465785
|
A | G | 1 | a0001c0001t0058 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 718 | chr6 | 18465785 | |||||
| chr6:18465873
|
G | A | 2 | a0001c0001t0091a0001c0001t0099 | 2 | HG03130.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*806G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 806 | chr6 | 18465873 | |||||
| chr6:18466177
|
G | A | 8 | a0001c0001t0038a0001c0001t0064a0001c0001t0074others(5): Show | 10 | HG01515.hp2 HG02559.hp2 HG02897.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1110 | chr6 | 18466177 | |||||
| chr6:18466382
|
T | C | 1 | a0001c0001t0081 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1315 | chr6 | 18466382 | |||||
| chr6:18466383
|
T | C | 1 | a0001c0001t0065 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1316T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1316 | chr6 | 18466383 | |||||
| chr6:18466446
|
A | T | 106 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(103): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*1379A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1379 | chr6 | 18466446 | |||||
| chr6:18466451
|
G | C | 1 | a0001c0001t0081 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1384G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1384 | chr6 | 18466451 | |||||
| chr6:18466519
|
C | T | 25 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(22): Show | 80 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1452C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1452 | chr6 | 18466519 | |||||
| chr6:18466587
|
C | T | 1 | a0001c0001t0070 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1520C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1520 | chr6 | 18466587 | |||||
| chr6:18466632
|
G | A | 1 | a0001c0001t0094 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1565G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1565 | chr6 | 18466632 | |||||
| chr6:18466877
|
G | A | 1 | a0001c0001t0081 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1810G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1810 | chr6 | 18466877 | |||||
| chr6:18466929
|
A | G | 2 | a0001c0001t0026a0002c0004t0078 | 5 | HG01358.hp1 HG01975.hp2 HG02071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1862A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1862 | chr6 | 18466929 | |||||
| chr6:18466973
|
T | C | 2 | a0001c0001t0066a0001c0001t0083 | 2 | HG01361.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1906T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1906 | chr6 | 18466973 | |||||
| chr6:18467009
|
C | A | 5 | a0001c0001t0022a0001c0001t0046a0001c0001t0056others(2): Show | 10 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1942C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1942 | chr6 | 18467009 | |||||
| chr6:18467025
|
CAT | C | 25 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(22): Show | 80 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1959_*1960delAT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1959 | chr6 | 18467025 | |||||
| chr6:18467097
|
C | G | 1 | a0001c0001t0053 | 2 | HG00423.hp1 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2030C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2030 | chr6 | 18467097 | |||||
| chr6:18467225
|
T | C | 106 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(103): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*2158T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2158 | chr6 | 18467225 | |||||
| chr6:18467291
|
G | A | 16 | a0001c0001t0002a0001c0001t0009a0001c0001t0013others(13): Show | 72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2224G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2224 | chr6 | 18467291 | |||||
| chr6:18467303
|
G | T | 9 | a0001c0001t0011a0001c0001t0025a0001c0001t0042others(6): Show | 22 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2236G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2236 | chr6 | 18467303 | |||||
| chr6:18467351
|
A | G | 106 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(103): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*2284A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2284 | chr6 | 18467351 | |||||
| chr6:18467395
|
C | CTTT | 3 | a0001c0001t0052a0001c0001t0077a0001c0001t0079 | 4 | HG01257.hp1 HG01258.hp2 HG02074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2330_*2332dupTTT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2333 | INFO_REALIGN_3_PRIME | chr6 | 18467395 | ||||
| chr6:18467400
|
G | GTTT | 41 | a0001c0001t0003a0001c0001t0005a0001c0001t0008others(38): Show | 120 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2350_*2352dupTTT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2353 | INFO_REALIGN_3_PRIME | chr6 | 18467400 | ||||
| chr6:18467400
|
G | GTTTT | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(34): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*2349_*2352dupTTTT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2353 | INFO_REALIGN_3_PRIME | chr6 | 18467400 | ||||
| chr6:18467400
|
G | GTTTTT | 14 | a0001c0001t0014a0001c0001t0023a0001c0001t0026others(11): Show | 30 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2348_*2352dupTTTT others(1): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2353 | INFO_REALIGN_3_PRIME | chr6 | 18467400 | ||||
| chr6:18467400
|
G | T | 3 | a0001c0001t0052a0001c0001t0077a0001c0001t0079 | 4 | HG01257.hp1 HG01258.hp2 HG02074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2333G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2333 | chr6 | 18467400 | |||||
| chr6:18467408
|
T | TG | 8 | a0001c0001t0007a0001c0001t0012a0001c0001t0015others(5): Show | 42 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2341_*2342insG | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2342 | chr6 | 18467408 | |||||
| chr6:18467422
|
C | T | 1 | a0001c0001t0085 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2355C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2355 | chr6 | 18467422 | |||||
| chr6:18467647
|
A | AT | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(22): Show | 100 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2585dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2586 | INFO_REALIGN_3_PRIME | chr6 | 18467647 | ||||
| chr6:18467653
|
A | T | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*2586A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2586 | chr6 | 18467653 | |||||
| chr6:18467688
|
C | T | 3 | a0001c0001t0049a0001c0001t0098a0001c0001t0107 | 4 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2621C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2621 | chr6 | 18467688 | |||||
| chr6:18467723
|
C | T | 1 | a0001c0001t0096 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2656C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2656 | chr6 | 18467723 | |||||
| chr6:18467880
|
A | G | 4 | a0001c0001t0038a0001c0001t0092a0001c0001t0093others(1): Show | 6 | HG02897.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2813A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2813 | chr6 | 18467880 | |||||
| chr6:18467883
|
C | T | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0023others(12): Show | 77 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2816C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2816 | chr6 | 18467883 | |||||
| chr6:18467988
|
G | A | 1 | a0001c0001t0058 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2921G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2921 | chr6 | 18467988 | |||||
| chr6:18468123
|
CA | C | 9 | a0001c0001t0024a0001c0001t0028a0001c0001t0062others(6): Show | 15 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3058delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3058 | INFO_REALIGN_3_PRIME | chr6 | 18468123 | ||||
| chr6:18468138
|
G | T | 9 | a0001c0001t0011a0001c0001t0025a0001c0001t0042others(6): Show | 22 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3071G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3071 | chr6 | 18468138 | |||||
| chr6:18468176
|
T | C | 9 | a0001c0001t0024a0001c0001t0028a0001c0001t0062others(6): Show | 15 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3109T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3109 | chr6 | 18468176 | |||||
| chr6:18468233
|
C | T | 106 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(103): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*3166C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3166 | chr6 | 18468233 | |||||
| chr6:18468267
|
A | C | 1 | a0001c0001t0057 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3200A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3200 | chr6 | 18468267 | |||||
| chr6:18468384
|
G | A | 2 | a0001c0001t0055a0003c0006t0055 | 2 | NA18941.hp1 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3317G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3317 | chr6 | 18468384 | |||||
| chr6:18468578
|
C | T | 1 | a0001c0001t0075 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3511C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3511 | chr6 | 18468578 | |||||
| chr6:18468736
|
A | G | 1 | a0001c0001t0081 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3669A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3669 | chr6 | 18468736 | |||||
| chr6:18468750
|
T | A | 14 | a0001c0001t0020a0001c0001t0021a0001c0001t0024others(11): Show | 29 | HG01109.hp2 HG01167.hp2 HG01496.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3683T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3683 | chr6 | 18468750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:18387664
|
G | C | 1 | a0001c0001t0001g0010 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-37+34G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387664 | ||||||
| chr6:18387722
|
A | C | 80 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(77): Show | 84 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-37+92A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387722 | ||||||
| chr6:18387864
|
C | T | 2 | a0001c0001t0007g0298a0001c0001t0071g0299 | 2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-37+234C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387864 | ||||||
| chr6:18387871
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-37+241A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387871 | ||||||
| chr6:18387890
|
G | A | 2 | a0001c0001t0012g0011a0001c0001t0012g0012 | 2 | NA18969.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-37+260G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387890 | ||||||
| chr6:18388062
|
G | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37+432G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388062 | ||||||
| chr6:18388139
|
T | C | 6 | a0001c0001t0028g0097a0001c0001t0028g0100a0001c0001t0038g0098others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+509T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388139 | ||||||
| chr6:18388314
|
C | G | 153 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(150): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.-37+684C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388314 | ||||||
| chr6:18388608
|
C | T | 1 | a0001c0001t0095g0225 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-37+978C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388608 | ||||||
| chr6:18388775
|
C | A | 4 | a0001c0001t0010g0228a0001c0001t0057g0229a0001c0001t0058g0227others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+1145C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388775 | ||||||
| chr6:18388806
|
A | AT | 69 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0007g0234others(66): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-37+1187dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18388806 | |||||
| chr6:18388806
|
AT | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37+1187delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18388806 | |||||
| chr6:18389070
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-37+1440C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389070 | ||||||
| chr6:18389079
|
G | A | 1 | a0001c0001t0036g0301 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-37+1449G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389079 | ||||||
| chr6:18389132
|
C | T | 1 | a0001c0001t0011g0375 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-37+1502C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389132 | ||||||
| chr6:18389258
|
A | G | 4 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(1): Show | 4 | NA18949.hp2 NA18964.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+1628A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389258 | ||||||
| chr6:18389539
|
G | C | 1 | a0001c0001t0054g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-37+1909G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389539 | ||||||
| chr6:18389602
|
C | A | 58 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0007g0234others(55): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-37+1972C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389602 | ||||||
| chr6:18389680
|
C | G | 350 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(347): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.-37+2050C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389680 | ||||||
| chr6:18389868
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-37+2238T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389868 | ||||||
| chr6:18389970
|
A | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37+2340A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389970 | ||||||
| chr6:18390406
|
T | C | 1 | a0001c0001t0082g0102 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-37+2776T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390406 | ||||||
| chr6:18390442
|
T | C | 4 | a0001c0001t0010g0228a0001c0001t0057g0229a0001c0001t0058g0227others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+2812T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390442 | ||||||
| chr6:18390574
|
A | C | 1 | a0001c0001t0015g0374 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-37+2944A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390574 | ||||||
| chr6:18390692
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(85): Show | 90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37+3062A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390692 | ||||||
| chr6:18390705
|
C | T | 1 | a0001c0001t0018g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-37+3075C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390705 | ||||||
| chr6:18390801
|
G | A | 1 | a0001c0001t0013g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-37+3171G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390801 | ||||||
| chr6:18391015
|
A | G | 1 | a0001c0001t0006g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-37+3385A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391015 | ||||||
| chr6:18391160
|
C | G | 79 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(76): Show | 80 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-37+3530C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391160 | ||||||
| chr6:18391202
|
C | T | 4 | a0001c0001t0010g0228a0001c0001t0057g0229a0001c0001t0058g0227others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+3572C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391202 | ||||||
| chr6:18391513
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-37+3883A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391513 | ||||||
| chr6:18391683
|
C | T | 1 | a0001c0001t0073g0373 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-37+4053C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391683 | ||||||
| chr6:18391817
|
G | A | 20 | a0001c0001t0002g0133a0001c0001t0004g0130a0001c0001t0004g0131others(17): Show | 20 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37+4187G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391817 | ||||||
| chr6:18391872
|
A | G | 2 | a0001c0001t0015g0138a0001c0001t0074g0139 | 2 | HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-37+4242A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391872 | ||||||
| chr6:18391910
|
T | C | 1 | a0001c0001t0102g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-37+4280T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391910 | ||||||
| chr6:18391995
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-37+4365C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391995 | ||||||
| chr6:18392035
|
T | TA | 54 | a0001c0001t0001g0074a0001c0001t0003g0152a0001c0001t0003g0221others(51): Show | 54 | HG00609.hp2 HG00639.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.-37+4432dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | |||||
| chr6:18392035
|
T | TAA | 86 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(83): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-37+4431_-37+4432d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | |||||
| chr6:18392035
|
TA | T | 38 | a0001c0001t0002g0133a0001c0001t0002g0308a0001c0001t0003g0216others(35): Show | 38 | HG00323.hp2 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-37+4432delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | |||||
| chr6:18392035
|
TAA | T | 68 | a0001c0001t0002g0311a0001c0001t0002g0313a0001c0001t0002g0314others(65): Show | 72 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37+4431_-37+4432d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | |||||
| chr6:18392035
|
TAAAAAAA others(2): Show |
T | 15 | a0001c0001t0008g0094a0001c0001t0013g0082a0001c0001t0013g0083others(12): Show | 16 | HG00642.hp1 HG01257.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37+4424_-37+4432d others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | |||||
| chr6:18392489
|
A | C | 1 | a0001c0001t0028g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-37+4859A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392489 | ||||||
| chr6:18392573
|
G | C | 152 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(149): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.-37+4943G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392573 | ||||||
| chr6:18392795
|
G | C | 58 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0007g0234others(55): Show | 59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-37+5165G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392795 | ||||||
| chr6:18392851
|
A | G | 20 | a0001c0001t0002g0133a0001c0001t0004g0130a0001c0001t0004g0131others(17): Show | 20 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37+5221A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392851 | ||||||
| chr6:18392855
|
A | T | 7 | a0001c0001t0009g0292a0001c0001t0024g0290a0001c0001t0024g0291others(4): Show | 7 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37+5225A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392855 | ||||||
| chr6:18392936
|
T | A | 1 | a0001c0001t0001g0015 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-37+5306T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392936 | ||||||
| chr6:18393040
|
G | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-37+5410G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393040 | ||||||
| chr6:18393097
|
G | A | 3 | a0001c0001t0002g0302a0001c0001t0002g0311a0001c0001t0011g0312 | 3 | HG01123.hp1 HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-37+5467G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393097 | ||||||
| chr6:18393119
|
C | CA | 13 | a0001c0001t0013g0082a0001c0001t0013g0083a0001c0001t0013g0085others(10): Show | 14 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37+5506dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18393119 | |||||
| chr6:18393119
|
CA | C | 169 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(166): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-37+5506delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18393119 | |||||
| chr6:18393147
|
G | A | 1 | a0001c0001t0007g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-37+5517G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393147 | ||||||
| chr6:18393181
|
G | C | 1 | a0001c0001t0081g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-37+5551G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393181 | ||||||
| chr6:18393241
|
A | G | 2 | a0001c0001t0057g0229a0001c0001t0058g0227 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-37+5611A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393241 | ||||||
| chr6:18393375
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-37+5745T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393375 | ||||||
| chr6:18393409
|
C | T | 2 | a0001c0001t0051g0006a0001c0001t0091g0215 | 3 | HG03453.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-37+5779C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393409 | ||||||
| chr6:18393635
|
G | C | 1 | a0001c0001t0002g0313 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-36-5864G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393635 | ||||||
| chr6:18393647
|
G | A | 4 | a0001c0001t0010g0228a0001c0001t0057g0229a0001c0001t0058g0227others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-5852G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393647 | ||||||
| chr6:18393829
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-36-5670C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393829 | ||||||
| chr6:18393944
|
C | T | 4 | a0001c0001t0043g0140a0001c0001t0043g0141a0001c0001t0059g0142others(1): Show | 4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-5555C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393944 | ||||||
| chr6:18394058
|
C | G | 78 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(75): Show | 82 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-36-5441C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394058 | ||||||
| chr6:18394177
|
T | C | 2 | a0001c0001t0057g0229a0001c0001t0058g0227 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-36-5322T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394177 | ||||||
| chr6:18394297
|
T | C | 1 | a0001c0001t0010g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-36-5202T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394297 | ||||||
| chr6:18394496
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-5003G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394496 | ||||||
| chr6:18394523
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-36-4976G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394523 | ||||||
| chr6:18394562
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(66): Show | 70 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-36-4937C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394562 | ||||||
| chr6:18394592
|
C | T | 1 | a0001c0001t0050g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-36-4907C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394592 | ||||||
| chr6:18394613
|
GA | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(104): Show | 109 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-36-4872delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18394613 | |||||
| chr6:18394614
|
A | G | 76 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(73): Show | 80 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.-36-4885A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394614 | ||||||
| chr6:18394615
|
A | G | 1 | a0001c0001t0005g0310 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-36-4884A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394615 | ||||||
| chr6:18394692
|
C | G | 2 | a0001c0001t0015g0138a0001c0001t0074g0139 | 2 | HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-36-4807C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394692 | ||||||
| chr6:18394753
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-36-4746T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394753 | ||||||
| chr6:18394761
|
C | T | 16 | a0001c0001t0008g0094a0001c0001t0013g0082a0001c0001t0013g0083others(13): Show | 17 | HG00642.hp1 HG01257.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-36-4738C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394761 | ||||||
| chr6:18394898
|
T | A | 4 | a0001c0001t0043g0140a0001c0001t0043g0141a0001c0001t0059g0142others(1): Show | 4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-4601T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394898 | ||||||
| chr6:18394904
|
G | A | 1 | a0001c0001t0025g0280 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-36-4595G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394904 | ||||||
| chr6:18394952
|
T | C | 1 | a0001c0001t0031g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-36-4547T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394952 | ||||||
| chr6:18395000
|
G | C | 157 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(154): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-36-4499G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395000 | ||||||
| chr6:18395091
|
G | A | 5 | a0001c0001t0013g0091a0001c0001t0017g0092a0001c0001t0042g0089others(2): Show | 5 | HG01257.hp2 HG02280.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-4408G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395091 | ||||||
| chr6:18395359
|
C | T | 1 | a0001c0001t0008g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-36-4140C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395359 | ||||||
| chr6:18395386
|
G | A | 2 | a0001c0001t0005g0306a0001c0001t0005g0315 | 2 | HG01928.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-36-4113G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395386 | ||||||
| chr6:18395439
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-36-4060T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395439 | ||||||
| chr6:18395566
|
T | C | 1 | a0001c0001t0008g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-36-3933T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395566 | ||||||
| chr6:18395578
|
C | CT | 173 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(170): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-36-3909dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18395578 | |||||
| chr6:18395798
|
A | G | 1 | a0001c0001t0037g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-36-3701A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395798 | ||||||
| chr6:18396086
|
C | T | 169 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-36-3413C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396086 | ||||||
| chr6:18396122
|
G | A | 5 | a0001c0001t0009g0288a0001c0001t0033g0284a0001c0001t0033g0286others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-3377G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396122 | ||||||
| chr6:18396194
|
A | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-3305A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396194 | ||||||
| chr6:18396230
|
A | T | 4 | a0001c0001t0010g0228a0001c0001t0057g0229a0001c0001t0058g0227others(1): Show | 4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-3269A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396230 | ||||||
| chr6:18396352
|
C | T | 1 | a0001c0001t0070g0226 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-36-3147C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396352 | ||||||
| chr6:18396375
|
A | T | 74 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(71): Show | 74 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-36-3124A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396375 | ||||||
| chr6:18396458
|
C | T | 169 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-36-3041C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396458 | ||||||
| chr6:18396554
|
G | A | 1 | a0001c0001t0003g0163 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-36-2945G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396554 | ||||||
| chr6:18396665
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | NA18986.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-36-2834T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396665 | ||||||
| chr6:18396806
|
C | A | 1 | a0001c0001t0013g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-36-2693C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396806 | ||||||
| chr6:18396888
|
C | T | 2 | a0001c0001t0014g0135a0001c0001t0037g0136 | 2 | HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-36-2611C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396888 | ||||||
| chr6:18396899
|
C | T | 169 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-36-2600C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396899 | ||||||
| chr6:18396964
|
G | A | 1 | a0001c0001t0048g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-36-2535G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396964 | ||||||
| chr6:18396986
|
G | A | 1 | a0001c0001t0010g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-36-2513G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396986 | ||||||
| chr6:18397018
|
A | G | 1 | a0001c0001t0011g0312 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-36-2481A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397018 | ||||||
| chr6:18397298
|
G | A | 4 | a0001c0001t0043g0140a0001c0001t0043g0141a0001c0001t0059g0142others(1): Show | 4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-2201G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397298 | ||||||
| chr6:18397359
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-36-2140C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397359 | ||||||
| chr6:18397569
|
C | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-1930C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397569 | ||||||
| chr6:18397592
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-1907G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397592 | ||||||
| chr6:18397698
|
T | G | 6 | a0001c0001t0002g0302a0001c0001t0002g0311a0001c0001t0004g0318others(3): Show | 6 | HG00099.hp2 HG01123.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-1801T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397698 | ||||||
| chr6:18397756
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-36-1743G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397756 | ||||||
| chr6:18398041
|
C | T | 1 | a0001c0001t0054g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-36-1458C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398041 | ||||||
| chr6:18398104
|
T | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(238): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-36-1395T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398104 | ||||||
| chr6:18398122
|
C | A | 2 | a0001c0001t0052g0150a0001c0001t0052g0151 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-36-1377C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398122 | ||||||
| chr6:18398148
|
C | T | 1 | a0001c0001t0054g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-36-1351C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398148 | ||||||
| chr6:18398160
|
G | A | 1 | a0001c0001t0102g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-36-1339G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398160 | ||||||
| chr6:18398164
|
C | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-1335C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398164 | ||||||
| chr6:18398287
|
G | T | 1 | a0001c0001t0011g0372 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-36-1212G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398287 | ||||||
| chr6:18398579
|
A | C | 5 | a0001c0001t0013g0091a0001c0001t0017g0092a0001c0001t0042g0089others(2): Show | 5 | HG01257.hp2 HG02280.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-920A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398579 | ||||||
| chr6:18398646
|
G | A | 12 | a0001c0001t0002g0319a0001c0001t0002g0320a0001c0001t0005g0306others(9): Show | 14 | HG01069.hp2 HG01123.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-853G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398646 | ||||||
| chr6:18398669
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-36-830C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398669 | ||||||
| chr6:18398732
|
G | T | 16 | a0001c0001t0008g0094a0001c0001t0013g0082a0001c0001t0013g0083others(13): Show | 17 | HG00642.hp1 HG01257.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-36-767G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398732 | ||||||
| chr6:18398934
|
C | T | 169 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.-36-565C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398934 | ||||||
| chr6:18399163
|
C | T | 241 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(238): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-36-336C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18399163 | ||||||
| chr6:18399335
|
G | A | 1 | a0001c0001t0104g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-36-164G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18399335 | ||||||
| chr6:18399992
|
C | A | 9 | a0001c0001t0002g0303a0001c0001t0002g0327a0001c0001t0002g0329others(6): Show | 9 | HG00423.hp2 HG02080.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+293C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18399992 | ||||||
| chr6:18399999
|
C | T | 14 | a0001c0001t0008g0094a0001c0001t0013g0083a0001c0001t0013g0085others(11): Show | 15 | HG00642.hp1 HG01257.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+300C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18399999 | ||||||
| chr6:18400042
|
C | T | 167 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(164): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.165+343C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400042 | ||||||
| chr6:18400046
|
C | T | 1 | a0001c0001t0013g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.165+347C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400046 | ||||||
| chr6:18400047
|
G | A | 1 | a0001c0001t0068g0281 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.165+348G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400047 | ||||||
| chr6:18400147
|
C | T | 1 | a0001c0001t0010g0279 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.165+448C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400147 | ||||||
| chr6:18400272
|
CA | C | 169 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.165+590delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18400272 | |||||
| chr6:18400312
|
C | G | 169 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(166): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.165+613C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400312 | ||||||
| chr6:18400330
|
C | G | 1 | a0001c0001t0034g0247 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.165+631C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400330 | ||||||
| chr6:18400740
|
C | T | 3 | a0001c0001t0002g0302a0001c0001t0002g0311a0001c0001t0011g0312 | 3 | HG01123.hp1 HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.165+1041C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400740 | ||||||
| chr6:18401102
|
T | A | 1 | a0001c0001t0083g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.165+1403T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401102 | ||||||
| chr6:18401150
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(147): Show | 155 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.165+1451A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401150 | ||||||
| chr6:18401194
|
G | A | 1 | a0001c0001t0023g0025 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.165+1495G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401194 | ||||||
| chr6:18401332
|
T | A | 154 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.165+1633T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401332 | ||||||
| chr6:18401377
|
T | G | 71 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(68): Show | 72 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.165+1678T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401377 | ||||||
| chr6:18401632
|
T | C | 2 | a0001c0001t0046g0124a0001c0001t0046g0125 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.165+1933T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401632 | ||||||
| chr6:18401856
|
CCCCAGGG others(773): Show |
C | 241 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(238): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.165+2161_165+2940d others(2): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18401856 | |||||
| chr6:18402718
|
C | A | 2 | a0001c0001t0005g0008a0001c0001t0036g0337 | 3 | HG03490.hp2 HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.165+3019C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402718 | ||||||
| chr6:18402761
|
T | A | 14 | a0001c0001t0008g0094a0001c0001t0013g0082a0001c0001t0013g0083others(11): Show | 14 | HG01257.hp2 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+3062T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402761 | ||||||
| chr6:18402764
|
G | T | 1 | a0001c0001t0030g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+3065G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402764 | ||||||
| chr6:18402884
|
A | G | 1 | a0001c0001t0082g0102 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.165+3185A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402884 | ||||||
| chr6:18402950
|
G | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(165): Show | 174 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.165+3251G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402950 | ||||||
| chr6:18402973
|
C | T | 1 | a0001c0001t0054g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+3274C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402973 | ||||||
| chr6:18403028
|
A | G | 78 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(75): Show | 82 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.165+3329A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403028 | ||||||
| chr6:18403045
|
G | A | 19 | a0001c0001t0002g0133a0001c0001t0004g0130a0001c0001t0004g0131others(16): Show | 19 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.165+3346G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403045 | ||||||
| chr6:18403109
|
T | C | 1 | a0001c0001t0054g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+3410T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403109 | ||||||
| chr6:18403479
|
T | G | 1 | a0001c0001t0054g0013 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+3780T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403479 | ||||||
| chr6:18403496
|
C | T | 4 | a0001c0001t0043g0140a0001c0001t0043g0141a0001c0001t0059g0142others(1): Show | 4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+3797C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403496 | ||||||
| chr6:18403566
|
T | C | 1 | a0001c0001t0002g0319 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.165+3867T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403566 | ||||||
| chr6:18403711
|
G | A | 10 | a0001c0001t0009g0288a0001c0001t0017g0003a0001c0001t0017g0088others(7): Show | 11 | HG00642.hp1 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+4012G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403711 | ||||||
| chr6:18403773
|
G | T | 1 | a0001c0001t0017g0065 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.165+4074G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403773 | ||||||
| chr6:18403789
|
A | G | 103 | a0001c0001t0001g0080a0001c0001t0002g0133a0001c0001t0002g0302others(100): Show | 108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.165+4090A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403789 | ||||||
| chr6:18403817
|
C | T | 4 | a0001c0001t0028g0134a0001c0001t0047g0132a0001c0001t0081g0122others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+4118C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403817 | ||||||
| chr6:18403902
|
C | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(211): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.165+4203C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403902 | ||||||
| chr6:18403912
|
A | G | 3 | a0001c0001t0013g0083a0001c0001t0099g0084a0001c0001t0102g0081 | 3 | HG03130.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.165+4213A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403912 | ||||||
| chr6:18403937
|
C | A | 6 | a0001c0001t0003g0164a0001c0001t0003g0166a0001c0001t0003g0216others(3): Show | 6 | HG00621.hp1 HG02040.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+4238C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403937 | ||||||
| chr6:18404219
|
C | T | 19 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0004g0309others(16): Show | 19 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.165+4520C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404219 | ||||||
| chr6:18404261
|
C | G | 1 | a0001c0001t0044g0268 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.165+4562C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404261 | ||||||
| chr6:18404706
|
G | GA | 65 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(62): Show | 68 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.165+5015dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18404706 | |||||
| chr6:18404781
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+5082A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404781 | ||||||
| chr6:18404813
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(127): Show | 133 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.165+5114C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404813 | ||||||
| chr6:18404886
|
T | A | 218 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+5187T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404886 | ||||||
| chr6:18404913
|
A | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+5214A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404913 | ||||||
| chr6:18404957
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+5258T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404957 | ||||||
| chr6:18405070
|
G | A | 343 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(340): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.165+5371G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405070 | ||||||
| chr6:18405117
|
T | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+5418T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405117 | ||||||
| chr6:18405150
|
T | A | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+5451T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405150 | ||||||
| chr6:18405150
|
T | TTTA | 80 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(77): Show | 82 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.165+5475_165+5477d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | |||||
| chr6:18405150
|
T | TTTATTA | 55 | a0001c0001t0002g0363a0001c0001t0003g0166a0001c0001t0003g0203others(52): Show | 57 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.165+5472_165+5477d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | |||||
| chr6:18405150
|
T | TTTATTAT others(2): Show |
5 | a0001c0001t0032g0200a0001c0001t0041g0031a0001c0001t0042g0071others(2): Show | 5 | HG00323.hp1 HG01255.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+5469_165+5477d others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | |||||
| chr6:18405150
|
T | TTTATTAT others(5): Show |
58 | a0001c0001t0003g0164a0001c0001t0003g0181a0001c0001t0003g0184others(55): Show | 58 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.165+5466_165+5477d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | |||||
| chr6:18405150
|
T | TTTATTAT others(8): Show |
17 | a0001c0001t0003g0176a0001c0001t0005g0341a0001c0001t0008g0030others(14): Show | 17 | HG00738.hp2 HG01361.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+5463_165+5477d others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | |||||
| chr6:18405150
|
T | TTTATTAT others(14): Show |
1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+5457_165+5477d others(23): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | |||||
| chr6:18405150
|
TTTA | T | 119 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(116): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.165+5475_165+5477d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | |||||
| chr6:18405174
|
A | ATTATTAT others(11): Show |
4 | a0001c0001t0009g0288a0001c0001t0033g0284a0001c0001t0033g0286others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+5477_165+5478i others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405174 | |||||
| chr6:18405174
|
A | ATTATTAT others(8): Show |
1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+5477_165+5478i others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405174 | |||||
| chr6:18405174
|
A | ATTATTAT others(2): Show |
2 | a0001c0001t0010g0228a0001c0001t0019g0004 | 3 | HG01256.hp2 HG01258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.165+5477_165+5478i others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405174 | |||||
| chr6:18405177
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.165+5478G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405177 | ||||||
| chr6:18405180
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.165+5481A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405180 | ||||||
| chr6:18405266
|
C | G | 2 | a0001c0001t0076g0371a0001c0001t0105g0063 | 2 | HG00735.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.165+5567C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405266 | ||||||
| chr6:18405319
|
A | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(217): Show | 224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+5620A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405319 | ||||||
| chr6:18405426
|
C | T | 1 | a0001c0001t0012g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.165+5727C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405426 | ||||||
| chr6:18405540
|
G | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(342): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.165+5841G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405540 | ||||||
| chr6:18405553
|
A | G | 133 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(130): Show | 136 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.165+5854A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405553 | ||||||
| chr6:18405576
|
C | A | 7 | a0001c0001t0009g0288a0001c0001t0010g0228a0001c0001t0016g0087others(4): Show | 8 | HG01256.hp2 HG01258.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+5877C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405576 | ||||||
| chr6:18405619
|
T | C | 1 | a0001c0001t0048g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165+5920T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405619 | ||||||
| chr6:18405654
|
C | T | 1 | a0001c0001t0047g0132 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.165+5955C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405654 | ||||||
| chr6:18405771
|
G | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0068 | 2 | NA18940.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.165+6072G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405771 | ||||||
| chr6:18405772
|
A | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0068 | 2 | NA18940.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.165+6073A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405772 | ||||||
| chr6:18405774
|
G | A | 1 | a0001c0001t0018g0269 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.165+6075G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405774 | ||||||
| chr6:18405864
|
A | G | 1 | a0001c0001t0013g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+6165A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405864 | ||||||
| chr6:18406084
|
A | G | 1 | a0001c0001t0098g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.165+6385A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406084 | ||||||
| chr6:18406156
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+6457G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406156 | ||||||
| chr6:18406269
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+6570A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406269 | ||||||
| chr6:18406405
|
G | A | 1 | a0001c0001t0013g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+6706G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406405 | ||||||
| chr6:18406433
|
A | G | 5 | a0001c0001t0009g0230a0001c0001t0009g0252a0001c0001t0009g0253others(2): Show | 5 | NA18939.hp2 NA18941.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+6734A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406433 | ||||||
| chr6:18406457
|
A | AGT | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(88): Show | 93 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.165+6801_165+6802d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
A | AGTGT | 20 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0057others(17): Show | 20 | HG00140.hp2 HG00735.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+6799_165+6802d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
A | AGTGTGT | 8 | a0001c0001t0004g0300a0001c0001t0006g0153a0001c0001t0006g0168others(5): Show | 9 | HG01261.hp2 HG01993.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+6797_165+6802d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
A | AGTGTGTG others(1): Show |
23 | a0001c0001t0001g0079a0001c0001t0003g0152a0001c0001t0004g0338others(20): Show | 24 | HG00642.hp1 HG01081.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.165+6795_165+6802d others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
A | AGTGTGTG others(3): Show |
6 | a0001c0001t0004g0309a0001c0001t0018g0271a0001c0001t0030g0162others(3): Show | 6 | HG01243.hp2 HG02132.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+6793_165+6802d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
A | AGTGTGTG others(5): Show |
4 | a0001c0001t0013g0082a0001c0001t0013g0083a0001c0001t0018g0269others(1): Show | 4 | HG02280.hp2 HG03225.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+6791_165+6802d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0053g0205 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.165+6789_165+6802d others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
A | AGTGTGTG others(9): Show |
3 | a0001c0001t0013g0014a0001c0001t0018g0261a0001c0001t0054g0086 | 3 | HG03209.hp2 HG03516.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.165+6787_165+6802d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGT | A | 16 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0004g0366others(13): Show | 17 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+6801_165+6802d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGT | A | 16 | a0001c0001t0008g0094a0001c0001t0009g0292a0001c0001t0024g0290others(13): Show | 16 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+6799_165+6802d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGTGT | A | 9 | a0001c0001t0002g0308a0001c0001t0002g0313a0001c0001t0002g0331others(6): Show | 9 | HG00140.hp1 HG03669.hp1 HG04115.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+6797_165+6802d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGTGTG others(1): Show |
A | 68 | a0001c0001t0002g0133a0001c0001t0002g0303a0001c0001t0002g0311others(65): Show | 70 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.165+6795_165+6802d others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGTGTG others(3): Show |
A | 76 | a0001c0001t0002g0302a0001c0001t0003g0176a0001c0001t0003g0181others(73): Show | 76 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.165+6793_165+6802d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0070g0226 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165+6791_165+6802d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0038 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.165+6789_165+6802d others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0013g0091 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.165+6787_165+6802d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGTGTG others(11): Show |
A | 1 | a0001c0001t0019g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+6785_165+6802d others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406457
|
AGTGTGTG others(13): Show |
A | 6 | a0001c0001t0002g0345a0001c0001t0002g0346a0001c0001t0004g0009others(3): Show | 7 | HG00408.hp2 NA18971.hp1 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+6783_165+6802d others(22): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | |||||
| chr6:18406504
|
G | T | 79 | a0001c0001t0003g0176a0001c0001t0003g0181a0001c0001t0003g0184others(76): Show | 79 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.165+6805G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406504 | ||||||
| chr6:18406507
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+6808G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406507 | ||||||
| chr6:18406623
|
G | A | 344 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(341): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.165+6924G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406623 | ||||||
| chr6:18406749
|
C | G | 1 | a0001c0001t0098g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.165+7050C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406749 | ||||||
| chr6:18406974
|
C | T | 2 | a0001c0001t0002g0133a0001c0001t0002g0314 | 2 | HG02738.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.165+7275C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406974 | ||||||
| chr6:18406995
|
G | A | 1 | a0001c0001t0019g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+7296G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406995 | ||||||
| chr6:18407068
|
T | C | 14 | a0001c0001t0008g0094a0001c0001t0009g0292a0001c0001t0024g0290others(11): Show | 14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+7369T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407068 | ||||||
| chr6:18407085
|
G | T | 73 | a0001c0001t0003g0176a0001c0001t0003g0181a0001c0001t0003g0184others(70): Show | 73 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.165+7386G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407085 | ||||||
| chr6:18407091
|
A | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+7392A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407091 | ||||||
| chr6:18407170
|
A | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(217): Show | 224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+7471A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407170 | ||||||
| chr6:18407322
|
G | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(129): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.165+7623G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407322 | ||||||
| chr6:18407359
|
T | C | 53 | a0001c0001t0003g0176a0001c0001t0003g0181a0001c0001t0003g0184others(50): Show | 53 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.165+7660T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407359 | ||||||
| chr6:18407483
|
A | G | 1 | a0001c0001t0015g0374 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.165+7784A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407483 | ||||||
| chr6:18407487
|
A | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(211): Show | 217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.165+7788A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407487 | ||||||
| chr6:18407512
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+7813T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407512 | ||||||
| chr6:18407675
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.165+7976A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407675 | ||||||
| chr6:18407868
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+8169T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407868 | ||||||
| chr6:18407901
|
G | A | 1 | a0001c0001t0091g0215 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165+8202G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407901 | ||||||
| chr6:18407966
|
TTTTC | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(216): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+8279_165+8282d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18407966 | |||||
| chr6:18407984
|
C | CT | 13 | a0001c0001t0009g0230a0001c0001t0009g0292a0001c0001t0010g0279others(10): Show | 13 | HG01167.hp2 HG01256.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+8302dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18407984 | |||||
| chr6:18407984
|
C | CTT | 61 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(58): Show | 64 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.165+8301_165+8302d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18407984 | |||||
| chr6:18407984
|
CTT | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(214): Show | 220 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.165+8301_165+8302d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18407984 | |||||
| chr6:18407986
|
T | C | 1 | a0001c0002t0022g0180 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165+8287T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407986 | ||||||
| chr6:18407987
|
T | C | 1 | a0003c0006t0055g0067 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.165+8288T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407987 | ||||||
| chr6:18408001
|
T | C | 3 | a0001c0001t0049g0116a0001c0001t0051g0006a0001c0001t0098g0206 | 4 | HG02109.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+8302T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408001 | ||||||
| chr6:18408092
|
C | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+8393C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408092 | ||||||
| chr6:18408135
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+8436T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408135 | ||||||
| chr6:18408145
|
C | T | 19 | a0001c0001t0007g0233a0001c0001t0007g0234a0001c0001t0007g0239others(16): Show | 20 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+8446C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408145 | ||||||
| chr6:18408186
|
T | C | 5 | a0001c0001t0013g0014a0001c0001t0013g0082a0001c0001t0013g0085others(2): Show | 5 | HG01243.hp2 HG02280.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+8487T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408186 | ||||||
| chr6:18408187
|
G | A | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+8488G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408187 | ||||||
| chr6:18408192
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+8493T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408192 | ||||||
| chr6:18408284
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+8585T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408284 | ||||||
| chr6:18408317
|
T | G | 3 | a0001c0001t0034g0272a0001c0001t0059g0142a0001c0001t0060g0147 | 3 | HG00735.hp1 HG01993.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.165+8618T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408317 | ||||||
| chr6:18408511
|
A | C | 11 | a0001c0001t0009g0292a0001c0001t0024g0290a0001c0001t0024g0291others(8): Show | 11 | HG01167.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+8812A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408511 | ||||||
| chr6:18408544
|
G | A | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+8845G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408544 | ||||||
| chr6:18408546
|
A | C | 1 | a0001c0001t0032g0200 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.165+8847A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408546 | ||||||
| chr6:18408660
|
G | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(211): Show | 217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.165+8961G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408660 | ||||||
| chr6:18408698
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(129): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.165+8999G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408698 | ||||||
| chr6:18408772
|
T | A | 73 | a0001c0001t0003g0176a0001c0001t0003g0181a0001c0001t0003g0184others(70): Show | 73 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.165+9073T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408772 | ||||||
| chr6:18408772
|
T | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(145): Show | 152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.165+9073T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408772 | ||||||
| chr6:18408938
|
G | GT | 64 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(61): Show | 67 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.165+9257dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18408938 | |||||
| chr6:18408938
|
GT | G | 26 | a0001c0001t0003g0152a0001c0001t0004g0309a0001c0001t0004g0338others(23): Show | 26 | HG01256.hp1 HG01261.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.165+9257delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18408938 | |||||
| chr6:18408938
|
GTTTTTT | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(213): Show | 220 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.165+9252_165+9257d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18408938 | |||||
| chr6:18409042
|
T | C | 1 | a0001c0001t0062g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.165+9343T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409042 | ||||||
| chr6:18409073
|
G | A | 1 | a0001c0001t0005g0365 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.165+9374G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409073 | ||||||
| chr6:18409091
|
A | G | 10 | a0001c0001t0007g0232a0001c0001t0007g0244a0001c0001t0007g0245others(7): Show | 10 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+9392A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409091 | ||||||
| chr6:18409246
|
C | T | 1 | a0001c0001t0006g0171 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.165+9547C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409246 | ||||||
| chr6:18409247
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165+9548G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409247 | ||||||
| chr6:18409298
|
A | G | 1 | a0001c0001t0038g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.165+9599A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409298 | ||||||
| chr6:18409302
|
C | T | 1 | a0001c0001t0004g0130 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.165+9603C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409302 | ||||||
| chr6:18409303
|
G | A | 1 | a0001c0001t0007g0298 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.165+9604G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409303 | ||||||
| chr6:18409353
|
G | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(219): Show | 226 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.165+9654G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409353 | ||||||
| chr6:18409375
|
C | CA | 8 | a0001c0001t0013g0014a0001c0001t0014g0357a0001c0001t0017g0088others(5): Show | 8 | HG00140.hp1 HG00642.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+9704dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409375
|
C | CAA | 40 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0308others(37): Show | 41 | HG01074.hp1 HG01081.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.165+9703_165+9704d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409375
|
C | CAAA | 51 | a0001c0001t0002g0133a0001c0001t0002g0311a0001c0001t0002g0313others(48): Show | 54 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.165+9702_165+9704d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409375
|
C | CAAAA | 17 | a0001c0001t0003g0152a0001c0001t0004g0338a0001c0001t0005g0306others(14): Show | 17 | HG01261.hp2 HG01891.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+9701_165+9704d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409375
|
CA | C | 12 | a0001c0001t0001g0040a0001c0001t0003g0166a0001c0001t0005g0362others(9): Show | 12 | HG00621.hp1 HG00642.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+9704delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409375
|
CAA | C | 45 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0002g0363others(42): Show | 46 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.165+9703_165+9704d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409375
|
CAAA | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(89): Show | 95 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.165+9702_165+9704d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409375
|
CAAAA | C | 12 | a0001c0001t0004g0366a0001c0001t0007g0239a0001c0001t0007g0240others(9): Show | 13 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+9701_165+9704d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409375
|
CAAAAA | C | 8 | a0001c0001t0007g0233a0001c0001t0007g0234a0001c0001t0007g0241others(5): Show | 8 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+9700_165+9704d others(7): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | |||||
| chr6:18409402
|
A | AG | 17 | a0001c0001t0003g0184a0001c0001t0003g0186a0001c0001t0003g0221others(14): Show | 17 | HG00438.hp1 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+9703_165+9704i others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409402 | ||||||
| chr6:18409402
|
A | G | 205 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(202): Show | 209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.165+9703A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409402 | ||||||
| chr6:18409429
|
G | T | 1 | a0001c0001t0091g0215 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165+9730G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409429 | ||||||
| chr6:18409463
|
C | A | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+9764C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409463 | ||||||
| chr6:18409492
|
G | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+9793G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409492 | ||||||
| chr6:18409560
|
C | A | 1 | a0001c0002t0022g0180 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165+9861C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409560 | ||||||
| chr6:18409561
|
C | CT | 39 | a0001c0001t0002g0314a0001c0001t0003g0152a0001c0001t0004g0309others(36): Show | 39 | HG00735.hp2 HG01175.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.165+9881dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | |||||
| chr6:18409561
|
C | CTTT | 19 | a0001c0001t0019g0145a0001c0001t0019g0148a0001c0001t0020g0005others(16): Show | 19 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.165+9879_165+9881d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | |||||
| chr6:18409561
|
C | CTTTT | 15 | a0001c0001t0009g0288a0001c0001t0010g0228a0001c0001t0019g0004others(12): Show | 16 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+9878_165+9881d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | |||||
| chr6:18409561
|
C | CTTTTT | 161 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(158): Show | 164 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.165+9877_165+9881d others(7): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | |||||
| chr6:18409561
|
C | CTTTTTT | 24 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0043others(21): Show | 24 | HG00423.hp1 HG00621.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.165+9876_165+9881d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | |||||
| chr6:18409762
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+10063A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409762 | ||||||
| chr6:18409856
|
C | T | 1 | a0001c0001t0018g0269 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.165+10157C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409856 | ||||||
| chr6:18409861
|
C | T | 73 | a0001c0001t0003g0176a0001c0001t0003g0181a0001c0001t0003g0184others(70): Show | 73 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.165+10162C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409861 | ||||||
| chr6:18409922
|
G | A | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.165+10223G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409922 | ||||||
| chr6:18409987
|
G | A | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+10288G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409987 | ||||||
| chr6:18410047
|
A | G | 1 | a0001c0001t0083g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.165+10348A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410047 | ||||||
| chr6:18410194
|
G | A | 2 | a0001c0001t0024g0290a0001c0001t0028g0097 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.165+10495G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410194 | ||||||
| chr6:18410219
|
C | T | 14 | a0001c0001t0008g0094a0001c0001t0009g0292a0001c0001t0024g0290others(11): Show | 14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+10520C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410219 | ||||||
| chr6:18410390
|
A | G | 365 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(362): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.165+10691A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410390 | ||||||
| chr6:18410546
|
GT | G | 11 | a0001c0001t0011g0372a0001c0001t0025g0276a0001c0001t0025g0278others(8): Show | 11 | HG00323.hp1 HG01257.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+10848delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410546 | ||||||
| chr6:18410550
|
G | T | 101 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(98): Show | 104 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.165+10851G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410550 | ||||||
| chr6:18410693
|
T | TA | 63 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(60): Show | 66 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.165+11001dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18410693 | |||||
| chr6:18410753
|
G | C | 5 | a0001c0001t0006g0172a0001c0001t0017g0003a0001c0001t0017g0088others(2): Show | 6 | HG00642.hp1 HG01081.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11054G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410753 | ||||||
| chr6:18410755
|
C | CGGTACAG others(17): Show |
1 | a0001c0002t0022g0180 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165+11057_165+1108 others(28): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18410755 | |||||
| chr6:18410757
|
G | A | 24 | a0001c0001t0003g0152a0001c0001t0004g0309a0001c0001t0004g0338others(21): Show | 24 | HG01261.hp2 HG01928.hp1 HG02004.hp2 others(21): Show |
intron_variant | MODIFIER | c.165+11058G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410757 | ||||||
| chr6:18410907
|
A | G | 3 | a0001c0001t0034g0272a0001c0001t0059g0142a0001c0001t0060g0147 | 3 | HG00735.hp1 HG01993.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.165+11208A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410907 | ||||||
| chr6:18410982
|
T | C | 5 | a0001c0001t0081g0122a0001c0001t0083g0123a0001c0001t0092g0179others(2): Show | 5 | HG01361.hp2 HG02559.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+11283T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410982 | ||||||
| chr6:18410994
|
C | CT | 219 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(216): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+11304dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18410994 | |||||
| chr6:18411077
|
C | T | 1 | a0001c0001t0005g0306 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.165+11378C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411077 | ||||||
| chr6:18411089
|
G | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(216): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+11390G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411089 | ||||||
| chr6:18411150
|
A | G | 7 | a0001c0001t0009g0288a0001c0001t0010g0228a0001c0001t0016g0087others(4): Show | 8 | HG01256.hp2 HG01258.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+11451A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411150 | ||||||
| chr6:18411173
|
C | T | 218 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+11474C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411173 | ||||||
| chr6:18411174
|
G | T | 1 | a0001c0002t0022g0180 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165+11475G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411174 | ||||||
| chr6:18411211
|
C | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(209): Show | 215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.165+11512C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411211 | ||||||
| chr6:18411230
|
G | A | 1 | a0001c0001t0006g0187 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.165+11531G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411230 | ||||||
| chr6:18411241
|
C | T | 1 | a0001c0001t0019g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+11542C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411241 | ||||||
| chr6:18411276
|
C | G | 1 | a0001c0001t0004g0333 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.165+11577C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411276 | ||||||
| chr6:18411334
|
T | TG | 373 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(370): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.165+11635_165+1163 others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411334 | ||||||
| chr6:18411361
|
G | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(216): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+11662G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411361 | ||||||
| chr6:18411378
|
C | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(216): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+11679C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411378 | ||||||
| chr6:18411380
|
T | C | 1 | a0001c0001t0066g0285 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.165+11681T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411380 | ||||||
| chr6:18411456
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.165+11757A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411456 | ||||||
| chr6:18411460
|
T | G | 219 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(216): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+11761T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411460 | ||||||
| chr6:18411462
|
C | CAT | 4 | a0001c0001t0016g0087a0001c0001t0026g0282a0001c0001t0054g0013others(1): Show | 4 | HG01975.hp2 HG02071.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+11798_165+1179 others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411462
|
C | CATATAT | 3 | a0001c0001t0026g0262a0001c0001t0026g0263a0001c0001t0107g0019 | 3 | HG01358.hp1 HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.165+11794_165+1179 others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411462
|
C | CATATATA others(3): Show |
1 | a0001c0001t0101g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.165+11790_165+1179 others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411462
|
CATATAT | C | 7 | a0001c0001t0002g0363a0001c0001t0004g0366a0001c0001t0015g0128others(4): Show | 7 | HG00438.hp2 HG01074.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+11794_165+1179 others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411462
|
CATATATA others(1): Show |
C | 78 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0016others(75): Show | 82 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.165+11792_165+1179 others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411462
|
CATATATA others(3): Show |
C | 15 | a0001c0001t0011g0372a0001c0001t0017g0029a0001c0001t0025g0276others(12): Show | 15 | HG01167.hp1 HG01257.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.165+11790_165+1179 others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411462
|
CATATATA others(5): Show |
C | 45 | a0001c0001t0002g0302a0001c0001t0002g0311a0001c0001t0002g0319others(42): Show | 47 | HG01123.hp1 HG01175.hp1 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.165+11788_165+1179 others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411462
|
CATATATA others(7): Show |
C | 14 | a0001c0001t0007g0234a0001c0001t0007g0242a0001c0001t0010g0235others(11): Show | 14 | HG00099.hp1 HG01168.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+11786_165+1179 others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411462
|
CATATATA others(9): Show |
C | 1 | a0001c0001t0008g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+11784_165+1179 others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | |||||
| chr6:18411478
|
TATATATA others(8): Show |
T | 1 | a0001c0001t0062g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.165+11780_165+1179 others(19): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411478 | ||||||
| chr6:18411480
|
TATATATA others(6): Show |
T | 12 | a0001c0001t0007g0233a0001c0001t0007g0240a0001c0001t0007g0241others(9): Show | 13 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+11782_165+1179 others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411480 | ||||||
| chr6:18411480
|
TATATATA others(8): Show |
T | 2 | a0001c0001t0009g0292a0001c0001t0024g0295 | 2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.165+11782_165+1179 others(19): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411480 | ||||||
| chr6:18411481
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.165+11784_165+1180 others(22): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411481 | |||||
| chr6:18411481
|
ATATATAT others(13): Show |
A | 3 | a0001c0001t0001g0050a0001c0001t0023g0064a0001c0001t0060g0147 | 3 | HG01993.hp2 HG02132.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.165+11784_165+1180 others(24): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411481 | |||||
| chr6:18411481
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0034g0272a0001c0001t0059g0142 | 2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.165+11784_165+1180 others(25): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411481 | |||||
| chr6:18411482
|
TATATATA | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0060a0001c0001t0001g0069others(4): Show | 7 | HG04184.hp1 NA18949.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+11784_165+1179 others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411482 | ||||||
| chr6:18411482
|
TATATATA others(2): Show |
T | 9 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0053others(6): Show | 9 | HG00558.hp1 HG01169.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+11784_165+1179 others(13): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411482 | ||||||
| chr6:18411482
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0006g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+11784_165+1179 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411482 | ||||||
| chr6:18411482
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0024g0296 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.165+11784_165+1179 others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411482 | ||||||
| chr6:18411484
|
TATATATA | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG02040.hp1 HG02165.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+11786_165+1179 others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411484 | ||||||
| chr6:18411484
|
TATATATA others(2): Show |
T | 3 | a0001c0001t0016g0073a0001c0001t0042g0089a0003c0006t0055g0067 | 3 | HG01070.hp1 HG02738.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.165+11786_165+1179 others(13): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411484 | ||||||
| chr6:18411484
|
TATATATA others(4): Show |
T | 2 | a0001c0001t0037g0339a0001c0001t0042g0071 | 2 | HG00323.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.165+11786_165+1179 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411484 | ||||||
| chr6:18411485
|
ATATATAT others(6): Show |
A | 3 | a0001c0001t0002g0320a0001c0001t0002g0349a0001c0001t0013g0027 | 3 | HG01943.hp2 NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.165+11788_165+1180 others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411485 | |||||
| chr6:18411486
|
TATATATA | T | 3 | a0001c0001t0006g0172a0001c0001t0056g0056a0001c0001t0106g0045 | 3 | HG01433.hp1 HG03098.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.165+11788_165+1179 others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411486 | ||||||
| chr6:18411486
|
TATATATA others(2): Show |
T | 9 | a0001c0001t0003g0203a0001c0001t0005g0359a0001c0001t0005g0365others(6): Show | 9 | HG00140.hp2 HG02132.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+11788_165+1179 others(13): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411486 | ||||||
| chr6:18411486
|
TATATATA others(4): Show |
T | 3 | a0001c0001t0019g0148a0001c0001t0038g0101a0001c0001t0038g0143 | 3 | HG02965.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.165+11788_165+1179 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411486 | ||||||
| chr6:18411487
|
A | AT | 6 | a0001c0001t0003g0192a0001c0001t0003g0217a0001c0001t0005g0341others(3): Show | 6 | NA18942.hp1 NA18975.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11789dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411487 | |||||
| chr6:18411487
|
A | T | 3 | a0001c0001t0003g0176a0001c0001t0008g0030a0001c0001t0023g0042 | 3 | HG00438.hp2 NA18991.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.165+11788A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411487 | ||||||
| chr6:18411487
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0346a0001c0001t0036g0336 | 2 | NA19000.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.165+11790_165+1180 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411487 | |||||
| chr6:18411487
|
ATATATAT others(5): Show |
A | 25 | a0001c0001t0002g0133a0001c0001t0002g0303a0001c0001t0002g0313others(22): Show | 26 | HG00408.hp2 HG00621.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.165+11790_165+1180 others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411487 | |||||
| chr6:18411487
|
ATATATAT others(6): Show |
A | 7 | a0001c0001t0002g0329a0001c0001t0002g0331a0001c0001t0002g0340others(4): Show | 7 | HG02523.hp1 HG02723.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+11790_165+1180 others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411487 | |||||
| chr6:18411489
|
A | AT | 13 | a0001c0001t0003g0181a0001c0001t0003g0186a0001c0001t0005g0358others(10): Show | 13 | HG01106.hp1 HG01175.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+11791dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | |||||
| chr6:18411489
|
A | ATT | 4 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(1): Show | 4 | NA18949.hp2 NA18964.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+11791_165+1179 others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | |||||
| chr6:18411489
|
A | T | 18 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0068others(15): Show | 18 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+11790A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411489 | ||||||
| chr6:18411489
|
ATATATAT others(3): Show |
A | 4 | a0001c0001t0020g0005a0001c0001t0044g0265a0001c0001t0085g0114others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+11792_165+1180 others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | |||||
| chr6:18411489
|
ATATATAT others(4): Show |
A | 5 | a0001c0001t0002g0308a0001c0001t0005g0352a0001c0001t0020g0127others(2): Show | 5 | HG01074.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+11792_165+1180 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | |||||
| chr6:18411489
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0034g0231 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.165+11792_165+1180 others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | |||||
| chr6:18411491
|
A | ATT | 6 | a0001c0001t0012g0188a0001c0001t0012g0189a0001c0001t0016g0076others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11793_165+1179 others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411491 | |||||
| chr6:18411491
|
A | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0016others(74): Show | 78 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.165+11792A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411491 | ||||||
| chr6:18411491
|
ATATATAT others(1): Show |
A | 9 | a0001c0001t0013g0014a0001c0001t0013g0082a0001c0001t0013g0085others(6): Show | 9 | HG01243.hp2 HG02280.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+11794_165+1180 others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411491 | |||||
| chr6:18411493
|
A | ATT | 3 | a0001c0001t0039g0146a0001c0001t0039g0149a0001c0001t0072g0275 | 3 | HG02896.hp1 HG02897.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.165+11795_165+1179 others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411493 | |||||
| chr6:18411493
|
A | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(119): Show | 124 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.165+11794A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411493 | ||||||
| chr6:18411495
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0022g0158a0001c0001t0022g0159 | 2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.165+11797_165+1179 others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411495 | |||||
| chr6:18411495
|
A | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(208): Show | 216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.165+11796A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411495 | ||||||
| chr6:18411497
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+11799_165+1180 others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411497 | |||||
| chr6:18411497
|
A | ATTTTTTT others(4): Show |
1 | a0001c0002t0022g0194 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.165+11812_165+1182 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411497 | |||||
| chr6:18411497
|
A | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(244): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.165+11798A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411497 | ||||||
| chr6:18411499
|
T | A | 6 | a0001c0001t0026g0262a0001c0001t0026g0282a0001c0001t0047g0106others(3): Show | 6 | HG01975.hp2 HG02071.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11800T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411499 | ||||||
| chr6:18411501
|
T | A | 1 | a0001c0001t0026g0262 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.165+11802T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411501 | ||||||
| chr6:18411592
|
C | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(216): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+11893C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411592 | ||||||
| chr6:18411659
|
G | A | 5 | a0001c0001t0025g0276a0001c0001t0025g0278a0001c0001t0025g0280others(2): Show | 5 | NA18945.hp2 NA18948.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+11960G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411659 | ||||||
| chr6:18411787
|
C | T | 3 | a0001c0001t0034g0272a0001c0001t0059g0142a0001c0001t0060g0147 | 3 | HG00735.hp1 HG01993.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.165+12088C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411787 | ||||||
| chr6:18411795
|
A | G | 1 | a0001c0001t0074g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.165+12096A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411795 | ||||||
| chr6:18411797
|
C | T | 1 | a0001c0001t0019g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.165+12098C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411797 | ||||||
| chr6:18411834
|
G | A | 101 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(98): Show | 104 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.165+12135G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411834 | ||||||
| chr6:18412104
|
G | T | 1 | a0001c0001t0060g0147 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.165+12405G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412104 | ||||||
| chr6:18412148
|
A | G | 1 | a0001c0001t0079g0361 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.165+12449A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412148 | ||||||
| chr6:18412176
|
A | G | 1 | a0001c0001t0030g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+12477A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412176 | ||||||
| chr6:18412238
|
C | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(73): Show | 77 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.165+12539C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412238 | ||||||
| chr6:18412247
|
C | G | 5 | a0001c0001t0081g0122a0001c0001t0083g0123a0001c0001t0092g0179others(2): Show | 5 | HG01361.hp2 HG02559.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+12548C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412247 | ||||||
| chr6:18412346
|
A | G | 3 | a0001c0001t0038g0098a0001c0001t0038g0101a0001c0001t0038g0143 | 3 | HG02897.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.165+12647A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412346 | ||||||
| chr6:18412410
|
A | G | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.165+12711A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412410 | ||||||
| chr6:18412559
|
CA | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+12867delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18412559 | |||||
| chr6:18412678
|
T | C | 19 | a0001c0001t0007g0233a0001c0001t0007g0234a0001c0001t0007g0239others(16): Show | 20 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+12979T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412678 | ||||||
| chr6:18412795
|
A | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(84): Show | 88 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.165+13096A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412795 | ||||||
| chr6:18412858
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | NA18986.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.165+13159G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412858 | ||||||
| chr6:18412993
|
A | G | 1 | a0001c0001t0019g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+13294A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412993 | ||||||
| chr6:18413013
|
A | G | 1 | a0001c0001t0013g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+13314A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413013 | ||||||
| chr6:18413207
|
A | AT | 73 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(70): Show | 75 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.165+13516dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18413207 | |||||
| chr6:18413397
|
T | A | 2 | a0001c0001t0064g0376a0001c0001t0082g0102 | 2 | HG01515.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.165+13698T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413397 | ||||||
| chr6:18413437
|
TG | T | 12 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(9): Show | 13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+13740delG | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18413437 | |||||
| chr6:18413444
|
G | A | 2 | a0001c0001t0030g0201a0001c0001t0084g0107 | 2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.165+13745G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413444 | ||||||
| chr6:18413663
|
T | A | 2 | a0001c0001t0066g0285a0001c0001t0083g0123 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-13918T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413663 | ||||||
| chr6:18413758
|
T | C | 20 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(17): Show | 20 | HG01261.hp2 HG02004.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.166-13823T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413758 | ||||||
| chr6:18413801
|
T | C | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-13780T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413801 | ||||||
| chr6:18413953
|
T | G | 1 | a0001c0001t0001g0297 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.166-13628T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413953 | ||||||
| chr6:18414061
|
C | G | 1 | a0001c0001t0070g0226 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.166-13520C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414061 | ||||||
| chr6:18414093
|
G | A | 2 | a0001c0001t0020g0120a0001c0001t0021g0195 | 2 | HG01496.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.166-13488G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414093 | ||||||
| chr6:18414240
|
A | T | 1 | a0001c0001t0008g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.166-13341A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414240 | ||||||
| chr6:18414458
|
G | A | 1 | a0001c0001t0023g0025 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.166-13123G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414458 | ||||||
| chr6:18414560
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.166-13021C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414560 | ||||||
| chr6:18415154
|
T | A | 2 | a0001c0001t0066g0285a0001c0001t0083g0123 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-12427T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415154 | ||||||
| chr6:18415163
|
T | C | 1 | a0002c0004t0078g0317 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.166-12418T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415163 | ||||||
| chr6:18415275
|
C | T | 1 | a0001c0001t0010g0279 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.166-12306C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415275 | ||||||
| chr6:18415298
|
A | G | 1 | a0001c0001t0066g0285 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.166-12283A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415298 | ||||||
| chr6:18415341
|
T | C | 5 | a0001c0001t0027g0129a0001c0001t0027g0305a0001c0001t0027g0364others(2): Show | 5 | HG01243.hp1 HG01433.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-12240T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415341 | ||||||
| chr6:18415347
|
C | T | 1 | a0001c0001t0042g0089 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.166-12234C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415347 | ||||||
| chr6:18415378
|
G | A | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-12203G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415378 | ||||||
| chr6:18415385
|
T | C | 1 | a0001c0001t0076g0371 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.166-12196T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415385 | ||||||
| chr6:18415386
|
G | A | 19 | a0001c0001t0011g0001a0001c0001t0011g0321a0001c0001t0011g0324others(16): Show | 21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.166-12195G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415386 | ||||||
| chr6:18415445
|
C | T | 4 | a0001c0001t0091g0215a0001c0001t0092g0179a0001c0001t0093g0178others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-12136C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415445 | ||||||
| chr6:18415482
|
T | C | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-12099T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415482 | ||||||
| chr6:18415482
|
T | G | 81 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(78): Show | 82 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.166-12099T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415482 | ||||||
| chr6:18415495
|
C | G | 120 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.166-12086C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415495 | ||||||
| chr6:18415640
|
C | G | 1 | a0001c0001t0047g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.166-11941C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415640 | ||||||
| chr6:18415766
|
A | G | 1 | a0001c0001t0032g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.166-11815A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415766 | ||||||
| chr6:18415777
|
A | G | 1 | a0001c0001t0023g0064 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.166-11804A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415777 | ||||||
| chr6:18415898
|
G | A | 13 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(10): Show | 14 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-11683G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415898 | ||||||
| chr6:18416013
|
G | T | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-11568G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416013 | ||||||
| chr6:18416137
|
CAGTT | C | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-11442_166-1143 others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18416137 | |||||
| chr6:18416206
|
A | T | 120 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.166-11375A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416206 | ||||||
| chr6:18416384
|
G | T | 80 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(77): Show | 81 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.166-11197G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416384 | ||||||
| chr6:18416461
|
C | T | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-11120C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416461 | ||||||
| chr6:18416539
|
A | G | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-11042A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416539 | ||||||
| chr6:18416565
|
C | G | 1 | a0001c0001t0079g0361 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.166-11016C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416565 | ||||||
| chr6:18416612
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.166-10969A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416612 | ||||||
| chr6:18416613
|
A | G | 2 | a0001c0001t0089g0182a0001c0001t0090g0174 | 2 | HG00438.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.166-10968A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416613 | ||||||
| chr6:18416646
|
G | A | 6 | a0001c0001t0005g0008a0001c0001t0005g0352a0001c0001t0008g0028others(3): Show | 7 | HG00140.hp2 HG01074.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-10935G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416646 | ||||||
| chr6:18416868
|
T | C | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-10713T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416868 | ||||||
| chr6:18416972
|
A | C | 1 | a0001c0001t0101g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.166-10609A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416972 | ||||||
| chr6:18417066
|
T | C | 1 | a0001c0001t0012g0188 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-10515T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417066 | ||||||
| chr6:18417260
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.166-10321T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417260 | ||||||
| chr6:18417264
|
A | G | 1 | a0001c0001t0050g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.166-10317A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417264 | ||||||
| chr6:18417302
|
C | G | 1 | a0001c0001t0002g0349 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.166-10279C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417302 | ||||||
| chr6:18417335
|
G | C | 4 | a0001c0001t0091g0215a0001c0001t0092g0179a0001c0001t0093g0178others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-10246G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417335 | ||||||
| chr6:18417456
|
G | T | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-10125G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417456 | ||||||
| chr6:18417501
|
G | A | 1 | a0001c0001t0002g0349 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.166-10080G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417501 | ||||||
| chr6:18417566
|
G | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0297 | 3 | NA18747.hp1 NA18986.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.166-10015G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417566 | ||||||
| chr6:18417612
|
T | G | 2 | a0001c0001t0005g0360a0001c0001t0079g0361 | 2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.166-9969T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417612 | ||||||
| chr6:18417898
|
A | G | 2 | a0001c0001t0005g0008a0001c0001t0036g0337 | 3 | HG03490.hp2 HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.166-9683A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417898 | ||||||
| chr6:18417934
|
G | C | 1 | a0001c0001t0002g0302 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.166-9647G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417934 | ||||||
| chr6:18417959
|
G | A | 42 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(39): Show | 42 | HG00408.hp2 HG00423.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.166-9622G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417959 | ||||||
| chr6:18417979
|
T | C | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-9602T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417979 | ||||||
| chr6:18418005
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.166-9576C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418005 | ||||||
| chr6:18418112
|
T | C | 1 | a0001c0001t0008g0032 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.166-9469T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418112 | ||||||
| chr6:18418152
|
G | A | 1 | a0001c0001t0070g0226 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.166-9429G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418152 | ||||||
| chr6:18418165
|
A | G | 1 | a0001c0001t0030g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.166-9416A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418165 | ||||||
| chr6:18418376
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.166-9205A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418376 | ||||||
| chr6:18418385
|
A | G | 19 | a0001c0001t0011g0001a0001c0001t0011g0321a0001c0001t0011g0324others(16): Show | 21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.166-9196A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418385 | ||||||
| chr6:18418477
|
T | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(265): Show | 275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.166-9104T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418477 | ||||||
| chr6:18418495
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(143): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.166-9086A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418495 | ||||||
| chr6:18418574
|
T | A | 1 | a0001c0001t0070g0226 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.166-9007T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418574 | ||||||
| chr6:18418577
|
G | A | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-9004G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418577 | ||||||
| chr6:18418658
|
G | A | 4 | a0001c0001t0016g0046a0001c0001t0016g0048a0001c0001t0016g0049others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-8923G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418658 | ||||||
| chr6:18418717
|
A | G | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-8864A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418717 | ||||||
| chr6:18418838
|
A | C | 91 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(88): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.166-8743A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418838 | ||||||
| chr6:18418842
|
A | G | 1 | a0001c0001t0033g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.166-8739A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418842 | ||||||
| chr6:18418963
|
A | G | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-8618A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418963 | ||||||
| chr6:18419087
|
A | G | 1 | a0001c0001t0003g0181 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.166-8494A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419087 | ||||||
| chr6:18419208
|
C | T | 8 | a0001c0001t0038g0098a0001c0001t0038g0101a0001c0001t0038g0143others(5): Show | 8 | HG01515.hp2 HG02559.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-8373C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419208 | ||||||
| chr6:18419318
|
G | A | 7 | a0001c0001t0020g0005a0001c0001t0020g0127a0001c0001t0021g0177others(4): Show | 7 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-8263G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419318 | ||||||
| chr6:18419459
|
G | A | 4 | a0001c0001t0049g0116a0001c0001t0049g0144a0001c0001t0098g0206others(1): Show | 4 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-8122G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419459 | ||||||
| chr6:18419562
|
G | A | 356 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(353): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.166-8019G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419562 | ||||||
| chr6:18419713
|
G | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(72): Show | 77 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.166-7868G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419713 | ||||||
| chr6:18419840
|
T | C | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-7741T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419840 | ||||||
| chr6:18419995
|
A | G | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-7586A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419995 | ||||||
| chr6:18420134
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.166-7447G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420134 | ||||||
| chr6:18420155
|
C | T | 1 | a0001c0001t0030g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.166-7426C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420155 | ||||||
| chr6:18420158
|
A | AT | 154 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(151): Show | 158 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.166-7413dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18420158 | |||||
| chr6:18420158
|
A | ATT | 127 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(124): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.166-7414_166-7413d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18420158 | |||||
| chr6:18420158
|
A | ATTT | 84 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(81): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.166-7415_166-7413d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18420158 | |||||
| chr6:18420215
|
C | A | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-7366C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420215 | ||||||
| chr6:18420278
|
A | T | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-7303A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420278 | ||||||
| chr6:18420483
|
G | A | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-7098G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420483 | ||||||
| chr6:18420527
|
C | A | 5 | a0001c0001t0002g0308a0001c0001t0002g0313a0001c0001t0002g0354others(2): Show | 5 | NA18940.hp2 NA18965.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-7054C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420527 | ||||||
| chr6:18420566
|
T | C | 1 | a0001c0001t0024g0295 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.166-7015T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420566 | ||||||
| chr6:18420789
|
G | A | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-6792G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420789 | ||||||
| chr6:18420849
|
C | T | 1 | a0001c0001t0037g0334 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.166-6732C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420849 | ||||||
| chr6:18421079
|
A | T | 1 | a0001c0001t0012g0175 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.166-6502A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421079 | ||||||
| chr6:18421123
|
C | T | 2 | a0001c0001t0005g0360a0001c0001t0079g0361 | 2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.166-6458C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421123 | ||||||
| chr6:18421270
|
TTA | T | 3 | a0001c0001t0002g0355a0001c0001t0026g0263a0001c0001t0026g0264 | 3 | HG01358.hp1 HG03239.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.166-6308_166-6307d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421270 | |||||
| chr6:18421271
|
T | TAC | 18 | a0001c0001t0002g0302a0001c0001t0002g0308a0001c0001t0002g0311others(15): Show | 18 | HG00140.hp1 HG01123.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.166-6309_166-6308i others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
T | TACAC | 29 | a0001c0001t0002g0133a0001c0001t0002g0303a0001c0001t0002g0314others(26): Show | 29 | HG00408.hp2 HG00423.hp2 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.166-6309_166-6308i others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
T | TACACAC | 9 | a0001c0001t0002g0313a0001c0001t0002g0331a0001c0001t0009g0230others(6): Show | 9 | HG01243.hp2 HG02602.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-6309_166-6308i others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
T | TACACACA others(1): Show |
3 | a0001c0001t0009g0254a0001c0001t0009g0288a0001c0001t0019g0148 | 3 | HG02965.hp2 NA19081.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.166-6309_166-6308i others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
T | TACACACA others(3): Show |
1 | a0001c0001t0002g0363 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-6309_166-6308i others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
T | TACACACA others(5): Show |
1 | a0001c0001t0019g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.166-6309_166-6308i others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
T | TACACACA others(9): Show |
1 | a0001c0005t0009g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.166-6309_166-6308i others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
TATACACA others(9): Show |
T | 99 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(96): Show | 100 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.166-6308_166-6293d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
TATACACA others(11): Show |
T | 44 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(41): Show | 47 | HG00323.hp1 HG00642.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.166-6308_166-6291d others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421271
|
TATACACA others(13): Show |
T | 14 | a0001c0001t0020g0005a0001c0001t0020g0113a0001c0001t0020g0120others(11): Show | 14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-6308_166-6289d others(22): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | |||||
| chr6:18421273
|
T | C | 71 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(68): Show | 72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.166-6308T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421273 | ||||||
| chr6:18421273
|
T | TAC | 18 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0052others(15): Show | 21 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.166-6266_166-6265d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | |||||
| chr6:18421273
|
T | TACAC | 6 | a0001c0001t0001g0047a0001c0001t0001g0080a0001c0001t0010g0228others(3): Show | 6 | HG01256.hp1 HG02922.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-6268_166-6265d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | |||||
| chr6:18421273
|
TAC | T | 28 | a0001c0001t0004g0131a0001c0001t0004g0309a0001c0001t0004g0332others(25): Show | 28 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.166-6266_166-6265d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | |||||
| chr6:18421273
|
TACAC | T | 19 | a0001c0001t0004g0009a0001c0001t0007g0232a0001c0001t0007g0234others(16): Show | 20 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.166-6268_166-6265d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | |||||
| chr6:18421273
|
TACACAC | T | 9 | a0001c0001t0004g0367a0001c0001t0007g0233a0001c0001t0027g0129others(6): Show | 9 | HG00280.hp1 HG00558.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-6270_166-6265d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | |||||
| chr6:18421313
|
C | T | 1 | a0001c0001t0056g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.166-6268C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421313 | ||||||
| chr6:18421315
|
C | T | 157 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(154): Show | 161 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.166-6266C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421315 | ||||||
| chr6:18421315
|
CAT | C | 3 | a0001c0001t0010g0237a0001c0001t0068g0281a0001c0001t0076g0371 | 3 | HG00735.hp2 HG03669.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.166-6258_166-6257d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421315 | |||||
| chr6:18421317
|
T | C | 13 | a0001c0001t0001g0041a0001c0001t0002g0303a0001c0001t0010g0007others(10): Show | 14 | HG00099.hp1 HG00280.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-6264T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421317 | ||||||
| chr6:18421319
|
T | C | 1 | a0001c0001t0010g0236 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.166-6262T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421319 | ||||||
| chr6:18421571
|
C | T | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166-6010C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421571 | ||||||
| chr6:18421582
|
A | G | 1 | a0001c0001t0014g0307 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.166-5999A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421582 | ||||||
| chr6:18421611
|
C | T | 1 | a0001c0001t0006g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.166-5970C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421611 | ||||||
| chr6:18421745
|
G | A | 2 | a0001c0001t0040g0109a0001c0001t0040g0110 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.166-5836G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421745 | ||||||
| chr6:18421797
|
C | T | 1 | a0001c0001t0101g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.166-5784C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421797 | ||||||
| chr6:18422226
|
A | G | 3 | a0001c0001t0027g0129a0001c0001t0027g0370a0001c0001t0048g0103 | 3 | HG02683.hp2 HG03834.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.166-5355A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422226 | ||||||
| chr6:18422242
|
G | T | 58 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(55): Show | 59 | HG00408.hp2 HG00423.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.166-5339G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422242 | ||||||
| chr6:18422318
|
T | C | 91 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.166-5263T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422318 | ||||||
| chr6:18422421
|
G | A | 358 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(355): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.166-5160G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422421 | ||||||
| chr6:18422574
|
C | CT | 4 | a0001c0001t0016g0087a0001c0001t0033g0284a0001c0001t0033g0286others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-5005dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18422574 | |||||
| chr6:18422617
|
C | T | 1 | a0001c0001t0028g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.166-4964C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422617 | ||||||
| chr6:18422951
|
C | CA | 70 | a0001c0001t0002g0133a0001c0001t0002g0303a0001c0001t0002g0308others(67): Show | 72 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.166-4615dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18422951 | |||||
| chr6:18422951
|
C | CAA | 18 | a0001c0001t0002g0302a0001c0001t0002g0313a0001c0001t0002g0319others(15): Show | 18 | HG00140.hp1 HG01358.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.166-4616_166-4615d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18422951 | |||||
| chr6:18422951
|
CA | C | 158 | a0001c0001t0001g0055a0001c0001t0003g0152a0001c0001t0003g0163others(155): Show | 163 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.166-4615delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18422951 | |||||
| chr6:18423174
|
C | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(101): Show | 106 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.166-4407C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423174 | ||||||
| chr6:18423189
|
G | A | 3 | a0001c0001t0005g0341a0001c0001t0005g0342a0001c0001t0005g0343 | 3 | NA18975.hp1 NA18982.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.166-4392G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423189 | ||||||
| chr6:18423334
|
A | T | 366 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(363): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.166-4247A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423334 | ||||||
| chr6:18423357
|
T | C | 1 | a0001c0001t0089g0182 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.166-4224T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423357 | ||||||
| chr6:18423358
|
T | C | 1 | a0001c0001t0008g0078 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.166-4223T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423358 | ||||||
| chr6:18423395
|
T | C | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-4186T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423395 | ||||||
| chr6:18423419
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.166-4162C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423419 | ||||||
| chr6:18423436
|
A | G | 81 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(78): Show | 82 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.166-4145A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423436 | ||||||
| chr6:18423517
|
A | G | 13 | a0001c0001t0010g0228a0001c0001t0033g0284a0001c0001t0033g0286others(10): Show | 14 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-4064A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423517 | ||||||
| chr6:18423561
|
G | A | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-4020G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423561 | ||||||
| chr6:18423577
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-4004G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423577 | ||||||
| chr6:18423766
|
C | CT | 88 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(85): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.166-3815_166-3814i others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423766 | ||||||
| chr6:18423767
|
C | A | 88 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(85): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.166-3814C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423767 | ||||||
| chr6:18423847
|
A | G | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-3734A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423847 | ||||||
| chr6:18424038
|
G | T | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-3543G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424038 | ||||||
| chr6:18424047
|
G | A | 3 | a0001c0001t0029g0117a0001c0001t0029g0121a0001c0001t0041g0051 | 3 | HG01167.hp1 HG01169.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.166-3534G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424047 | ||||||
| chr6:18424068
|
A | G | 269 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(266): Show | 276 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.166-3513A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424068 | ||||||
| chr6:18424077
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-3504G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424077 | ||||||
| chr6:18424170
|
G | T | 1 | a0001c0001t0094g0209 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-3411G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424170 | ||||||
| chr6:18424171
|
A | T | 1 | a0001c0001t0094g0209 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-3410A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424171 | ||||||
| chr6:18424199
|
G | T | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-3382G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424199 | ||||||
| chr6:18424349
|
A | G | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-3232A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424349 | ||||||
| chr6:18424370
|
A | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.166-3211A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424370 | ||||||
| chr6:18424374
|
C | T | 1 | a0001c0001t0094g0209 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-3207C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424374 | ||||||
| chr6:18424385
|
G | A | 1 | a0001c0001t0009g0250 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.166-3196G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424385 | ||||||
| chr6:18424495
|
A | G | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-3086A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424495 | ||||||
| chr6:18424609
|
GA | G | 16 | a0001c0001t0014g0135a0001c0001t0014g0357a0001c0001t0026g0262others(13): Show | 16 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.166-2970delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18424609 | |||||
| chr6:18424648
|
C | G | 2 | a0001c0001t0007g0246a0001c0001t0007g0274 | 2 | HG00639.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.166-2933C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424648 | ||||||
| chr6:18424691
|
T | C | 1 | a0001c0001t0020g0113 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.166-2890T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424691 | ||||||
| chr6:18424783
|
T | TAAG | 269 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(266): Show | 276 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.166-2796_166-2794d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18424783 | |||||
| chr6:18424951
|
C | A | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-2630C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424951 | ||||||
| chr6:18424970
|
A | G | 4 | a0001c0001t0038g0098a0001c0001t0038g0101a0001c0001t0038g0143others(1): Show | 4 | HG02897.hp1 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-2611A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424970 | ||||||
| chr6:18425056
|
G | GGTGT | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-2510_166-2507d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18425056 | |||||
| chr6:18425056
|
G | T | 1 | a0001c0001t0045g0258 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.166-2525G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425056 | ||||||
| chr6:18425056
|
GGT | G | 37 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(34): Show | 39 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.166-2508_166-2507d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18425056 | |||||
| chr6:18425064
|
T | A | 3 | a0001c0001t0064g0376a0001c0001t0074g0139a0001c0001t0082g0102 | 3 | HG01515.hp2 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.166-2517T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425064 | ||||||
| chr6:18425079
|
A | C | 358 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(355): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.166-2502A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425079 | ||||||
| chr6:18425109
|
G | A | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-2472G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425109 | ||||||
| chr6:18425135
|
C | T | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-2446C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425135 | ||||||
| chr6:18425184
|
T | C | 30 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(27): Show | 32 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.166-2397T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425184 | ||||||
| chr6:18425472
|
G | C | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-2109G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425472 | ||||||
| chr6:18425723
|
A | G | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-1858A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425723 | ||||||
| chr6:18425725
|
A | G | 6 | a0001c0001t0002g0302a0001c0001t0002g0311a0001c0001t0002g0319others(3): Show | 6 | HG01123.hp1 HG01361.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-1856A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425725 | ||||||
| chr6:18425751
|
C | T | 12 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(9): Show | 13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-1830C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425751 | ||||||
| chr6:18425912
|
T | C | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-1669T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425912 | ||||||
| chr6:18425989
|
A | T | 1 | a0001c0001t0062g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.166-1592A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425989 | ||||||
| chr6:18426093
|
G | A | 4 | a0001c0001t0010g0228a0001c0001t0051g0006a0001c0001t0058g0227others(1): Show | 5 | HG02055.hp1 HG02922.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-1488G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426093 | ||||||
| chr6:18426168
|
G | A | 1 | a0001c0001t0072g0275 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.166-1413G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426168 | ||||||
| chr6:18426181
|
T | C | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-1400T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426181 | ||||||
| chr6:18426193
|
A | C | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166-1388A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426193 | ||||||
| chr6:18426316
|
A | G | 1 | a0001c0001t0100g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.166-1265A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426316 | ||||||
| chr6:18426344
|
T | C | 66 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(63): Show | 70 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.166-1237T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426344 | ||||||
| chr6:18426365
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-1216G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426365 | ||||||
| chr6:18426377
|
A | G | 229 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(226): Show | 233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.166-1204A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426377 | ||||||
| chr6:18426390
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-1191G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426390 | ||||||
| chr6:18426470
|
T | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.166-1111T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426470 | ||||||
| chr6:18426494
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0004g0369 | 2 | HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.166-1087G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426494 | ||||||
| chr6:18426506
|
T | C | 12 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(9): Show | 13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-1075T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426506 | ||||||
| chr6:18426744
|
CTTTTTTC others(25): Show |
C | 12 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(9): Show | 13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-789_166-758del others(32): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18426744 | |||||
| chr6:18426792
|
GTCTTCTC others(25): Show |
G | 1 | a0001c0001t0047g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.166-773_166-742del others(32): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18426792 | |||||
| chr6:18426794
|
C | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-787C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426794 | ||||||
| chr6:18426896
|
C | T | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-685C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426896 | ||||||
| chr6:18426967
|
G | GAGA | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-612_166-611ins others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18426967 | |||||
| chr6:18427021
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-560G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427021 | ||||||
| chr6:18427081
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-500T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427081 | ||||||
| chr6:18427101
|
A | G | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-480A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427101 | ||||||
| chr6:18427186
|
C | T | 1 | a0001c0001t0050g0214 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.166-395C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427186 | ||||||
| chr6:18427207
|
A | G | 1 | a0001c0001t0100g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.166-374A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427207 | ||||||
| chr6:18427256
|
A | AT | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.166-314dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18427256 | |||||
| chr6:18427256
|
AT | A | 16 | a0001c0001t0013g0083a0001c0001t0014g0135a0001c0001t0014g0357others(13): Show | 16 | HG00140.hp1 HG01358.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.166-314delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18427256 | |||||
| chr6:18427256
|
ATT | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-315_166-314del others(2): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18427256 | |||||
| chr6:18427321
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.166-260T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427321 | ||||||
| chr6:18427445
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-136G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427445 | ||||||
| chr6:18427522
|
T | C | 13 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(10): Show | 14 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-59T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427522 | ||||||
| chr6:18427553
|
C | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-28C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427553 | ||||||
| chr6:18427824
|
G | T | 95 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(92): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.270+139G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427824 | ||||||
| chr6:18427877
|
C | T | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.270+192C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427877 | ||||||
| chr6:18427886
|
T | C | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.270+201T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427886 | ||||||
| chr6:18427940
|
A | G | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+255A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427940 | ||||||
| chr6:18427946
|
C | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+261C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427946 | ||||||
| chr6:18428011
|
T | C | 2 | a0001c0001t0013g0026a0001c0001t0013g0027 | 2 | NA18986.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.270+326T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428011 | ||||||
| chr6:18428101
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+416G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428101 | ||||||
| chr6:18428102
|
T | G | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.270+417T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428102 | ||||||
| chr6:18428115
|
T | A | 2 | a0001c0001t0014g0135a0001c0001t0014g0357 | 2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.270+430T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428115 | ||||||
| chr6:18428198
|
C | T | 1 | a0001c0001t0014g0316 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.270+513C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428198 | ||||||
| chr6:18428199
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(255): Show | 265 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.270+514T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428199 | ||||||
| chr6:18428247
|
C | A | 81 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(78): Show | 82 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.270+562C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428247 | ||||||
| chr6:18428280
|
T | C | 1 | a0001c0001t0021g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.270+595T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428280 | ||||||
| chr6:18428307
|
A | G | 322 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(319): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.270+622A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428307 | ||||||
| chr6:18428467
|
C | G | 16 | a0001c0001t0014g0135a0001c0001t0014g0357a0001c0001t0026g0262others(13): Show | 16 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.270+782C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428467 | ||||||
| chr6:18428485
|
A | ATG | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+801_270+802ins others(2): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18428485 | |||||
| chr6:18428513
|
C | T | 1 | a0001c0001t0005g0359 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.270+828C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428513 | ||||||
| chr6:18428514
|
G | A | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+829G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428514 | ||||||
| chr6:18428549
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.270+864A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428549 | ||||||
| chr6:18428627
|
G | A | 95 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(92): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.270+942G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428627 | ||||||
| chr6:18428755
|
C | T | 14 | a0001c0001t0020g0005a0001c0001t0020g0113a0001c0001t0020g0120others(11): Show | 14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.270+1070C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428755 | ||||||
| chr6:18428824
|
C | T | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+1139C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428824 | ||||||
| chr6:18428825
|
A | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+1140A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428825 | ||||||
| chr6:18428849
|
A | G | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.270+1164A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428849 | ||||||
| chr6:18429062
|
G | A | 1 | a0001c0001t0014g0328 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.270+1377G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429062 | ||||||
| chr6:18429202
|
A | G | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+1517A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429202 | ||||||
| chr6:18429229
|
A | G | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.270+1544A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429229 | ||||||
| chr6:18429342
|
T | C | 2 | a0001c0001t0006g0168a0001c0001t0017g0065 | 2 | NA19011.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.270+1657T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429342 | ||||||
| chr6:18429344
|
CTTTG | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.270+1663_270+1666d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18429344 | |||||
| chr6:18429483
|
T | G | 94 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(91): Show | 95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.270+1798T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429483 | ||||||
| chr6:18429496
|
T | C | 38 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(35): Show | 39 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.270+1811T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429496 | ||||||
| chr6:18429580
|
T | C | 88 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(85): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.270+1895T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429580 | ||||||
| chr6:18429597
|
AC | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.270+1915delC | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18429597 | |||||
| chr6:18429612
|
A | G | 1 | a0001c0001t0032g0193 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.270+1927A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429612 | ||||||
| chr6:18429627
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+1942G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429627 | ||||||
| chr6:18429689
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2004G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429689 | ||||||
| chr6:18429860
|
C | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2175C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429860 | ||||||
| chr6:18429881
|
G | A | 37 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(34): Show | 39 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.270+2196G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429881 | ||||||
| chr6:18429885
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2200G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429885 | ||||||
| chr6:18429974
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2289G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429974 | ||||||
| chr6:18430004
|
A | G | 1 | a0001c0001t0006g0168 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.270+2319A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430004 | ||||||
| chr6:18430084
|
GA | G | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2400delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430084 | ||||||
| chr6:18430258
|
C | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2573C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430258 | ||||||
| chr6:18430356
|
T | C | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2671T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430356 | ||||||
| chr6:18430486
|
TTC | T | 364 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(361): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.270+2821_270+2822d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18430486 | |||||
| chr6:18430586
|
C | T | 1 | a0001c0001t0010g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.270+2901C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430586 | ||||||
| chr6:18430657
|
AT | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(230): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.270+2987delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18430657 | |||||
| chr6:18430663
|
T | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.270+2978T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430663 | ||||||
| chr6:18430700
|
G | A | 3 | a0001c0001t0010g0243a0001c0001t0076g0371a0001c0001t0105g0063 | 3 | HG00280.hp2 HG00735.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.270+3015G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430700 | ||||||
| chr6:18430720
|
A | C | 2 | a0001c0001t0053g0204a0001c0001t0053g0205 | 2 | HG00423.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.270+3035A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430720 | ||||||
| chr6:18430731
|
C | T | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+3046C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430731 | ||||||
| chr6:18430787
|
G | C | 4 | a0001c0001t0091g0215a0001c0001t0092g0179a0001c0001t0093g0178others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+3102G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430787 | ||||||
| chr6:18430788
|
AATAG | A | 4 | a0001c0001t0091g0215a0001c0001t0092g0179a0001c0001t0093g0178others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+3105_270+3108d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18430788 | |||||
| chr6:18430852
|
C | T | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.270+3167C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430852 | ||||||
| chr6:18430879
|
T | C | 1 | a0001c0001t0008g0030 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.270+3194T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430879 | ||||||
| chr6:18431005
|
G | A | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3320G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431005 | ||||||
| chr6:18431008
|
T | C | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3323T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431008 | ||||||
| chr6:18431048
|
C | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3363C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431048 | ||||||
| chr6:18431199
|
C | G | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3514C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431199 | ||||||
| chr6:18431225
|
C | CA | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3549dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18431225 | |||||
| chr6:18431242
|
TA | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3567delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18431242 | |||||
| chr6:18431423
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.270+3738A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431423 | ||||||
| chr6:18431429
|
A | G | 1 | a0001c0001t0002g0340 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.270+3744A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431429 | ||||||
| chr6:18431464
|
A | C | 173 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(170): Show | 176 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.270+3779A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431464 | ||||||
| chr6:18431519
|
C | T | 358 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(355): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.270+3834C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431519 | ||||||
| chr6:18431572
|
A | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+3887A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431572 | ||||||
| chr6:18431663
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.270+3978A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431663 | ||||||
| chr6:18431666
|
C | G | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.270+3981C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431666 | ||||||
| chr6:18431674
|
T | C | 357 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(354): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.270+3989T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431674 | ||||||
| chr6:18431841
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4156C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431841 | ||||||
| chr6:18431960
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4275T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431960 | ||||||
| chr6:18431985
|
G | A | 1 | a0001c0001t0002g0303 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.270+4300G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431985 | ||||||
| chr6:18432012
|
G | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4327G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432012 | ||||||
| chr6:18432130
|
T | C | 1 | a0001c0001t0047g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.270+4445T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432130 | ||||||
| chr6:18432181
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4496T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432181 | ||||||
| chr6:18432237
|
C | T | 5 | a0001c0001t0005g0310a0001c0001t0005g0323a0001c0001t0005g0358others(2): Show | 5 | HG01496.hp1 HG01928.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+4552C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432237 | ||||||
| chr6:18432315
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(93): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.270+4630C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432315 | ||||||
| chr6:18432316
|
G | A | 12 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(9): Show | 13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.270+4631G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432316 | ||||||
| chr6:18432349
|
G | T | 1 | a0001c0001t0001g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.270+4664G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432349 | ||||||
| chr6:18432355
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4670C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432355 | ||||||
| chr6:18432482
|
T | C | 1 | a0001c0001t0003g0181 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.270+4797T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432482 | ||||||
| chr6:18432498
|
A | G | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+4813A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432498 | ||||||
| chr6:18432538
|
C | A | 1 | a0001c0001t0005g0343 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+4853C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432538 | ||||||
| chr6:18432631
|
T | C | 4 | a0001c0001t0091g0215a0001c0001t0092g0179a0001c0001t0093g0178others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+4946T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432631 | ||||||
| chr6:18432870
|
G | C | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5185G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432870 | ||||||
| chr6:18433128
|
C | T | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5443C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433128 | ||||||
| chr6:18433224
|
T | A | 2 | a0001c0001t0014g0316a0001c0001t0019g0104 | 2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.270+5539T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433224 | ||||||
| chr6:18433360
|
A | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5675A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433360 | ||||||
| chr6:18433438
|
A | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5753A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433438 | ||||||
| chr6:18433504
|
A | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5819A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433504 | ||||||
| chr6:18433568
|
A | G | 2 | a0001c0001t0015g0335a0001c0001t0016g0066 | 2 | NA18951.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.270+5883A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433568 | ||||||
| chr6:18433676
|
C | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+5991C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433676 | ||||||
| chr6:18433859
|
G | A | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5825G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433859 | ||||||
| chr6:18433867
|
C | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5817C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433867 | ||||||
| chr6:18433918
|
G | A | 42 | a0001c0001t0003g0191a0001c0001t0007g0266a0001c0001t0007g0298others(39): Show | 45 | HG00323.hp1 HG00609.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.271-5766G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433918 | ||||||
| chr6:18433922
|
A | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5762A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433922 | ||||||
| chr6:18433969
|
C | A | 2 | a0001c0001t0010g0228a0001c0001t0051g0006 | 3 | HG02922.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.271-5715C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433969 | ||||||
| chr6:18433993
|
G | A | 20 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0007g0234others(17): Show | 20 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-5691G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433993 | ||||||
| chr6:18434005
|
C | T | 358 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(355): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.271-5679C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434005 | ||||||
| chr6:18434101
|
A | T | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5583A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434101 | ||||||
| chr6:18434204
|
T | G | 2 | a0001c0001t0034g0272a0001c0001t0059g0142 | 2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.271-5480T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434204 | ||||||
| chr6:18434224
|
G | A | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-5460G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434224 | ||||||
| chr6:18434235
|
T | A | 1 | a0001c0001t0015g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.271-5449T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434235 | ||||||
| chr6:18434359
|
T | C | 1 | a0001c0001t0026g0282 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.271-5325T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434359 | ||||||
| chr6:18434366
|
G | A | 95 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(92): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-5318G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434366 | ||||||
| chr6:18434366
|
GA | G | 20 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0007g0234others(17): Show | 20 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-5317delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434366 | ||||||
| chr6:18434445
|
G | A | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5239G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434445 | ||||||
| chr6:18434470
|
G | T | 1 | a0001c0001t0008g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.271-5214G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434470 | ||||||
| chr6:18434576
|
T | C | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.271-5108T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434576 | ||||||
| chr6:18434621
|
T | TTTTG | 5 | a0001c0001t0010g0228a0001c0001t0011g0324a0001c0001t0051g0006others(2): Show | 6 | HG01993.hp1 HG02055.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-5051_271-5048d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18434621 | |||||
| chr6:18434633
|
G | GTTTT | 35 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(32): Show | 37 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.271-5047_271-5044d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18434633 | |||||
| chr6:18434690
|
C | T | 1 | a0001c0001t0003g0203 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.271-4994C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434690 | ||||||
| chr6:18434753
|
C | T | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4931C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434753 | ||||||
| chr6:18434807
|
G | C | 1 | a0001c0001t0062g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.271-4877G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434807 | ||||||
| chr6:18434903
|
A | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4781A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434903 | ||||||
| chr6:18434925
|
T | C | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4759T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434925 | ||||||
| chr6:18434982
|
A | G | 1 | a0001c0001t0011g0372 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.271-4702A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434982 | ||||||
| chr6:18434998
|
A | G | 2 | a0001c0002t0022g0180a0001c0002t0022g0194 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.271-4686A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434998 | ||||||
| chr6:18435041
|
T | C | 1 | a0001c0001t0062g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.271-4643T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435041 | ||||||
| chr6:18435089
|
G | A | 3 | a0001c0001t0020g0005a0001c0001t0020g0127a0001c0001t0086g0005 | 3 | HG02258.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.271-4595G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435089 | ||||||
| chr6:18435096
|
T | C | 95 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(92): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-4588T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435096 | ||||||
| chr6:18435136
|
A | G | 3 | a0001c0001t0002g0363a0001c0001t0009g0288a0001c0001t0019g0148 | 3 | HG02965.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.271-4548A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435136 | ||||||
| chr6:18435304
|
G | A | 358 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(355): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.271-4380G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435304 | ||||||
| chr6:18435406
|
A | G | 1 | a0001c0001t0006g0156 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.271-4278A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435406 | ||||||
| chr6:18435409
|
GAATA | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4270_271-4267d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18435409 | |||||
| chr6:18435447
|
A | C | 2 | a0001c0001t0042g0090a0001c0001t0052g0151 | 2 | HG01257.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.271-4237A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435447 | ||||||
| chr6:18435483
|
AG | A | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-4200delG | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435483 | ||||||
| chr6:18435559
|
C | A | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4125C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435559 | ||||||
| chr6:18435573
|
A | C | 10 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(7): Show | 10 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-4111A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435573 | ||||||
| chr6:18435779
|
A | C | 1 | a0001c0001t0037g0339 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.271-3905A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435779 | ||||||
| chr6:18435787
|
C | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-3897C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435787 | ||||||
| chr6:18435837
|
C | A | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-3847C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435837 | ||||||
| chr6:18435885
|
G | C | 4 | a0001c0001t0010g0228a0001c0001t0051g0006a0001c0001t0058g0227others(1): Show | 5 | HG02055.hp1 HG02922.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3799G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435885 | ||||||
| chr6:18435888
|
G | T | 81 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(78): Show | 82 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.271-3796G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435888 | ||||||
| chr6:18435889
|
G | A | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271-3795G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435889 | ||||||
| chr6:18435892
|
G | A | 1 | a0001c0001t0007g0244 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.271-3792G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435892 | ||||||
| chr6:18435957
|
G | T | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.271-3727G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435957 | ||||||
| chr6:18436058
|
T | TA | 24 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(21): Show | 25 | HG01261.hp2 HG02004.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.271-3613dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436058 | |||||
| chr6:18436058
|
TA | T | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.271-3613delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436058 | |||||
| chr6:18436281
|
A | G | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-3403A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436281 | ||||||
| chr6:18436294
|
T | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.271-3390T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436294 | ||||||
| chr6:18436312
|
C | T | 10 | a0001c0001t0009g0292a0001c0001t0013g0014a0001c0001t0013g0082others(7): Show | 10 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-3372C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436312 | ||||||
| chr6:18436318
|
C | T | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-3366C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436318 | ||||||
| chr6:18436344
|
G | A | 95 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(92): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-3340G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436344 | ||||||
| chr6:18436519
|
G | A | 4 | a0001c0001t0002g0345a0001c0001t0002g0346a0001c0001t0013g0026others(1): Show | 4 | HG00408.hp2 NA18986.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3165G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436519 | ||||||
| chr6:18436807
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(94): Show | 99 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.271-2877A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436807 | ||||||
| chr6:18436851
|
G | C | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-2833G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436851 | ||||||
| chr6:18436905
|
G | GTT | 20 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(17): Show | 20 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-2770_271-2769d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436905 | |||||
| chr6:18436905
|
G | GTTT | 20 | a0001c0001t0011g0001a0001c0001t0011g0321a0001c0001t0011g0324others(17): Show | 23 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.271-2771_271-2769d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436905 | |||||
| chr6:18436905
|
GT | G | 305 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(302): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.271-2769delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436905 | |||||
| chr6:18437167
|
A | C | 1 | a0001c0001t0001g0074 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.271-2517A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437167 | ||||||
| chr6:18437245
|
C | G | 2 | a0001c0001t0006g0170a0001c0001t0006g0171 | 2 | HG02071.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.271-2439C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437245 | ||||||
| chr6:18437328
|
A | G | 1 | a0001c0001t0006g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.271-2356A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437328 | ||||||
| chr6:18437376
|
C | T | 4 | a0001c0001t0002g0345a0001c0001t0002g0346a0001c0001t0013g0026others(1): Show | 4 | HG00408.hp2 NA18986.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-2308C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437376 | ||||||
| chr6:18437384
|
G | A | 22 | a0001c0001t0004g0130a0001c0001t0004g0344a0001c0001t0007g0232others(19): Show | 22 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-2300G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437384 | ||||||
| chr6:18437391
|
T | C | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-2293T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437391 | ||||||
| chr6:18437534
|
A | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(70): Show | 75 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.271-2150A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437534 | ||||||
| chr6:18437576
|
G | A | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-2108G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437576 | ||||||
| chr6:18437603
|
T | C | 22 | a0001c0001t0004g0130a0001c0001t0004g0344a0001c0001t0007g0232others(19): Show | 22 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-2081T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437603 | ||||||
| chr6:18437614
|
C | T | 1 | a0001c0001t0023g0061 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.271-2070C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437614 | ||||||
| chr6:18437615
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.271-2069G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437615 | ||||||
| chr6:18437717
|
A | G | 4 | a0001c0001t0091g0215a0001c0001t0092g0179a0001c0001t0093g0178others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1967A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437717 | ||||||
| chr6:18437789
|
C | A | 7 | a0001c0001t0038g0098a0001c0001t0038g0101a0001c0001t0038g0143others(4): Show | 7 | HG01515.hp2 HG02897.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-1895C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437789 | ||||||
| chr6:18437801
|
A | G | 1 | a0001c0001t0081g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-1883A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437801 | ||||||
| chr6:18437835
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1849C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437835 | ||||||
| chr6:18437843
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1841T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437843 | ||||||
| chr6:18438047
|
G | T | 1 | a0001c0001t0016g0049 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.271-1637G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438047 | ||||||
| chr6:18438061
|
A | T | 2 | a0001c0001t0012g0011a0001c0001t0012g0012 | 2 | NA18969.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.271-1623A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438061 | ||||||
| chr6:18438094
|
G | A | 4 | a0001c0001t0091g0215a0001c0001t0092g0179a0001c0001t0093g0178others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1590G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438094 | ||||||
| chr6:18438256
|
G | A | 95 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(92): Show | 96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-1428G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438256 | ||||||
| chr6:18438274
|
C | T | 4 | a0001c0001t0091g0215a0001c0001t0092g0179a0001c0001t0093g0178others(1): Show | 4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1410C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438274 | ||||||
| chr6:18438361
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1323C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438361 | ||||||
| chr6:18438367
|
A | G | 121 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(118): Show | 123 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.271-1317A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438367 | ||||||
| chr6:18438453
|
A | G | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-1231A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438453 | ||||||
| chr6:18438497
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1187C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438497 | ||||||
| chr6:18438601
|
G | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1083G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438601 | ||||||
| chr6:18438645
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(73): Show | 78 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.271-1039T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438645 | ||||||
| chr6:18438731
|
G | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-953G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438731 | ||||||
| chr6:18438796
|
T | C | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.271-888T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438796 | ||||||
| chr6:18438876
|
T | G | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.271-808T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438876 | ||||||
| chr6:18439308
|
T | G | 40 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0010g0228others(37): Show | 43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-376T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439308 | ||||||
| chr6:18439327
|
A | G | 90 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(87): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.271-357A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439327 | ||||||
| chr6:18439404
|
G | C | 1 | a0001c0001t0014g0316 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.271-280G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439404 | ||||||
| chr6:18439443
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.271-241T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439443 | ||||||
| chr6:18439508
|
T | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.271-176T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439508 | ||||||
| chr6:18439580
|
G | T | 1 | a0001c0001t0100g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.271-104G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439580 | ||||||
| chr6:18439788
|
A | G | 2 | a0001c0001t0010g0228a0001c0001t0051g0006 | 3 | HG02922.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331+44A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18439788 | ||||||
| chr6:18439802
|
C | T | 6 | a0001c0001t0002g0340a0001c0001t0009g0230a0001c0001t0009g0252others(3): Show | 6 | NA18939.hp2 NA18941.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+58C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18439802 | ||||||
| chr6:18439982
|
T | C | 65 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(62): Show | 68 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.331+238T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18439982 | ||||||
| chr6:18440016
|
A | G | 19 | a0001c0001t0011g0001a0001c0001t0011g0321a0001c0001t0011g0324others(16): Show | 21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.331+272A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440016 | ||||||
| chr6:18440069
|
A | G | 14 | a0001c0001t0020g0005a0001c0001t0020g0113a0001c0001t0020g0120others(11): Show | 14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+325A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440069 | ||||||
| chr6:18440081
|
C | T | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+337C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440081 | ||||||
| chr6:18440162
|
A | G | 1 | a0001c0001t0041g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.331+418A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440162 | ||||||
| chr6:18440269
|
C | CTT | 64 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(61): Show | 67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+525_331+526ins others(2): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440269 | ||||||
| chr6:18440377
|
G | C | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+633G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440377 | ||||||
| chr6:18440409
|
A | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.331+665A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440409 | ||||||
| chr6:18440436
|
G | C | 64 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(61): Show | 67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+692G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440436 | ||||||
| chr6:18440525
|
A | G | 1 | a0001c0001t0006g0156 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.331+781A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440525 | ||||||
| chr6:18440663
|
GA | G | 64 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(61): Show | 67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+927delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440663 | |||||
| chr6:18440672
|
C | T | 1 | a0001c0001t0041g0031 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.331+928C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440672 | ||||||
| chr6:18440680
|
G | A | 96 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(93): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+936G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440680 | ||||||
| chr6:18440710
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(93): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.331+966T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440710 | ||||||
| chr6:18440723
|
G | GGTT | 357 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(354): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.331+980_331+982dup others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440723 | |||||
| chr6:18440729
|
T | C | 1 | a0001c0001t0015g0335 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.331+985T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440729 | ||||||
| chr6:18440795
|
G | GT | 194 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(191): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.331+1065dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440795 | |||||
| chr6:18440810
|
A | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(157): Show | 165 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.331+1066A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440810 | ||||||
| chr6:18440811
|
A | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(133): Show | 141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.331+1067A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440811 | ||||||
| chr6:18440836
|
T | C | 65 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(62): Show | 68 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.331+1092T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440836 | ||||||
| chr6:18440891
|
C | CA | 7 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(4): Show | 7 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.331+1158dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440891 | |||||
| chr6:18440891
|
C | CAA | 46 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(43): Show | 46 | HG00408.hp2 HG00423.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.331+1157_331+1158d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440891 | |||||
| chr6:18440891
|
C | CAAA | 64 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(61): Show | 67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+1156_331+1158d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440891 | |||||
| chr6:18440980
|
T | G | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+1236T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440980 | ||||||
| chr6:18441101
|
T | C | 37 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(34): Show | 39 | HG00323.hp1 HG00741.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.331+1357T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441101 | ||||||
| chr6:18441105
|
T | C | 58 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(55): Show | 59 | HG00408.hp2 HG00423.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.331+1361T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441105 | ||||||
| chr6:18441214
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+1470C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441214 | ||||||
| chr6:18441296
|
T | C | 2 | a0001c0001t0015g0347a0001c0001t0015g0348 | 2 | HG00621.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.331+1552T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441296 | ||||||
| chr6:18441331
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+1587T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441331 | ||||||
| chr6:18441377
|
A | G | 64 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(61): Show | 67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+1633A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441377 | ||||||
| chr6:18441393
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(130): Show | 137 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.331+1649G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441393 | ||||||
| chr6:18441575
|
CT | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+1837delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18441575 | |||||
| chr6:18441696
|
T | C | 1 | a0001c0001t0003g0166 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.331+1952T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441696 | ||||||
| chr6:18441723
|
G | T | 1 | a0001c0001t0049g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.331+1979G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441723 | ||||||
| chr6:18441752
|
G | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2008G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441752 | ||||||
| chr6:18441825
|
G | A | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331+2081G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441825 | ||||||
| chr6:18442086
|
G | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2342G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442086 | ||||||
| chr6:18442248
|
G | C | 1 | a0001c0001t0077g0304 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.331+2504G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442248 | ||||||
| chr6:18442259
|
A | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2515A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442259 | ||||||
| chr6:18442325
|
G | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2581G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442325 | ||||||
| chr6:18442366
|
G | A | 1 | a0001c0001t0005g0365 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.331+2622G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442366 | ||||||
| chr6:18442385
|
C | T | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331+2641C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442385 | ||||||
| chr6:18442541
|
T | G | 2 | a0001c0001t0050g0161a0001c0001t0088g0111 | 2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.331+2797T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442541 | ||||||
| chr6:18442554
|
A | G | 1 | a0001c0001t0062g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.331+2810A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442554 | ||||||
| chr6:18442573
|
C | T | 3 | a0001c0001t0010g0243a0001c0001t0076g0371a0001c0001t0105g0063 | 3 | HG00280.hp2 HG00735.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.331+2829C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442573 | ||||||
| chr6:18442617
|
C | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.331+2873C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442617 | ||||||
| chr6:18442723
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2979C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442723 | ||||||
| chr6:18442728
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.331+2984A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442728 | ||||||
| chr6:18442805
|
G | C | 3 | a0001c0001t0016g0076a0001c0001t0043g0140a0001c0001t0043g0141 | 3 | HG01109.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.331+3061G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442805 | ||||||
| chr6:18442969
|
T | C | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.331+3225T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442969 | ||||||
| chr6:18442988
|
G | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3244G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442988 | ||||||
| chr6:18443027
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3283T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443027 | ||||||
| chr6:18443160
|
T | C | 1 | a0001c0001t0031g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.331+3416T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443160 | ||||||
| chr6:18443169
|
G | A | 1 | a0001c0001t0006g0154 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.331+3425G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443169 | ||||||
| chr6:18443290
|
T | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3546T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443290 | ||||||
| chr6:18443316
|
G | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3572G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443316 | ||||||
| chr6:18443326
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.331+3582G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443326 | ||||||
| chr6:18443459
|
A | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3715A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443459 | ||||||
| chr6:18443593
|
G | A | 3 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287 | 3 | HG02109.hp1 HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.331+3849G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443593 | ||||||
| chr6:18443615
|
G | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3871G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443615 | ||||||
| chr6:18443705
|
A | G | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331+3961A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443705 | ||||||
| chr6:18443706
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3962C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443706 | ||||||
| chr6:18443729
|
C | G | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3985C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443729 | ||||||
| chr6:18443828
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.331+4084T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443828 | ||||||
| chr6:18443942
|
A | G | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.331+4198A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443942 | ||||||
| chr6:18444045
|
T | C | 11 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(8): Show | 11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.331+4301T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444045 | ||||||
| chr6:18444151
|
C | T | 1 | a0001c0001t0031g0211 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.331+4407C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444151 | ||||||
| chr6:18444157
|
A | T | 2 | a0001c0001t0018g0271a0001c0001t0018g0283 | 2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.331+4413A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444157 | ||||||
| chr6:18444158
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+4414T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444158 | ||||||
| chr6:18444201
|
G | A | 12 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(9): Show | 13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.331+4457G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444201 | ||||||
| chr6:18444244
|
G | A | 64 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(61): Show | 67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+4500G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444244 | ||||||
| chr6:18444389
|
C | T | 1 | a0001c0001t0019g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.331+4645C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444389 | ||||||
| chr6:18444468
|
T | TG | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.331+4724_331+4725i others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444468 | ||||||
| chr6:18444673
|
T | TA | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+4937dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18444673 | |||||
| chr6:18444703
|
CT | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+4963delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18444703 | |||||
| chr6:18444719
|
A | C | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+4975A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444719 | ||||||
| chr6:18444790
|
C | A | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+5046C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444790 | ||||||
| chr6:18444803
|
T | G | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5059T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444803 | ||||||
| chr6:18444846
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5102C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444846 | ||||||
| chr6:18444877
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5133C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444877 | ||||||
| chr6:18444953
|
A | G | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5209A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444953 | ||||||
| chr6:18444997
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5253C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444997 | ||||||
| chr6:18445016
|
CTTTTAGT others(5): Show |
C | 1 | a0001c0001t0002g0327 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.331+5276_331+5287d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18445016 | |||||
| chr6:18445024
|
G | GT | 39 | a0001c0001t0004g0344a0001c0001t0007g0266a0001c0001t0007g0298others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.331+5287dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18445024 | |||||
| chr6:18445084
|
A | AT | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5347dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18445084 | |||||
| chr6:18445119
|
T | C | 1 | a0001c0001t0003g0186 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.331+5375T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445119 | ||||||
| chr6:18445189
|
C | T | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.331+5445C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445189 | ||||||
| chr6:18445274
|
G | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5530G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445274 | ||||||
| chr6:18445308
|
T | G | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5564T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445308 | ||||||
| chr6:18445351
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(143): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.331+5607G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445351 | ||||||
| chr6:18445519
|
C | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.331+5775C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445519 | ||||||
| chr6:18445563
|
A | G | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.331+5819A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445563 | ||||||
| chr6:18445608
|
T | A | 1 | a0001c0001t0035g0270 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.331+5864T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445608 | ||||||
| chr6:18445661
|
A | G | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5917A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445661 | ||||||
| chr6:18445688
|
G | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(143): Show | 150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.331+5944G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445688 | ||||||
| chr6:18445727
|
C | T | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+5983C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445727 | ||||||
| chr6:18445743
|
A | G | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5999A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445743 | ||||||
| chr6:18445816
|
T | G | 1 | a0001c0001t0008g0034 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.331+6072T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445816 | ||||||
| chr6:18445839
|
C | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+6095C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445839 | ||||||
| chr6:18445863
|
G | T | 12 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(9): Show | 13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.331+6119G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445863 | ||||||
| chr6:18445936
|
A | G | 1 | a0001c0001t0013g0091 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.331+6192A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445936 | ||||||
| chr6:18445982
|
GCACTC | G | 2 | a0001c0001t0010g0228a0001c0001t0051g0006 | 3 | HG02922.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331+6243_331+6247d others(7): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18445982 | |||||
| chr6:18446020
|
T | C | 92 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(89): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.331+6276T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446020 | ||||||
| chr6:18446029
|
A | C | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+6285A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446029 | ||||||
| chr6:18446113
|
G | C | 1 | a0001c0001t0002g0319 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.331+6369G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446113 | ||||||
| chr6:18446145
|
G | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+6401G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446145 | ||||||
| chr6:18446207
|
A | C | 366 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(363): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.331+6463A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446207 | ||||||
| chr6:18446253
|
T | C | 19 | a0001c0001t0011g0001a0001c0001t0011g0321a0001c0001t0011g0324others(16): Show | 21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.331+6509T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446253 | ||||||
| chr6:18446277
|
T | TA | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+6539dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446277 | |||||
| chr6:18446359
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.331+6615T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446359 | ||||||
| chr6:18446516
|
G | A | 82 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(79): Show | 83 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.331+6772G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446516 | ||||||
| chr6:18446530
|
A | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+6786A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446530 | ||||||
| chr6:18446567
|
TACTATGG others(25): Show |
T | 1 | a0001c0001t0008g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331+6824_331+6855d others(34): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446567 | ||||||
| chr6:18446619
|
C | T | 1 | a0001c0001t0008g0034 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.331+6875C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446619 | ||||||
| chr6:18446637
|
A | G | 2 | a0001c0001t0041g0033a0001c0001t0104g0024 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.331+6893A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446637 | ||||||
| chr6:18446735
|
G | A | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+6991G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446735 | ||||||
| chr6:18446739
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(107): Show | 112 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.331+6995C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446739 | ||||||
| chr6:18446746
|
G | T | 5 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(2): Show | 5 | HG01261.hp2 HG02004.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+7002G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446746 | ||||||
| chr6:18446840
|
G | GGT | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(88): Show | 95 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.331+7129_331+7130d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446840
|
G | GGTGT | 20 | a0001c0001t0002g0303a0001c0001t0002g0327a0001c0001t0002g0329others(17): Show | 20 | HG00140.hp1 HG00423.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.331+7127_331+7130d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446840
|
G | GGTGTGT | 11 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0058others(8): Show | 11 | HG01884.hp1 HG02040.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.331+7125_331+7130d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446840
|
G | GGTGTGTG others(9): Show |
2 | a0001c0001t0033g0284a0001c0001t0033g0287 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.331+7115_331+7130d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446840
|
G | GGTGTGTG others(11): Show |
1 | a0001c0001t0033g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.331+7113_331+7130d others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446840
|
GGTGT | G | 9 | a0001c0001t0002g0308a0001c0001t0002g0313a0001c0001t0002g0355others(6): Show | 9 | HG01361.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.331+7127_331+7130d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446840
|
GGTGTGT | G | 15 | a0001c0001t0002g0354a0001c0001t0020g0005a0001c0001t0020g0113others(12): Show | 15 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.331+7125_331+7130d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446840
|
GGTGTGTG others(3): Show |
G | 117 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(114): Show | 120 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.331+7121_331+7130d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446840
|
GGTGTGTG others(5): Show |
G | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+7119_331+7130d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | |||||
| chr6:18446865
|
G | C | 1 | a0001c0001t0008g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331+7121G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446865 | ||||||
| chr6:18447379
|
T | C | 360 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(357): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.331+7635T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447379 | ||||||
| chr6:18447473
|
G | A | 5 | a0001c0001t0002g0308a0001c0001t0002g0313a0001c0001t0002g0354others(2): Show | 5 | NA18940.hp2 NA18965.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+7729G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447473 | ||||||
| chr6:18447521
|
G | A | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.331+7777G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447521 | ||||||
| chr6:18447624
|
G | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.331+7880G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447624 | ||||||
| chr6:18447794
|
G | A | 1 | a0001c0001t0015g0128 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.331+8050G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447794 | ||||||
| chr6:18447853
|
T | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+8109T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447853 | ||||||
| chr6:18447890
|
A | G | 1 | a0001c0001t0002g0340 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.331+8146A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447890 | ||||||
| chr6:18448218
|
G | A | 14 | a0001c0001t0020g0005a0001c0001t0020g0113a0001c0001t0020g0120others(11): Show | 14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+8474G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448218 | ||||||
| chr6:18448290
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+8546T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448290 | ||||||
| chr6:18448317
|
C | T | 1 | a0001c0001t0013g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.331+8573C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448317 | ||||||
| chr6:18448345
|
G | T | 5 | a0001c0001t0009g0292a0001c0001t0013g0014a0001c0001t0013g0082others(2): Show | 5 | HG02280.hp2 HG03209.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+8601G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448345 | ||||||
| chr6:18448598
|
T | C | 37 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(34): Show | 39 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.332-8557T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448598 | ||||||
| chr6:18448672
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-8483T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448672 | ||||||
| chr6:18448680
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.332-8475G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448680 | ||||||
| chr6:18448688
|
G | GCA | 99 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(96): Show | 102 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.332-8439_332-8438d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | |||||
| chr6:18448688
|
G | GCACA | 22 | a0001c0001t0001g0038a0001c0001t0009g0230a0001c0001t0009g0252others(19): Show | 22 | HG00140.hp1 HG00621.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.332-8441_332-8438d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | |||||
| chr6:18448688
|
G | GCACACA | 48 | a0001c0001t0001g0060a0001c0001t0002g0133a0001c0001t0002g0302others(45): Show | 49 | HG00423.hp2 HG01123.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.332-8443_332-8438d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | |||||
| chr6:18448688
|
G | GCACACAC others(1): Show |
10 | a0001c0001t0002g0308a0001c0001t0002g0345a0001c0001t0002g0346others(7): Show | 10 | HG00408.hp2 HG02809.hp2 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-8445_332-8438d others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | |||||
| chr6:18448688
|
G | GCACACAC others(3): Show |
2 | a0001c0001t0010g0228a0001c0001t0051g0006 | 3 | HG02922.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.332-8447_332-8438d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | |||||
| chr6:18448688
|
G | GCACACAC others(5): Show |
1 | a0001c0001t0013g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-8449_332-8438d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | |||||
| chr6:18448688
|
GCA | G | 5 | a0001c0001t0031g0211a0001c0001t0049g0116a0001c0001t0049g0144others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-8439_332-8438d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | |||||
| chr6:18448688
|
GCACACA | G | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.332-8443_332-8438d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | |||||
| chr6:18448716
|
A | ACACACAC others(1): Show |
11 | a0001c0001t0010g0007a0001c0001t0010g0235a0001c0001t0010g0236others(8): Show | 12 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.332-8438_332-8437i others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448716 | |||||
| chr6:18448718
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0072g0275 | 2 | NA19083.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.332-8437C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448718 | ||||||
| chr6:18448785
|
C | T | 1 | a0001c0001t0095g0225 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.332-8370C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448785 | ||||||
| chr6:18448795
|
T | C | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-8360T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448795 | ||||||
| chr6:18448910
|
C | T | 1 | a0001c0001t0014g0356 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.332-8245C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448910 | ||||||
| chr6:18449025
|
T | A | 1 | a0001c0001t0008g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.332-8130T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449025 | ||||||
| chr6:18449269
|
T | C | 1 | a0001c0001t0037g0334 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.332-7886T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449269 | ||||||
| chr6:18449376
|
G | A | 1 | a0001c0001t0002g0330 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.332-7779G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449376 | ||||||
| chr6:18449592
|
T | A | 3 | a0001c0001t0027g0129a0001c0001t0027g0370a0001c0001t0048g0103 | 3 | HG02683.hp2 HG03834.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.332-7563T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449592 | ||||||
| chr6:18449653
|
A | C | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-7502A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449653 | ||||||
| chr6:18449697
|
G | GTA | 87 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(84): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.332-7443_332-7442d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | |||||
| chr6:18449697
|
G | GTATATAT others(3): Show |
17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.332-7451_332-7442d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | |||||
| chr6:18449697
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-7453_332-7442d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | |||||
| chr6:18449697
|
G | GTATATAT others(7): Show |
17 | a0001c0001t0011g0001a0001c0001t0011g0321a0001c0001t0011g0324others(14): Show | 19 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.332-7455_332-7442d others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | |||||
| chr6:18449697
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0025g0276a0001c0001t0025g0280 | 2 | NA18945.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.332-7457_332-7442d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | |||||
| chr6:18449745
|
G | A | 1 | a0001c0001t0010g0237 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.332-7410G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449745 | ||||||
| chr6:18449750
|
C | T | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-7405C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449750 | ||||||
| chr6:18449877
|
G | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-7278G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449877 | ||||||
| chr6:18449968
|
A | C | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.332-7187A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449968 | ||||||
| chr6:18449968
|
A | T | 2 | a0001c0001t0043g0140a0001c0001t0043g0141 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.332-7187A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449968 | ||||||
| chr6:18449986
|
G | A | 1 | a0001c0001t0016g0066 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.332-7169G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449986 | ||||||
| chr6:18449990
|
T | C | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-7165T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449990 | ||||||
| chr6:18450039
|
A | G | 1 | a0001c0001t0009g0250 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.332-7116A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450039 | ||||||
| chr6:18450057
|
T | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-7098T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450057 | ||||||
| chr6:18450078
|
G | A | 3 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287 | 3 | HG02109.hp1 HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.332-7077G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450078 | ||||||
| chr6:18450255
|
C | G | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-6900C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450255 | ||||||
| chr6:18450304
|
G | C | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-6851G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450304 | ||||||
| chr6:18450304
|
G | GT | 26 | a0001c0001t0002g0302a0001c0001t0002g0311a0001c0001t0002g0319others(23): Show | 26 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.332-6839dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18450304 | |||||
| chr6:18450304
|
G | GTT | 19 | a0001c0001t0011g0001a0001c0001t0011g0321a0001c0001t0011g0324others(16): Show | 21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.332-6840_332-6839d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18450304 | |||||
| chr6:18450376
|
C | T | 20 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0007g0234others(17): Show | 20 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.332-6779C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450376 | ||||||
| chr6:18450383
|
C | T | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-6772C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450383 | ||||||
| chr6:18450440
|
C | T | 1 | a0001c0001t0040g0109 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.332-6715C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450440 | ||||||
| chr6:18450450
|
A | G | 4 | a0001c0001t0015g0335a0001c0001t0015g0347a0001c0001t0015g0348others(1): Show | 4 | HG00621.hp2 HG02523.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-6705A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450450 | ||||||
| chr6:18450550
|
C | T | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.332-6605C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450550 | ||||||
| chr6:18450689
|
A | G | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-6466A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450689 | ||||||
| chr6:18450720
|
A | G | 1 | a0002c0004t0078g0317 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.332-6435A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450720 | ||||||
| chr6:18450829
|
C | T | 36 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(33): Show | 38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.332-6326C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450829 | ||||||
| chr6:18450897
|
A | T | 1 | a0001c0001t0008g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.332-6258A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450897 | ||||||
| chr6:18451022
|
A | G | 14 | a0001c0001t0020g0005a0001c0001t0020g0113a0001c0001t0020g0120others(11): Show | 14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-6133A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451022 | ||||||
| chr6:18451266
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(92): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.332-5889G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451266 | ||||||
| chr6:18451326
|
T | A | 1 | a0001c0001t0006g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.332-5829T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451326 | ||||||
| chr6:18451501
|
T | C | 13 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(10): Show | 13 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-5654T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451501 | ||||||
| chr6:18451519
|
G | T | 1 | a0001c0001t0008g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.332-5636G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451519 | ||||||
| chr6:18451554
|
A | C | 1 | a0001c0001t0003g0191 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.332-5601A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451554 | ||||||
| chr6:18451732
|
C | T | 1 | a0001c0001t0002g0350 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.332-5423C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451732 | ||||||
| chr6:18451760
|
T | G | 1 | a0001c0001t0002g0355 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.332-5395T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451760 | ||||||
| chr6:18451771
|
A | T | 1 | a0001c0001t0008g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.332-5384A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451771 | ||||||
| chr6:18451888
|
G | A | 1 | a0001c0001t0047g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.332-5267G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451888 | ||||||
| chr6:18452004
|
A | C | 2 | a0001c0001t0027g0305a0001c0001t0027g0364 | 2 | HG01243.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.332-5151A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452004 | ||||||
| chr6:18452023
|
T | G | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-5132T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452023 | ||||||
| chr6:18452135
|
A | C | 1 | a0001c0001t0003g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.332-5020A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452135 | ||||||
| chr6:18452380
|
T | C | 1 | a0001c0001t0081g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332-4775T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452380 | ||||||
| chr6:18452387
|
C | T | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-4768C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452387 | ||||||
| chr6:18452423
|
G | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-4732G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452423 | ||||||
| chr6:18452504
|
G | A | 1 | a0001c0001t0048g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.332-4651G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452504 | ||||||
| chr6:18452650
|
A | T | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-4505A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452650 | ||||||
| chr6:18452659
|
T | A | 1 | a0001c0001t0013g0036 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.332-4496T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452659 | ||||||
| chr6:18452739
|
TA | T | 5 | a0001c0001t0002g0308a0001c0001t0002g0313a0001c0001t0002g0354others(2): Show | 5 | NA18940.hp2 NA18965.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-4414delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18452739 | |||||
| chr6:18452952
|
T | A | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-4203T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452952 | ||||||
| chr6:18453029
|
G | T | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-4126G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453029 | ||||||
| chr6:18453124
|
CTCTT | C | 19 | a0001c0001t0011g0001a0001c0001t0011g0321a0001c0001t0011g0324others(16): Show | 21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.332-4027_332-4024d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453124 | |||||
| chr6:18453137
|
C | CT | 68 | a0001c0001t0002g0329a0001c0001t0006g0187a0001c0001t0007g0266others(65): Show | 70 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.332-3999dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | |||||
| chr6:18453137
|
C | CTT | 64 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(61): Show | 65 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.332-4000_332-3999d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | |||||
| chr6:18453137
|
C | CTTT | 15 | a0001c0001t0003g0184a0001c0001t0005g0306a0001c0001t0005g0310others(12): Show | 15 | HG00438.hp1 HG01255.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-4001_332-3999d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | |||||
| chr6:18453137
|
CT | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(90): Show | 95 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.332-3999delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | |||||
| chr6:18453137
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0041g0033a0001c0001t0104g0024 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.332-4009_332-3999d others(13): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | |||||
| chr6:18453359
|
G | A | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-3796G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453359 | ||||||
| chr6:18453385
|
G | A | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-3770G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453385 | ||||||
| chr6:18453386
|
C | T | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-3769C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453386 | ||||||
| chr6:18453422
|
G | A | 1 | a0001c0001t0017g0029 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.332-3733G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453422 | ||||||
| chr6:18453430
|
A | C | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-3725A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453430 | ||||||
| chr6:18453538
|
C | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(92): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.332-3617C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453538 | ||||||
| chr6:18453588
|
T | C | 1 | a0001c0001t0062g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332-3567T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453588 | ||||||
| chr6:18453658
|
G | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(92): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.332-3497G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453658 | ||||||
| chr6:18453669
|
G | A | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.332-3486G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453669 | ||||||
| chr6:18453790
|
G | A | 1 | a0001c0001t0033g0286 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.332-3365G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453790 | ||||||
| chr6:18453851
|
T | A | 1 | a0001c0001t0085g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.332-3304T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453851 | ||||||
| chr6:18453932
|
A | G | 17 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0012g0183others(14): Show | 17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.332-3223A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453932 | ||||||
| chr6:18454060
|
C | G | 2 | a0001c0001t0006g0156a0001c0001t0018g0269 | 2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.332-3095C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454060 | ||||||
| chr6:18454096
|
T | G | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-3059T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454096 | ||||||
| chr6:18454179
|
T | C | 1 | a0001c0001t0008g0028 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.332-2976T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454179 | ||||||
| chr6:18454264
|
T | C | 1 | a0001c0001t0004g0367 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.332-2891T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454264 | ||||||
| chr6:18454294
|
G | T | 1 | a0001c0001t0004g0332 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.332-2861G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454294 | ||||||
| chr6:18454354
|
A | G | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-2801A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454354 | ||||||
| chr6:18454574
|
A | T | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-2581A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454574 | ||||||
| chr6:18454612
|
T | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(267): Show | 276 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.332-2543T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454612 | ||||||
| chr6:18454640
|
T | C | 1 | a0001c0001t0004g0130 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.332-2515T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454640 | ||||||
| chr6:18454654
|
G | A | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-2501G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454654 | ||||||
| chr6:18454660
|
T | TGCCATAG others(9): Show |
1 | a0001c0001t0013g0083 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-2478_332-2463d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18454660 | |||||
| chr6:18454738
|
T | G | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-2417T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454738 | ||||||
| chr6:18454814
|
G | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-2341G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454814 | ||||||
| chr6:18455093
|
A | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(144): Show | 151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.332-2062A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455093 | ||||||
| chr6:18455316
|
A | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(92): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.332-1839A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455316 | ||||||
| chr6:18455342
|
T | A | 2 | a0001c0001t0092g0179a0001c0001t0093g0178 | 2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.332-1813T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455342 | ||||||
| chr6:18455383
|
G | C | 82 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(79): Show | 83 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.332-1772G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455383 | ||||||
| chr6:18455404
|
G | A | 1 | a0001c0001t0013g0091 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.332-1751G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455404 | ||||||
| chr6:18455610
|
C | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-1545C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455610 | ||||||
| chr6:18455683
|
G | C | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-1472G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455683 | ||||||
| chr6:18455710
|
G | A | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-1445G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455710 | ||||||
| chr6:18455730
|
G | C | 1 | a0001c0001t0010g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.332-1425G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455730 | ||||||
| chr6:18455750
|
CA | C | 10 | a0001c0001t0003g0163a0001c0001t0003g0184a0001c0001t0003g0190others(7): Show | 10 | HG00558.hp2 NA18942.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-1402delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18455750 | |||||
| chr6:18455771
|
G | T | 1 | a0001c0001t0045g0258 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.332-1384G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455771 | ||||||
| chr6:18455814
|
A | C | 10 | a0001c0001t0003g0163a0001c0001t0003g0184a0001c0001t0003g0190others(7): Show | 10 | HG00558.hp2 NA18942.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-1341A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455814 | ||||||
| chr6:18456124
|
C | G | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-1031C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456124 | ||||||
| chr6:18456164
|
C | T | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.332-991C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456164 | ||||||
| chr6:18456190
|
G | A | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-965G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456190 | ||||||
| chr6:18456390
|
A | G | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-765A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456390 | ||||||
| chr6:18456587
|
C | T | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-568C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456587 | ||||||
| chr6:18456610
|
A | T | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.332-545A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456610 | ||||||
| chr6:18456732
|
G | C | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.332-423G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456732 | ||||||
| chr6:18456779
|
G | A | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-376G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456779 | ||||||
| chr6:18456839
|
G | A | 2 | a0001c0001t0034g0272a0001c0001t0059g0142 | 2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.332-316G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456839 | ||||||
| chr6:18456890
|
T | C | 39 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(36): Show | 41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-265T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456890 | ||||||
| chr6:18456996
|
G | A | 13 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(10): Show | 13 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-159G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456996 | ||||||
| chr6:18457022
|
C | T | 1 | a0001c0001t0101g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.332-133C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18457022 | ||||||
| chr6:18457024
|
G | C | 2 | a0001c0001t0039g0146a0001c0001t0039g0149 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.332-131G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18457024 | ||||||
| chr6:18457463
|
G | A | 1 | a0001c0001t0030g0213 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.536+104G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457463 | ||||||
| chr6:18457543
|
C | A | 38 | a0001c0001t0007g0266a0001c0001t0007g0298a0001c0001t0011g0001others(35): Show | 40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.536+184C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457543 | ||||||
| chr6:18457560
|
A | T | 1 | a0001c0001t0008g0037 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.536+201A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457560 | ||||||
| chr6:18457587
|
G | A | 1 | a0001c0001t0034g0231 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.536+228G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457587 | ||||||
| chr6:18457606
|
G | T | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.536+247G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457606 | ||||||
| chr6:18457660
|
C | A | 360 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(357): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.536+301C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457660 | ||||||
| chr6:18457801
|
A | G | 1 | a0001c0001t0096g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.536+442A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457801 | ||||||
| chr6:18457896
|
A | G | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.536+537A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457896 | ||||||
| chr6:18457930
|
G | GT | 17 | a0001c0001t0005g0358a0001c0001t0007g0240a0001c0001t0008g0032others(14): Show | 17 | HG01243.hp1 HG01515.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.536+580dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 18457930 | |||||
| chr6:18457935
|
T | G | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.536+576T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457935 | ||||||
| chr6:18457940
|
G | T | 1 | a0001c0001t0103g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.536+581G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457940 | ||||||
| chr6:18458014
|
T | A | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.536+655T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458014 | ||||||
| chr6:18458030
|
T | C | 187 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(184): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.536+671T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458030 | ||||||
| chr6:18458063
|
G | A | 1 | a0001c0001t0008g0028 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.536+704G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458063 | ||||||
| chr6:18458125
|
A | T | 1 | a0001c0001t0023g0025 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.536+766A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458125 | ||||||
| chr6:18458263
|
G | A | 3 | a0001c0001t0003g0163a0001c0001t0003g0190a0001c0001t0003g0192 | 3 | HG00558.hp2 NA19004.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.536+904G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458263 | ||||||
| chr6:18458305
|
T | C | 14 | a0001c0001t0014g0135a0001c0001t0014g0357a0001c0001t0026g0262others(11): Show | 14 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.536+946T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458305 | ||||||
| chr6:18458356
|
T | C | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.536+997T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458356 | ||||||
| chr6:18458406
|
C | T | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.536+1047C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458406 | ||||||
| chr6:18458446
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.536+1087T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458446 | ||||||
| chr6:18458530
|
C | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(108): Show | 113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.537-1077C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458530 | ||||||
| chr6:18458541
|
A | G | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-1066A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458541 | ||||||
| chr6:18458567
|
C | T | 12 | a0001c0001t0003g0164a0001c0001t0003g0166a0001c0001t0003g0203others(9): Show | 12 | HG00621.hp1 HG02040.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.537-1040C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458567 | ||||||
| chr6:18458980
|
A | C | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-627A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458980 | ||||||
| chr6:18459029
|
C | G | 10 | a0001c0001t0009g0292a0001c0001t0013g0014a0001c0001t0013g0082others(7): Show | 10 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.537-578C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459029 | ||||||
| chr6:18459088
|
T | TCACCTAT others(10): Show |
3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-516_537-515ins others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 18459088 | |||||
| chr6:18459093
|
C | G | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.537-514C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459093 | ||||||
| chr6:18459168
|
G | A | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.537-439G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459168 | ||||||
| chr6:18459191
|
A | G | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.537-416A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459191 | ||||||
| chr6:18459250
|
G | A | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-357G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459250 | ||||||
| chr6:18459255
|
A | T | 1 | a0001c0001t0012g0175 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.537-352A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459255 | ||||||
| chr6:18459269
|
G | A | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-338G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459269 | ||||||
| chr6:18459395
|
G | GTAAT | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.537-209_537-206dup others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 18459395 | |||||
| chr6:18459449
|
G | A | 1 | a0001c0001t0065g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.537-158G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459449 | ||||||
| chr6:18459505
|
A | C | 91 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(88): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.537-102A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459505 | ||||||
| chr6:18459972
|
T | A | 96 | a0001c0001t0003g0152a0001c0001t0003g0163a0001c0001t0003g0164others(93): Show | 97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.681+221T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18459972 | ||||||
| chr6:18460088
|
C | A | 1 | a0001c0001t0047g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.681+337C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460088 | ||||||
| chr6:18460096
|
T | C | 1 | a0001c0001t0003g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.681+345T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460096 | ||||||
| chr6:18460257
|
A | G | 1 | a0001c0001t0058g0227 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.681+506A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460257 | ||||||
| chr6:18460346
|
G | A | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.681+595G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460346 | ||||||
| chr6:18460365
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(93): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.681+614A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460365 | ||||||
| chr6:18460505
|
A | T | 6 | a0001c0001t0007g0232a0001c0001t0007g0244a0001c0001t0007g0245others(3): Show | 6 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+754A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460505 | ||||||
| chr6:18460581
|
C | T | 1 | a0001c0001t0057g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.681+830C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460581 | ||||||
| chr6:18460588
|
C | A | 1 | a0001c0001t0001g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.681+837C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460588 | ||||||
| chr6:18460611
|
T | C | 1 | a0001c0001t0016g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.681+860T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460611 | ||||||
| chr6:18460614
|
A | G | 360 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(357): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.681+863A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460614 | ||||||
| chr6:18460753
|
T | C | 360 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(357): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.681+1002T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460753 | ||||||
| chr6:18460800
|
TA | T | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.681+1054delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 18460800 | |||||
| chr6:18460865
|
G | T | 1 | a0001c0001t0037g0339 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.681+1114G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460865 | ||||||
| chr6:18460890
|
A | T | 5 | a0001c0001t0016g0046a0001c0001t0016g0048a0001c0001t0016g0049others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+1139A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460890 | ||||||
| chr6:18460927
|
A | C | 13 | a0001c0001t0033g0284a0001c0001t0033g0286a0001c0001t0033g0287others(10): Show | 13 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.681+1176A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460927 | ||||||
| chr6:18461113
|
T | C | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.681+1362T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461113 | ||||||
| chr6:18461233
|
G | T | 2 | a0001c0001t0066g0285a0001c0001t0083g0123 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.681+1482G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461233 | ||||||
| chr6:18461236
|
C | T | 2 | a0001c0001t0015g0128a0001c0001t0015g0137 | 2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.681+1485C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461236 | ||||||
| chr6:18461302
|
A | G | 2 | a0001c0001t0053g0204a0001c0001t0053g0205 | 2 | HG00423.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.681+1551A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461302 | ||||||
| chr6:18461590
|
C | T | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.682-1701C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461590 | ||||||
| chr6:18461622
|
G | T | 1 | a0001c0001t0015g0374 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.682-1669G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461622 | ||||||
| chr6:18461761
|
G | A | 2 | a0001c0001t0058g0227a0001c0001t0065g0289 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.682-1530G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461761 | ||||||
| chr6:18461854
|
G | A | 26 | a0001c0001t0006g0153a0001c0001t0006g0154a0001c0001t0006g0155others(23): Show | 27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.682-1437G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461854 | ||||||
| chr6:18461867
|
A | G | 1 | a0001c0001t0081g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.682-1424A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461867 | ||||||
| chr6:18461871
|
A | G | 2 | a0001c0001t0019g0145a0001c0001t0057g0229 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.682-1420A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461871 | ||||||
| chr6:18461940
|
G | GGTGTAGT others(8): Show |
1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1350_682-1349i others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 18461940 | |||||
| chr6:18461956
|
A | T | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1335A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461956 | ||||||
| chr6:18462022
|
T | C | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1269T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462022 | ||||||
| chr6:18462024
|
C | T | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1267C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462024 | ||||||
| chr6:18462027
|
T | G | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1264T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462027 | ||||||
| chr6:18462028
|
C | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1263C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462028 | ||||||
| chr6:18462037
|
T | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1254T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462037 | ||||||
| chr6:18462057
|
T | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1234T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462057 | ||||||
| chr6:18462058
|
C | T | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1233C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462058 | ||||||
| chr6:18462059
|
T | C | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1232T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462059 | ||||||
| chr6:18462061
|
A | T | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1230A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462061 | ||||||
| chr6:18462069
|
C | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1222C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462069 | ||||||
| chr6:18462071
|
T | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1220T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462071 | ||||||
| chr6:18462071
|
T | C | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.682-1220T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462071 | ||||||
| chr6:18462078
|
G | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1213G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462078 | ||||||
| chr6:18462082
|
G | T | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1209G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462082 | ||||||
| chr6:18462083
|
T | C | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1208T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462083 | ||||||
| chr6:18462084
|
G | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1207G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462084 | ||||||
| chr6:18462087
|
A | G | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1204A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462087 | ||||||
| chr6:18462088
|
C | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1203C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462088 | ||||||
| chr6:18462089
|
A | G | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1202A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462089 | ||||||
| chr6:18462092
|
T | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1199T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462092 | ||||||
| chr6:18462094
|
A | C | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1197A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462094 | ||||||
| chr6:18462114
|
T | G | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1177T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462114 | ||||||
| chr6:18462125
|
T | A | 359 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(356): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.682-1166T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462125 | ||||||
| chr6:18462145
|
C | T | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1146C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462145 | ||||||
| chr6:18462146
|
T | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1145T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462146 | ||||||
| chr6:18462147
|
A | C | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1144A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462147 | ||||||
| chr6:18462150
|
T | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1141T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462150 | ||||||
| chr6:18462152
|
T | A | 1 | a0001c0001t0009g0254 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1139T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462152 | ||||||
| chr6:18462261
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.682-1030G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462261 | ||||||
| chr6:18462457
|
C | T | 3 | a0001c0001t0016g0087a0001c0001t0058g0227a0001c0001t0065g0289 | 3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.682-834C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462457 | ||||||
| chr6:18462560
|
C | T | 1 | a0001c0001t0004g0009 | 2 | NA18971.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.682-731C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462560 | ||||||
| chr6:18462622
|
T | C | 1 | a0001c0001t0004g0367 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.682-669T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462622 | ||||||
| chr6:18462648
|
C | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(105): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.682-643C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462648 | ||||||
| chr6:18462662
|
G | GT | 135 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(132): Show | 138 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.682-616dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 18462662 | |||||
| chr6:18462697
|
A | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(320): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.682-594A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462697 | ||||||
| chr6:18462848
|
G | C | 1 | a0001c0001t0005g0342 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.682-443G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462848 | ||||||
| chr6:18462879
|
C | T | 1 | a0001c0001t0039g0173 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.682-412C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462879 | ||||||
| chr6:18463012
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.682-279G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463012 | ||||||
| chr6:18463034
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.682-257A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463034 | ||||||
| chr6:18463040
|
T | A | 75 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(72): Show | 76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.682-251T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463040 | ||||||
| chr6:18463056
|
C | CT | 96 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(93): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.682-226dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 18463056 | |||||
| chr6:18463063
|
T | A | 2 | a0001c0001t0091g0215a0001c0001t0099g0084 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.682-228T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463063 | ||||||
| chr6:18463129
|
C | G | 185 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(182): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.682-162C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463129 | ||||||
| chr6:18463155
|
G | T | 2 | a0001c0001t0002g0133a0001c0001t0002g0314 | 2 | HG02738.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.682-136G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463155 | ||||||
| chr6:18463402
|
C | T | 90 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(87): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.771+22C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463402 | ||||||
| chr6:18463592
|
A | G | 362 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0015others(359): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.771+212A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463592 | ||||||
| chr6:18463718
|
A | G | 1 | a0001c0001t0015g0374 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.771+338A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463718 | ||||||
| chr6:18463719
|
G | A | 20 | a0001c0001t0011g0001a0001c0001t0011g0312a0001c0001t0011g0321others(17): Show | 22 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.771+339G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463719 | ||||||
| chr6:18463968
|
G | A | 2 | a0001c0001t0066g0285a0001c0001t0083g0123 | 2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.771+588G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463968 | ||||||
| chr6:18464320
|
C | T | 1 | a0001c0001t0004g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.772-607C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18464320 | ||||||
| chr6:18464417
|
G | T | 76 | a0001c0001t0002g0133a0001c0001t0002g0302a0001c0001t0002g0303others(73): Show | 78 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.772-510G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18464417 | ||||||
| chr6:18464676
|
A | C | 1 | a0001c0001t0005g0341 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.772-251A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18464676 | ||||||
| chr6:18464878
|
A | C | 1 | a0001c0001t0047g0132 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.772-49A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18464878 |