| geneid | 64919 |
|---|---|
| ensemblid | ENSG00000127152.18 |
| hgncid | 13222 |
| symbol | BCL11B |
| name | BCL11 transcription factor B |
| refseq_nuc | NM_138576.4 |
| refseq_prot | NP_612808.1 |
| ensembl_nuc | ENST00000357195.8 |
| ensembl_prot | ENSP00000349723.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 99169287 |
| end | 99272197 |
| strand | - |
| ver | v1.2 |
| region | chr14:99169287-99272197 |
| region5000 | chr14:99164287-99277197 |
| regionname0 | BCL11B_chr14_99169287_99272197 |
| regionname5000 | BCL11B_chr14_99164287_99277197 |
| 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 | 894 | 347 | 94 | 70 | 124 | 12 | 45 | 94 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0002 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0003 | 0/0 | 894 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0004 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| 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 | 2685 | 249 | 66 | 50 | 88 | 8 | 35 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0002 | 0/0 | 2685 | 84 | 20 | 17 | 35 | 4 | 8 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0003 | 0/0 | 2685 | 6 | 1 | 3 | 0 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0004 | 0/0 | 2685 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0005 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0006 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0007 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0008 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0009 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| c0010 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| 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 | 0/1 | 5845 | 62 | 6 | 8 | 37 | 2 | 8 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0002 | 1/0 | 5844 | 37 | 9 | 6 | 15 | 2 | 4 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0003 | 0/0 | 5846 | 34 | 6 | 6 | 15 | 0 | 7 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0004 | 0/0 | 5845 | 23 | 6 | 5 | 9 | 1 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0005 | 0/0 | 5846 | 19 | 1 | 5 | 7 | 1 | 5 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0006 | 0/0 | 5855 | 18 | 0 | 9 | 0 | 3 | 6 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0007 | 0/0 | 5847 | 14 | 0 | 6 | 5 | 0 | 3 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0008 | 0/0 | 5843 | 9 | 9 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0009 | 0/0 | 5845 | 9 | 9 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0010 | 0/0 | 5856 | 9 | 0 | 5 | 1 | 1 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0011 | 0/0 | 5846 | 6 | 1 | 1 | 3 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0012 | 0/0 | 5850 | 5 | 0 | 0 | 5 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0013 | 0/0 | 5857 | 5 | 0 | 4 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0014 | 0/0 | 5844 | 4 | 4 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0015 | 0/0 | 5846 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0016 | 0/0 | 5845 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0017 | 0/0 | 5848 | 3 | 1 | 1 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0018 | 0/0 | 5831 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0019 | 0/0 | 5845 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0020 | 0/0 | 5845 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0021 | 0/0 | 5837 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0022 | 0/0 | 5852 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0023 | 0/0 | 5847 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0024 | 0/0 | 5846 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0025 | 0/0 | 5846 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0026 | 0/0 | 5847 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0027 | 0/0 | 5848 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0028 | 0/0 | 5847 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0029 | 0/0 | 5856 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0030 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0031 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0032 | 0/0 | 5842 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0033 | 0/0 | 5844 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0034 | 0/0 | 5844 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0035 | 0/0 | 5845 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0036 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0037 | 0/0 | 5844 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0038 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0039 | 0/0 | 5802 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0040 | 0/0 | 5844 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0041 | 0/0 | 5844 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0042 | 0/0 | 5844 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0043 | 0/0 | 5844 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0044 | 0/0 | 5845 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0045 | 0/0 | 5845 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0046 | 0/0 | 5845 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0047 | 0/0 | 5845 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0048 | 0/0 | 5844 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0049 | 0/0 | 5845 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0050 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0051 | 0/0 | 5845 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0052 | 0/0 | 5847 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0053 | 0/0 | 5853 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0054 | 0/0 | 5853 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0055 | 0/0 | 5854 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0056 | 0/0 | 5855 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0057 | 0/0 | 5836 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0058 | 0/0 | 5851 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0059 | 0/0 | 5817 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0060 | 0/0 | 5845 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0061 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0062 | 0/0 | 5845 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0063 | 0/0 | 5845 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0064 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0065 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0066 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0067 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0068 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0069 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0070 | 0/0 | 5847 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0071 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0072 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0073 | 0/0 | 5847 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0074 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0075 | 0/0 | 5866 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0076 | 0/0 | 5867 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0077 | 0/0 | 5845 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0078 | 0/0 | 5847 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0079 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0080 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0081 | 0/0 | 5856 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0082 | 0/0 | 5856 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0083 | 0/0 | 5856 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0084 | 0/0 | 5856 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0085 | 0/0 | 5856 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0086 | 0/0 | 5868 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0087 | 0/0 | 5867 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0088 | 0/0 | 5845 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0089 | 0/0 | 5845 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0090 | 0/0 | 5846 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0091 | 0/0 | 5845 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| t0092 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| 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 | 2685 | 249 | 66 | 50 | 88 | 8 | 35 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002 | 0/0 | 2685 | 84 | 20 | 17 | 35 | 4 | 8 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0003 | 0/0 | 2685 | 6 | 1 | 3 | 0 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0004 | 0/0 | 2685 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0005 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0006 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0008 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0002c0009 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0003c0007 | 0/0 | 2685 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0004c0010 | 0/0 | 2685 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8529 | 58 | 3 | 8 | 36 | 2 | 8 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0002 | 1/0 | 8528 | 37 | 9 | 6 | 15 | 2 | 4 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0003 | 0/0 | 8530 | 5 | 1 | 1 | 0 | 0 | 3 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0004 | 0/0 | 8529 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0005 | 0/0 | 8530 | 18 | 1 | 5 | 7 | 0 | 5 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0006 | 0/0 | 8539 | 18 | 0 | 9 | 0 | 3 | 6 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0007 | 0/0 | 8531 | 10 | 0 | 4 | 4 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0008 | 0/0 | 8527 | 9 | 9 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0009 | 0/0 | 8529 | 7 | 7 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0011 | 0/0 | 8530 | 6 | 1 | 1 | 3 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0012 | 0/0 | 8534 | 5 | 0 | 0 | 5 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0013 | 0/0 | 8541 | 5 | 0 | 4 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0014 | 0/0 | 8528 | 4 | 4 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0015 | 0/0 | 8530 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0016 | 0/0 | 8529 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0017 | 0/0 | 8532 | 2 | 0 | 1 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0020 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0022 | 0/0 | 8536 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0023 | 0/0 | 8531 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0024 | 0/0 | 8530 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0026 | 0/0 | 8531 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0027 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0029 | 0/0 | 8540 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0030 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0031 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0032 | 0/0 | 8526 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0034 | 0/0 | 8528 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0035 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0036 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0037 | 0/0 | 8528 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0038 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0039 | 0/0 | 8486 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0040 | 0/0 | 8528 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0041 | 0/0 | 8528 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0042 | 0/0 | 8528 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0043 | 0/0 | 8528 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0048 | 0/0 | 8528 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0050 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0051 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0052 | 0/0 | 8531 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0053 | 0/0 | 8537 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0054 | 0/0 | 8537 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0056 | 0/0 | 8539 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0058 | 0/0 | 8535 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0059 | 0/0 | 8501 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0060 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0061 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0062 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0063 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0069 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0070 | 0/0 | 8531 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0071 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0072 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0074 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0075 | 0/0 | 8550 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0076 | 0/0 | 8551 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0077 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0078 | 0/0 | 8531 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0080 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0081 | 0/0 | 8540 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0084 | 0/0 | 8540 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0085 | 0/0 | 8540 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0086 | 0/0 | 8552 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0087 | 0/0 | 8551 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0090 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0091 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0001t0092 | 0/0 | 8518 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0001 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0003 | 0/0 | 8530 | 26 | 5 | 5 | 14 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0004 | 0/0 | 8529 | 21 | 5 | 4 | 9 | 1 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0005 | 0/0 | 8530 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0007 | 0/0 | 8531 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0010 | 0/0 | 8540 | 7 | 0 | 3 | 1 | 1 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0017 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0018 | 0/0 | 8515 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0019 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0021 | 0/0 | 8521 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0028 | 0/0 | 8531 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0033 | 0/0 | 8528 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0044 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0046 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0047 | 0/0 | 8529 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0049 | 0/0 | 8529 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0057 | 0/0 | 8520 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0064 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0065 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0066 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0067 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0068 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0073 | 0/0 | 8531 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0079 | 0/0 | 8530 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0082 | 0/0 | 8540 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0083 | 0/0 | 8540 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0088 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0002t0089 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0003t0003 | 0/0 | 8530 | 2 | 0 | 0 | 0 | 0 | 2 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0003t0004 | 0/0 | 8529 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0003t0010 | 0/0 | 8540 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0003t0055 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0004t0001 | 0/0 | 8529 | 3 | 3 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0005t0009 | 0/0 | 8529 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0006t0025 | 0/0 | 8530 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0001c0008t0045 | 0/0 | 8529 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0002c0009t0003 | 0/0 | 8530 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0003c0007t0007 | 0/0 | 8531 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| a0004c0010t0007 | 0/0 | 8531 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | copy fasta | chr14 | 99164287 | 99277197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0002g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0011g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0011g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0011g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0011g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0011g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0012g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0012g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0012g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0012g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0013g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0013g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0013g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0013g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0013g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0014g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0014g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0015g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0015g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0015g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0016g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0016g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0017g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0017g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0020g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0022g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0022g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0023g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0023g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0024g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0026g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0026g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0027g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0027g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0029g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0029g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0030g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0031g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0032g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0034g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0035g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0036g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0037g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0038g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0039g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0040g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0041g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0042g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0043g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0048g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0050g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0051g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0052g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0053g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0054g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0056g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0058g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0059g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0060g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0061g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0062g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0063g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0069g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0070g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0071g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0072g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0074g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0075g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0076g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0077g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0078g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0080g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0081g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0084g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0085g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0086g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0087g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0090g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0091g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0001t0092g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0007g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0010g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0010g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0010g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0010g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0010g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0010g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0010g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0017g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0018g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0018g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0019g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0021g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0021g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0028g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0028g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0033g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0044g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0046g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0047g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0049g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0057g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0064g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0065g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0066g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0067g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0068g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0073g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0079g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0082g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0083g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0088g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0002t0089g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0003t0010g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0003t0010g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0003t0055g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0004t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0005t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0005t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0006t0025g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0006t0025g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0001c0008t0045g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0002c0009t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0003c0007t0007g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| a0004c0010t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0084 | g0308 | EUR | GBR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0321 | EUR | GBR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0310 | EUR | GBR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | GBR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0002 | EUR | FIN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00280 | hp2 | a0001 | c0002 | t0005 | g0103 | EUR | FIN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0197 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00438 | hp2 | a0001 | c0001 | t0042 | g0072 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0121 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0250 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00621 | hp1 | a0001 | c0001 | t0017 | g0304 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00621 | hp2 | a0001 | c0001 | t0080 | g0303 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00639 | hp1 | a0001 | c0002 | t0018 | g0011 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00639 | hp2 | a0001 | c0002 | t0049 | g0057 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00642 | hp2 | a0001 | c0002 | t0018 | g0012 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | CHS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00733 | hp1 | a0001 | c0001 | t0039 | g0038 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00733 | hp2 | a0001 | c0001 | t0011 | g0295 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0316 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00738 | hp1 | a0001 | c0001 | t0026 | g0251 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0037 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00741 | hp1 | a0001 | c0001 | t0054 | g0138 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0338 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0317 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01070 | hp1 | a0001 | c0002 | t0010 | g0325 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01070 | hp2 | a0001 | c0001 | t0029 | g0322 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0332 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01071 | hp2 | a0001 | c0001 | t0029 | g0314 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0066 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0329 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0268 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01099 | hp1 | a0001 | c0001 | t0043 | g0120 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0335 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0152 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01168 | hp1 | a0001 | c0002 | t0010 | g0333 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01168 | hp2 | a0001 | c0002 | t0007 | g0256 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01169 | hp1 | a0001 | c0002 | t0007 | g0255 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01175 | hp2 | a0001 | c0001 | t0056 | g0136 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01192 | hp1 | a0001 | c0001 | t0026 | g0277 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0319 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0239 | AMR | PUR | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0257 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01257 | hp1 | a0001 | c0003 | t0010 | g0309 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0312 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01261 | hp1 | a0001 | c0001 | t0013 | g0339 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01261 | hp2 | a0001 | c0002 | t0004 | g0031 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0033 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01433 | hp2 | a0001 | c0003 | t0055 | g0135 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0220 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01496 | hp2 | a0001 | c0001 | t0013 | g0334 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | IBS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01517 | hp1 | a0001 | c0002 | t0047 | g0015 | EUR | IBS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | IBS | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01884 | hp1 | a0001 | c0002 | t0067 | g0177 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01884 | hp2 | a0001 | c0001 | t0070 | g0171 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01891 | hp1 | a0001 | c0002 | t0046 | g0014 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01891 | hp2 | a0001 | c0001 | t0034 | g0005 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01934 | hp2 | a0001 | c0002 | t0004 | g0075 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0201 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01943 | hp2 | a0001 | c0003 | t0010 | g0313 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01952 | hp1 | a0001 | c0001 | t0085 | g0340 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0215 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0206 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01975 | hp2 | a0001 | c0001 | t0081 | g0311 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0154 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02004 | hp2 | a0001 | c0002 | t0010 | g0318 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0249 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02027 | hp1 | a0001 | c0002 | t0004 | g0034 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02027 | hp2 | a0001 | c0001 | t0011 | g0298 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02055 | hp1 | a0001 | c0002 | t0088 | g0344 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0264 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02056 | hp1 | a0001 | c0002 | t0028 | g0293 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02056 | hp2 | a0001 | c0001 | t0063 | g0153 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02071 | hp2 | a0001 | c0002 | t0028 | g0297 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02145 | hp2 | a0001 | c0001 | t0048 | g0096 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02148 | hp1 | a0001 | c0001 | t0013 | g0331 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CDX | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02257 | hp1 | a0001 | c0001 | t0090 | g0346 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02257 | hp2 | a0001 | c0002 | t0017 | g0300 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0175 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02258 | hp2 | a0001 | c0001 | t0027 | g0230 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0119 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02451 | hp1 | a0001 | c0001 | t0036 | g0007 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0064 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0050 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02602 | hp2 | a0001 | c0001 | t0076 | g0289 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0079 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02615 | hp2 | a0001 | c0001 | t0016 | g0073 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0286 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02630 | hp1 | a0001 | c0002 | t0089 | g0345 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02630 | hp2 | a0001 | c0002 | t0068 | g0170 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0260 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02683 | hp1 | a0001 | c0001 | t0075 | g0288 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0078 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0076 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02698 | hp2 | a0001 | c0002 | t0082 | g0336 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02723 | hp1 | a0001 | c0001 | t0016 | g0030 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0123 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0169 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02809 | hp1 | a0001 | c0001 | t0024 | g0226 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0301 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02886 | hp2 | a0001 | c0005 | t0009 | g0029 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0001 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0001 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02896 | hp2 | a0001 | c0006 | t0025 | g0192 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0179 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02897 | hp2 | a0001 | c0006 | t0025 | g0191 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02922 | hp2 | a0001 | c0001 | t0077 | g0290 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02965 | hp1 | a0001 | c0001 | t0050 | g0108 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0060 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02976 | hp1 | a0001 | c0001 | t0051 | g0082 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0131 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03017 | hp2 | a0001 | c0002 | t0010 | g0320 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03041 | hp1 | a0001 | c0001 | t0072 | g0166 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03041 | hp2 | a0001 | c0001 | t0078 | g0291 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03098 | hp1 | a0001 | c0001 | t0027 | g0165 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0090 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03130 | hp1 | a0001 | c0002 | t0079 | g0292 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03130 | hp2 | a0001 | c0001 | t0071 | g0187 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0099 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03139 | hp2 | a0001 | c0001 | t0035 | g0008 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0174 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0182 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0088 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0080 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03453 | hp1 | a0001 | c0001 | t0015 | g0083 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03453 | hp2 | a0001 | c0001 | t0030 | g0003 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0087 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03486 | hp2 | a0001 | c0002 | t0019 | g0130 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03490 | hp1 | a0001 | c0001 | t0041 | g0105 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0315 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0306 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0324 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03492 | hp2 | a0001 | c0001 | t0006 | g0305 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03516 | hp1 | a0001 | c0001 | t0031 | g0004 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03516 | hp2 | a0001 | c0002 | t0033 | g0006 | AFR | ESN | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03540 | hp2 | a0001 | c0001 | t0032 | g0009 | AFR | GWD | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0046 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0114 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03654 | hp2 | a0001 | c0001 | t0006 | g0341 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03669 | hp2 | a0001 | c0003 | t0003 | g0263 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0071 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03688 | hp2 | a0001 | c0003 | t0003 | g0270 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03710 | hp1 | a0001 | c0001 | t0086 | g0342 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03710 | hp2 | a0001 | c0001 | t0087 | g0343 | SAS | PJL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0168 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0262 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03834 | hp1 | a0001 | c0002 | t0010 | g0330 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0296 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0104 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0275 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG04115 | hp1 | a0001 | c0001 | t0053 | g0137 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG04115 | hp2 | a0001 | c0002 | t0004 | g0041 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG04184 | hp2 | a0001 | c0002 | t0073 | g0281 | SAS | BEB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0285 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0326 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG04204 | hp2 | a0003 | c0007 | t0007 | g0283 | SAS | STU | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0063 | AFR | YRI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | YRI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18942 | hp1 | a0001 | c0002 | t0003 | g0209 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0133 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18948 | hp2 | a0001 | c0002 | t0021 | g0139 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18950 | hp1 | a0001 | c0002 | t0083 | g0328 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18950 | hp2 | a0001 | c0002 | t0065 | g0245 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0274 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18953 | hp2 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18960 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18960 | hp2 | a0001 | c0001 | t0059 | g0150 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18962 | hp1 | a0001 | c0001 | t0092 | g0348 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18965 | hp2 | a0001 | c0001 | t0074 | g0259 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18966 | hp2 | a0001 | c0001 | t0012 | g0149 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18968 | hp1 | a0001 | c0001 | t0058 | g0145 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18968 | hp2 | a0001 | c0002 | t0010 | g0323 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18969 | hp1 | a0001 | c0001 | t0012 | g0143 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18969 | hp2 | a0001 | c0001 | t0023 | g0216 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18970 | hp2 | a0001 | c0001 | t0013 | g0327 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18977 | hp1 | a0002 | c0009 | t0003 | g0195 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18978 | hp1 | a0001 | c0001 | t0061 | g0196 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0023 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18979 | hp2 | a0001 | c0002 | t0044 | g0106 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0227 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18995 | hp1 | a0001 | c0001 | t0022 | g0144 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18998 | hp2 | a0004 | c0010 | t0007 | g0287 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19002 | hp1 | a0001 | c0001 | t0023 | g0280 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19002 | hp2 | a0001 | c0002 | t0004 | g0091 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19003 | hp1 | a0001 | c0008 | t0045 | g0085 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19007 | hp1 | a0001 | c0001 | t0062 | g0273 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19007 | hp2 | a0001 | c0002 | t0064 | g0269 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19009 | hp2 | a0001 | c0001 | t0040 | g0134 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19012 | hp2 | a0001 | c0001 | t0012 | g0147 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0117 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0176 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19043 | hp1 | a0001 | c0001 | t0024 | g0211 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19043 | hp2 | a0001 | c0001 | t0037 | g0010 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19058 | hp1 | a0001 | c0002 | t0057 | g0141 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19060 | hp1 | a0001 | c0001 | t0011 | g0294 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19063 | hp1 | a0001 | c0001 | t0011 | g0299 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0258 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19064 | hp2 | a0001 | c0001 | t0038 | g0095 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0142 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0254 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19068 | hp2 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19074 | hp1 | a0001 | c0001 | t0012 | g0148 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19074 | hp2 | a0001 | c0001 | t0060 | g0161 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0265 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19080 | hp2 | a0001 | c0002 | t0066 | g0247 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0132 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19082 | hp2 | a0001 | c0001 | t0022 | g0146 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19088 | hp2 | a0001 | c0002 | t0021 | g0140 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19090 | hp1 | a0001 | c0002 | t0004 | g0126 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0089 | AFR | YRI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | YRI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0049 | AFR | ASW | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA20129 | hp2 | a0001 | c0001 | t0052 | g0124 | AFR | ASW | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA20752 | hp1 | a0001 | c0002 | t0010 | g0307 | EUR | TSI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0070 | EUR | TSI | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | GIH | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0278 | SAS | GIH | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0337 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG01123 | hp2 | a0001 | c0001 | t0017 | g0302 | AMR | CLM | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02109 | hp1 | a0001 | c0002 | t0019 | g0062 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0084 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02486 | hp1 | a0001 | c0001 | t0091 | g0347 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02486 | hp2 | a0001 | c0003 | t0004 | g0109 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02559 | hp1 | a0001 | c0005 | t0009 | g0013 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG02559 | hp2 | a0001 | c0001 | t0020 | g0021 | AFR | ACB | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0183 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG03471 | hp2 | a0001 | c0001 | t0020 | g0086 | AFR | MSL | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | USA | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| HG06807 | hp2 | a0001 | c0001 | t0014 | g0190 | AFR | USA | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0077 | AFR | USA | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA20300 | hp2 | a0001 | c0001 | t0069 | g0221 | AFR | USA | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | LWK | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0212 | REF | REF | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0127 | REF | REF | BCL11B_chr14_99164287_99277197 | BCL11B | chr14 | 99164287 | 99277197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99174951
|
C | A | 1 | a0002 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.1885G>T | p.Gly629Cys | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2864/8528 | 1885/2685 | 629/894 | chr14 | 99174951 | ||
| chr14:99257616
|
G | T | 1 | a0003 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.282C>A | p.Asp94Glu | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/4 | 1261/8528 | 282/2685 | 94/894 | chr14 | 99257616 | ||
| chr14:99257827
|
T | A | 1 | a0004 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.71A>T | p.His24Leu | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/4 | 1050/8528 | 71/2685 | 24/894 | chr14 | 99257827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99174568
|
G | A | 1 | a0001c0003 | 6 | HG01257.hp1 HG01433.hp2 HG01943.hp2 others(3): Show |
synonymous_variant | LOW | c.2268C>T | p.Pro756Pro | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3247/8528 | 2268/2685 | 756/894 | chr14 | 99174568 | ||
| chr14:99174601
|
G | T | 1 | a0001c0004 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.2235C>A | p.Ser745Ser | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3214/8528 | 2235/2685 | 745/894 | chr14 | 99174601 | ||
| chr14:99174931
|
G | A | 1 | a0001c0005 | 2 | HG02559.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.1905C>T | p.Asp635Asp | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2884/8528 | 1905/2685 | 635/894 | chr14 | 99174931 | ||
| chr14:99174934
|
G | A | 1 | a0001c0008 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.1902C>T | p.Gly634Gly | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2881/8528 | 1902/2685 | 634/894 | chr14 | 99174934 | ||
| chr14:99175399
|
G | A | 1 | a0001c0006 | 2 | HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.1437C>T | p.His479His | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2416/8528 | 1437/2685 | 479/894 | chr14 | 99175399 | ||
| chr14:99176023
|
C | G | 4 | a0001c0002a0001c0003a0001c0008others(1): Show | 92 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(89): Show |
synonymous_variant | LOW | c.813G>C | p.Pro271Pro | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1792/8528 | 813/2685 | 271/894 | chr14 | 99176023 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99169889
|
A | T | 1 | a0001c0006t0025 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4262T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 4262 | chr14 | 99169889 | |||||
| chr14:99169996
|
G | A | 4 | a0001c0002t0019a0001c0002t0067a0001c0002t0079others(1): Show | 5 | HG01884.hp1 HG02109.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4155C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 4155 | chr14 | 99169996 | |||||
| chr14:99170058
|
T | C | 2 | a0001c0001t0063a0001c0001t0080 | 2 | HG00621.hp2 HG02056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4093A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 4093 | chr14 | 99170058 | |||||
| chr14:99170262
|
T | G | 1 | a0001c0001t0085 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3889A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3889 | chr14 | 99170262 | |||||
| chr14:99170310
|
G | A | 1 | a0001c0001t0041 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3841C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3841 | chr14 | 99170310 | |||||
| chr14:99170353
|
A | T | 1 | a0001c0001t0026 | 2 | HG00738.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3798T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3798 | chr14 | 99170353 | |||||
| chr14:99170552
|
A | G | 2 | a0001c0001t0040a0001c0001t0062 | 2 | NA19007.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3599T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3599 | chr14 | 99170552 | |||||
| chr14:99170997
|
TCTCTCGC others(35): Show |
T | 1 | a0001c0001t0039 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3112_*3153delGCCA others(38): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3112 | chr14 | 99170997 | |||||
| chr14:99170998
|
C | G | 1 | a0001c0002t0066 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3153G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 3153 | chr14 | 99170998 | |||||
| chr14:99171171
|
G | A | 1 | a0001c0001t0071 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2980C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2980 | chr14 | 99171171 | |||||
| chr14:99171314
|
C | T | 6 | a0001c0001t0034a0001c0001t0071a0001c0001t0076others(3): Show | 6 | HG00099.hp1 HG00639.hp2 HG01891.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2837G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2837 | chr14 | 99171314 | |||||
| chr14:99171334
|
G | A | 2 | a0001c0002t0046a0001c0002t0068 | 2 | HG01891.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2817C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2817 | chr14 | 99171334 | |||||
| chr14:99171639
|
A | C | 1 | a0001c0001t0070 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2512T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2512 | chr14 | 99171639 | |||||
| chr14:99171760
|
A | G | 1 | a0001c0008t0045 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2391T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2391 | chr14 | 99171760 | |||||
| chr14:99172013
|
T | G | 1 | a0001c0001t0081 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2138A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 2138 | chr14 | 99172013 | |||||
| chr14:99172159
|
T | C | 1 | a0001c0001t0031 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1992A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1992 | chr14 | 99172159 | |||||
| chr14:99172399
|
A | AT | 11 | a0001c0001t0015a0001c0001t0027a0001c0001t0035others(8): Show | 14 | HG01884.hp2 HG01975.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1751dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1751 | chr14 | 99172399 | |||||
| chr14:99172409
|
T | C | 3 | a0001c0001t0008a0001c0001t0014a0001c0001t0032 | 14 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1742A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1742 | chr14 | 99172409 | |||||
| chr14:99172529
|
A | G | 3 | a0001c0002t0044a0001c0002t0065a0001c0002t0083 | 3 | NA18950.hp1 NA18950.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1622T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1622 | chr14 | 99172529 | |||||
| chr14:99172681
|
C | T | 1 | a0001c0002t0064 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1470G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1470 | chr14 | 99172681 | |||||
| chr14:99172706
|
G | C | 1 | a0001c0001t0042 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1445C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1445 | chr14 | 99172706 | |||||
| chr14:99172845
|
GA | G | 4 | a0001c0001t0008a0001c0001t0014a0001c0001t0032others(1): Show | 15 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1305delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1305 | chr14 | 99172845 | |||||
| chr14:99172913
|
C | T | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1238G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1238 | chr14 | 99172913 | |||||
| chr14:99172933
|
T | G | 28 | a0001c0001t0005a0001c0001t0007a0001c0001t0009others(25): Show | 74 | HG00280.hp2 HG00423.hp1 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1218A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1218 | chr14 | 99172933 | |||||
| chr14:99173019
|
C | G | 1 | a0001c0001t0060 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1132G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1132 | chr14 | 99173019 | |||||
| chr14:99173063
|
A | G | 1 | a0001c0002t0082 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1088T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 1088 | chr14 | 99173063 | |||||
| chr14:99173552
|
A | G | 1 | a0001c0001t0069 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*599T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 599 | chr14 | 99173552 | |||||
| chr14:99173554
|
C | A | 1 | a0001c0001t0048 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*597G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 597 | chr14 | 99173554 | |||||
| chr14:99173554
|
C | CA | 49 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(46): Show | 146 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*596dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 596 | chr14 | 99173554 | |||||
| chr14:99173575
|
A | AT | 2 | a0001c0001t0023a0001c0001t0038 | 3 | NA18969.hp2 NA19002.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*575dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 575 | chr14 | 99173575 | |||||
| chr14:99173577
|
T | TA | 40 | a0001c0001t0005a0001c0001t0007a0001c0001t0009others(37): Show | 88 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*573dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 573 | chr14 | 99173577 | |||||
| chr14:99173805
|
T | TA | 9 | a0001c0001t0016a0001c0001t0027a0001c0001t0035others(6): Show | 12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*345dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 345 | chr14 | 99173805 | |||||
| chr14:99173963
|
C | G | 1 | a0001c0001t0053 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 4/4 | 188 | chr14 | 99173963 | |||||
| chr14:99271290
|
CCGCCGCC others(1): Show |
C | 2 | a0001c0002t0021a0001c0002t0057 | 3 | NA18948.hp2 NA19058.hp1 NA19088.hp2 |
5_prime_UTR_variant | MODIFIER | c.-80_-73delCGGCGGCG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 73 | chr14 | 99271290 | |||||
| chr14:99271298
|
G | GCGCCGCT others(2): Show |
14 | a0001c0001t0006a0001c0001t0013a0001c0001t0029others(11): Show | 43 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(40): Show |
5_prime_UTR_variant | MODIFIER | c.-89_-81dupGCAGCGGC others(1): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 81 | chr14 | 99271298 | |||||
| chr14:99271298
|
G | GCGCGCTG others(13): Show |
1 | a0001c0001t0086 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81_-80insGCGGCAGC others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 81 | chr14 | 99271298 | |||||
| chr14:99271298
|
GCGCCGCT others(23): Show |
G | 1 | a0001c0001t0059 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110_-81delGCGGCGG others(23): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 81 | chr14 | 99271298 | |||||
| chr14:99271305
|
T | C | 1 | a0001c0001t0086 | 1 | HG03710.hp1 | 5_prime_UTR_variant | MODIFIER | c.-87A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 87 | chr14 | 99271305 | |||||
| chr14:99271305
|
T | TGCCGCCG others(14): Show |
3 | a0001c0001t0075a0001c0001t0076a0001c0001t0087 | 3 | HG02602.hp2 HG02683.hp1 HG03710.hp2 |
5_prime_UTR_variant | MODIFIER | c.-108_-88dupGGCGGCG others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 88 | chr14 | 99271305 | |||||
| chr14:99271314
|
T | C | 4 | a0001c0001t0030a0001c0001t0031a0001c0001t0077others(1): Show | 4 | HG02922.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-96A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 96 | chr14 | 99271314 | |||||
| chr14:99271314
|
T | TGCCGCC | 3 | a0001c0001t0012a0001c0001t0022a0001c0001t0058 | 8 | NA18966.hp2 NA18968.hp1 NA18969.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-102_-97dupGGCGGC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 97 | chr14 | 99271314 | |||||
| chr14:99271314
|
TGCCGCCG others(8): Show |
T | 1 | a0001c0002t0018 | 2 | HG00639.hp1 HG00642.hp2 |
5_prime_UTR_variant | MODIFIER | c.-111_-97delGGCGGCG others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 97 | chr14 | 99271314 | |||||
| chr14:99271384
|
T | G | 1 | a0001c0001t0037 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-166A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 166 | chr14 | 99271384 | |||||
| chr14:99271467
|
G | A | 4 | a0001c0001t0090a0001c0001t0091a0001c0002t0079others(1): Show | 4 | HG02257.hp1 HG02486.hp1 HG02630.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-249C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 249 | chr14 | 99271467 | |||||
| chr14:99271515
|
C | CA | 43 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(40): Show | 150 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(147): Show |
5_prime_UTR_variant | MODIFIER | c.-298dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 298 | chr14 | 99271515 | |||||
| chr14:99271515
|
C | CAA | 18 | a0001c0001t0006a0001c0001t0011a0001c0001t0013others(15): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-299_-298dupTT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 298 | chr14 | 99271515 | |||||
| chr14:99271515
|
CA | C | 6 | a0001c0001t0032a0001c0001t0034a0001c0001t0035others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG03139.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-298delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 298 | chr14 | 99271515 | |||||
| chr14:99271656
|
C | T | 2 | a0001c0001t0030a0001c0001t0031 | 2 | HG03453.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-438G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 438 | chr14 | 99271656 | |||||
| chr14:99271755
|
AT | A | 4 | a0001c0001t0090a0001c0001t0091a0001c0002t0088others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-538delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 538 | chr14 | 99271755 | |||||
| chr14:99271899
|
CTGTTTTT others(5): Show |
C | 1 | a0001c0001t0092 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-693_-682delAAAACA others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/4 | 682 | chr14 | 99271899 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99176310
|
T | A | 147 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.641-115A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176310 | ||||||
| chr14:99176377
|
G | C | 1 | a0001c0001t0086g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.641-182C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176377 | ||||||
| chr14:99176430
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0012g0147a0001c0001t0012g0148 | 3 | NA18953.hp1 NA19012.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.641-235C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176430 | ||||||
| chr14:99176467
|
C | A | 1 | a0001c0001t0043g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.641-272G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176467 | ||||||
| chr14:99176472
|
A | G | 11 | a0001c0001t0002g0067a0001c0001t0009g0043a0001c0001t0009g0063others(8): Show | 11 | HG02559.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.641-277T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176472 | ||||||
| chr14:99176507
|
C | T | 1 | a0001c0001t0002g0097 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.641-312G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176507 | ||||||
| chr14:99176577
|
C | T | 1 | a0001c0002t0073g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.641-382G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176577 | ||||||
| chr14:99176632
|
C | T | 1 | a0001c0001t0080g0303 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.641-437G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176632 | ||||||
| chr14:99176635
|
C | T | 72 | a0001c0001t0008g0046a0001c0001t0008g0053a0001c0001t0008g0084others(69): Show | 72 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.641-440G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176635 | ||||||
| chr14:99176684
|
G | T | 1 | a0001c0001t0051g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.641-489C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176684 | ||||||
| chr14:99176844
|
A | G | 3 | a0001c0001t0020g0086a0001c0001t0031g0004a0001c0001t0036g0007 | 3 | HG02451.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641-649T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176844 | ||||||
| chr14:99176873
|
C | T | 2 | a0001c0001t0029g0314a0001c0001t0029g0322 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.641-678G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176873 | ||||||
| chr14:99176920
|
C | CT | 12 | a0001c0001t0001g0189a0001c0001t0002g0056a0001c0001t0003g0267others(9): Show | 12 | HG01175.hp1 HG01884.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-726dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176920 | ||||||
| chr14:99176920
|
CT | C | 13 | a0001c0001t0001g0172a0001c0001t0006g0312a0001c0001t0029g0314others(10): Show | 13 | HG01071.hp2 HG01169.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-726delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99176920 | ||||||
| chr14:99177462
|
C | G | 7 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0125others(4): Show | 7 | HG00099.hp1 HG01952.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-1267G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177462 | ||||||
| chr14:99177481
|
T | A | 1 | a0001c0002t0010g0323 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.641-1286A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177481 | ||||||
| chr14:99177517
|
A | G | 262 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.641-1322T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177517 | ||||||
| chr14:99177598
|
T | C | 82 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0167others(79): Show | 82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.641-1403A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177598 | ||||||
| chr14:99177623
|
C | G | 3 | a0001c0001t0020g0086a0001c0001t0031g0004a0001c0001t0036g0007 | 3 | HG02451.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641-1428G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177623 | ||||||
| chr14:99177715
|
A | C | 7 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0125others(4): Show | 7 | HG00099.hp1 HG01952.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-1520T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177715 | ||||||
| chr14:99177818
|
T | C | 3 | a0001c0001t0020g0086a0001c0001t0031g0004a0001c0001t0036g0007 | 3 | HG02451.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641-1623A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177818 | ||||||
| chr14:99177950
|
T | C | 26 | a0001c0001t0001g0189a0001c0001t0002g0067a0001c0001t0002g0068others(23): Show | 26 | HG00099.hp1 HG01099.hp1 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.641-1755A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99177950 | ||||||
| chr14:99178152
|
C | T | 1 | a0001c0002t0010g0333 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.641-1957G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178152 | ||||||
| chr14:99178236
|
G | A | 1 | a0001c0001t0012g0142 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.641-2041C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178236 | ||||||
| chr14:99178252
|
G | A | 1 | a0001c0001t0015g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.641-2057C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178252 | ||||||
| chr14:99178275
|
T | G | 4 | a0001c0001t0014g0190a0001c0002t0046g0014a0001c0002t0049g0057others(1): Show | 4 | HG00639.hp2 HG01891.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-2080A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178275 | ||||||
| chr14:99178385
|
T | C | 233 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(230): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.641-2190A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178385 | ||||||
| chr14:99178480
|
G | A | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-2285C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178480 | ||||||
| chr14:99178492
|
C | CCA | 3 | a0001c0001t0020g0086a0001c0001t0031g0004a0001c0001t0036g0007 | 3 | HG02451.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.641-2299_641-2298d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178492 | ||||||
| chr14:99178500
|
C | G | 139 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(136): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.641-2305G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178500 | ||||||
| chr14:99178617
|
G | A | 233 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(230): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.641-2422C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178617 | ||||||
| chr14:99178675
|
C | G | 80 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0167others(77): Show | 80 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.641-2480G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178675 | ||||||
| chr14:99178756
|
C | T | 25 | a0001c0001t0005g0024a0001c0001t0005g0028a0001c0001t0005g0074others(22): Show | 25 | HG00733.hp2 HG00738.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.641-2561G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178756 | ||||||
| chr14:99178823
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-2628A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178823 | ||||||
| chr14:99178849
|
G | A | 1 | a0001c0001t0008g0084 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.641-2654C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178849 | ||||||
| chr14:99178851
|
C | T | 1 | a0001c0001t0052g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.641-2656G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178851 | ||||||
| chr14:99178895
|
C | T | 1 | a0001c0001t0052g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.641-2700G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99178895 | ||||||
| chr14:99179043
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.641-2848C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179043 | ||||||
| chr14:99179083
|
A | C | 137 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(134): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.641-2888T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179083 | ||||||
| chr14:99179240
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.641-3045C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179240 | ||||||
| chr14:99179330
|
C | T | 3 | a0001c0001t0008g0054a0001c0001t0009g0043a0001c0001t0015g0083 | 3 | HG02572.hp1 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.641-3135G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179330 | ||||||
| chr14:99179341
|
G | T | 1 | a0001c0003t0003g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.641-3146C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179341 | ||||||
| chr14:99179473
|
T | TA | 64 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0173others(61): Show | 64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.641-3279dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | ||||||
| chr14:99179473
|
T | TAA | 8 | a0001c0001t0001g0203a0001c0001t0002g0100a0001c0001t0005g0028others(5): Show | 8 | HG00423.hp1 HG00438.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-3280_641-3279d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | ||||||
| chr14:99179473
|
TA | T | 144 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.641-3279delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | ||||||
| chr14:99179473
|
TAA | T | 19 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0218others(16): Show | 19 | HG01069.hp2 HG01099.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.641-3280_641-3279d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | ||||||
| chr14:99179473
|
TAAA | T | 10 | a0001c0001t0009g0064a0001c0001t0009g0080a0001c0001t0009g0123others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.641-3281_641-3279d others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | ||||||
| chr14:99179473
|
TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0027g0165a0001c0001t0027g0230 | 2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.641-3288_641-3279d others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179473 | ||||||
| chr14:99179500
|
GCTT | G | 6 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0125others(3): Show | 6 | HG01952.hp1 HG02602.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-3308_641-3306d others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179500 | ||||||
| chr14:99179609
|
G | A | 5 | a0001c0001t0014g0176a0001c0001t0016g0030a0001c0001t0016g0073others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-3414C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179609 | ||||||
| chr14:99179716
|
C | T | 1 | a0001c0001t0052g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.641-3521G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179716 | ||||||
| chr14:99179767
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0052g0124 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.641-3572G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179767 | ||||||
| chr14:99179796
|
A | C | 131 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0167others(128): Show | 131 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.641-3601T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179796 | ||||||
| chr14:99179803
|
T | C | 4 | a0001c0001t0001g0228a0001c0001t0001g0238a0001c0001t0001g0253others(1): Show | 4 | HG00609.hp2 NA18981.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-3608A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99179803 | ||||||
| chr14:99180162
|
G | A | 1 | a0001c0001t0006g0338 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.641-3967C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180162 | ||||||
| chr14:99180229
|
C | T | 264 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.641-4034G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180229 | ||||||
| chr14:99180504
|
T | C | 1 | a0001c0002t0003g0194 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.641-4309A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180504 | ||||||
| chr14:99180562
|
A | C | 1 | a0001c0002t0083g0328 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.641-4367T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180562 | ||||||
| chr14:99180691
|
C | T | 5 | a0001c0002t0004g0036a0001c0002t0004g0049a0001c0002t0033g0006others(2): Show | 5 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-4496G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180691 | ||||||
| chr14:99180711
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0006g0337 | 2 | HG01106.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.641-4516C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180711 | ||||||
| chr14:99180718
|
T | C | 3 | a0001c0002t0010g0320a0001c0003t0003g0263a0001c0003t0004g0109 | 3 | HG02486.hp2 HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.641-4523A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180718 | ||||||
| chr14:99180724
|
A | C | 1 | a0001c0001t0008g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.641-4529T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180724 | ||||||
| chr14:99180877
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-4682C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180877 | ||||||
| chr14:99180992
|
T | G | 88 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0167others(85): Show | 88 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.641-4797A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99180992 | ||||||
| chr14:99181049
|
C | T | 113 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(110): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.641-4854G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181049 | ||||||
| chr14:99181191
|
G | A | 4 | a0001c0001t0002g0040a0001c0001t0003g0233a0001c0001t0027g0165others(1): Show | 4 | HG00733.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-4996C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181191 | ||||||
| chr14:99181202
|
G | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0279 | 2 | HG00558.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.641-5007C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181202 | ||||||
| chr14:99181218
|
G | A | 1 | a0001c0002t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.641-5023C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181218 | ||||||
| chr14:99181427
|
C | T | 98 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(95): Show | 98 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.641-5232G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181427 | ||||||
| chr14:99181553
|
C | A | 305 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(302): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.641-5358G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181553 | ||||||
| chr14:99181709
|
C | T | 2 | a0001c0001t0016g0089a0001c0001t0069g0221 | 2 | NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.641-5514G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181709 | ||||||
| chr14:99181881
|
G | A | 88 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.641-5686C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181881 | ||||||
| chr14:99181891
|
T | G | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-5696A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181891 | ||||||
| chr14:99181917
|
C | T | 1 | a0001c0001t0020g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.641-5722G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181917 | ||||||
| chr14:99181919
|
G | A | 91 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(88): Show | 91 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.641-5724C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181919 | ||||||
| chr14:99181975
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.641-5780G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181975 | ||||||
| chr14:99181988
|
T | C | 1 | a0001c0002t0033g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.641-5793A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99181988 | ||||||
| chr14:99182051
|
G | A | 1 | a0001c0001t0027g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-5856C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182051 | ||||||
| chr14:99182157
|
C | A | 101 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(98): Show | 102 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.641-5962G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182157 | ||||||
| chr14:99182428
|
C | T | 222 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.641-6233G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182428 | ||||||
| chr14:99182443
|
C | T | 16 | a0001c0001t0001g0184a0001c0001t0001g0266a0001c0001t0002g0125others(13): Show | 16 | HG00597.hp2 HG01884.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-6248G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182443 | ||||||
| chr14:99182505
|
A | T | 1 | a0001c0001t0008g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.641-6310T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182505 | ||||||
| chr14:99182689
|
G | A | 2 | a0001c0001t0034g0005a0001c0002t0033g0006 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.641-6494C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182689 | ||||||
| chr14:99182693
|
A | G | 102 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(99): Show | 102 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.641-6498T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182693 | ||||||
| chr14:99182727
|
T | C | 89 | a0001c0001t0001g0189a0001c0001t0001g0193a0001c0001t0001g0200others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.641-6532A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182727 | ||||||
| chr14:99182731
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-6536G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99182731 | ||||||
| chr14:99183057
|
AG | A | 127 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(124): Show | 127 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.641-6863delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183057 | ||||||
| chr14:99183059
|
G | C | 2 | a0001c0001t0003g0233a0001c0001t0008g0119 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.641-6864C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183059 | ||||||
| chr14:99183170
|
C | A | 257 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.641-6975G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183170 | ||||||
| chr14:99183226
|
C | A | 60 | a0001c0001t0001g0205a0001c0001t0001g0210a0001c0001t0001g0213others(57): Show | 60 | HG00621.hp1 HG00621.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.641-7031G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183226 | ||||||
| chr14:99183243
|
C | T | 34 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(31): Show | 34 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.641-7048G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183243 | ||||||
| chr14:99183260
|
G | A | 17 | a0001c0001t0001g0178a0001c0001t0001g0272a0001c0001t0002g0042others(14): Show | 17 | HG00738.hp2 HG01069.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.641-7065C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183260 | ||||||
| chr14:99183337
|
A | G | 1 | a0001c0001t0007g0204 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.641-7142T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183337 | ||||||
| chr14:99183376
|
T | C | 154 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0162others(151): Show | 154 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.641-7181A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183376 | ||||||
| chr14:99183575
|
C | T | 1 | a0001c0001t0007g0197 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.641-7380G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183575 | ||||||
| chr14:99183644
|
G | A | 1 | a0001c0001t0077g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.641-7449C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183644 | ||||||
| chr14:99183665
|
T | C | 1 | a0001c0001t0005g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.641-7470A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183665 | ||||||
| chr14:99183673
|
CACATACA others(5): Show |
C | 1 | a0001c0001t0043g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.641-7490_641-7479d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183673 | ||||||
| chr14:99183728
|
T | G | 1 | a0001c0001t0009g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.641-7533A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183728 | ||||||
| chr14:99183770
|
A | G | 17 | a0001c0001t0001g0178a0001c0001t0002g0042a0001c0001t0009g0043others(14): Show | 17 | HG00738.hp2 HG01069.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.641-7575T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183770 | ||||||
| chr14:99183797
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-7602G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183797 | ||||||
| chr14:99183890
|
C | A | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-7695G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183890 | ||||||
| chr14:99183958
|
C | A | 93 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(90): Show | 93 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.641-7763G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99183958 | ||||||
| chr14:99184251
|
C | T | 18 | a0001c0001t0001g0178a0001c0001t0002g0042a0001c0001t0009g0043others(15): Show | 18 | HG00738.hp2 HG01069.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.641-8056G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184251 | ||||||
| chr14:99184582
|
G | A | 6 | a0001c0001t0015g0083a0001c0001t0024g0211a0001c0001t0024g0226others(3): Show | 7 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-8387C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184582 | ||||||
| chr14:99184596
|
C | T | 13 | a0001c0001t0001g0184a0001c0001t0001g0266a0001c0002t0001g0237others(10): Show | 13 | HG00597.hp2 HG02056.hp1 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-8401G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184596 | ||||||
| chr14:99184597
|
G | C | 257 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.641-8402C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184597 | ||||||
| chr14:99184603
|
TG | T | 67 | a0001c0001t0001g0178a0001c0001t0001g0184a0001c0001t0001g0266others(64): Show | 67 | HG00597.hp2 HG00738.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.641-8409delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184603 | ||||||
| chr14:99184681
|
G | A | 4 | a0001c0001t0001g0224a0001c0001t0002g0058a0001c0001t0002g0112others(1): Show | 4 | HG02071.hp1 HG02523.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-8486C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184681 | ||||||
| chr14:99184714
|
T | C | 68 | a0001c0001t0001g0178a0001c0001t0001g0184a0001c0001t0001g0266others(65): Show | 68 | HG00597.hp2 HG00738.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.641-8519A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184714 | ||||||
| chr14:99184793
|
C | T | 1 | a0001c0001t0011g0295 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.641-8598G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184793 | ||||||
| chr14:99184812
|
G | A | 1 | a0001c0001t0086g0342 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.641-8617C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184812 | ||||||
| chr14:99184828
|
T | C | 1 | a0001c0001t0017g0302 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.641-8633A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99184828 | ||||||
| chr14:99185378
|
G | A | 1 | a0001c0001t0077g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.641-9183C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185378 | ||||||
| chr14:99185446
|
G | A | 1 | a0001c0001t0027g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-9251C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185446 | ||||||
| chr14:99185446
|
GA | G | 229 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.641-9252delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185446 | ||||||
| chr14:99185446
|
GAA | G | 12 | a0001c0001t0002g0056a0001c0001t0014g0176a0001c0001t0015g0079others(9): Show | 13 | HG02615.hp1 HG02809.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-9253_641-9252d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185446 | ||||||
| chr14:99185447
|
A | G | 2 | a0001c0001t0027g0165a0001c0002t0010g0325 | 2 | HG01070.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.641-9252T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185447 | ||||||
| chr14:99185456
|
A | G | 6 | a0001c0001t0015g0083a0001c0001t0024g0211a0001c0001t0024g0226others(3): Show | 7 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-9261T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185456 | ||||||
| chr14:99185459
|
A | C | 155 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(152): Show | 155 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.641-9264T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185459 | ||||||
| chr14:99185466
|
T | C | 44 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0186others(41): Show | 44 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.641-9271A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185466 | ||||||
| chr14:99185473
|
AGTAATGT others(298): Show |
A | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.641-9583_641-9279d others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185473 | ||||||
| chr14:99185532
|
C | A | 1 | a0001c0001t0043g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.641-9337G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185532 | ||||||
| chr14:99185564
|
G | C | 3 | a0001c0002t0007g0255a0001c0002t0007g0256a0001c0002t0017g0300 | 3 | HG01168.hp2 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.641-9369C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185564 | ||||||
| chr14:99185586
|
G | A | 1 | a0001c0002t0003g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.641-9391C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185586 | ||||||
| chr14:99185601
|
T | C | 1 | a0001c0003t0003g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.641-9406A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185601 | ||||||
| chr14:99185632
|
G | A | 1 | a0001c0001t0009g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.641-9437C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185632 | ||||||
| chr14:99185734
|
T | C | 170 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(167): Show | 170 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.641-9539A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185734 | ||||||
| chr14:99185740
|
C | T | 2 | a0001c0001t0009g0064a0001c0001t0009g0123 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.641-9545G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185740 | ||||||
| chr14:99185772
|
T | C | 2 | a0001c0001t0008g0131a0001c0001t0009g0060 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.641-9577A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185772 | ||||||
| chr14:99185856
|
G | A | 2 | a0001c0001t0009g0064a0001c0001t0009g0123 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.641-9661C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185856 | ||||||
| chr14:99185913
|
C | T | 1 | a0001c0002t0028g0293 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.641-9718G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185913 | ||||||
| chr14:99185973
|
G | A | 1 | a0001c0001t0005g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.641-9778C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99185973 | ||||||
| chr14:99186031
|
G | T | 1 | a0001c0001t0077g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.641-9836C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186031 | ||||||
| chr14:99186153
|
A | T | 1 | a0001c0001t0043g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.641-9958T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186153 | ||||||
| chr14:99186224
|
T | G | 268 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159others(265): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.641-10029A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186224 | ||||||
| chr14:99186376
|
C | A | 1 | a0001c0003t0003g0263 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.641-10181G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186376 | ||||||
| chr14:99186399
|
A | G | 13 | a0001c0001t0001g0184a0001c0001t0001g0266a0001c0002t0001g0237others(10): Show | 13 | HG00597.hp2 HG02056.hp1 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-10204T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186399 | ||||||
| chr14:99186445
|
T | G | 1 | a0001c0001t0002g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.641-10250A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186445 | ||||||
| chr14:99186475
|
G | A | 1 | a0001c0001t0042g0072 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.641-10280C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186475 | ||||||
| chr14:99186736
|
C | T | 345 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(342): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.641-10541G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186736 | ||||||
| chr14:99186769
|
C | T | 3 | a0001c0001t0008g0087a0001c0001t0008g0090a0001c0001t0009g0080 | 3 | HG03098.hp2 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.641-10574G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186769 | ||||||
| chr14:99186786
|
C | T | 16 | a0001c0001t0001g0178a0001c0001t0002g0042a0001c0001t0005g0047others(13): Show | 16 | HG00738.hp1 HG01069.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.641-10591G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186786 | ||||||
| chr14:99186863
|
CTTTCCAT others(6): Show |
C | 1 | a0001c0002t0003g0227 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.641-10681_641-1066 others(17): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99186863 | ||||||
| chr14:99187104
|
T | G | 2 | a0001c0001t0009g0064a0001c0001t0009g0123 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.641-10909A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187104 | ||||||
| chr14:99187412
|
G | A | 1 | a0001c0002t0089g0345 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.641-11217C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187412 | ||||||
| chr14:99187588
|
T | G | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-11393A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187588 | ||||||
| chr14:99187662
|
C | CA | 234 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0164others(231): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.641-11468dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187662 | ||||||
| chr14:99187662
|
C | CAA | 8 | a0001c0001t0001g0229a0001c0001t0001g0261a0001c0001t0009g0060others(5): Show | 8 | HG00673.hp2 HG01109.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-11469_641-1146 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187662 | ||||||
| chr14:99187739
|
G | A | 4 | a0001c0001t0002g0040a0001c0001t0002g0044a0001c0001t0039g0038others(1): Show | 4 | HG00639.hp2 HG00733.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-11544C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187739 | ||||||
| chr14:99187758
|
A | C | 3 | a0001c0001t0005g0047a0001c0001t0006g0337a0001c0001t0013g0334 | 3 | HG01123.hp1 HG01496.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.641-11563T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187758 | ||||||
| chr14:99187778
|
T | TTCCTCCT others(2): Show |
266 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0164others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.641-11592_641-1158 others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187778 | ||||||
| chr14:99187870
|
A | C | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-11675T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187870 | ||||||
| chr14:99187886
|
G | A | 20 | a0001c0001t0002g0061a0001c0001t0005g0129a0001c0001t0008g0046others(17): Show | 20 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.641-11691C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187886 | ||||||
| chr14:99187886
|
G | T | 1 | a0001c0001t0038g0095 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.641-11691C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187886 | ||||||
| chr14:99187985
|
T | C | 264 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0164others(261): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.641-11790A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187985 | ||||||
| chr14:99187989
|
G | A | 1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.641-11794C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99187989 | ||||||
| chr14:99188058
|
T | C | 1 | a0001c0001t0008g0131 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.641-11863A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188058 | ||||||
| chr14:99188095
|
G | A | 8 | a0001c0001t0001g0164a0001c0001t0001g0266a0001c0001t0002g0058others(5): Show | 8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-11900C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188095 | ||||||
| chr14:99188099
|
T | C | 261 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0164others(258): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.641-11904A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188099 | ||||||
| chr14:99188176
|
T | C | 1 | a0001c0003t0003g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.641-11981A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188176 | ||||||
| chr14:99188293
|
A | C | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-12098T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188293 | ||||||
| chr14:99188386
|
C | A | 3 | a0001c0001t0027g0230a0001c0001t0078g0291a0001c0002t0019g0062 | 3 | HG02109.hp1 HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.641-12191G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188386 | ||||||
| chr14:99188437
|
C | T | 2 | a0001c0001t0015g0079a0001c0001t0069g0221 | 2 | HG02615.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.641-12242G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188437 | ||||||
| chr14:99188440
|
G | A | 1 | a0001c0001t0005g0048 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.641-12245C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188440 | ||||||
| chr14:99188537
|
C | CCTGGGG | 60 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0178others(57): Show | 61 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.641-12348_641-1234 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | ||||||
| chr14:99188537
|
C | CCTGGGGC others(5): Show |
2 | a0001c0001t0001g0180a0001c0002t0003g0194 | 2 | HG02451.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.641-12354_641-1234 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | ||||||
| chr14:99188537
|
CCTGGGG | C | 61 | a0001c0001t0001g0164a0001c0001t0001g0210a0001c0001t0001g0212others(58): Show | 61 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.641-12348_641-1234 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | ||||||
| chr14:99188537
|
CCTGGGGC others(5): Show |
C | 5 | a0001c0001t0001g0228a0001c0001t0001g0253a0001c0001t0011g0299others(2): Show | 5 | HG00609.hp2 HG03831.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-12354_641-1234 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | ||||||
| chr14:99188537
|
CCTGGGGC others(11): Show |
C | 1 | a0001c0001t0002g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.641-12360_641-1234 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188537 | ||||||
| chr14:99188866
|
T | G | 1 | a0001c0002t0010g0330 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.641-12671A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99188866 | ||||||
| chr14:99189011
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.641-12816C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189011 | ||||||
| chr14:99189433
|
T | G | 1 | a0001c0001t0011g0296 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.641-13238A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189433 | ||||||
| chr14:99189622
|
G | A | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-13427C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189622 | ||||||
| chr14:99189689
|
GAGGGCAG others(5): Show |
G | 2 | a0001c0001t0012g0148a0001c0002t0003g0209 | 2 | NA18942.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.641-13506_641-1349 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189689 | ||||||
| chr14:99189883
|
T | C | 1 | a0001c0002t0010g0333 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.641-13688A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189883 | ||||||
| chr14:99189901
|
G | T | 3 | a0001c0001t0013g0329a0001c0001t0013g0331a0001c0001t0056g0136 | 3 | HG01081.hp1 HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.641-13706C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189901 | ||||||
| chr14:99189908
|
G | C | 39 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0218others(36): Show | 40 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.641-13713C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189908 | ||||||
| chr14:99189942
|
G | A | 39 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0218others(36): Show | 40 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.641-13747C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99189942 | ||||||
| chr14:99190111
|
C | T | 8 | a0001c0001t0001g0164a0001c0001t0001g0266a0001c0001t0002g0058others(5): Show | 8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-13916G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190111 | ||||||
| chr14:99190219
|
TG | T | 122 | a0001c0001t0001g0185a0001c0001t0001g0210a0001c0001t0001g0212others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.641-14025delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190219 | ||||||
| chr14:99190315
|
C | T | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.641-14120G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190315 | ||||||
| chr14:99190350
|
G | A | 1 | a0001c0002t0066g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.641-14155C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190350 | ||||||
| chr14:99190482
|
C | T | 5 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0011g0298others(2): Show | 5 | HG02027.hp2 HG02056.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-14287G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190482 | ||||||
| chr14:99190517
|
T | A | 40 | a0001c0001t0001g0214a0001c0001t0002g0056a0001c0001t0002g0061others(37): Show | 40 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.641-14322A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190517 | ||||||
| chr14:99190541
|
T | A | 1 | a0001c0002t0003g0265 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.641-14346A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190541 | ||||||
| chr14:99190550
|
T | C | 41 | a0001c0001t0001g0214a0001c0001t0002g0056a0001c0001t0002g0061others(38): Show | 41 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.641-14355A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190550 | ||||||
| chr14:99190600
|
A | C | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.641-14405T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190600 | ||||||
| chr14:99190855
|
G | A | 39 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0180others(36): Show | 40 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.641-14660C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190855 | ||||||
| chr14:99190890
|
C | T | 26 | a0001c0001t0001g0210a0001c0001t0001g0212a0001c0001t0001g0228others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.641-14695G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190890 | ||||||
| chr14:99190907
|
C | CG | 229 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0164others(226): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.641-14713dupC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99190907 | ||||||
| chr14:99191169
|
G | A | 21 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0236others(18): Show | 21 | HG00609.hp1 HG00673.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.641-14974C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191169 | ||||||
| chr14:99191174
|
T | C | 1 | a0001c0001t0071g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.641-14979A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191174 | ||||||
| chr14:99191217
|
CT | C | 282 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0164others(279): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.641-15023delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191217 | ||||||
| chr14:99191221
|
G | C | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.641-15026C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191221 | ||||||
| chr14:99191291
|
C | T | 1 | a0001c0001t0016g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.641-15096G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191291 | ||||||
| chr14:99191402
|
T | TA | 8 | a0001c0001t0001g0164a0001c0001t0001g0266a0001c0001t0002g0058others(5): Show | 8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-15208dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191402 | ||||||
| chr14:99191402
|
TA | T | 181 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0167others(178): Show | 182 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.641-15208delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191402 | ||||||
| chr14:99191520
|
C | T | 8 | a0001c0001t0001g0164a0001c0001t0001g0266a0001c0001t0002g0058others(5): Show | 8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-15325G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191520 | ||||||
| chr14:99191708
|
G | A | 8 | a0001c0001t0001g0164a0001c0001t0001g0266a0001c0001t0002g0058others(5): Show | 8 | HG00423.hp2 HG02523.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-15513C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191708 | ||||||
| chr14:99191720
|
C | CA | 31 | a0001c0001t0001g0210a0001c0001t0001g0212a0001c0001t0001g0213others(28): Show | 31 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.641-15526dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99191720 | ||||||
| chr14:99192395
|
G | A | 1 | a0001c0002t0003g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.641-16200C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192395 | ||||||
| chr14:99192400
|
A | G | 1 | a0001c0001t0070g0171 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.641-16205T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192400 | ||||||
| chr14:99192480
|
G | A | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.641-16285C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192480 | ||||||
| chr14:99192550
|
G | A | 1 | a0001c0001t0078g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.641-16355C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192550 | ||||||
| chr14:99192673
|
G | T | 1 | a0001c0001t0006g0338 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.641-16478C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192673 | ||||||
| chr14:99192869
|
GTGAA | G | 208 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0167others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.641-16678_641-1667 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192869 | ||||||
| chr14:99192885
|
A | T | 1 | a0001c0001t0001g0156 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-16690T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192885 | ||||||
| chr14:99192905
|
A | G | 211 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0167others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.641-16710T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192905 | ||||||
| chr14:99192935
|
A | T | 9 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(6): Show | 9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-16740T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192935 | ||||||
| chr14:99192939
|
TAGTGAAT others(1): Show |
T | 111 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0172others(108): Show | 111 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.641-16752_641-1674 others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99192939 | ||||||
| chr14:99193034
|
G | A | 112 | a0001c0001t0001g0185a0001c0001t0001g0210a0001c0001t0001g0212others(109): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.641-16839C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193034 | ||||||
| chr14:99193185
|
C | G | 2 | a0001c0001t0005g0129a0001c0001t0009g0128 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.641-16990G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193185 | ||||||
| chr14:99193327
|
T | C | 9 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(6): Show | 9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-17132A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193327 | ||||||
| chr14:99193372
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-17177T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193372 | ||||||
| chr14:99193413
|
G | A | 1 | a0001c0001t0013g0334 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.641-17218C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193413 | ||||||
| chr14:99193546
|
G | A | 5 | a0001c0001t0001g0222a0001c0001t0001g0284a0001c0001t0011g0294others(2): Show | 5 | HG00597.hp1 NA18969.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-17351C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193546 | ||||||
| chr14:99193645
|
G | A | 2 | a0001c0001t0001g0203a0001c0002t0010g0318 | 2 | HG00438.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.641-17450C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99193645 | ||||||
| chr14:99194122
|
C | T | 2 | a0001c0006t0025g0191a0001c0006t0025g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.641-17927G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194122 | ||||||
| chr14:99194152
|
C | T | 1 | a0001c0001t0013g0339 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.641-17957G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194152 | ||||||
| chr14:99194314
|
G | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0052 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.641-18119C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194314 | ||||||
| chr14:99194546
|
G | A | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.641-18351C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194546 | ||||||
| chr14:99194697
|
C | T | 2 | a0001c0001t0005g0129a0001c0001t0009g0128 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.641-18502G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194697 | ||||||
| chr14:99194805
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-18610C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194805 | ||||||
| chr14:99194830
|
G | C | 1 | a0001c0001t0008g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.641-18635C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194830 | ||||||
| chr14:99194924
|
C | T | 2 | a0001c0001t0071g0187a0001c0002t0003g0152 | 2 | HG01109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.641-18729G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194924 | ||||||
| chr14:99194965
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-18770T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99194965 | ||||||
| chr14:99195089
|
A | C | 1 | a0001c0001t0027g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-18894T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195089 | ||||||
| chr14:99195313
|
G | C | 1 | a0001c0002t0004g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.641-19118C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195313 | ||||||
| chr14:99195567
|
C | G | 1 | a0001c0001t0007g0268 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.641-19372G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195567 | ||||||
| chr14:99195752
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.641-19557G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195752 | ||||||
| chr14:99195952
|
T | C | 5 | a0001c0001t0002g0061a0001c0001t0008g0046a0001c0001t0024g0211others(2): Show | 5 | HG02809.hp1 HG02922.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-19757A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99195952 | ||||||
| chr14:99196164
|
A | C | 238 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0167others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.641-19969T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196164 | ||||||
| chr14:99196394
|
G | A | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.641-20199C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196394 | ||||||
| chr14:99196531
|
GA | G | 93 | a0001c0001t0001g0185a0001c0001t0001g0214a0001c0001t0001g0223others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.641-20337delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196531 | ||||||
| chr14:99196639
|
G | A | 1 | a0001c0001t0007g0257 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.641-20444C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196639 | ||||||
| chr14:99196768
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.641-20573C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196768 | ||||||
| chr14:99196864
|
C | A | 1 | a0001c0001t0002g0093 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.641-20669G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99196864 | ||||||
| chr14:99197124
|
T | A | 1 | a0001c0001t0001g0156 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.641-20929A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197124 | ||||||
| chr14:99197214
|
C | T | 2 | a0001c0002t0044g0106a0001c0002t0065g0245 | 2 | NA18950.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.641-21019G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197214 | ||||||
| chr14:99197379
|
A | G | 4 | a0001c0001t0002g0125a0001c0001t0090g0346a0001c0002t0003g0286others(1): Show | 4 | HG02257.hp1 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-21184T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197379 | ||||||
| chr14:99197464
|
A | G | 2 | a0001c0001t0005g0129a0001c0001t0009g0128 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.641-21269T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197464 | ||||||
| chr14:99197510
|
A | G | 283 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0164others(280): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.641-21315T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197510 | ||||||
| chr14:99197551
|
G | T | 10 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0002g0093others(7): Show | 10 | HG00597.hp2 HG00639.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.641-21356C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197551 | ||||||
| chr14:99197588
|
G | C | 1 | a0001c0001t0078g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.641-21393C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197588 | ||||||
| chr14:99197651
|
C | T | 2 | a0001c0001t0001g0212a0001c0002t0003g0220 | 2 | HG01496.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.641-21456G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197651 | ||||||
| chr14:99197747
|
C | T | 3 | a0001c0001t0008g0090a0001c0001t0009g0080a0001c0001t0016g0089 | 3 | HG03098.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.641-21552G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197747 | ||||||
| chr14:99197865
|
G | A | 5 | a0001c0001t0002g0125a0001c0001t0032g0009a0001c0001t0090g0346others(2): Show | 5 | HG02257.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-21670C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197865 | ||||||
| chr14:99197919
|
T | C | 1 | a0001c0001t0002g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.641-21724A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99197919 | ||||||
| chr14:99198227
|
C | T | 9 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(6): Show | 9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-22032G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198227 | ||||||
| chr14:99198321
|
T | C | 3 | a0001c0001t0040g0134a0001c0002t0003g0274a0001c0002t0004g0132 | 3 | NA18951.hp1 NA19009.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.641-22126A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198321 | ||||||
| chr14:99198333
|
G | C | 3 | a0001c0001t0001g0235a0001c0001t0002g0051a0001c0001t0002g0052 | 3 | HG01516.hp1 HG01517.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.641-22138C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198333 | ||||||
| chr14:99198646
|
C | T | 9 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(6): Show | 9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-22451G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198646 | ||||||
| chr14:99198647
|
G | A | 136 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0185others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.641-22452C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198647 | ||||||
| chr14:99198679
|
A | G | 1 | a0001c0001t0007g0257 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.641-22484T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198679 | ||||||
| chr14:99198686
|
TGCACCTT others(2): Show |
T | 7 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0009g0043others(4): Show | 7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-22500_641-2249 others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198686 | ||||||
| chr14:99198705
|
G | A | 98 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0186others(95): Show | 98 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.641-22510C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198705 | ||||||
| chr14:99198858
|
G | C | 1 | a0001c0002t0010g0330 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.641-22663C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198858 | ||||||
| chr14:99198994
|
G | A | 245 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0167others(242): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.641-22799C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99198994 | ||||||
| chr14:99199003
|
G | A | 1 | a0001c0001t0016g0089 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.641-22808C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199003 | ||||||
| chr14:99199423
|
T | C | 1 | a0001c0001t0005g0116 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.641-23228A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199423 | ||||||
| chr14:99199462
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.641-23267C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199462 | ||||||
| chr14:99199639
|
G | GCT | 20 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0261others(17): Show | 20 | HG00438.hp1 HG00738.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.641-23446_641-2344 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199639 | ||||||
| chr14:99199640
|
C | CTCTG | 16 | a0001c0001t0001g0186a0001c0001t0001g0225a0001c0001t0001g0236others(13): Show | 16 | HG01257.hp1 HG01934.hp1 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.641-23446_641-2344 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | ||||||
| chr14:99199640
|
C | CTCTGTG | 8 | a0001c0001t0001g0213a0001c0001t0001g0234a0001c0001t0005g0101others(5): Show | 8 | HG00609.hp1 HG00673.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-23446_641-2344 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | ||||||
| chr14:99199640
|
C | CTCTGTGT others(3): Show |
1 | a0001c0001t0002g0097 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.641-23446_641-2344 others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | ||||||
| chr14:99199640
|
C | CTG | 15 | a0001c0001t0001g0212a0001c0001t0001g0222a0001c0001t0001g0228others(12): Show | 15 | HG00609.hp2 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.641-23447_641-2344 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | ||||||
| chr14:99199640
|
CTG | C | 27 | a0001c0001t0001g0173a0001c0001t0001g0184a0001c0001t0001g0208others(24): Show | 27 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.641-23447_641-2344 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | ||||||
| chr14:99199640
|
CTGTG | C | 25 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(22): Show | 25 | HG01433.hp1 HG01975.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.641-23449_641-2344 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | ||||||
| chr14:99199640
|
CTGTGTG | C | 7 | a0001c0001t0004g0110a0001c0001t0007g0197a0001c0002t0003g0209others(4): Show | 7 | HG00423.hp1 HG01175.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.641-23451_641-2344 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | ||||||
| chr14:99199640
|
CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0013g0329a0001c0001t0013g0331a0001c0001t0056g0136 | 3 | HG01081.hp1 HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.641-23453_641-2344 others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199640 | ||||||
| chr14:99199642
|
G | C | 185 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0167others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.641-23447C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199642 | ||||||
| chr14:99199644
|
G | C | 2 | a0001c0002t0007g0255a0001c0002t0017g0300 | 2 | HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.641-23449C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199644 | ||||||
| chr14:99199646
|
G | C | 1 | a0001c0006t0025g0192 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.641-23451C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199646 | ||||||
| chr14:99199648
|
G | C | 1 | a0001c0006t0025g0191 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.641-23453C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199648 | ||||||
| chr14:99199650
|
G | C | 3 | a0001c0001t0013g0329a0001c0001t0013g0331a0001c0001t0056g0136 | 3 | HG01081.hp1 HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.641-23455C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199650 | ||||||
| chr14:99199661
|
TGTGTGTG others(37): Show |
T | 1 | a0001c0002t0089g0345 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.641-23510_641-2346 others(48): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199661 | ||||||
| chr14:99199669
|
TGTGTGTG others(29): Show |
T | 8 | a0001c0001t0001g0218a0001c0001t0001g0229a0001c0001t0008g0054others(5): Show | 8 | HG02572.hp1 NA18948.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.641-23510_641-2347 others(40): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199669 | ||||||
| chr14:99199670
|
GTGTGTGT others(51): Show |
G | 2 | a0001c0001t0006g0335a0001c0001t0007g0239 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.641-23533_641-2347 others(62): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199670 | ||||||
| chr14:99199671
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0001t0017g0304 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.641-23490_641-2347 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199671 | ||||||
| chr14:99199671
|
TGTGTGTG others(27): Show |
T | 12 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(9): Show | 12 | HG00423.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-23510_641-2347 others(38): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199671 | ||||||
| chr14:99199672
|
GTGTGTGT others(49): Show |
G | 2 | a0001c0001t0026g0251a0001c0001t0026g0277 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.641-23533_641-2347 others(60): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199672 | ||||||
| chr14:99199673
|
TGTGTGTG others(25): Show |
T | 8 | a0001c0001t0006g0326a0001c0001t0006g0338a0001c0001t0011g0298others(5): Show | 8 | HG00099.hp1 HG00741.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-23510_641-2347 others(36): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199673 | ||||||
| chr14:99199673
|
TGTGTGTG others(33): Show |
T | 1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.641-23518_641-2347 others(44): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199673 | ||||||
| chr14:99199675
|
T | TGCGC | 4 | a0001c0001t0001g0178a0001c0001t0002g0045a0001c0001t0075g0288others(1): Show | 4 | HG00673.hp1 HG02683.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-23481_641-2348 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199675 | ||||||
| chr14:99199675
|
TGTGTGTG others(23): Show |
T | 4 | a0001c0001t0001g0231a0001c0001t0002g0055a0001c0001t0005g0078others(1): Show | 4 | HG02015.hp1 HG02683.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-23510_641-2348 others(34): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199675 | ||||||
| chr14:99199677
|
T | C | 10 | a0001c0001t0001g0178a0001c0001t0002g0045a0001c0001t0005g0024others(7): Show | 10 | HG00673.hp1 HG01074.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.641-23482A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199677 | ||||||
| chr14:99199677
|
TGTGTGTG others(15): Show |
T | 5 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0260others(2): Show | 5 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-23504_641-2348 others(26): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199677 | ||||||
| chr14:99199677
|
TGTGTGTG others(21): Show |
T | 29 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0279others(26): Show | 30 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.641-23510_641-2348 others(32): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199677 | ||||||
| chr14:99199679
|
T | C | 17 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0002g0045others(14): Show | 17 | HG00673.hp1 HG01070.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.641-23484A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199679 | ||||||
| chr14:99199679
|
TGTGTGCG others(19): Show |
T | 8 | a0001c0001t0001g0282a0001c0001t0002g0016a0001c0001t0002g0040others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-23510_641-2348 others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199679 | ||||||
| chr14:99199681
|
T | C | 34 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0214others(31): Show | 34 | HG00642.hp1 HG00673.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.641-23486A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | ||||||
| chr14:99199681
|
T | TGCGCGCG others(4): Show |
1 | a0001c0002t0004g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.641-23487_641-2348 others(15): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | ||||||
| chr14:99199681
|
T | TGCGCGCG others(5): Show |
1 | a0001c0002t0010g0333 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.641-23487_641-2348 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | ||||||
| chr14:99199681
|
TGTGC | T | 5 | a0001c0001t0001g0163a0001c0001t0005g0047a0001c0001t0006g0337others(2): Show | 5 | HG01123.hp1 HG01496.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-23490_641-2348 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | ||||||
| chr14:99199681
|
TGTGCGCG others(11): Show |
T | 1 | a0001c0002t0010g0330 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.641-23504_641-2348 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | ||||||
| chr14:99199681
|
TGTGCGCG others(17): Show |
T | 2 | a0001c0001t0001g0189a0001c0001t0030g0003 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.641-23510_641-2348 others(28): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199681 | ||||||
| chr14:99199683
|
T | C | 70 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0178others(67): Show | 70 | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.641-23488A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGCGCGCG others(11): Show |
1 | a0001c0001t0001g0200 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGCG others(7): Show |
1 | a0001c0005t0009g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.641-23489_641-2348 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0244 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0008g0131 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.641-23489_641-2348 others(20): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(11): Show |
2 | a0001c0001t0003g0275a0001c0001t0003g0285 | 2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.641-23489_641-2348 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(3): Show |
1 | a0001c0002t0067g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0003g0248 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0027g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0199 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.641-23489_641-2348 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0036g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.641-23489_641-2348 others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(13): Show |
1 | a0001c0002t0004g0133 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.641-23489_641-2348 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
T | TGTGTGTG others(21): Show |
3 | a0001c0002t0068g0170a0001c0004t0001g0001a0001c0004t0001g0179 | 4 | HG02630.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-23489_641-2348 others(32): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
TGCGCGCG others(9): Show |
T | 5 | a0001c0001t0001g0167a0001c0001t0003g0233a0001c0001t0007g0155others(2): Show | 5 | HG01978.hp2 HG02559.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-23504_641-2348 others(20): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199683
|
TGCGCGCG others(15): Show |
T | 2 | a0001c0002t0003g0181a0001c0002t0004g0117 | 2 | NA18983.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.641-23510_641-2348 others(26): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199683 | ||||||
| chr14:99199684
|
GCGCGCGC others(7): Show |
G | 5 | a0001c0001t0002g0067a0001c0001t0002g0069a0001c0001t0012g0147others(2): Show | 5 | HG02004.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-23503_641-2349 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199684 | ||||||
| chr14:99199684
|
GCGCGCGC others(13): Show |
G | 8 | a0001c0001t0001g0235a0001c0001t0002g0051a0001c0001t0002g0052others(5): Show | 8 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-23509_641-2349 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199684 | ||||||
| chr14:99199685
|
C | CGCGT | 8 | a0001c0001t0002g0061a0001c0001t0005g0116a0001c0001t0008g0046others(5): Show | 8 | HG02258.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.641-23491_641-2349 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199685 | ||||||
| chr14:99199685
|
C | CGT | 14 | a0001c0001t0001g0214a0001c0001t0002g0056a0001c0001t0002g0115others(11): Show | 14 | HG00597.hp2 HG00639.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.641-23491_641-2349 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199685 | ||||||
| chr14:99199685
|
C | T | 29 | a0001c0001t0001g0172a0001c0001t0001g0186a0001c0001t0001g0243others(26): Show | 29 | HG01074.hp1 HG01943.hp1 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.641-23490G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199685 | ||||||
| chr14:99199686
|
GCGCGCGC others(5): Show |
G | 4 | a0001c0001t0002g0068a0001c0001t0031g0004a0001c0002t0003g0217others(1): Show | 4 | HG03516.hp1 NA18999.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-23503_641-2349 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199686 | ||||||
| chr14:99199686
|
GCGCGCGC others(11): Show |
G | 5 | a0001c0001t0001g0172a0001c0001t0005g0066a0001c0001t0007g0201others(2): Show | 5 | HG01074.hp1 HG01943.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-23509_641-2349 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199686 | ||||||
| chr14:99199687
|
C | T | 2 | a0001c0001t0011g0301a0001c0001t0050g0108 | 2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.641-23492G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199687 | ||||||
| chr14:99199689
|
C | CGCGCGCG others(10): Show |
1 | a0001c0001t0014g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.641-23495_641-2349 others(21): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199689 | ||||||
| chr14:99199689
|
C | T | 3 | a0001c0001t0002g0122a0001c0001t0011g0301a0001c0001t0050g0108 | 3 | HG02886.hp1 HG02965.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.641-23494G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199689 | ||||||
| chr14:99199693
|
CGCGCACG others(11): Show |
C | 2 | a0001c0001t0011g0301a0001c0001t0050g0108 | 2 | HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.641-23516_641-2349 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199693 | ||||||
| chr14:99199696
|
G | A | 29 | a0001c0001t0001g0188a0001c0001t0001g0212a0001c0001t0001g0222others(26): Show | 29 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.641-23501C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199696 | ||||||
| chr14:99199696
|
G | C | 1 | a0001c0001t0011g0294 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.641-23501C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199696 | ||||||
| chr14:99199696
|
G | GCA | 4 | a0001c0001t0001g0210a0001c0001t0020g0021a0001c0001t0070g0171others(1): Show | 4 | HG01496.hp1 HG01516.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.641-23503_641-2350 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199696 | ||||||
| chr14:99199697
|
C | G | 1 | a0001c0001t0011g0294 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.641-23502G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199697 | ||||||
| chr14:99199699
|
C | T | 9 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(6): Show | 9 | HG02004.hp2 HG02809.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.641-23504G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199699 | ||||||
| chr14:99199703
|
C | T | 12 | a0001c0001t0001g0167a0001c0001t0002g0067a0001c0001t0002g0068others(9): Show | 12 | HG01978.hp2 HG02559.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-23508G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199703 | ||||||
| chr14:99199704
|
A | G | 12 | a0001c0001t0001g0167a0001c0001t0002g0067a0001c0001t0002g0068others(9): Show | 12 | HG01978.hp2 HG02559.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-23509T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199704 | ||||||
| chr14:99199705
|
C | T | 25 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0235others(22): Show | 25 | HG01074.hp1 HG01516.hp1 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.641-23510G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199705 | ||||||
| chr14:99199711
|
T | C | 13 | a0001c0001t0001g0164a0001c0001t0001g0172a0001c0001t0001g0189others(10): Show | 13 | HG00423.hp2 HG01261.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.641-23516A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199711 | ||||||
| chr14:99199713
|
C | T | 2 | a0001c0001t0001g0178a0001c0002t0004g0070 | 2 | HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.641-23518G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199713 | ||||||
| chr14:99199733
|
T | G | 7 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0009g0043others(4): Show | 7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-23538A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99199733 | ||||||
| chr14:99200063
|
C | T | 147 | a0001c0001t0001g0159a0001c0001t0001g0172a0001c0001t0001g0178others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.641-23868G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200063 | ||||||
| chr14:99200108
|
CT | C | 11 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0224others(8): Show | 11 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.641-23914delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200108 | ||||||
| chr14:99200120
|
T | A | 1 | a0001c0001t0006g0321 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.641-23925A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200120 | ||||||
| chr14:99200142
|
T | A | 1 | a0001c0001t0002g0039 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.641-23947A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200142 | ||||||
| chr14:99200234
|
T | C | 4 | a0001c0001t0002g0040a0001c0001t0002g0044a0001c0001t0039g0038others(1): Show | 4 | HG00639.hp2 HG00733.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.641-24039A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200234 | ||||||
| chr14:99200329
|
C | G | 7 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0009g0043others(4): Show | 7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-24134G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200329 | ||||||
| chr14:99200329
|
C | T | 1 | a0001c0001t0002g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.641-24134G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200329 | ||||||
| chr14:99200382
|
C | T | 200 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0172others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.641-24187G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200382 | ||||||
| chr14:99200411
|
G | A | 9 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(6): Show | 9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-24216C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200411 | ||||||
| chr14:99200451
|
G | A | 2 | a0001c0001t0061g0196a0001c0002t0064g0269 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.641-24256C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200451 | ||||||
| chr14:99200507
|
G | A | 1 | a0001c0001t0004g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.641-24312C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200507 | ||||||
| chr14:99200594
|
C | A | 7 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0009g0043others(4): Show | 7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-24399G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200594 | ||||||
| chr14:99200598
|
G | A | 2 | a0001c0001t0026g0251a0001c0001t0026g0277 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.641-24403C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200598 | ||||||
| chr14:99200603
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.641-24408C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200603 | ||||||
| chr14:99200709
|
G | A | 99 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0186others(96): Show | 99 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.641-24514C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200709 | ||||||
| chr14:99200781
|
G | A | 1 | a0001c0001t0005g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.641-24586C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200781 | ||||||
| chr14:99200842
|
G | A | 45 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(42): Show | 46 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(43): Show |
intron_variant | MODIFIER | c.641-24647C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200842 | ||||||
| chr14:99200882
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.641-24687G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99200882 | ||||||
| chr14:99201016
|
G | C | 1 | a0001c0001t0001g0244 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.641-24821C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201016 | ||||||
| chr14:99201127
|
G | A | 1 | a0001c0001t0008g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.641-24932C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201127 | ||||||
| chr14:99201137
|
G | C | 102 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0180others(99): Show | 102 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.641-24942C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201137 | ||||||
| chr14:99201179
|
C | T | 7 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0009g0043others(4): Show | 7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-24984G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201179 | ||||||
| chr14:99201288
|
T | G | 1 | a0001c0001t0015g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.641-25093A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201288 | ||||||
| chr14:99201316
|
C | T | 5 | a0001c0001t0001g0178a0001c0001t0013g0329a0001c0001t0013g0331others(2): Show | 5 | HG01081.hp1 HG01175.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-25121G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201316 | ||||||
| chr14:99201347
|
G | C | 1 | a0001c0001t0027g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.641-25152C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201347 | ||||||
| chr14:99201349
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.641-25154G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201349 | ||||||
| chr14:99201350
|
G | A | 102 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0180others(99): Show | 102 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.641-25155C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201350 | ||||||
| chr14:99201506
|
G | A | 1 | a0001c0001t0005g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.641-25311C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201506 | ||||||
| chr14:99201514
|
C | T | 1 | a0001c0002t0010g0320 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.641-25319G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201514 | ||||||
| chr14:99201536
|
T | G | 2 | a0001c0001t0040g0134a0001c0002t0004g0132 | 2 | NA19009.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.641-25341A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99201536 | ||||||
| chr14:99202304
|
G | A | 7 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0009g0043others(4): Show | 7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.641-26109C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202304 | ||||||
| chr14:99202333
|
C | T | 107 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(104): Show | 107 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.641-26138G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202333 | ||||||
| chr14:99202368
|
C | T | 5 | a0001c0001t0081g0311a0001c0002t0004g0037a0001c0002t0010g0307others(2): Show | 5 | HG00738.hp2 HG01975.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.641-26173G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202368 | ||||||
| chr14:99202614
|
A | G | 98 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(95): Show | 98 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.641-26419T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202614 | ||||||
| chr14:99202668
|
G | C | 77 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0210others(74): Show | 78 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.641-26473C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202668 | ||||||
| chr14:99202683
|
T | C | 107 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(104): Show | 107 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.641-26488A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202683 | ||||||
| chr14:99202774
|
G | A | 1 | a0001c0003t0003g0263 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.641-26579C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202774 | ||||||
| chr14:99202806
|
G | T | 9 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(6): Show | 9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-26611C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202806 | ||||||
| chr14:99202862
|
G | A | 1 | a0001c0001t0038g0095 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.641-26667C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99202862 | ||||||
| chr14:99203016
|
G | A | 6 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0253others(3): Show | 6 | HG00609.hp2 HG03831.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-26821C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203016 | ||||||
| chr14:99203167
|
T | C | 253 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.641-26972A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203167 | ||||||
| chr14:99203194
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.641-26999G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203194 | ||||||
| chr14:99203199
|
G | T | 105 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(102): Show | 105 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.641-27004C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203199 | ||||||
| chr14:99203530
|
C | T | 9 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(6): Show | 9 | HG00423.hp2 HG02071.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.641-27335G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203530 | ||||||
| chr14:99203604
|
G | T | 1 | a0001c0002t0003g0249 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.641-27409C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203604 | ||||||
| chr14:99203631
|
T | C | 3 | a0001c0001t0002g0125a0001c0001t0090g0346a0001c0002t0003g0286 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.641-27436A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203631 | ||||||
| chr14:99203668
|
A | C | 103 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(100): Show | 103 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.641-27473T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203668 | ||||||
| chr14:99203695
|
A | G | 267 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(264): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.641-27500T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203695 | ||||||
| chr14:99203705
|
C | G | 1 | a0001c0001t0051g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.641-27510G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203705 | ||||||
| chr14:99203754
|
C | A | 1 | a0001c0002t0004g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.641-27559G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203754 | ||||||
| chr14:99203791
|
C | G | 2 | a0001c0001t0014g0182a0001c0001t0015g0099 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.640+27554G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203791 | ||||||
| chr14:99203827
|
G | A | 2 | a0001c0001t0005g0047a0001c0001t0013g0334 | 2 | HG01496.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.640+27518C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203827 | ||||||
| chr14:99203891
|
G | A | 5 | a0001c0001t0014g0176a0001c0001t0016g0030a0001c0001t0020g0086others(2): Show | 5 | HG02723.hp1 HG02886.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+27454C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203891 | ||||||
| chr14:99203895
|
C | T | 1 | a0001c0002t0003g0194 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.640+27450G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203895 | ||||||
| chr14:99203913
|
A | AC | 99 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(96): Show | 99 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.640+27431dupG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99203913 | ||||||
| chr14:99204019
|
A | G | 57 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(54): Show | 57 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.640+27326T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204019 | ||||||
| chr14:99204037
|
C | T | 1 | a0001c0002t0019g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640+27308G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204037 | ||||||
| chr14:99204108
|
G | A | 50 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0001g0214others(47): Show | 50 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+27237C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204108 | ||||||
| chr14:99204190
|
A | C | 50 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0001g0214others(47): Show | 50 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+27155T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204190 | ||||||
| chr14:99204198
|
T | A | 114 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(111): Show | 114 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.640+27147A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204198 | ||||||
| chr14:99204302
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.640+27043G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204302 | ||||||
| chr14:99204408
|
C | G | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+26937G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204408 | ||||||
| chr14:99204454
|
G | A | 52 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(49): Show | 53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.640+26891C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204454 | ||||||
| chr14:99204572
|
T | C | 50 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0001g0214others(47): Show | 50 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+26773A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204572 | ||||||
| chr14:99204639
|
G | A | 54 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(51): Show | 54 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.640+26706C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204639 | ||||||
| chr14:99204674
|
A | G | 10 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(7): Show | 10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+26671T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204674 | ||||||
| chr14:99204828
|
G | A | 53 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(50): Show | 53 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.640+26517C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99204828 | ||||||
| chr14:99205108
|
G | A | 4 | a0001c0001t0027g0165a0001c0001t0034g0005a0001c0001t0077g0290others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+26237C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205108 | ||||||
| chr14:99205238
|
G | A | 10 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(7): Show | 10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+26107C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205238 | ||||||
| chr14:99205252
|
C | T | 1 | a0001c0001t0008g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.640+26093G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205252 | ||||||
| chr14:99205350
|
C | A | 45 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0001g0214others(42): Show | 45 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.640+25995G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205350 | ||||||
| chr14:99205392
|
C | T | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+25953G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205392 | ||||||
| chr14:99205451
|
G | A | 51 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(48): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.640+25894C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205451 | ||||||
| chr14:99205456
|
A | T | 14 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(11): Show | 14 | HG00423.hp2 HG01884.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+25889T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205456 | ||||||
| chr14:99205811
|
C | T | 1 | a0001c0002t0066g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.640+25534G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205811 | ||||||
| chr14:99205995
|
G | C | 1 | a0001c0001t0001g0271 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.640+25350C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99205995 | ||||||
| chr14:99206068
|
T | C | 2 | a0001c0001t0008g0114a0001c0002t0046g0014 | 2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.640+25277A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206068 | ||||||
| chr14:99206201
|
C | T | 246 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.640+25144G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206201 | ||||||
| chr14:99206460
|
C | G | 130 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0172others(127): Show | 131 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.640+24885G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206460 | ||||||
| chr14:99206572
|
A | G | 1 | a0001c0001t0007g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.640+24773T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206572 | ||||||
| chr14:99206580
|
C | T | 132 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0172others(129): Show | 133 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.640+24765G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206580 | ||||||
| chr14:99206591
|
G | A | 50 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0001g0214others(47): Show | 50 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+24754C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206591 | ||||||
| chr14:99206611
|
G | A | 1 | a0001c0002t0017g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.640+24734C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206611 | ||||||
| chr14:99206629
|
C | T | 251 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.640+24716G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206629 | ||||||
| chr14:99206718
|
T | C | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+24627A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206718 | ||||||
| chr14:99206937
|
G | C | 1 | a0001c0001t0081g0311 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.640+24408C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206937 | ||||||
| chr14:99206941
|
T | C | 191 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(188): Show | 192 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.640+24404A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206941 | ||||||
| chr14:99206987
|
A | C | 80 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0178others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.640+24358T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206987 | ||||||
| chr14:99206997
|
A | G | 80 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0178others(77): Show | 81 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.640+24348T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99206997 | ||||||
| chr14:99207185
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.640+24160T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207185 | ||||||
| chr14:99207369
|
G | A | 41 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0218others(38): Show | 42 | HG00621.hp1 HG00673.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.640+23976C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207369 | ||||||
| chr14:99207466
|
T | C | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+23879A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207466 | ||||||
| chr14:99207520
|
A | G | 67 | a0001c0001t0001g0164a0001c0001t0001g0172a0001c0001t0001g0189others(64): Show | 67 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.640+23825T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207520 | ||||||
| chr14:99207658
|
C | A | 2 | a0001c0001t0027g0230a0001c0001t0071g0187 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.640+23687G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207658 | ||||||
| chr14:99207669
|
C | T | 2 | a0001c0001t0006g0305a0001c0001t0006g0306 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.640+23676G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207669 | ||||||
| chr14:99207742
|
C | G | 42 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0002g0056others(39): Show | 42 | HG00639.hp1 HG00642.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.640+23603G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207742 | ||||||
| chr14:99207778
|
G | A | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+23567C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207778 | ||||||
| chr14:99207863
|
C | G | 1 | a0001c0001t0011g0294 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.640+23482G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207863 | ||||||
| chr14:99207967
|
G | A | 39 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0002g0056others(36): Show | 39 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.640+23378C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99207967 | ||||||
| chr14:99208159
|
T | C | 33 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0002g0056others(30): Show | 33 | HG01099.hp1 HG01496.hp2 HG01952.hp2 others(30): Show |
intron_variant | MODIFIER | c.640+23186A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99208159 | ||||||
| chr14:99208336
|
C | T | 55 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(52): Show | 55 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.640+23009G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99208336 | ||||||
| chr14:99208574
|
G | A | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+22771C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99208574 | ||||||
| chr14:99209096
|
C | T | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+22249G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209096 | ||||||
| chr14:99209242
|
G | A | 58 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.640+22103C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209242 | ||||||
| chr14:99209244
|
T | C | 1 | a0001c0002t0004g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.640+22101A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209244 | ||||||
| chr14:99209287
|
A | G | 11 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(8): Show | 11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+22058T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209287 | ||||||
| chr14:99209313
|
G | A | 1 | a0001c0001t0009g0063 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.640+22032C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209313 | ||||||
| chr14:99209369
|
C | T | 1 | a0001c0001t0014g0260 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.640+21976G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209369 | ||||||
| chr14:99209611
|
C | G | 87 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.640+21734G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209611 | ||||||
| chr14:99209632
|
T | C | 1 | a0001c0002t0004g0133 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.640+21713A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209632 | ||||||
| chr14:99209678
|
A | T | 1 | a0001c0001t0007g0155 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.640+21667T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209678 | ||||||
| chr14:99209696
|
G | A | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+21649C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209696 | ||||||
| chr14:99209711
|
G | A | 184 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.640+21634C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209711 | ||||||
| chr14:99209849
|
G | A | 35 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0002g0056others(32): Show | 35 | HG01099.hp1 HG01496.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.640+21496C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99209849 | ||||||
| chr14:99210269
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.640+21076C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210269 | ||||||
| chr14:99210286
|
T | C | 184 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.640+21059A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210286 | ||||||
| chr14:99210392
|
C | T | 1 | a0001c0002t0003g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.640+20953G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210392 | ||||||
| chr14:99210418
|
C | A | 1 | a0001c0001t0005g0116 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.640+20927G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210418 | ||||||
| chr14:99210467
|
T | C | 3 | a0001c0001t0007g0169a0001c0002t0003g0168a0001c0002t0082g0336 | 3 | HG02698.hp2 HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.640+20878A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210467 | ||||||
| chr14:99210470
|
A | G | 184 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(181): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.640+20875T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210470 | ||||||
| chr14:99210613
|
C | T | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+20732G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210613 | ||||||
| chr14:99210708
|
G | A | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+20637C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210708 | ||||||
| chr14:99210791
|
C | T | 24 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0228others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.640+20554G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210791 | ||||||
| chr14:99210867
|
A | T | 64 | a0001c0001t0001g0210a0001c0001t0001g0214a0001c0001t0001g0219others(61): Show | 64 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.640+20478T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210867 | ||||||
| chr14:99210887
|
A | AAGACACC others(42): Show |
1 | a0001c0001t0001g0238 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.640+20409_640+2045 others(53): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99210887 | ||||||
| chr14:99211017
|
G | A | 2 | a0001c0001t0030g0003a0001c0001t0031g0004 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.640+20328C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211017 | ||||||
| chr14:99211098
|
G | A | 4 | a0001c0001t0027g0165a0001c0001t0034g0005a0001c0001t0077g0290others(1): Show | 4 | HG01891.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+20247C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211098 | ||||||
| chr14:99211225
|
C | T | 1 | a0001c0001t0013g0334 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.640+20120G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211225 | ||||||
| chr14:99211339
|
A | G | 11 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(8): Show | 11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+20006T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211339 | ||||||
| chr14:99211355
|
G | A | 1 | a0001c0001t0009g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.640+19990C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211355 | ||||||
| chr14:99211396
|
C | G | 20 | a0001c0001t0002g0061a0001c0001t0008g0046a0001c0001t0008g0087others(17): Show | 20 | HG01099.hp1 HG02258.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.640+19949G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211396 | ||||||
| chr14:99211531
|
T | C | 1 | a0001c0001t0008g0087 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.640+19814A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211531 | ||||||
| chr14:99211569
|
T | C | 55 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(52): Show | 55 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.640+19776A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211569 | ||||||
| chr14:99211628
|
C | T | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+19717G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211628 | ||||||
| chr14:99211713
|
C | T | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+19632G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99211713 | ||||||
| chr14:99212179
|
G | A | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+19166C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212179 | ||||||
| chr14:99212282
|
A | C | 190 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.640+19063T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212282 | ||||||
| chr14:99212308
|
G | A | 32 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0002g0056others(29): Show | 32 | HG01099.hp1 HG01496.hp2 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.640+19037C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212308 | ||||||
| chr14:99212335
|
TGCA | T | 50 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(47): Show | 51 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(48): Show |
intron_variant | MODIFIER | c.640+19007_640+1900 others(7): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212335 | ||||||
| chr14:99212343
|
C | T | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+19002G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212343 | ||||||
| chr14:99212450
|
C | T | 1 | a0001c0001t0075g0288 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.640+18895G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212450 | ||||||
| chr14:99212612
|
A | C | 1 | a0001c0001t0043g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.640+18733T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212612 | ||||||
| chr14:99212706
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.640+18639C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212706 | ||||||
| chr14:99212721
|
G | A | 3 | a0001c0001t0075g0288a0001c0001t0076g0289a0001c0001t0087g0343 | 3 | HG02602.hp2 HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.640+18624C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212721 | ||||||
| chr14:99212773
|
C | T | 1 | a0001c0002t0004g0033 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.640+18572G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212773 | ||||||
| chr14:99212825
|
G | C | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+18520C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212825 | ||||||
| chr14:99212844
|
C | A | 7 | a0001c0001t0008g0054a0001c0001t0027g0230a0001c0001t0071g0187others(4): Show | 7 | HG00639.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+18501G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212844 | ||||||
| chr14:99212911
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0090g0346a0001c0002t0003g0286 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.640+18434G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212911 | ||||||
| chr14:99212912
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0090g0346a0001c0002t0003g0286 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.640+18433G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99212912 | ||||||
| chr14:99213170
|
C | T | 48 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+18175G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213170 | ||||||
| chr14:99213248
|
G | A | 1 | a0001c0001t0048g0096 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.640+18097C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213248 | ||||||
| chr14:99213276
|
T | C | 1 | a0001c0001t0005g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.640+18069A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213276 | ||||||
| chr14:99213411
|
C | T | 2 | a0001c0001t0026g0251a0001c0001t0026g0277 | 2 | HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.640+17934G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213411 | ||||||
| chr14:99213438
|
A | G | 130 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(127): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.640+17907T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213438 | ||||||
| chr14:99213459
|
A | G | 189 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.640+17886T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213459 | ||||||
| chr14:99213700
|
C | T | 1 | a0001c0001t0002g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.640+17645G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213700 | ||||||
| chr14:99213921
|
G | A | 1 | a0001c0003t0004g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.640+17424C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99213921 | ||||||
| chr14:99214266
|
G | T | 23 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0228others(20): Show | 23 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.640+17079C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214266 | ||||||
| chr14:99214671
|
A | T | 4 | a0001c0001t0002g0067a0001c0003t0010g0309a0001c0003t0010g0313others(1): Show | 4 | HG01257.hp1 HG01433.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+16674T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214671 | ||||||
| chr14:99214674
|
AT | A | 3 | a0001c0001t0001g0279a0001c0001t0023g0216a0001c0001t0023g0280 | 3 | NA18969.hp2 NA19002.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.640+16670delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214674 | ||||||
| chr14:99214675
|
T | A | 42 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(39): Show | 43 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(40): Show |
intron_variant | MODIFIER | c.640+16670A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214675 | ||||||
| chr14:99214787
|
T | G | 2 | a0001c0001t0007g0204a0001c0002t0004g0121 | 2 | HG00597.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.640+16558A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214787 | ||||||
| chr14:99214889
|
C | T | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+16456G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214889 | ||||||
| chr14:99214913
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.640+16432G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214913 | ||||||
| chr14:99214914
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+16431C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214914 | ||||||
| chr14:99214952
|
G | A | 1 | a0001c0002t0004g0036 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.640+16393C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99214952 | ||||||
| chr14:99215348
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.640+15997G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99215348 | ||||||
| chr14:99215446
|
G | C | 11 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(8): Show | 11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+15899C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99215446 | ||||||
| chr14:99215812
|
A | G | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+15533T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99215812 | ||||||
| chr14:99215959
|
G | A | 1 | a0001c0001t0006g0326 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.640+15386C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99215959 | ||||||
| chr14:99216318
|
G | T | 2 | a0001c0001t0002g0061a0001c0001t0008g0046 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.640+15027C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216318 | ||||||
| chr14:99216319
|
C | T | 2 | a0001c0001t0002g0061a0001c0001t0008g0046 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.640+15026G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216319 | ||||||
| chr14:99216419
|
A | G | 1 | a0001c0002t0003g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.640+14926T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216419 | ||||||
| chr14:99216573
|
C | T | 42 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0001g0214others(39): Show | 42 | HG01074.hp1 HG01099.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.640+14772G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216573 | ||||||
| chr14:99216580
|
T | C | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+14765A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216580 | ||||||
| chr14:99216852
|
C | T | 47 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(44): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+14493G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216852 | ||||||
| chr14:99216859
|
A | G | 1 | a0001c0002t0004g0023 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.640+14486T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216859 | ||||||
| chr14:99216863
|
G | A | 1 | a0001c0002t0003g0250 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.640+14482C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216863 | ||||||
| chr14:99216874
|
C | T | 2 | a0001c0001t0005g0129a0001c0001t0009g0128 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.640+14471G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216874 | ||||||
| chr14:99216909
|
T | C | 48 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14436A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216909 | ||||||
| chr14:99216923
|
C | CAT | 48 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14420_640+1442 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216923 | ||||||
| chr14:99216954
|
C | A | 48 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14391G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216954 | ||||||
| chr14:99216960
|
A | C | 48 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14385T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216960 | ||||||
| chr14:99216965
|
T | A | 48 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14380A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99216965 | ||||||
| chr14:99217018
|
T | G | 1 | a0001c0002t0044g0106 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.640+14327A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217018 | ||||||
| chr14:99217084
|
C | T | 10 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0190others(7): Show | 11 | HG02109.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.640+14261G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217084 | ||||||
| chr14:99217281
|
TACAA | T | 11 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(8): Show | 11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+14060_640+1406 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217281 | ||||||
| chr14:99217301
|
CAT | C | 48 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+14042_640+1404 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217301 | ||||||
| chr14:99217363
|
T | C | 47 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(44): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+13982A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217363 | ||||||
| chr14:99217371
|
T | TACACACA others(11): Show |
9 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0006g0337others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.640+13956_640+1397 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217371 | ||||||
| chr14:99217381
|
T | TACAGACA others(17): Show |
1 | a0001c0001t0008g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.640+13963_640+1396 others(28): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217381 | ||||||
| chr14:99217385
|
G | GAC | 15 | a0001c0001t0001g0200a0001c0001t0001g0272a0001c0001t0002g0102others(12): Show | 15 | HG00558.hp1 HG01169.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.640+13958_640+1395 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
G | GACAC | 13 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0002g0040others(10): Show | 13 | HG00733.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+13956_640+1395 others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
G | GACACACA others(17): Show |
1 | a0001c0002t0004g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.640+13959_640+1396 others(28): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
G | GACACACA others(13): Show |
53 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0001g0214others(50): Show | 53 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.640+13959_640+1396 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
G | GACACACA others(15): Show |
65 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(62): Show | 65 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.640+13959_640+1396 others(26): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
G | GACACACA others(17): Show |
3 | a0001c0001t0008g0114a0001c0002t0003g0249a0001c0002t0046g0014 | 3 | HG01891.hp1 HG02015.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.640+13959_640+1396 others(28): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
G | GACACACA others(19): Show |
2 | a0001c0001t0001g0238a0001c0001t0001g0271 | 2 | NA19004.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.640+13959_640+1396 others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
G | GACACACA others(21): Show |
10 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(7): Show | 10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+13959_640+1396 others(32): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
G | GACACACA others(19): Show |
1 | a0001c0002t0067g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.640+13959_640+1396 others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217385
|
GACACACA others(11): Show |
G | 1 | a0001c0001t0001g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.640+13942_640+1395 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217385 | ||||||
| chr14:99217387
|
C | CACACACA others(9): Show |
1 | a0001c0001t0005g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.640+13957_640+1395 others(20): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217387 | ||||||
| chr14:99217389
|
C | CACACACA others(7): Show |
1 | a0001c0001t0059g0150 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.640+13955_640+1395 others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217389 | ||||||
| chr14:99217391
|
C | CACACACA others(5): Show |
7 | a0001c0001t0001g0279a0001c0001t0007g0258a0001c0001t0023g0216others(4): Show | 7 | HG03139.hp2 NA18969.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+13953_640+1395 others(16): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217391 | ||||||
| chr14:99217393
|
C | CACACATA others(3): Show |
40 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(37): Show | 41 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(38): Show |
intron_variant | MODIFIER | c.640+13951_640+1395 others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217393 | ||||||
| chr14:99217418
|
G | A | 49 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(46): Show | 50 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(47): Show |
intron_variant | MODIFIER | c.640+13927C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217418 | ||||||
| chr14:99217453
|
C | A | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+13892G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217453 | ||||||
| chr14:99217632
|
G | A | 193 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.640+13713C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217632 | ||||||
| chr14:99217932
|
T | C | 198 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.640+13413A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217932 | ||||||
| chr14:99217997
|
A | G | 1 | a0001c0001t0074g0259 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.640+13348T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99217997 | ||||||
| chr14:99218061
|
G | GT | 40 | a0001c0001t0001g0162a0001c0001t0001g0173a0001c0001t0001g0203others(37): Show | 40 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.640+13283dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218061 | ||||||
| chr14:99218061
|
GT | G | 24 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0228others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.640+13283delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218061 | ||||||
| chr14:99218084
|
G | A | 2 | a0001c0001t0005g0129a0001c0001t0009g0128 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.640+13261C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218084 | ||||||
| chr14:99218114
|
A | G | 4 | a0001c0001t0001g0188a0001c0001t0001g0232a0001c0001t0001g0271others(1): Show | 4 | NA19004.hp2 NA19063.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+13231T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218114 | ||||||
| chr14:99218152
|
G | A | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+13193C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218152 | ||||||
| chr14:99218232
|
A | AT | 100 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0162others(97): Show | 100 | HG00558.hp2 HG00621.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.640+13112dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218232 | ||||||
| chr14:99218232
|
A | ATT | 17 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(14): Show | 17 | HG00423.hp1 HG00423.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.640+13111_640+1311 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218232 | ||||||
| chr14:99218232
|
A | ATTTTT | 20 | a0001c0001t0001g0210a0001c0001t0001g0228a0001c0001t0001g0240others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(17): Show |
intron_variant | MODIFIER | c.640+13108_640+1311 others(9): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218232 | ||||||
| chr14:99218232
|
AT | A | 11 | a0001c0001t0003g0233a0001c0001t0003g0275a0001c0001t0003g0285others(8): Show | 11 | HG01168.hp2 HG01257.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.640+13112delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218232 | ||||||
| chr14:99218325
|
C | T | 1 | a0001c0001t0011g0299 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.640+13020G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218325 | ||||||
| chr14:99218332
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+13013C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218332 | ||||||
| chr14:99218375
|
C | T | 191 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.640+12970G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218375 | ||||||
| chr14:99218540
|
C | T | 1 | a0001c0002t0004g0018 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.640+12805G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218540 | ||||||
| chr14:99218669
|
T | C | 11 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0002g0040others(8): Show | 11 | HG00733.hp1 HG02145.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.640+12676A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218669 | ||||||
| chr14:99218764
|
G | A | 3 | a0001c0001t0008g0114a0001c0001t0052g0124a0001c0002t0046g0014 | 3 | HG01891.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.640+12581C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218764 | ||||||
| chr14:99218796
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+12549C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218796 | ||||||
| chr14:99218833
|
G | C | 27 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0162others(24): Show | 27 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.640+12512C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218833 | ||||||
| chr14:99218855
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.640+12490C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218855 | ||||||
| chr14:99218971
|
C | T | 1 | a0001c0001t0004g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.640+12374G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99218971 | ||||||
| chr14:99219045
|
CT | C | 167 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.640+12299delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219045 | ||||||
| chr14:99219049
|
T | C | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+12296A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219049 | ||||||
| chr14:99219094
|
T | C | 15 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(12): Show | 15 | HG00423.hp2 HG01884.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+12251A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219094 | ||||||
| chr14:99219095
|
G | A | 15 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(12): Show | 15 | HG00423.hp2 HG01884.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+12250C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219095 | ||||||
| chr14:99219291
|
CCCAAAGT others(10): Show |
C | 1 | a0001c0001t0011g0299 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.640+12037_640+1205 others(21): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219291 | ||||||
| chr14:99219314
|
G | A | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+12031C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219314 | ||||||
| chr14:99219411
|
G | A | 1 | a0001c0001t0005g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.640+11934C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219411 | ||||||
| chr14:99219692
|
C | T | 1 | a0001c0001t0030g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.640+11653G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219692 | ||||||
| chr14:99219811
|
A | T | 1 | a0001c0001t0074g0259 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.640+11534T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219811 | ||||||
| chr14:99219813
|
T | A | 1 | a0001c0001t0074g0259 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.640+11532A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219813 | ||||||
| chr14:99219813
|
T | TA | 55 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0205others(52): Show | 56 | HG00621.hp1 HG00673.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.640+11531dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219813 | ||||||
| chr14:99219813
|
T | TAA | 36 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0002g0061others(33): Show | 36 | HG01099.hp1 HG01168.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.640+11530_640+1153 others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219813 | ||||||
| chr14:99219813
|
TA | T | 13 | a0001c0001t0001g0172a0001c0001t0001g0189a0001c0001t0002g0040others(10): Show | 13 | HG00733.hp1 HG01256.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.640+11531delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219813 | ||||||
| chr14:99219928
|
A | G | 139 | a0001c0001t0001g0164a0001c0001t0001g0185a0001c0001t0001g0186others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.640+11417T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99219928 | ||||||
| chr14:99220035
|
C | G | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+11310G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220035 | ||||||
| chr14:99220051
|
T | G | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+11294A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220051 | ||||||
| chr14:99220071
|
T | C | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.640+11274A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220071 | ||||||
| chr14:99220107
|
G | A | 2 | a0001c0001t0009g0064a0001c0001t0009g0123 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.640+11238C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220107 | ||||||
| chr14:99220170
|
T | C | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+11175A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220170 | ||||||
| chr14:99220178
|
G | A | 1 | a0001c0001t0077g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.640+11167C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220178 | ||||||
| chr14:99220196
|
A | G | 96 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0212others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.640+11149T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220196 | ||||||
| chr14:99220199
|
A | G | 98 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0212others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.640+11146T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220199 | ||||||
| chr14:99220207
|
T | C | 26 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0228others(23): Show | 26 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.640+11138A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220207 | ||||||
| chr14:99220241
|
G | A | 1 | a0001c0002t0010g0330 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.640+11104C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220241 | ||||||
| chr14:99220277
|
A | G | 96 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0212others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.640+11068T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220277 | ||||||
| chr14:99220278
|
C | T | 197 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.640+11067G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220278 | ||||||
| chr14:99220281
|
A | G | 1 | a0001c0003t0004g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.640+11064T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220281 | ||||||
| chr14:99220285
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.640+11060A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220285 | ||||||
| chr14:99220297
|
G | A | 1 | a0001c0002t0021g0140 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.640+11048C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220297 | ||||||
| chr14:99220556
|
C | T | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+10789G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220556 | ||||||
| chr14:99220565
|
G | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0162others(4): Show | 7 | HG02083.hp1 NA18953.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+10780C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220565 | ||||||
| chr14:99220566
|
G | A | 7 | a0001c0001t0008g0054a0001c0001t0027g0230a0001c0001t0071g0187others(4): Show | 7 | HG00639.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+10779C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220566 | ||||||
| chr14:99220633
|
A | T | 102 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0212others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.640+10712T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220633 | ||||||
| chr14:99220665
|
G | A | 8 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(5): Show | 8 | HG02055.hp1 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.640+10680C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220665 | ||||||
| chr14:99220835
|
T | C | 2 | a0001c0002t0003g0168a0001c0002t0082g0336 | 2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.640+10510A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220835 | ||||||
| chr14:99220874
|
A | G | 166 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.640+10471T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220874 | ||||||
| chr14:99220919
|
C | T | 1 | a0001c0002t0049g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.640+10426G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99220919 | ||||||
| chr14:99221103
|
G | A | 3 | a0001c0001t0008g0054a0001c0002t0003g0264a0001c0002t0019g0130 | 3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.640+10242C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221103 | ||||||
| chr14:99221136
|
G | A | 1 | a0001c0002t0003g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.640+10209C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221136 | ||||||
| chr14:99221193
|
C | G | 1 | a0001c0001t0002g0039 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.640+10152G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221193 | ||||||
| chr14:99221436
|
C | T | 192 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.640+9909G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221436 | ||||||
| chr14:99221559
|
G | C | 3 | a0001c0002t0089g0345a0001c0006t0025g0191a0001c0006t0025g0192 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.640+9786C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221559 | ||||||
| chr14:99221560
|
C | T | 3 | a0001c0002t0089g0345a0001c0006t0025g0191a0001c0006t0025g0192 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.640+9785G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221560 | ||||||
| chr14:99221642
|
G | A | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.640+9703C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221642 | ||||||
| chr14:99221745
|
G | A | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+9600C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221745 | ||||||
| chr14:99221810
|
G | A | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+9535C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221810 | ||||||
| chr14:99221856
|
C | T | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+9489G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221856 | ||||||
| chr14:99221924
|
G | C | 201 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(198): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.640+9421C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99221924 | ||||||
| chr14:99222072
|
G | A | 177 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.640+9273C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222072 | ||||||
| chr14:99222097
|
G | A | 1 | a0001c0001t0043g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.640+9248C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222097 | ||||||
| chr14:99222261
|
GA | G | 179 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.640+9083delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222261 | ||||||
| chr14:99222333
|
G | A | 177 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.640+9012C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222333 | ||||||
| chr14:99222406
|
T | C | 67 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(64): Show | 67 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.640+8939A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222406 | ||||||
| chr14:99222434
|
G | A | 6 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0260others(3): Show | 6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+8911C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222434 | ||||||
| chr14:99222561
|
G | A | 46 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0001g0214others(43): Show | 46 | HG01074.hp1 HG01099.hp1 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.640+8784C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222561 | ||||||
| chr14:99222587
|
G | T | 10 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(7): Show | 10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+8758C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222587 | ||||||
| chr14:99222731
|
C | G | 64 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(61): Show | 64 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.640+8614G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222731 | ||||||
| chr14:99222836
|
C | CCTTT | 45 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0205others(42): Show | 46 | HG00621.hp1 HG00673.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.640+8505_640+8508d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222836 | ||||||
| chr14:99222836
|
C | CCTTTCTT others(5): Show |
1 | a0001c0001t0008g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.640+8497_640+8508d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222836 | ||||||
| chr14:99222836
|
C | CCTTTCTT others(21): Show |
1 | a0001c0002t0067g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.640+8508_640+8509i others(30): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222836 | ||||||
| chr14:99222836
|
CCTTT | C | 30 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0167others(27): Show | 30 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.640+8505_640+8508d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222836 | ||||||
| chr14:99222897
|
CTT | C | 3 | a0001c0001t0008g0054a0001c0002t0003g0264a0001c0002t0019g0130 | 3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.640+8446_640+8447d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99222897 | ||||||
| chr14:99223550
|
C | T | 3 | a0001c0002t0089g0345a0001c0006t0025g0191a0001c0006t0025g0192 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.640+7795G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99223550 | ||||||
| chr14:99223654
|
G | T | 4 | a0001c0001t0027g0230a0001c0001t0071g0187a0001c0002t0049g0057others(1): Show | 4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+7691C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99223654 | ||||||
| chr14:99223944
|
G | A | 1 | a0001c0002t0047g0015 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.640+7401C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99223944 | ||||||
| chr14:99223960
|
T | C | 1 | a0001c0001t0008g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.640+7385A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99223960 | ||||||
| chr14:99224048
|
C | T | 2 | a0001c0001t0002g0100a0001c0001t0006g0338 | 2 | HG00741.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.640+7297G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224048 | ||||||
| chr14:99224049
|
G | A | 1 | a0001c0001t0007g0155 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.640+7296C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224049 | ||||||
| chr14:99224129
|
A | G | 28 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0228others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.640+7216T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224129 | ||||||
| chr14:99224190
|
G | A | 46 | a0001c0001t0001g0164a0001c0001t0001g0210a0001c0001t0001g0219others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.640+7155C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224190 | ||||||
| chr14:99224532
|
C | T | 6 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0005g0066others(3): Show | 6 | HG00639.hp2 HG01074.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+6813G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224532 | ||||||
| chr14:99224533
|
G | A | 2 | a0001c0001t0002g0092a0001c0001t0005g0017 | 2 | NA18964.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.640+6812C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224533 | ||||||
| chr14:99224570
|
C | A | 252 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(249): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.640+6775G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224570 | ||||||
| chr14:99224598
|
C | T | 10 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(7): Show | 10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+6747G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224598 | ||||||
| chr14:99224616
|
G | A | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+6729C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224616 | ||||||
| chr14:99224648
|
T | C | 10 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(7): Show | 10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+6697A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224648 | ||||||
| chr14:99224696
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.640+6649T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224696 | ||||||
| chr14:99224753
|
A | G | 6 | a0001c0001t0012g0147a0001c0001t0012g0148a0001c0001t0022g0144others(3): Show | 6 | NA18968.hp1 NA18983.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+6592T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224753 | ||||||
| chr14:99224843
|
G | T | 200 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.640+6502C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224843 | ||||||
| chr14:99224992
|
G | T | 110 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.640+6353C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99224992 | ||||||
| chr14:99225086
|
G | C | 3 | a0001c0001t0008g0090a0001c0001t0016g0089a0001c0002t0004g0088 | 3 | HG03098.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.640+6259C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225086 | ||||||
| chr14:99225129
|
T | C | 2 | a0001c0001t0071g0187a0001c0002t0079g0292 | 2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.640+6216A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225129 | ||||||
| chr14:99225266
|
T | G | 7 | a0001c0001t0027g0230a0001c0001t0071g0187a0001c0002t0049g0057others(4): Show | 7 | HG00639.hp2 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+6079A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225266 | ||||||
| chr14:99225364
|
G | A | 2 | a0001c0001t0003g0248a0001c0001t0086g0342 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.640+5981C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225364 | ||||||
| chr14:99225406
|
C | T | 1 | a0001c0001t0038g0095 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.640+5939G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225406 | ||||||
| chr14:99225456
|
G | C | 28 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0228others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.640+5889C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225456 | ||||||
| chr14:99225642
|
A | T | 6 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0260others(3): Show | 6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+5703T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225642 | ||||||
| chr14:99225651
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.640+5694C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225651 | ||||||
| chr14:99225657
|
A | AAAAG | 4 | a0001c0001t0003g0267a0001c0001t0053g0137a0001c0002t0003g0152others(1): Show | 4 | HG01109.hp2 HG01981.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+5684_640+5687d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225657 | ||||||
| chr14:99225883
|
GCCCCAAC others(11): Show |
G | 1 | a0001c0001t0027g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.640+5444_640+5461d others(20): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225883 | ||||||
| chr14:99225917
|
T | C | 48 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(45): Show | 49 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(46): Show |
intron_variant | MODIFIER | c.640+5428A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225917 | ||||||
| chr14:99225934
|
T | C | 47 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(44): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+5411A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225934 | ||||||
| chr14:99225988
|
T | G | 11 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(8): Show | 11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+5357A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99225988 | ||||||
| chr14:99226057
|
C | T | 1 | a0001c0002t0003g0202 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.640+5288G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226057 | ||||||
| chr14:99226093
|
G | A | 148 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.640+5252C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226093 | ||||||
| chr14:99226318
|
G | A | 30 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0162others(27): Show | 30 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.640+5027C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226318 | ||||||
| chr14:99226350
|
C | T | 3 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0002t0004g0049 | 3 | HG02922.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.640+4995G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226350 | ||||||
| chr14:99226351
|
G | A | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+4994C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226351 | ||||||
| chr14:99226402
|
G | A | 47 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(44): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.640+4943C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99226402 | ||||||
| chr14:99227097
|
A | T | 10 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(7): Show | 10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.640+4248T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227097 | ||||||
| chr14:99227211
|
T | A | 1 | a0001c0002t0003g0207 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.640+4134A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227211 | ||||||
| chr14:99227250
|
G | A | 58 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(55): Show | 58 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.640+4095C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227250 | ||||||
| chr14:99227298
|
T | C | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+4047A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227298 | ||||||
| chr14:99227375
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0090g0346a0001c0002t0003g0286 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.640+3970G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227375 | ||||||
| chr14:99227482
|
C | T | 6 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0260others(3): Show | 6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+3863G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227482 | ||||||
| chr14:99227506
|
G | T | 27 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0228others(24): Show | 27 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.640+3839C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227506 | ||||||
| chr14:99227565
|
C | T | 3 | a0001c0002t0007g0255a0001c0002t0007g0256a0001c0002t0017g0300 | 3 | HG01168.hp2 HG01169.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.640+3780G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227565 | ||||||
| chr14:99227576
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.640+3769C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227576 | ||||||
| chr14:99227654
|
G | A | 3 | a0001c0001t0001g0222a0001c0001t0012g0142a0001c0001t0012g0143 | 3 | NA18969.hp1 NA18977.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.640+3691C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227654 | ||||||
| chr14:99227676
|
C | T | 3 | a0001c0001t0008g0114a0001c0001t0052g0124a0001c0002t0046g0014 | 3 | HG01891.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.640+3669G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227676 | ||||||
| chr14:99227855
|
C | T | 1 | a0001c0001t0002g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.640+3490G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227855 | ||||||
| chr14:99227881
|
T | G | 6 | a0001c0001t0008g0054a0001c0001t0008g0119a0001c0001t0077g0290others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+3464A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99227881 | ||||||
| chr14:99228112
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.640+3233A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228112 | ||||||
| chr14:99228379
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.640+2966A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228379 | ||||||
| chr14:99228423
|
C | A | 17 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(14): Show | 17 | HG00423.hp2 HG00639.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.640+2922G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228423 | ||||||
| chr14:99228537
|
A | C | 2 | a0001c0002t0004g0091a0001c0002t0004g0126 | 2 | NA19002.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.640+2808T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228537 | ||||||
| chr14:99228714
|
G | A | 2 | a0001c0001t0061g0196a0001c0002t0064g0269 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.640+2631C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228714 | ||||||
| chr14:99228931
|
G | A | 57 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(54): Show | 57 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.640+2414C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228931 | ||||||
| chr14:99228976
|
A | C | 1 | a0001c0002t0003g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.640+2369T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99228976 | ||||||
| chr14:99229003
|
A | AATGG | 15 | a0001c0001t0001g0205a0001c0001t0001g0218a0001c0001t0001g0229others(12): Show | 15 | HG01074.hp2 HG01934.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+2338_640+2341d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | ||||||
| chr14:99229003
|
A | AATGGAGG others(5): Show |
4 | a0001c0001t0008g0084a0001c0001t0014g0260a0001c0001t0015g0083others(1): Show | 4 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2341_640+2342i others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | ||||||
| chr14:99229003
|
A | AATGGATG others(1): Show |
11 | a0001c0001t0001g0188a0001c0001t0001g0208a0001c0001t0001g0234others(8): Show | 12 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.640+2334_640+2341d others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | ||||||
| chr14:99229003
|
A | AATGGATG others(5): Show |
5 | a0001c0001t0036g0007a0001c0001t0037g0010a0001c0002t0001g0237others(2): Show | 5 | HG02056.hp1 HG02451.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+2330_640+2341d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | ||||||
| chr14:99229003
|
A | G | 1 | a0001c0001t0013g0334 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.640+2342T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | ||||||
| chr14:99229003
|
AATGG | A | 3 | a0001c0001t0001g0272a0001c0002t0003g0152a0001c0002t0004g0050 | 3 | HG01109.hp2 HG01981.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.640+2338_640+2341d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | ||||||
| chr14:99229003
|
AATGGATG others(33): Show |
A | 1 | a0001c0002t0049g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.640+2302_640+2341d others(42): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229003 | ||||||
| chr14:99229007
|
GATGGATG others(29): Show |
G | 5 | a0001c0001t0027g0230a0001c0001t0071g0187a0001c0002t0089g0345others(2): Show | 5 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+2302_640+2337d others(38): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229007 | ||||||
| chr14:99229011
|
GATGGATG others(25): Show |
G | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.640+2302_640+2333d others(34): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229011 | ||||||
| chr14:99229031
|
G | GATGGATG others(9): Show |
2 | a0001c0001t0002g0056a0001c0001t0006g0319 | 2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.640+2313_640+2314i others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229031 | ||||||
| chr14:99229031
|
G | GATGGATG others(13): Show |
4 | a0001c0001t0001g0193a0001c0001t0001g0242a0001c0001t0061g0196others(1): Show | 4 | HG01109.hp1 HG02293.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2313_640+2314i others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229031 | ||||||
| chr14:99229035
|
G | C | 1 | a0001c0002t0019g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640+2310C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229035 | ||||||
| chr14:99229035
|
G | GATGGATG others(9): Show |
6 | a0001c0001t0002g0058a0001c0001t0091g0347a0001c0002t0003g0174others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2309_640+2310i others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229035 | ||||||
| chr14:99229039
|
G | GATGGATG others(1): Show |
4 | a0001c0001t0001g0203a0001c0001t0001g0271a0001c0001t0077g0290others(1): Show | 4 | HG00438.hp1 HG00609.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2305_640+2306i others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229039 | ||||||
| chr14:99229039
|
G | GATGGATG others(5): Show |
33 | a0001c0001t0001g0157a0001c0001t0001g0162a0001c0001t0001g0163others(30): Show | 33 | HG00621.hp2 HG01261.hp2 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.640+2305_640+2306i others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229039 | ||||||
| chr14:99229039
|
G | GATGGATG others(9): Show |
8 | a0001c0001t0001g0158a0001c0001t0002g0097a0001c0001t0004g0110others(5): Show | 8 | HG00423.hp1 HG01175.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.640+2305_640+2306i others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229039 | ||||||
| chr14:99229039
|
GATGC | G | 6 | a0001c0001t0008g0114a0001c0001t0052g0124a0001c0002t0003g0202others(3): Show | 6 | HG00673.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+2302_640+2305d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229039 | ||||||
| chr14:99229043
|
C | CATGG | 46 | a0001c0001t0001g0189a0001c0001t0001g0200a0001c0001t0001g0214others(43): Show | 46 | HG00558.hp1 HG00597.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.640+2298_640+2301d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | ||||||
| chr14:99229043
|
C | CATGGATG others(1): Show |
12 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0172others(9): Show | 12 | HG01099.hp1 HG02615.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.640+2294_640+2301d others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | ||||||
| chr14:99229043
|
C | CATGGATG others(5): Show |
6 | a0001c0001t0005g0116a0001c0001t0011g0301a0001c0001t0016g0073others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2290_640+2301d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | ||||||
| chr14:99229043
|
C | CATGGATG others(9): Show |
1 | a0001c0001t0002g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.640+2286_640+2301d others(18): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | ||||||
| chr14:99229043
|
C | CATGGATG others(13): Show |
1 | a0001c0001t0001g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.640+2282_640+2301d others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | ||||||
| chr14:99229043
|
C | G | 141 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.640+2302G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | ||||||
| chr14:99229043
|
CATGG | C | 4 | a0001c0001t0013g0334a0001c0001t0020g0086a0001c0002t0018g0011others(1): Show | 4 | HG00639.hp1 HG00642.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2298_640+2301d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229043 | ||||||
| chr14:99229047
|
G | C | 6 | a0001c0001t0002g0112a0001c0001t0012g0148a0001c0001t0014g0182others(3): Show | 6 | HG01884.hp1 HG02015.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2298C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229047 | ||||||
| chr14:99229047
|
G | GATGC | 38 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0001g0212others(35): Show | 38 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.640+2297_640+2298i others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229047 | ||||||
| chr14:99229047
|
G | GATGGATG others(1): Show |
7 | a0001c0001t0001g0186a0001c0001t0003g0267a0001c0001t0005g0076others(4): Show | 7 | HG01981.hp2 HG02698.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+2297_640+2298i others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229047 | ||||||
| chr14:99229047
|
G | GATGGATG others(5): Show |
3 | a0001c0001t0002g0016a0001c0001t0005g0028a0001c0001t0006g0341 | 3 | HG01243.hp1 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.640+2297_640+2298i others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229047 | ||||||
| chr14:99229051
|
G | C | 5 | a0001c0001t0001g0253a0001c0001t0001g0276a0001c0001t0063g0153others(2): Show | 5 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.640+2294C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229051 | ||||||
| chr14:99229051
|
G | GATGC | 15 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0240others(12): Show | 15 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.640+2293_640+2294i others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229051 | ||||||
| chr14:99229055
|
G | C | 7 | a0001c0001t0002g0042a0001c0001t0008g0114a0001c0001t0052g0124others(4): Show | 7 | HG00280.hp2 HG01069.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+2290C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229055 | ||||||
| chr14:99229055
|
G | GATGA | 4 | a0001c0001t0001g0238a0001c0002t0001g0237a0001c0002t0003g0265others(1): Show | 4 | HG02056.hp1 NA18952.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+2289_640+2290i others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229055 | ||||||
| chr14:99229055
|
G | GATGCATG others(13): Show |
6 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0266others(3): Show | 6 | HG00423.hp2 HG02071.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2289_640+2290i others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229055 | ||||||
| chr14:99229059
|
G | A | 1 | a0001c0002t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.640+2286C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229059 | ||||||
| chr14:99229059
|
G | C | 4 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0011g0296others(1): Show | 4 | HG01099.hp2 HG01516.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2286C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229059 | ||||||
| chr14:99229090
|
A | G | 7 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(4): Show | 7 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.640+2255T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229090 | ||||||
| chr14:99229094
|
G | A | 1 | a0001c0002t0003g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.640+2251C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229094 | ||||||
| chr14:99229098
|
G | A | 6 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2247C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229098 | ||||||
| chr14:99229110
|
A | G | 6 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2235T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229110 | ||||||
| chr14:99229111
|
C | G | 6 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2234G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229111 | ||||||
| chr14:99229113
|
G | T | 6 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2232C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229113 | ||||||
| chr14:99229113
|
GGGATGAA others(5): Show |
G | 4 | a0001c0002t0079g0292a0001c0002t0089g0345a0001c0006t0025g0191others(1): Show | 4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+2220_640+2231d others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229113 | ||||||
| chr14:99229115
|
GATGA | G | 11 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(8): Show | 11 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.640+2226_640+2229d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229115 | ||||||
| chr14:99229118
|
G | A | 6 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2227C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229118 | ||||||
| chr14:99229119
|
A | AATGG | 102 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0199others(99): Show | 103 | HG00558.hp1 HG00597.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.640+2222_640+2225d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | ||||||
| chr14:99229119
|
A | AATGGATG others(1): Show |
14 | a0001c0001t0001g0212a0001c0001t0002g0051a0001c0001t0002g0052others(11): Show | 14 | HG01074.hp1 HG01099.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+2218_640+2225d others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | ||||||
| chr14:99229119
|
A | C | 6 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2226T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | ||||||
| chr14:99229119
|
AATGG | A | 27 | a0001c0001t0001g0205a0001c0001t0001g0223a0001c0001t0002g0019others(24): Show | 28 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.640+2222_640+2225d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | ||||||
| chr14:99229119
|
AATGGATG others(1): Show |
A | 22 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0240others(19): Show | 22 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.640+2218_640+2225d others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229119 | ||||||
| chr14:99229121
|
T | G | 6 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2224A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229121 | ||||||
| chr14:99229127
|
G | A | 6 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0002g0042others(3): Show | 6 | HG00280.hp2 HG01069.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.640+2218C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229127 | ||||||
| chr14:99229153
|
T | C | 63 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(60): Show | 63 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.640+2192A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229153 | ||||||
| chr14:99229167
|
G | A | 1 | a0001c0002t0064g0269 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.640+2178C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229167 | ||||||
| chr14:99229337
|
G | A | 2 | a0001c0001t0006g0305a0001c0001t0006g0306 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.640+2008C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229337 | ||||||
| chr14:99229360
|
GGCAGA | G | 4 | a0001c0001t0027g0230a0001c0001t0071g0187a0001c0002t0049g0057others(1): Show | 4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1980_640+1984d others(7): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229360 | ||||||
| chr14:99229367
|
C | A | 4 | a0001c0001t0027g0230a0001c0001t0071g0187a0001c0002t0049g0057others(1): Show | 4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1978G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229367 | ||||||
| chr14:99229369
|
C | T | 4 | a0001c0001t0027g0230a0001c0001t0071g0187a0001c0002t0049g0057others(1): Show | 4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1976G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229369 | ||||||
| chr14:99229370
|
C | T | 4 | a0001c0001t0027g0230a0001c0001t0071g0187a0001c0002t0049g0057others(1): Show | 4 | HG00639.hp2 HG02258.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1975G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229370 | ||||||
| chr14:99229432
|
G | T | 1 | a0001c0001t0005g0024 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.640+1913C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229432 | ||||||
| chr14:99229504
|
C | T | 2 | a0001c0001t0003g0248a0001c0001t0086g0342 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.640+1841G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229504 | ||||||
| chr14:99229543
|
A | G | 10 | a0001c0001t0008g0054a0001c0001t0008g0119a0001c0001t0008g0131others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+1802T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229543 | ||||||
| chr14:99229604
|
T | C | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.640+1741A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229604 | ||||||
| chr14:99229732
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0002g0102 | 2 | HG01981.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.640+1613C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229732 | ||||||
| chr14:99229767
|
C | T | 199 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(196): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.640+1578G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229767 | ||||||
| chr14:99229801
|
G | A | 1 | a0001c0001t0027g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.640+1544C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99229801 | ||||||
| chr14:99230265
|
A | G | 6 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0260others(3): Show | 6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+1080T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230265 | ||||||
| chr14:99230371
|
C | T | 1 | a0001c0001t0005g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.640+974G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230371 | ||||||
| chr14:99230439
|
A | G | 1 | a0001c0002t0019g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.640+906T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230439 | ||||||
| chr14:99230774
|
C | T | 2 | a0001c0001t0074g0259a0001c0002t0003g0227 | 2 | NA18965.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.640+571G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230774 | ||||||
| chr14:99230820
|
G | A | 4 | a0001c0001t0006g0317a0001c0001t0006g0332a0001c0001t0006g0338others(1): Show | 4 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.640+525C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230820 | ||||||
| chr14:99230973
|
G | A | 6 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0260others(3): Show | 6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+372C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230973 | ||||||
| chr14:99230995
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.640+350C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99230995 | ||||||
| chr14:99231000
|
A | AG | 9 | a0001c0001t0001g0225a0001c0001t0001g0252a0001c0001t0002g0093others(6): Show | 9 | HG00438.hp2 HG01099.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.640+344dupC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99231000 | ||||||
| chr14:99231082
|
A | G | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.640+263T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99231082 | ||||||
| chr14:99231248
|
T | C | 1 | a0001c0001t0016g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.640+97A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99231248 | ||||||
| chr14:99231328
|
G | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0052 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.640+17C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 3/3 | chr14 | 99231328 | ||||||
| chr14:99231638
|
C | T | 1 | a0001c0001t0027g0230 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.428-81G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231638 | ||||||
| chr14:99231648
|
T | G | 8 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0005g0066others(5): Show | 8 | HG01074.hp1 HG02015.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-91A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231648 | ||||||
| chr14:99231653
|
A | G | 8 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0005g0066others(5): Show | 8 | HG01074.hp1 HG02015.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-96T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231653 | ||||||
| chr14:99231664
|
C | T | 6 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0260others(3): Show | 6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-107G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231664 | ||||||
| chr14:99231815
|
G | A | 1 | a0001c0002t0017g0300 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.428-258C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231815 | ||||||
| chr14:99231867
|
A | C | 1 | a0001c0002t0003g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.428-310T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231867 | ||||||
| chr14:99231874
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.428-317C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231874 | ||||||
| chr14:99231932
|
T | G | 1 | a0001c0001t0008g0131 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.428-375A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231932 | ||||||
| chr14:99231976
|
G | A | 3 | a0001c0001t0016g0030a0001c0001t0020g0086a0001c0005t0009g0029 | 3 | HG02723.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.428-419C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99231976 | ||||||
| chr14:99232158
|
C | T | 6 | a0001c0001t0008g0084a0001c0001t0014g0182a0001c0001t0014g0260others(3): Show | 6 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-601G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232158 | ||||||
| chr14:99232198
|
C | A | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.428-641G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232198 | ||||||
| chr14:99232454
|
T | C | 6 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0005g0066others(3): Show | 6 | HG01074.hp1 HG02015.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-897A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232454 | ||||||
| chr14:99232505
|
G | C | 4 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0006g0335others(1): Show | 4 | HG01106.hp2 HG01243.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-948C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232505 | ||||||
| chr14:99232594
|
C | A | 82 | a0001c0001t0001g0164a0001c0001t0001g0185a0001c0001t0001g0214others(79): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.428-1037G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232594 | ||||||
| chr14:99232595
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.428-1038C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232595 | ||||||
| chr14:99232740
|
T | C | 6 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0005g0066others(3): Show | 6 | HG01074.hp1 HG02015.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-1183A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232740 | ||||||
| chr14:99232776
|
C | T | 7 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0006g0002others(4): Show | 8 | HG00140.hp1 HG00280.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-1219G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232776 | ||||||
| chr14:99232866
|
C | T | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.428-1309G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99232866 | ||||||
| chr14:99233025
|
T | C | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.428-1468A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233025 | ||||||
| chr14:99233033
|
G | A | 1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.428-1476C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233033 | ||||||
| chr14:99233359
|
C | T | 11 | a0001c0001t0001g0210a0001c0001t0001g0252a0001c0001t0001g0276others(8): Show | 11 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.428-1802G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233359 | ||||||
| chr14:99233682
|
T | A | 47 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(44): Show | 47 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.428-2125A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233682 | ||||||
| chr14:99233743
|
C | T | 43 | a0001c0001t0001g0185a0001c0001t0001g0223a0001c0001t0001g0231others(40): Show | 44 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.428-2186G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233743 | ||||||
| chr14:99233778
|
G | A | 2 | a0001c0001t0003g0275a0001c0001t0003g0285 | 2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.428-2221C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233778 | ||||||
| chr14:99233794
|
G | A | 10 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(7): Show | 10 | HG00423.hp2 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.428-2237C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99233794 | ||||||
| chr14:99234117
|
C | T | 134 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(131): Show | 135 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.428-2560G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234117 | ||||||
| chr14:99234205
|
G | A | 1 | a0001c0001t0007g0197 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.428-2648C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234205 | ||||||
| chr14:99234482
|
C | G | 1 | a0001c0001t0042g0072 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.428-2925G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234482 | ||||||
| chr14:99234657
|
A | G | 2 | a0001c0001t0036g0007a0001c0001t0091g0347 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.428-3100T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234657 | ||||||
| chr14:99234677
|
G | A | 2 | a0001c0001t0001g0235a0001c0001t0005g0078 | 2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.428-3120C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234677 | ||||||
| chr14:99234759
|
G | T | 29 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0162others(26): Show | 29 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.428-3202C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234759 | ||||||
| chr14:99234855
|
C | CA | 48 | a0001c0001t0001g0193a0001c0001t0001g0199a0001c0001t0001g0203others(45): Show | 48 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.428-3299dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234855 | ||||||
| chr14:99234855
|
CA | C | 33 | a0001c0001t0001g0231a0001c0001t0002g0016a0001c0001t0002g0111others(30): Show | 34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.428-3299delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234855 | ||||||
| chr14:99234855
|
CAA | C | 34 | a0001c0001t0002g0061a0001c0001t0002g0067a0001c0001t0002g0068others(31): Show | 35 | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.428-3300_428-3299d others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234855 | ||||||
| chr14:99234880
|
A | AAAAG | 6 | a0001c0001t0007g0239a0001c0001t0011g0296a0001c0001t0011g0299others(3): Show | 6 | HG00673.hp2 HG01192.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-3324_428-3323i others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | ||||||
| chr14:99234880
|
A | AAAG | 25 | a0001c0001t0001g0164a0001c0001t0001g0210a0001c0001t0001g0219others(22): Show | 25 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.428-3324_428-3323i others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | ||||||
| chr14:99234880
|
A | AAG | 18 | a0001c0001t0001g0224a0001c0001t0001g0238a0001c0001t0001g0266others(15): Show | 18 | HG00621.hp1 HG01433.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.428-3324_428-3323i others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | ||||||
| chr14:99234880
|
A | AG | 24 | a0001c0001t0001g0157a0001c0001t0001g0212a0001c0001t0001g0214others(21): Show | 24 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.428-3324dupC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | ||||||
| chr14:99234880
|
A | G | 44 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0162others(41): Show | 44 | HG00558.hp2 HG00733.hp2 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.428-3323T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99234880 | ||||||
| chr14:99235038
|
T | C | 1 | a0001c0001t0002g0107 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.428-3481A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235038 | ||||||
| chr14:99235044
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.428-3487G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235044 | ||||||
| chr14:99235122
|
G | C | 199 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.428-3565C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235122 | ||||||
| chr14:99235171
|
G | A | 13 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(10): Show | 13 | HG00423.hp2 HG00621.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.428-3614C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235171 | ||||||
| chr14:99235238
|
C | T | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.428-3681G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235238 | ||||||
| chr14:99235344
|
G | A | 1 | a0001c0002t0003g0209 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.428-3787C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235344 | ||||||
| chr14:99235644
|
TC | T | 40 | a0001c0001t0002g0061a0001c0001t0002g0067a0001c0001t0002g0068others(37): Show | 41 | HG00639.hp2 HG01099.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.428-4088delG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235644 | ||||||
| chr14:99235746
|
G | T | 1 | a0001c0002t0019g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.428-4189C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235746 | ||||||
| chr14:99235831
|
A | AT | 13 | a0001c0001t0001g0164a0001c0001t0001g0224a0001c0001t0001g0238others(10): Show | 13 | HG00423.hp2 HG00621.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.428-4275dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235831 | ||||||
| chr14:99235898
|
A | T | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.428-4341T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235898 | ||||||
| chr14:99235906
|
TA | T | 195 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.428-4350delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235906 | ||||||
| chr14:99235953
|
T | A | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.428-4396A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235953 | ||||||
| chr14:99235961
|
G | C | 1 | a0001c0001t0054g0138 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.428-4404C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99235961 | ||||||
| chr14:99236171
|
G | A | 1 | a0001c0002t0004g0133 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.428-4614C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99236171 | ||||||
| chr14:99236253
|
A | T | 2 | a0001c0001t0007g0204a0001c0002t0004g0121 | 2 | HG00597.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.428-4696T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99236253 | ||||||
| chr14:99237041
|
C | T | 1 | a0001c0002t0004g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.428-5484G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237041 | ||||||
| chr14:99237137
|
G | A | 31 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(28): Show | 32 | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.428-5580C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237137 | ||||||
| chr14:99237236
|
CT | C | 43 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(40): Show | 44 | HG00639.hp2 HG00673.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.428-5680delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237236 | ||||||
| chr14:99237621
|
C | G | 14 | a0001c0001t0001g0164a0001c0001t0001g0199a0001c0001t0001g0224others(11): Show | 14 | HG00423.hp2 HG00621.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-6064G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237621 | ||||||
| chr14:99237631
|
C | T | 44 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.428-6074G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237631 | ||||||
| chr14:99237844
|
C | A | 160 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.428-6287G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237844 | ||||||
| chr14:99237860
|
C | A | 1 | a0001c0001t0009g0064 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.428-6303G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237860 | ||||||
| chr14:99237907
|
G | A | 31 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(28): Show | 32 | HG01099.hp1 HG01109.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.428-6350C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99237907 | ||||||
| chr14:99238090
|
A | G | 44 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.428-6533T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238090 | ||||||
| chr14:99238113
|
G | A | 1 | a0002c0009t0003g0195 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.428-6556C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238113 | ||||||
| chr14:99238115
|
G | A | 44 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.428-6558C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238115 | ||||||
| chr14:99238195
|
G | A | 1 | a0001c0002t0003g0202 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.428-6638C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238195 | ||||||
| chr14:99238344
|
G | A | 1 | a0001c0001t0052g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.428-6787C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238344 | ||||||
| chr14:99238432
|
C | T | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.428-6875G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238432 | ||||||
| chr14:99238954
|
T | A | 149 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(146): Show | 150 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.428-7397A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238954 | ||||||
| chr14:99238989
|
A | ACATATG | 14 | a0001c0001t0001g0164a0001c0001t0001g0199a0001c0001t0001g0224others(11): Show | 14 | HG00423.hp2 HG00621.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.428-7438_428-7433d others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238989 | ||||||
| chr14:99238994
|
T | C | 45 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(42): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.428-7437A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238994 | ||||||
| chr14:99238999
|
G | A | 201 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.428-7442C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99238999 | ||||||
| chr14:99239420
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.428-7863C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239420 | ||||||
| chr14:99239488
|
G | C | 5 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0253others(2): Show | 5 | HG00609.hp2 HG03831.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-7931C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239488 | ||||||
| chr14:99239617
|
G | A | 150 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(147): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.428-8060C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239617 | ||||||
| chr14:99239625
|
T | A | 2 | a0001c0001t0027g0230a0001c0001t0077g0290 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.428-8068A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239625 | ||||||
| chr14:99239785
|
A | G | 1 | a0001c0002t0003g0249 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.428-8228T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239785 | ||||||
| chr14:99239875
|
G | A | 7 | a0001c0001t0002g0039a0001c0001t0036g0007a0001c0001t0091g0347others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.428-8318C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99239875 | ||||||
| chr14:99240137
|
G | A | 45 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(42): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.428-8580C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240137 | ||||||
| chr14:99240283
|
G | A | 150 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(147): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.428-8726C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240283 | ||||||
| chr14:99240297
|
C | T | 4 | a0001c0001t0008g0119a0001c0001t0027g0230a0001c0001t0077g0290others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-8740G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240297 | ||||||
| chr14:99240369
|
T | C | 1 | a0001c0001t0006g0321 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.428-8812A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240369 | ||||||
| chr14:99240500
|
A | T | 24 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0240others(21): Show | 24 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.428-8943T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240500 | ||||||
| chr14:99240691
|
C | T | 1 | a0001c0001t0005g0078 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.428-9134G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240691 | ||||||
| chr14:99240774
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.428-9217G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240774 | ||||||
| chr14:99240849
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0070g0171 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.428-9292G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240849 | ||||||
| chr14:99240854
|
C | T | 1 | a0001c0001t0015g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.428-9297G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240854 | ||||||
| chr14:99240880
|
G | A | 199 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.428-9323C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240880 | ||||||
| chr14:99240991
|
T | C | 4 | a0001c0001t0009g0064a0001c0001t0009g0123a0001c0001t0034g0005others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-9434A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99240991 | ||||||
| chr14:99241018
|
AT | A | 61 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(58): Show | 61 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.428-9462delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241018 | ||||||
| chr14:99241487
|
A | G | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.428-9930T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241487 | ||||||
| chr14:99241492
|
C | T | 3 | a0001c0001t0009g0080a0001c0001t0015g0079a0001c0001t0069g0221 | 3 | HG02615.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.428-9935G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241492 | ||||||
| chr14:99241596
|
C | T | 53 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(50): Show | 54 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.428-10039G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241596 | ||||||
| chr14:99241677
|
C | T | 3 | a0001c0001t0001g0203a0001c0002t0003g0250a0001c0002t0010g0318 | 3 | HG00438.hp1 HG00609.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.428-10120G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241677 | ||||||
| chr14:99241936
|
C | T | 1 | a0001c0001t0002g0016 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.428-10379G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241936 | ||||||
| chr14:99241992
|
C | T | 1 | a0001c0001t0036g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.428-10435G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241992 | ||||||
| chr14:99241997
|
G | A | 3 | a0001c0002t0003g0174a0001c0002t0003g0175a0001c0002t0003g0183 | 3 | HG02258.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.428-10440C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99241997 | ||||||
| chr14:99242028
|
G | A | 15 | a0001c0001t0001g0199a0001c0001t0001g0224a0001c0001t0001g0238others(12): Show | 15 | HG00621.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.428-10471C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242028 | ||||||
| chr14:99242310
|
G | A | 8 | a0001c0001t0001g0276a0001c0001t0003g0267a0001c0001t0006g0337others(5): Show | 8 | HG00140.hp2 HG00738.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-10753C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242310 | ||||||
| chr14:99242334
|
C | T | 1 | a0001c0001t0050g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.428-10777G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242334 | ||||||
| chr14:99242400
|
G | A | 4 | a0001c0001t0009g0123a0001c0001t0034g0005a0001c0001t0051g0082others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-10843C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242400 | ||||||
| chr14:99242466
|
A | G | 2 | a0001c0001t0002g0019a0001c0002t0004g0034 | 2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.428-10909T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242466 | ||||||
| chr14:99242494
|
A | C | 1 | a0001c0001t0036g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.428-10937T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242494 | ||||||
| chr14:99242539
|
G | A | 116 | a0001c0001t0001g0159a0001c0001t0001g0172a0001c0001t0001g0178others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.428-10982C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242539 | ||||||
| chr14:99242598
|
C | T | 2 | a0001c0001t0008g0114a0001c0001t0037g0010 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428-11041G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99242598 | ||||||
| chr14:99243099
|
G | A | 58 | a0001c0001t0001g0159a0001c0001t0001g0172a0001c0001t0001g0178others(55): Show | 58 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.428-11542C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243099 | ||||||
| chr14:99243139
|
C | A | 3 | a0001c0001t0016g0030a0001c0001t0020g0086a0001c0005t0009g0029 | 3 | HG02723.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.428-11582G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243139 | ||||||
| chr14:99243281
|
C | T | 34 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0240others(31): Show | 34 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.428-11724G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243281 | ||||||
| chr14:99243365
|
A | C | 91 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0199others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.428-11808T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243365 | ||||||
| chr14:99243424
|
A | G | 30 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0240others(27): Show | 30 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.428-11867T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243424 | ||||||
| chr14:99243533
|
G | A | 1 | a0001c0001t0005g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.428-11976C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243533 | ||||||
| chr14:99243693
|
A | G | 3 | a0001c0001t0008g0114a0001c0001t0009g0060a0001c0001t0037g0010 | 3 | HG02970.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428-12136T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243693 | ||||||
| chr14:99243837
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.428-12280C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243837 | ||||||
| chr14:99243918
|
TAAAAA | T | 6 | a0001c0001t0001g0199a0001c0001t0017g0304a0001c0001t0040g0134others(3): Show | 6 | HG00621.hp1 HG02055.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.428-12366_428-1236 others(9): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | ||||||
| chr14:99243918
|
TAAAAAA | T | 19 | a0001c0001t0001g0185a0001c0001t0001g0224a0001c0001t0001g0231others(16): Show | 19 | HG01074.hp1 HG01106.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.428-12367_428-1236 others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | ||||||
| chr14:99243918
|
TAAAAAAA | T | 43 | a0001c0001t0002g0016a0001c0001t0002g0055a0001c0001t0002g0061others(40): Show | 44 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.428-12368_428-1236 others(11): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | ||||||
| chr14:99243918
|
TAAAAAAA others(11): Show |
T | 3 | a0001c0001t0008g0114a0001c0001t0009g0060a0001c0001t0037g0010 | 3 | HG02970.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.428-12379_428-1236 others(22): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | ||||||
| chr14:99243918
|
TAAAAAAA others(13): Show |
T | 2 | a0001c0001t0027g0230a0001c0001t0071g0187 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.428-12381_428-1236 others(24): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | ||||||
| chr14:99243918
|
TAAAAAAA others(16): Show |
T | 272 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(269): Show | 273 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.428-12384_428-1236 others(27): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243918 | ||||||
| chr14:99243942
|
A | T | 1 | a0001c0002t0089g0345 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.428-12385T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243942 | ||||||
| chr14:99243964
|
G | A | 1 | a0001c0001t0001g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.428-12407C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243964 | ||||||
| chr14:99243988
|
C | G | 1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.428-12431G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243988 | ||||||
| chr14:99243989
|
G | T | 1 | a0001c0001t0022g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.428-12432C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99243989 | ||||||
| chr14:99244009
|
A | T | 1 | a0001c0001t0080g0303 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.428-12452T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244009 | ||||||
| chr14:99244109
|
C | T | 1 | a0001c0001t0005g0047 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.428-12552G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244109 | ||||||
| chr14:99244121
|
T | C | 3 | a0001c0001t0008g0054a0001c0002t0003g0264a0001c0002t0019g0130 | 3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.428-12564A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244121 | ||||||
| chr14:99244295
|
C | A | 1 | a0001c0002t0004g0133 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.428-12738G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244295 | ||||||
| chr14:99244296
|
C | T | 1 | a0001c0002t0004g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.428-12739G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244296 | ||||||
| chr14:99244300
|
CT | C | 4 | a0001c0001t0001g0172a0001c0001t0002g0051a0001c0001t0002g0052others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.428-12744delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244300 | ||||||
| chr14:99244301
|
T | A | 3 | a0001c0002t0089g0345a0001c0006t0025g0191a0001c0006t0025g0192 | 3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.428-12744A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244301 | ||||||
| chr14:99244301
|
T | C | 6 | a0001c0001t0001g0158a0001c0001t0008g0114a0001c0001t0009g0060others(3): Show | 6 | HG02970.hp2 HG03579.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-12744A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244301 | ||||||
| chr14:99244303
|
A | C | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.428-12746T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244303 | ||||||
| chr14:99244303
|
A | T | 3 | a0001c0001t0001g0158a0001c0002t0003g0160a0004c0010t0007g0287 | 3 | NA18971.hp2 NA18998.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.428-12746T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244303 | ||||||
| chr14:99244350
|
C | T | 34 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(31): Show | 35 | HG01099.hp1 HG01109.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.428-12793G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244350 | ||||||
| chr14:99244506
|
C | T | 257 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(254): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.428-12949G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244506 | ||||||
| chr14:99244634
|
A | G | 1 | a0001c0001t0008g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.427+12837T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244634 | ||||||
| chr14:99244859
|
A | G | 347 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(344): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.427+12612T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244859 | ||||||
| chr14:99244994
|
G | A | 257 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(254): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.427+12477C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99244994 | ||||||
| chr14:99245057
|
T | C | 110 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0180others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.427+12414A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245057 | ||||||
| chr14:99245415
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.427+12056G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245415 | ||||||
| chr14:99245544
|
C | A | 1 | a0001c0001t0016g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427+11927G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245544 | ||||||
| chr14:99245545
|
C | A | 1 | a0001c0001t0016g0073 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.427+11926G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245545 | ||||||
| chr14:99245581
|
C | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+11890G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245581 | ||||||
| chr14:99245616
|
A | G | 110 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0180others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.427+11855T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245616 | ||||||
| chr14:99245686
|
A | AG | 347 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(344): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.427+11784_427+1178 others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245686 | ||||||
| chr14:99245695
|
G | A | 56 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(53): Show | 57 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.427+11776C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245695 | ||||||
| chr14:99245957
|
G | A | 1 | a0001c0001t0006g0341 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.427+11514C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245957 | ||||||
| chr14:99245964
|
G | A | 83 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0180others(80): Show | 83 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.427+11507C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99245964 | ||||||
| chr14:99246032
|
C | G | 46 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(43): Show | 46 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.427+11439G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246032 | ||||||
| chr14:99246069
|
G | A | 6 | a0001c0001t0007g0257a0001c0001t0007g0278a0001c0002t0007g0255others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.427+11402C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246069 | ||||||
| chr14:99246112
|
T | C | 32 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0240others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.427+11359A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246112 | ||||||
| chr14:99246276
|
A | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0242a0001c0001t0006g0319 | 3 | HG01109.hp1 HG01192.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.427+11195T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246276 | ||||||
| chr14:99246283
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.427+11188A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246283 | ||||||
| chr14:99246360
|
T | C | 15 | a0001c0001t0001g0199a0001c0001t0001g0224a0001c0001t0001g0238others(12): Show | 15 | HG00621.hp1 HG02056.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.427+11111A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246360 | ||||||
| chr14:99246457
|
C | T | 42 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.427+11014G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246457 | ||||||
| chr14:99246483
|
C | G | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+10988G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246483 | ||||||
| chr14:99246485
|
A | G | 2 | a0001c0001t0061g0196a0001c0002t0064g0269 | 2 | NA18978.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.427+10986T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246485 | ||||||
| chr14:99246556
|
T | C | 16 | a0001c0001t0001g0186a0001c0001t0001g0210a0001c0001t0001g0212others(13): Show | 16 | HG01070.hp2 HG01071.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.427+10915A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246556 | ||||||
| chr14:99246608
|
A | G | 54 | a0001c0001t0001g0185a0001c0001t0001g0231a0001c0001t0001g0282others(51): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.427+10863T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246608 | ||||||
| chr14:99246726
|
G | GT | 347 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(344): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.427+10744_427+1074 others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246726 | ||||||
| chr14:99246727
|
A | C | 347 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(344): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.427+10744T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246727 | ||||||
| chr14:99246911
|
A | G | 1 | a0001c0002t0003g0202 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.427+10560T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246911 | ||||||
| chr14:99246946
|
C | T | 2 | a0001c0001t0013g0327a0001c0002t0083g0328 | 2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.427+10525G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99246946 | ||||||
| chr14:99247662
|
C | T | 1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427+9809G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99247662 | ||||||
| chr14:99247694
|
C | T | 1 | a0001c0002t0010g0330 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.427+9777G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99247694 | ||||||
| chr14:99247827
|
G | C | 1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427+9644C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99247827 | ||||||
| chr14:99248096
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.427+9375C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99248096 | ||||||
| chr14:99248269
|
A | G | 2 | a0001c0001t0008g0119a0001c0002t0067g0177 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.427+9202T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99248269 | ||||||
| chr14:99248420
|
G | A | 260 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(257): Show | 261 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.427+9051C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99248420 | ||||||
| chr14:99248795
|
C | T | 1 | a0001c0001t0036g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427+8676G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99248795 | ||||||
| chr14:99249062
|
A | C | 1 | a0001c0001t0002g0032 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.427+8409T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249062 | ||||||
| chr14:99249070
|
G | A | 31 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0240others(28): Show | 31 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.427+8401C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249070 | ||||||
| chr14:99249237
|
A | G | 2 | a0001c0001t0008g0114a0001c0001t0009g0060 | 2 | HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.427+8234T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249237 | ||||||
| chr14:99249495
|
A | G | 4 | a0001c0001t0014g0190a0001c0002t0068g0170a0001c0004t0001g0001others(1): Show | 5 | HG02630.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+7976T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249495 | ||||||
| chr14:99249587
|
T | G | 70 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0210others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.427+7884A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249587 | ||||||
| chr14:99249594
|
T | G | 1 | a0001c0002t0004g0132 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.427+7877A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249594 | ||||||
| chr14:99249631
|
C | T | 2 | a0001c0001t0002g0019a0001c0002t0004g0034 | 2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.427+7840G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249631 | ||||||
| chr14:99249690
|
A | ATCTCTGG others(3): Show |
1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427+7771_427+7780d others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249690 | ||||||
| chr14:99249789
|
T | C | 17 | a0001c0001t0001g0193a0001c0001t0001g0242a0001c0001t0001g0244others(14): Show | 17 | HG00639.hp1 HG00642.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.427+7682A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99249789 | ||||||
| chr14:99250026
|
G | A | 1 | a0001c0002t0004g0077 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.427+7445C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250026 | ||||||
| chr14:99250033
|
C | CT | 37 | a0001c0001t0001g0219a0001c0001t0002g0067a0001c0001t0002g0068others(34): Show | 38 | HG01099.hp1 HG01175.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.427+7437dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250033 | ||||||
| chr14:99250033
|
CT | C | 136 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0180others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.427+7437delA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250033 | ||||||
| chr14:99250075
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.427+7396C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250075 | ||||||
| chr14:99250225
|
C | T | 47 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(44): Show | 47 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.427+7246G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250225 | ||||||
| chr14:99250241
|
T | C | 33 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0240others(30): Show | 33 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.427+7230A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250241 | ||||||
| chr14:99250413
|
G | A | 1 | a0001c0001t0036g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427+7058C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250413 | ||||||
| chr14:99250438
|
A | T | 1 | a0001c0002t0004g0132 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.427+7033T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250438 | ||||||
| chr14:99250481
|
C | T | 2 | a0001c0001t0001g0178a0001c0002t0004g0070 | 2 | HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.427+6990G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250481 | ||||||
| chr14:99250501
|
C | T | 1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.427+6970G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250501 | ||||||
| chr14:99250571
|
T | C | 72 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0210others(69): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.427+6900A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250571 | ||||||
| chr14:99250818
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+6653C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250818 | ||||||
| chr14:99250867
|
G | GA | 342 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(339): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.427+6603dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250867 | ||||||
| chr14:99250905
|
G | C | 332 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(329): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.427+6566C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99250905 | ||||||
| chr14:99251570
|
G | A | 332 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(329): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.427+5901C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99251570 | ||||||
| chr14:99251618
|
G | C | 347 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(344): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.427+5853C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99251618 | ||||||
| chr14:99251768
|
T | C | 71 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0210others(68): Show | 72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.427+5703A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99251768 | ||||||
| chr14:99251836
|
G | A | 56 | a0001c0001t0001g0159a0001c0001t0001g0172a0001c0001t0001g0178others(53): Show | 56 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.427+5635C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99251836 | ||||||
| chr14:99252179
|
G | A | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.427+5292C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252179 | ||||||
| chr14:99252261
|
G | A | 4 | a0001c0001t0008g0054a0001c0002t0003g0264a0001c0002t0004g0075others(1): Show | 4 | HG01934.hp2 HG02055.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+5210C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252261 | ||||||
| chr14:99252408
|
G | A | 1 | a0001c0002t0003g0194 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.427+5063C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252408 | ||||||
| chr14:99252526
|
G | C | 1 | a0001c0002t0004g0132 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.427+4945C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252526 | ||||||
| chr14:99252586
|
G | A | 245 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0167others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.427+4885C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252586 | ||||||
| chr14:99252588
|
G | A | 47 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(44): Show | 47 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.427+4883C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252588 | ||||||
| chr14:99252685
|
C | T | 1 | a0001c0002t0001g0237 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.427+4786G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252685 | ||||||
| chr14:99252695
|
C | G | 1 | a0001c0001t0001g0279 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.427+4776G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252695 | ||||||
| chr14:99252807
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+4664C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252807 | ||||||
| chr14:99252882
|
A | G | 268 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(265): Show | 269 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.427+4589T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99252882 | ||||||
| chr14:99253055
|
C | T | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+4416G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253055 | ||||||
| chr14:99253131
|
A | G | 9 | a0001c0001t0001g0229a0001c0001t0003g0275a0001c0001t0003g0285others(6): Show | 9 | HG00639.hp1 HG00642.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.427+4340T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253131 | ||||||
| chr14:99253343
|
T | C | 132 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0178others(129): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.427+4128A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253343 | ||||||
| chr14:99253362
|
A | G | 4 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0253others(1): Show | 4 | HG00609.hp2 NA18948.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.427+4109T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253362 | ||||||
| chr14:99253391
|
A | G | 22 | a0001c0001t0001g0186a0001c0001t0001g0210a0001c0001t0001g0212others(19): Show | 22 | HG01496.hp1 HG01516.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.427+4080T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253391 | ||||||
| chr14:99253465
|
C | T | 2 | a0001c0001t0009g0063a0001c0002t0019g0062 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.427+4006G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253465 | ||||||
| chr14:99253536
|
A | G | 167 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(164): Show | 167 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.427+3935T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253536 | ||||||
| chr14:99253537
|
T | G | 1 | a0001c0001t0005g0017 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.427+3934A>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253537 | ||||||
| chr14:99253858
|
A | G | 4 | a0001c0001t0008g0131a0001c0001t0009g0080a0001c0001t0015g0079others(1): Show | 4 | HG02615.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.427+3613T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99253858 | ||||||
| chr14:99254233
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.427+3238G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254233 | ||||||
| chr14:99254271
|
A | C | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.427+3200T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254271 | ||||||
| chr14:99254313
|
A | T | 2 | a0001c0001t0040g0134a0001c0002t0004g0132 | 2 | NA19009.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.427+3158T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254313 | ||||||
| chr14:99254414
|
G | A | 1 | a0001c0002t0003g0249 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.427+3057C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254414 | ||||||
| chr14:99254501
|
C | T | 1 | a0001c0001t0007g0257 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.427+2970G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254501 | ||||||
| chr14:99254583
|
G | C | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+2888C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254583 | ||||||
| chr14:99254642
|
G | A | 128 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0178others(125): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.427+2829C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254642 | ||||||
| chr14:99254738
|
G | A | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.427+2733C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254738 | ||||||
| chr14:99254871
|
C | CA | 7 | a0001c0001t0001g0189a0001c0001t0009g0123a0001c0001t0027g0165others(4): Show | 7 | HG01891.hp2 HG02723.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.427+2599dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254871 | ||||||
| chr14:99254890
|
A | G | 1 | a0001c0001t0036g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.427+2581T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99254890 | ||||||
| chr14:99255038
|
T | C | 1 | a0001c0001t0005g0078 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.427+2433A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255038 | ||||||
| chr14:99255154
|
G | A | 1 | a0001c0002t0066g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.427+2317C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255154 | ||||||
| chr14:99255178
|
G | A | 1 | a0001c0001t0008g0054 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.427+2293C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255178 | ||||||
| chr14:99255405
|
G | GAAAAAAA others(3): Show |
2 | a0001c0001t0001g0253a0001c0001t0011g0299 | 2 | HG00609.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.427+2056_427+2065d others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
G | GAAAAAAA others(6): Show |
1 | a0001c0002t0003g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.427+2053_427+2065d others(15): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
GA | G | 179 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(176): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.427+2065delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
GAAA | G | 26 | a0001c0001t0001g0178a0001c0001t0001g0214a0001c0001t0002g0019others(23): Show | 26 | HG00423.hp1 HG01517.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.427+2063_427+2065d others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
GAAAA | G | 68 | a0001c0001t0001g0180a0001c0001t0001g0185a0001c0001t0001g0189others(65): Show | 69 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.427+2062_427+2065d others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
GAAAAA | G | 11 | a0001c0001t0001g0188a0001c0001t0002g0025a0001c0001t0002g0026others(8): Show | 11 | HG00099.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.427+2061_427+2065d others(7): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
GAAAAAA | G | 7 | a0001c0001t0008g0131a0001c0001t0009g0080a0001c0001t0015g0079others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+2060_427+2065d others(8): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0011g0298 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.427+2056_427+2065d others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0005g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.427+2055_427+2065d others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255405
|
GAAAAAAA others(6): Show |
G | 2 | a0001c0001t0007g0169a0001c0002t0047g0015 | 2 | HG01517.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.427+2053_427+2065d others(15): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255405 | ||||||
| chr14:99255419
|
A | G | 1 | a0001c0001t0012g0148 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.427+2052T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255419 | ||||||
| chr14:99255424
|
A | C | 1 | a0001c0001t0001g0284 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.427+2047T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255424 | ||||||
| chr14:99255431
|
A | C | 220 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(217): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.427+2040T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255431 | ||||||
| chr14:99255542
|
G | C | 4 | a0001c0001t0008g0054a0001c0001t0037g0010a0001c0002t0003g0264others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.427+1929C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255542 | ||||||
| chr14:99255629
|
A | G | 1 | a0001c0001t0012g0147 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.427+1842T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255629 | ||||||
| chr14:99255678
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.427+1793G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255678 | ||||||
| chr14:99255795
|
G | C | 1 | a0001c0002t0003g0194 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.427+1676C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255795 | ||||||
| chr14:99255943
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.427+1528G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255943 | ||||||
| chr14:99255953
|
G | C | 36 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0282others(33): Show | 37 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.427+1518C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255953 | ||||||
| chr14:99255963
|
C | T | 1 | a0001c0001t0008g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.427+1508G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99255963 | ||||||
| chr14:99256068
|
A | G | 346 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(343): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.427+1403T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256068 | ||||||
| chr14:99256108
|
C | T | 2 | a0001c0002t0007g0255a0001c0002t0007g0256 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.427+1363G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256108 | ||||||
| chr14:99256299
|
A | G | 346 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(343): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.427+1172T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256299 | ||||||
| chr14:99256418
|
C | T | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.427+1053G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256418 | ||||||
| chr14:99256712
|
G | A | 6 | a0001c0001t0008g0087a0001c0001t0008g0090a0001c0001t0009g0064others(3): Show | 6 | HG02572.hp2 HG03098.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.427+759C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256712 | ||||||
| chr14:99256791
|
G | A | 1 | a0001c0002t0082g0336 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.427+680C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256791 | ||||||
| chr14:99256867
|
C | G | 2 | a0001c0001t0003g0248a0001c0001t0086g0342 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.427+604G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256867 | ||||||
| chr14:99256960
|
G | C | 85 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0188others(82): Show | 86 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.427+511C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99256960 | ||||||
| chr14:99257124
|
G | A | 346 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(343): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.427+347C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99257124 | ||||||
| chr14:99257216
|
G | A | 4 | a0001c0001t0014g0190a0001c0002t0068g0170a0001c0004t0001g0001others(1): Show | 5 | HG02630.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+255C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99257216 | ||||||
| chr14:99257346
|
G | A | 7 | a0001c0001t0001g0172a0001c0001t0002g0040a0001c0001t0002g0044others(4): Show | 7 | HG00733.hp1 HG02145.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.427+125C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 2/3 | chr14 | 99257346 | ||||||
| chr14:99258196
|
C | G | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-357G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258196 | ||||||
| chr14:99258264
|
A | G | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.59-425T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258264 | ||||||
| chr14:99258351
|
C | G | 2 | a0001c0001t0001g0180a0001c0001t0070g0171 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.59-512G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258351 | ||||||
| chr14:99258446
|
G | A | 2 | a0001c0001t0005g0047a0001c0001t0006g0321 | 2 | HG00099.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.59-607C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258446 | ||||||
| chr14:99258796
|
C | T | 41 | a0001c0001t0001g0224a0001c0001t0001g0235a0001c0001t0001g0238others(38): Show | 41 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.59-957G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258796 | ||||||
| chr14:99258894
|
G | GT | 218 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(215): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.59-1056dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258894 | ||||||
| chr14:99258894
|
G | T | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.59-1055C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258894 | ||||||
| chr14:99258912
|
A | G | 346 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(343): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.59-1073T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99258912 | ||||||
| chr14:99259005
|
C | CG | 210 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(207): Show | 210 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.59-1167_59-1166ins others(1): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259005 | ||||||
| chr14:99259006
|
A | G | 8 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0234others(5): Show | 8 | HG00609.hp2 HG03239.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1167T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259006 | ||||||
| chr14:99259076
|
C | T | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-1237G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259076 | ||||||
| chr14:99259214
|
G | A | 8 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0234others(5): Show | 8 | HG00609.hp2 HG03239.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1375C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259214 | ||||||
| chr14:99259394
|
A | G | 2 | a0001c0001t0003g0248a0001c0001t0086g0342 | 2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.59-1555T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259394 | ||||||
| chr14:99259589
|
G | A | 1 | a0001c0001t0078g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.59-1750C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259589 | ||||||
| chr14:99259663
|
G | C | 216 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(213): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.59-1824C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259663 | ||||||
| chr14:99259668
|
A | G | 8 | a0001c0001t0001g0222a0001c0001t0012g0142a0001c0001t0012g0143others(5): Show | 8 | NA18968.hp1 NA18969.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1829T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259668 | ||||||
| chr14:99259704
|
C | T | 2 | a0001c0001t0001g0158a0004c0010t0007g0287 | 2 | NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.59-1865G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259704 | ||||||
| chr14:99259793
|
C | T | 2 | a0001c0001t0005g0129a0001c0001t0009g0128 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.59-1954G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259793 | ||||||
| chr14:99259881
|
C | T | 3 | a0001c0001t0008g0054a0001c0002t0003g0264a0001c0002t0019g0130 | 3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.59-2042G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259881 | ||||||
| chr14:99259981
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-2142C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99259981 | ||||||
| chr14:99260072
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.59-2233C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260072 | ||||||
| chr14:99260220
|
G | A | 1 | a0001c0002t0046g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.59-2381C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260220 | ||||||
| chr14:99260311
|
G | A | 1 | a0001c0002t0066g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-2472C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260311 | ||||||
| chr14:99260382
|
T | C | 182 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(179): Show | 182 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.59-2543A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260382 | ||||||
| chr14:99260430
|
G | A | 4 | a0001c0001t0001g0223a0001c0001t0002g0065a0001c0001t0009g0080others(1): Show | 4 | HG01934.hp1 HG01978.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-2591C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260430 | ||||||
| chr14:99260584
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.59-2745G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260584 | ||||||
| chr14:99260627
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.59-2788G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260627 | ||||||
| chr14:99260748
|
C | T | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-2909G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260748 | ||||||
| chr14:99260749
|
G | A | 39 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0282others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.59-2910C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260749 | ||||||
| chr14:99260777
|
G | A | 182 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(179): Show | 182 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.59-2938C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99260777 | ||||||
| chr14:99261254
|
A | G | 184 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(181): Show | 184 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.59-3415T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261254 | ||||||
| chr14:99261255
|
A | G | 82 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0188others(79): Show | 83 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.59-3416T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261255 | ||||||
| chr14:99261283
|
G | A | 6 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0234others(3): Show | 6 | HG00609.hp2 HG03239.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-3444C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261283 | ||||||
| chr14:99261452
|
A | G | 1 | a0001c0001t0035g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-3613T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261452 | ||||||
| chr14:99261478
|
T | C | 1 | a0001c0001t0007g0278 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.59-3639A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261478 | ||||||
| chr14:99261513
|
C | T | 1 | a0001c0001t0008g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.59-3674G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261513 | ||||||
| chr14:99261805
|
G | A | 1 | a0001c0002t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-3966C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261805 | ||||||
| chr14:99261832
|
G | A | 2 | a0001c0001t0013g0327a0001c0002t0083g0328 | 2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.59-3993C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261832 | ||||||
| chr14:99261878
|
T | TAC | 28 | a0001c0001t0001g0180a0001c0001t0001g0214a0001c0001t0002g0019others(25): Show | 28 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.59-4041_59-4040dup others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261878 | ||||||
| chr14:99261903
|
G | A | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.59-4064C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99261903 | ||||||
| chr14:99262111
|
C | T | 11 | a0001c0001t0002g0019a0001c0001t0002g0035a0001c0001t0004g0110others(8): Show | 11 | HG01109.hp2 HG01175.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-4272G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262111 | ||||||
| chr14:99262112
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0070g0171 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.59-4273C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262112 | ||||||
| chr14:99262172
|
G | A | 1 | a0001c0001t0002g0112 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.59-4333C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262172 | ||||||
| chr14:99262192
|
C | A | 1 | a0001c0001t0011g0299 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.59-4353G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262192 | ||||||
| chr14:99262219
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0090g0346a0001c0002t0003g0286 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.59-4380G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262219 | ||||||
| chr14:99262280
|
G | A | 1 | a0001c0001t0050g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59-4441C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262280 | ||||||
| chr14:99262456
|
C | T | 77 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0188others(74): Show | 78 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.59-4617G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262456 | ||||||
| chr14:99262465
|
T | C | 1 | a0001c0001t0002g0093 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.59-4626A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262465 | ||||||
| chr14:99262479
|
C | T | 1 | a0001c0001t0003g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.59-4640G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262479 | ||||||
| chr14:99262549
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-4710G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262549 | ||||||
| chr14:99262571
|
G | A | 1 | a0001c0001t0007g0169 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59-4732C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262571 | ||||||
| chr14:99262693
|
C | T | 1 | a0001c0002t0004g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-4854G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262693 | ||||||
| chr14:99262708
|
A | G | 8 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-4869T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262708 | ||||||
| chr14:99262740
|
G | A | 1 | a0001c0002t0066g0247 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-4901C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262740 | ||||||
| chr14:99262756
|
C | T | 1 | a0001c0001t0011g0298 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.59-4917G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262756 | ||||||
| chr14:99262768
|
C | T | 1 | a0003c0007t0007g0283 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.59-4929G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262768 | ||||||
| chr14:99262783
|
C | T | 8 | a0001c0001t0005g0022a0001c0001t0006g0341a0001c0001t0013g0339others(5): Show | 8 | HG00735.hp2 HG00741.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-4944G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262783 | ||||||
| chr14:99262967
|
C | G | 2 | a0001c0001t0008g0114a0001c0001t0050g0108 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59-5128G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262967 | ||||||
| chr14:99262973
|
C | A | 2 | a0001c0001t0005g0129a0001c0001t0009g0128 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.59-5134G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99262973 | ||||||
| chr14:99263050
|
G | A | 7 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0231others(4): Show | 7 | HG01074.hp1 HG01106.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-5211C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263050 | ||||||
| chr14:99263212
|
A | G | 28 | a0001c0001t0001g0180a0001c0001t0001g0214a0001c0001t0002g0019others(25): Show | 28 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.59-5373T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263212 | ||||||
| chr14:99263390
|
C | G | 1 | a0001c0001t0009g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.59-5551G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263390 | ||||||
| chr14:99263436
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.59-5597C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263436 | ||||||
| chr14:99263470
|
C | A | 21 | a0001c0001t0001g0214a0001c0001t0002g0019a0001c0001t0002g0035others(18): Show | 21 | HG00099.hp2 HG00597.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-5631G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263470 | ||||||
| chr14:99263480
|
G | C | 1 | a0001c0002t0046g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.59-5641C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263480 | ||||||
| chr14:99263626
|
A | G | 211 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(208): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.59-5787T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263626 | ||||||
| chr14:99263874
|
C | T | 6 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0234others(3): Show | 6 | HG00609.hp2 HG03239.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-6035G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99263874 | ||||||
| chr14:99264141
|
CG | C | 38 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0282others(35): Show | 39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.59-6303delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264141 | ||||||
| chr14:99264288
|
G | GC | 73 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0223others(70): Show | 74 | HG00438.hp2 HG00639.hp1 HG01106.hp2 others(71): Show |
intron_variant | MODIFIER | c.59-6450dupG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264288 | ||||||
| chr14:99264288
|
G | GCC | 14 | a0001c0001t0002g0026a0001c0001t0002g0102a0001c0001t0004g0110others(11): Show | 14 | HG00423.hp1 HG00642.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-6451_59-6450dup others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264288 | ||||||
| chr14:99264288
|
GC | G | 15 | a0001c0001t0001g0157a0001c0001t0001g0224a0001c0001t0001g0266others(12): Show | 15 | HG02071.hp1 HG02486.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-6450delG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264288 | ||||||
| chr14:99264295
|
C | CG | 11 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0231others(8): Show | 11 | HG01074.hp1 HG01106.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-6457_59-6456ins others(1): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264295 | ||||||
| chr14:99264339
|
T | A | 1 | a0001c0002t0079g0292 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.59-6500A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264339 | ||||||
| chr14:99264497
|
A | AT | 212 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(209): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.59-6659dupA | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264497 | ||||||
| chr14:99264538
|
T | A | 7 | a0001c0001t0001g0172a0001c0001t0002g0040a0001c0001t0002g0044others(4): Show | 7 | HG00733.hp1 HG02145.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+6623A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264538 | ||||||
| chr14:99264546
|
G | A | 4 | a0001c0001t0008g0054a0001c0001t0037g0010a0001c0002t0003g0264others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+6615C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264546 | ||||||
| chr14:99264683
|
C | G | 1 | a0001c0001t0051g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58+6478G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264683 | ||||||
| chr14:99264698
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+6463C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264698 | ||||||
| chr14:99264703
|
T | C | 10 | a0001c0001t0001g0252a0001c0001t0001g0276a0001c0001t0006g0337others(7): Show | 10 | HG00140.hp2 HG00738.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+6458A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264703 | ||||||
| chr14:99264827
|
C | T | 1 | a0001c0002t0003g0220 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.58+6334G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264827 | ||||||
| chr14:99264934
|
G | C | 216 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(213): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.58+6227C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99264934 | ||||||
| chr14:99265070
|
C | T | 1 | a0001c0001t0071g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.58+6091G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265070 | ||||||
| chr14:99265097
|
G | A | 1 | a0001c0002t0010g0307 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.58+6064C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265097 | ||||||
| chr14:99265112
|
C | G | 1 | a0001c0001t0001g0235 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+6049G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265112 | ||||||
| chr14:99265330
|
C | A | 8 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0001t0002g0069others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+5831G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265330 | ||||||
| chr14:99265394
|
A | C | 38 | a0001c0001t0001g0151a0001c0001t0001g0167a0001c0001t0001g0282others(35): Show | 39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.58+5767T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265394 | ||||||
| chr14:99265443
|
C | T | 1 | a0001c0001t0008g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58+5718G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265443 | ||||||
| chr14:99265483
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.58+5678T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265483 | ||||||
| chr14:99265508
|
T | C | 1 | a0001c0001t0002g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.58+5653A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265508 | ||||||
| chr14:99265625
|
G | T | 1 | a0001c0001t0022g0146 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.58+5536C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265625 | ||||||
| chr14:99265789
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0009g0080a0001c0001t0015g0079others(1): Show | 4 | HG02615.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5372C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265789 | ||||||
| chr14:99265804
|
T | C | 5 | a0001c0001t0001g0180a0001c0001t0008g0053a0001c0001t0070g0171others(2): Show | 5 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+5357A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265804 | ||||||
| chr14:99265824
|
C | A | 5 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0253others(2): Show | 5 | HG00609.hp2 NA18948.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+5337G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99265824 | ||||||
| chr14:99266079
|
G | C | 215 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(212): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.58+5082C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266079 | ||||||
| chr14:99266155
|
G | T | 4 | a0001c0001t0008g0131a0001c0001t0009g0080a0001c0001t0015g0079others(1): Show | 4 | HG02615.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5006C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266155 | ||||||
| chr14:99266159
|
C | T | 5 | a0001c0001t0001g0279a0001c0001t0007g0258a0001c0001t0023g0216others(2): Show | 5 | NA18960.hp2 NA18969.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+5002G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266159 | ||||||
| chr14:99266543
|
G | A | 4 | a0001c0001t0008g0131a0001c0001t0009g0080a0001c0001t0015g0079others(1): Show | 4 | HG02615.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4618C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266543 | ||||||
| chr14:99266605
|
G | A | 2 | a0001c0001t0091g0347a0001c0002t0004g0036 | 2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.58+4556C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266605 | ||||||
| chr14:99266660
|
C | T | 5 | a0001c0001t0007g0257a0001c0001t0007g0278a0001c0002t0007g0255others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+4501G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99266660 | ||||||
| chr14:99267047
|
G | C | 57 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0228others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.58+4114C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267047 | ||||||
| chr14:99267270
|
CA | C | 8 | a0001c0001t0009g0060a0001c0001t0011g0299a0001c0001t0014g0182others(5): Show | 8 | HG02258.hp1 HG02970.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+3890delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267270 | ||||||
| chr14:99267271
|
A | C | 3 | a0001c0001t0008g0054a0001c0002t0003g0264a0001c0002t0019g0130 | 3 | HG02055.hp2 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.58+3890T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267271 | ||||||
| chr14:99267327
|
T | A | 1 | a0001c0001t0006g0337 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.58+3834A>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267327 | ||||||
| chr14:99267544
|
A | ACC | 31 | a0001c0001t0001g0167a0001c0001t0006g0002a0001c0001t0006g0305others(28): Show | 32 | HG00099.hp1 HG00280.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.58+3615_58+3616dup others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267544 | ||||||
| chr14:99267544
|
AC | A | 19 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0061others(16): Show | 19 | HG01074.hp1 HG01074.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+3616delG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267544 | ||||||
| chr14:99267544
|
ACC | A | 268 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(265): Show | 269 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.58+3615_58+3616del others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267544 | ||||||
| chr14:99267552
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58+3609G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267552 | ||||||
| chr14:99267554
|
C | A | 2 | a0001c0001t0008g0053a0001c0002t0049g0057 | 2 | HG00639.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.58+3607G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267554 | ||||||
| chr14:99267554
|
C | CA | 4 | a0001c0001t0002g0056a0001c0001t0008g0054a0001c0002t0003g0264others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3606dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267554 | ||||||
| chr14:99267565
|
C | CA | 8 | a0001c0001t0002g0056a0001c0001t0008g0053a0001c0001t0008g0054others(5): Show | 8 | HG00639.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+3595dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267565 | ||||||
| chr14:99267617
|
C | T | 296 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(293): Show | 297 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.58+3544G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267617 | ||||||
| chr14:99267649
|
C | T | 1 | a0001c0001t0043g0120 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.58+3512G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99267649 | ||||||
| chr14:99268020
|
C | T | 1 | a0001c0001t0014g0182 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.58+3141G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268020 | ||||||
| chr14:99268102
|
C | G | 1 | a0001c0002t0046g0014 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58+3059G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268102 | ||||||
| chr14:99268262
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.58+2899C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268262 | ||||||
| chr14:99268274
|
C | T | 326 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(323): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.58+2887G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268274 | ||||||
| chr14:99268320
|
T | C | 48 | a0001c0001t0001g0151a0001c0001t0001g0180a0001c0001t0002g0016others(45): Show | 48 | HG00642.hp1 HG00673.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.58+2841A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268320 | ||||||
| chr14:99268390
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.58+2771C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268390 | ||||||
| chr14:99268547
|
G | A | 9 | a0001c0001t0001g0222a0001c0001t0012g0142a0001c0001t0012g0143others(6): Show | 9 | NA18966.hp2 NA18968.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+2614C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268547 | ||||||
| chr14:99268647
|
A | G | 286 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0157others(283): Show | 287 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.58+2514T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268647 | ||||||
| chr14:99268794
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.58+2367G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268794 | ||||||
| chr14:99268896
|
T | C | 59 | a0001c0001t0001g0167a0001c0001t0001g0222a0001c0001t0002g0055others(56): Show | 60 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(57): Show |
intron_variant | MODIFIER | c.58+2265A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99268896 | ||||||
| chr14:99269143
|
T | C | 50 | a0001c0001t0001g0167a0001c0001t0002g0055a0001c0001t0002g0056others(47): Show | 51 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(48): Show |
intron_variant | MODIFIER | c.58+2018A>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269143 | ||||||
| chr14:99269156
|
A | AC | 37 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(34): Show | 37 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.58+2004dupG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269156 | ||||||
| chr14:99269205
|
G | A | 6 | a0001c0001t0001g0172a0001c0001t0011g0301a0001c0001t0014g0176others(3): Show | 6 | HG02886.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+1956C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269205 | ||||||
| chr14:99269515
|
T | TC | 103 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0186others(100): Show | 103 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+1645dupG | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269515 | ||||||
| chr14:99269515
|
T | TCC | 35 | a0001c0001t0001g0172a0001c0001t0001g0180a0001c0001t0001g0188others(32): Show | 36 | HG00733.hp1 HG01109.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.58+1644_58+1645dup others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269515 | ||||||
| chr14:99269515
|
T | TTC | 4 | a0001c0001t0014g0182a0001c0002t0003g0174a0001c0002t0003g0175others(1): Show | 4 | HG02258.hp1 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1645_58+1646ins others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269515 | ||||||
| chr14:99269518
|
C | G | 4 | a0001c0001t0014g0182a0001c0002t0003g0174a0001c0002t0003g0175others(1): Show | 4 | HG02258.hp1 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1643G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269518 | ||||||
| chr14:99269524
|
C | CG | 37 | a0001c0001t0001g0167a0001c0001t0006g0002a0001c0001t0006g0310others(34): Show | 38 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(35): Show |
intron_variant | MODIFIER | c.58+1636_58+1637ins others(1): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269524 | ||||||
| chr14:99269526
|
C | A | 7 | a0001c0001t0006g0341a0001c0001t0008g0114a0001c0001t0013g0339others(4): Show | 7 | HG00741.hp1 HG01123.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1635G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269526 | ||||||
| chr14:99269527
|
A | C | 12 | a0001c0001t0001g0222a0001c0001t0002g0061a0001c0001t0009g0063others(9): Show | 12 | HG02109.hp1 NA18522.hp1 NA18522.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+1634T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269527 | ||||||
| chr14:99269651
|
A | C | 10 | a0001c0001t0001g0222a0001c0001t0012g0142a0001c0001t0012g0143others(7): Show | 10 | NA18966.hp2 NA18968.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+1510T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269651 | ||||||
| chr14:99269658
|
A | ATATT | 8 | a0001c0001t0006g0002a0001c0001t0006g0310a0001c0001t0006g0312others(5): Show | 9 | HG00140.hp1 HG00280.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+1499_58+1502dup others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269658 | ||||||
| chr14:99269875
|
T | TA | 34 | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0272others(31): Show | 34 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.58+1285dupT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TA | T | 43 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0203others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.58+1285delT | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAA | T | 11 | a0001c0001t0001g0193a0001c0001t0002g0115a0001c0001t0002g0118others(8): Show | 11 | HG02293.hp1 HG02293.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+1284_58+1285del others(2): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAA | T | 40 | a0001c0001t0001g0173a0001c0001t0001g0184a0001c0001t0001g0185others(37): Show | 40 | HG00280.hp2 HG01106.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.58+1283_58+1285del others(3): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAA | T | 45 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0002g0051others(42): Show | 46 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.58+1282_58+1285del others(4): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAA | T | 16 | a0001c0001t0001g0172a0001c0001t0002g0039a0001c0001t0002g0040others(13): Show | 16 | HG00673.hp1 HG01069.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.58+1281_58+1285del others(5): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAA | T | 29 | a0001c0001t0001g0151a0001c0001t0002g0016a0001c0001t0002g0019others(26): Show | 29 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.58+1280_58+1285del others(6): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAAA others(2): Show |
T | 9 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0006g0338others(6): Show | 9 | HG00639.hp2 HG00741.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+1277_58+1285del others(9): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAAA others(3): Show |
T | 37 | a0001c0001t0001g0167a0001c0001t0006g0002a0001c0001t0006g0310others(34): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.58+1276_58+1285del others(10): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0084g0308a0001c0002t0010g0307 | 2 | HG00099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.58+1275_58+1285del others(11): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0005t0009g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+1274_58+1285del others(12): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAAA others(6): Show |
T | 12 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(9): Show | 12 | HG00423.hp2 HG02056.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+1273_58+1285del others(13): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0001g0156 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.58+1272_58+1285del others(14): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0005g0059 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.58+1271_58+1285del others(15): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269875
|
TAAAAAAA others(12): Show |
T | 1 | a0001c0001t0077g0290 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.58+1267_58+1285del others(19): Show |
BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269875 | ||||||
| chr14:99269876
|
A | T | 2 | a0001c0001t0011g0294a0002c0009t0003g0195 | 2 | NA18977.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.58+1285T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269876 | ||||||
| chr14:99269878
|
A | T | 1 | a0001c0002t0003g0181 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.58+1283T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269878 | ||||||
| chr14:99269879
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.58+1282T>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99269879 | ||||||
| chr14:99270091
|
G | T | 1 | a0001c0001t0002g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58+1070C>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270091 | ||||||
| chr14:99270521
|
G | A | 1 | a0004c0010t0007g0287 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.58+640C>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270521 | ||||||
| chr14:99270635
|
AG | A | 8 | a0001c0001t0012g0142a0001c0001t0012g0143a0001c0001t0012g0147others(5): Show | 8 | NA18966.hp2 NA18968.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+525delC | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270635 | ||||||
| chr14:99270647
|
C | T | 5 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0001t0008g0053others(2): Show | 5 | HG00639.hp2 HG02280.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+514G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270647 | ||||||
| chr14:99270664
|
C | A | 1 | a0001c0005t0009g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+497G>T | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270664 | ||||||
| chr14:99270672
|
C | G | 1 | a0001c0001t0037g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58+489G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270672 | ||||||
| chr14:99270706
|
C | T | 1 | a0001c0001t0007g0155 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.58+455G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270706 | ||||||
| chr14:99270792
|
C | G | 1 | a0001c0001t0091g0347 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+369G>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270792 | ||||||
| chr14:99270812
|
C | T | 2 | a0001c0001t0002g0051a0001c0001t0002g0052 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.58+349G>A | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270812 | ||||||
| chr14:99270868
|
A | G | 43 | a0001c0001t0001g0151a0001c0001t0002g0016a0001c0001t0002g0019others(40): Show | 43 | HG00642.hp1 HG00673.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.58+293T>C | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270868 | ||||||
| chr14:99270942
|
G | C | 3 | a0001c0001t0034g0005a0001c0002t0033g0006a0001c0005t0009g0013 | 3 | HG01891.hp2 HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.58+219C>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99270942 | ||||||
| chr14:99271072
|
A | C | 12 | a0001c0001t0012g0142a0001c0001t0012g0143a0001c0001t0012g0147others(9): Show | 12 | HG01891.hp2 HG02559.hp1 HG03516.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+89T>G | BCL11B | ENSG00000127152.18 | transcript | ENST00000357195.8 | protein_coding | 1/3 | chr14 | 99271072 |