Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 53335 |
|---|---|
| ensemblid | ENSG00000119866.22 |
| hgncid | 13221 |
| symbol | BCL11A |
| name | BCL11 transcription factor A |
| refseq_nuc | NM_022893.4 |
| refseq_prot | NP_075044.2 |
| ensembl_nuc | ENST00000642384.2 |
| ensembl_prot | ENSP00000496168.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 60457194 |
| end | 60553654 |
| strand | - |
| ver | v1.2 |
| region | chr2:60457194-60553654 |
| region5000 | chr2:60452194-60558654 |
| regionname0 | BCL11A_chr2_60457194_60553654 |
| regionname5000 | BCL11A_chr2_60452194_60558654 |
| 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 | 835 | 259 | 71 | 60 | 72 | 13 | 41 | 48 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0002 | 0/0 | 835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0003 | 0/0 | 835 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0004 | 0/0 | 835 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2508 | 213 | 65 | 42 | 66 | 10 | 29 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| c0002 | 1/0 | 2508 | 29 | 4 | 10 | 0 | 3 | 11 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| c0003 | 0/0 | 2508 | 13 | 0 | 7 | 6 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| c0004 | 0/0 | 2508 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| c0005 | 0/0 | 2508 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| c0006 | 0/0 | 2508 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| c0007 | 0/0 | 2508 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| c0008 | 0/0 | 2508 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| c0009 | 0/0 | 2508 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3597 | 38 | 9 | 12 | 6 | 2 | 9 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0002 | 0/0 | 3599 | 33 | 3 | 13 | 12 | 2 | 3 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0003 | 0/0 | 3600 | 32 | 7 | 2 | 16 | 1 | 6 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0004 | 0/0 | 3598 | 19 | 4 | 5 | 4 | 0 | 6 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0005 | 0/0 | 3604 | 15 | 2 | 5 | 5 | 2 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0006 | 0/0 | 3605 | 9 | 0 | 3 | 4 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0007 | 0/0 | 3597 | 8 | 5 | 2 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0008 | 0/0 | 3600 | 7 | 1 | 1 | 3 | 0 | 2 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0009 | 0/0 | 3601 | 7 | 0 | 1 | 4 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0010 | 0/0 | 3595 | 5 | 2 | 1 | 0 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0011 | 0/0 | 3598 | 5 | 1 | 4 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0012 | 0/0 | 3603 | 5 | 2 | 1 | 0 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0013 | 0/0 | 3606 | 5 | 2 | 1 | 1 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0014 | 0/0 | 3595 | 4 | 1 | 0 | 0 | 1 | 2 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0015 | 0/0 | 3601 | 4 | 3 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0016 | 0/0 | 3607 | 4 | 1 | 2 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0017 | 0/0 | 3596 | 3 | 1 | 1 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0018 | 0/0 | 3602 | 3 | 2 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0019 | 0/0 | 3597 | 2 | 1 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0020 | 0/0 | 3598 | 2 | 0 | 1 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0021 | 0/0 | 3599 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0022 | 0/0 | 3601 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0023 | 0/0 | 3602 | 2 | 1 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0024 | 0/0 | 3606 | 2 | 0 | 1 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0025 | 0/0 | 3593 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0026 | 1/0 | 3595 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0027 | 0/0 | 3584 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0028 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0029 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0030 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0031 | 0/0 | 3596 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0032 | 0/0 | 3598 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0033 | 0/0 | 3598 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0034 | 0/0 | 3598 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0035 | 0/0 | 3596 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0036 | 0/0 | 3596 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0037 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0038 | 0/0 | 3598 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0039 | 0/0 | 3598 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0040 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0041 | 0/0 | 3598 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0042 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0043 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0044 | 0/0 | 3598 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0045 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0046 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0047 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0048 | 0/0 | 3613 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0049 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0050 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0051 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0052 | 0/0 | 3599 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0053 | 0/0 | 3602 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0054 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0055 | 0/0 | 3602 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0056 | 0/0 | 3601 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0057 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0058 | 0/0 | 3604 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0059 | 0/0 | 3603 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0060 | 0/0 | 3601 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0061 | 0/0 | 3603 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0062 | 0/0 | 3607 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0063 | 0/0 | 3605 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0064 | 0/0 | 3606 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0065 | 0/0 | 3608 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0066 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0067 | 0/1 | 3595 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| t0068 | 0/0 | 3595 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| 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 | 0 | 2 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| 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 | 0/1 | 2508 | 213 | 65 | 42 | 66 | 10 | 29 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002 | 1/0 | 2508 | 29 | 4 | 10 | 0 | 3 | 11 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0003 | 0/0 | 2508 | 13 | 0 | 7 | 6 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0004 | 0/0 | 2508 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0007 | 0/0 | 2508 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0009 | 0/0 | 2508 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0002c0006 | 0/0 | 2508 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0003c0008 | 0/0 | 2508 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0004c0005 | 0/0 | 2508 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6104 | 26 | 9 | 7 | 6 | 0 | 4 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0002 | 0/0 | 6106 | 22 | 2 | 8 | 9 | 1 | 2 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0003 | 0/0 | 6107 | 25 | 6 | 0 | 14 | 1 | 4 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0004 | 0/0 | 6105 | 15 | 3 | 4 | 4 | 0 | 4 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0005 | 0/0 | 6111 | 15 | 2 | 5 | 5 | 2 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0006 | 0/0 | 6112 | 9 | 0 | 3 | 4 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0007 | 0/0 | 6104 | 8 | 5 | 2 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0008 | 0/0 | 6107 | 6 | 1 | 0 | 3 | 0 | 2 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0009 | 0/0 | 6108 | 6 | 0 | 1 | 3 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0010 | 0/0 | 6102 | 5 | 2 | 1 | 0 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0011 | 0/0 | 6105 | 5 | 1 | 4 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0012 | 0/0 | 6110 | 4 | 1 | 1 | 0 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0013 | 0/0 | 6113 | 5 | 2 | 1 | 1 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0014 | 0/0 | 6102 | 2 | 1 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0015 | 0/0 | 6108 | 4 | 3 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0016 | 0/0 | 6114 | 3 | 1 | 1 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0017 | 0/0 | 6103 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0018 | 0/0 | 6109 | 3 | 2 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0019 | 0/0 | 6104 | 2 | 1 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0020 | 0/0 | 6105 | 2 | 0 | 1 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0021 | 0/0 | 6106 | 2 | 2 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0022 | 0/0 | 6108 | 2 | 0 | 0 | 2 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0023 | 0/0 | 6109 | 2 | 1 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0024 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0025 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0027 | 0/0 | 6091 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0029 | 0/0 | 6104 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0030 | 0/0 | 6104 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0032 | 0/0 | 6105 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0033 | 0/0 | 6105 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0034 | 0/0 | 6105 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0035 | 0/0 | 6103 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0036 | 0/0 | 6103 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0037 | 0/0 | 6106 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0038 | 0/0 | 6105 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0039 | 0/0 | 6105 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0040 | 0/0 | 6106 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0042 | 0/0 | 6106 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0043 | 0/0 | 6106 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0044 | 0/0 | 6105 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0045 | 0/0 | 6107 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0046 | 0/0 | 6107 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0047 | 0/0 | 6107 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0048 | 0/0 | 6120 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0049 | 0/0 | 6107 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0050 | 0/0 | 6107 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0051 | 0/0 | 6107 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0052 | 0/0 | 6106 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0053 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0054 | 0/0 | 6107 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0055 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0056 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0057 | 0/0 | 6110 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0059 | 0/0 | 6110 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0060 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0061 | 0/0 | 6110 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0063 | 0/0 | 6112 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0064 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0065 | 0/0 | 6115 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0066 | 0/0 | 6116 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0067 | 0/1 | 6102 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0001t0068 | 0/0 | 6102 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0001 | 0/0 | 6104 | 11 | 0 | 5 | 0 | 2 | 4 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0002 | 0/0 | 6106 | 3 | 1 | 1 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0003 | 0/0 | 6107 | 2 | 1 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0004 | 0/0 | 6105 | 3 | 1 | 0 | 0 | 0 | 2 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0008 | 0/0 | 6107 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0014 | 0/0 | 6102 | 2 | 0 | 0 | 0 | 1 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0016 | 0/0 | 6114 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0017 | 0/0 | 6103 | 2 | 1 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0024 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0026 | 1/0 | 6102 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0028 | 0/0 | 6104 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0002t0031 | 0/0 | 6103 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0003t0002 | 0/0 | 6106 | 6 | 0 | 3 | 3 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0003t0003 | 0/0 | 6107 | 4 | 0 | 2 | 2 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0003t0004 | 0/0 | 6105 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0003t0009 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0003t0041 | 0/0 | 6105 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0004t0058 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0004t0062 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0007t0002 | 0/0 | 6106 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0001c0009t0001 | 0/0 | 6104 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0002c0006t0012 | 0/0 | 6110 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0003c0008t0003 | 0/0 | 6107 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| a0004c0005t0002 | 0/0 | 6106 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | copy fasta | chr2 | 60452194 | 60558654 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0010g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0010g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0011g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0011g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0011g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0012g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0012g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0012g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0013g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0013g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0013g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0013g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0014g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0015g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0015g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0016g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0016g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0016g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0017g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0018g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0018g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0019g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0019g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0020g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0020g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0021g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0021g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0022g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0023g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0023g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0024g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0025g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0027g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0029g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0030g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0032g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0033g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0034g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0035g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0036g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0037g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0038g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0039g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0040g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0042g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0043g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0044g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0045g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0046g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0047g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0048g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0049g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0050g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0051g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0052g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0053g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0054g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0055g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0056g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0057g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0059g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0060g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0061g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0063g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0064g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0065g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0066g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0067g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0001t0068g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0014g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0014g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0016g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0017g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0017g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0024g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0026g0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0028g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0002t0031g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0009g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0003t0041g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0004t0058g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0004t0062g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0007t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0001c0009t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0002c0006t0012g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0003c0008t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| a0004c0005t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0057 | EUR | GBR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0062 | EUR | GBR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0051 | EUR | GBR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00140 | hp2 | a0001 | c0001 | t0012 | g0217 | EUR | GBR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0239 | EUR | FIN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00280 | hp2 | a0001 | c0001 | t0025 | g0003 | EUR | FIN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0101 | EUR | FIN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00323 | hp2 | a0001 | c0001 | t0009 | g0205 | EUR | FIN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00423 | hp1 | a0001 | c0001 | t0020 | g0047 | EAS | CHS | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00423 | hp2 | a0001 | c0001 | t0008 | g0137 | EAS | CHS | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0134 | EAS | CHS | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | CHS | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | CHS | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0198 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00735 | hp1 | a0001 | c0001 | t0020 | g0041 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00735 | hp2 | a0001 | c0003 | t0004 | g0079 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0242 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00738 | hp2 | a0001 | c0007 | t0002 | g0096 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00741 | hp1 | a0001 | c0002 | t0008 | g0115 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0092 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0223 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01071 | hp2 | a0001 | c0003 | t0041 | g0135 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0095 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01167 | hp1 | a0001 | c0001 | t0013 | g0248 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01168 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01169 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01243 | hp2 | a0001 | c0001 | t0054 | g0194 | AMR | PUR | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01256 | hp1 | a0001 | c0001 | t0011 | g0150 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01258 | hp2 | a0001 | c0001 | t0011 | g0151 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0241 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01261 | hp2 | a0001 | c0001 | t0010 | g0050 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01358 | hp1 | a0001 | c0002 | t0017 | g0010 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01361 | hp2 | a0001 | c0002 | t0016 | g0255 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0120 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01515 | hp1 | a0001 | c0002 | t0014 | g0007 | EUR | IBS | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0221 | EUR | IBS | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0245 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0164 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01943 | hp2 | a0001 | c0001 | t0027 | g0005 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01975 | hp1 | a0001 | c0003 | t0002 | g0108 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01975 | hp2 | a0001 | c0001 | t0016 | g0256 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01978 | hp1 | a0001 | c0003 | t0002 | g0143 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0107 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0229 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01981 | hp2 | a0001 | c0001 | t0039 | g0142 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0230 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02027 | hp2 | a0001 | c0001 | t0018 | g0207 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02055 | hp1 | a0001 | c0001 | t0014 | g0006 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02055 | hp2 | a0001 | c0001 | t0053 | g0191 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02056 | hp1 | a0001 | c0001 | t0022 | g0180 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02056 | hp2 | a0001 | c0001 | t0022 | g0179 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0184 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0243 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0225 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02074 | hp2 | a0001 | c0001 | t0043 | g0109 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02080 | hp2 | a0001 | c0001 | t0048 | g0148 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0227 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0104 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02145 | hp1 | a0001 | c0001 | t0038 | g0069 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0077 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02258 | hp1 | a0001 | c0001 | t0035 | g0080 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0185 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02293 | hp1 | a0001 | c0003 | t0003 | g0155 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0226 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0231 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02300 | hp2 | a0001 | c0001 | t0012 | g0215 | AMR | PEL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0116 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02572 | hp2 | a0001 | c0001 | t0032 | g0037 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02630 | hp1 | a0001 | c0001 | t0023 | g0203 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02683 | hp1 | a0001 | c0002 | t0028 | g0044 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02698 | hp1 | a0003 | c0008 | t0003 | g0154 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0204 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0102 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02723 | hp2 | a0001 | c0001 | t0063 | g0234 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02738 | hp2 | a0001 | c0002 | t0004 | g0073 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02809 | hp1 | a0001 | c0001 | t0037 | g0068 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02809 | hp2 | a0001 | c0001 | t0021 | g0093 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02818 | hp1 | a0001 | c0001 | t0065 | g0251 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0169 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0099 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02965 | hp1 | a0001 | c0001 | t0055 | g0202 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02965 | hp2 | a0001 | c0004 | t0058 | g0206 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02970 | hp2 | a0001 | c0001 | t0040 | g0117 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02976 | hp2 | a0001 | c0004 | t0062 | g0235 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0070 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03041 | hp1 | a0001 | c0001 | t0068 | g0260 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03041 | hp2 | a0001 | c0002 | t0017 | g0011 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03098 | hp1 | a0001 | c0001 | t0016 | g0254 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0060 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03130 | hp1 | a0001 | c0001 | t0018 | g0211 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03130 | hp2 | a0002 | c0006 | t0012 | g0214 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0193 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0253 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | ESN | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03225 | hp2 | a0001 | c0001 | t0045 | g0114 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03239 | hp1 | a0001 | c0001 | t0014 | g0009 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03239 | hp2 | a0001 | c0002 | t0014 | g0008 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0190 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0139 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03490 | hp2 | a0001 | c0001 | t0013 | g0252 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0098 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0219 | AFR | GWD | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0188 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03579 | hp2 | a0001 | c0001 | t0046 | g0186 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03654 | hp2 | a0001 | c0001 | t0019 | g0013 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0236 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03688 | hp1 | a0001 | c0002 | t0004 | g0075 | SAS | STU | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0129 | SAS | STU | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03704 | hp1 | a0001 | c0001 | t0029 | g0056 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0220 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0133 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0218 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03834 | hp2 | a0001 | c0002 | t0031 | g0053 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03927 | hp2 | a0001 | c0009 | t0001 | g0017 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0167 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG04115 | hp1 | a0001 | c0001 | t0024 | g0237 | SAS | STU | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0132 | SAS | STU | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | BEB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG04199 | hp2 | a0001 | c0001 | t0017 | g0014 | SAS | STU | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | STU | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | STU | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | YRI | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | YRI | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18962 | hp1 | a0001 | c0001 | t0015 | g0162 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18962 | hp2 | a0001 | c0001 | t0023 | g0200 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0224 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18969 | hp2 | a0001 | c0001 | t0042 | g0138 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18970 | hp1 | a0001 | c0001 | t0044 | g0105 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18971 | hp1 | a0001 | c0001 | t0050 | g0161 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0240 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0244 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18974 | hp1 | a0001 | c0003 | t0009 | g0199 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18979 | hp1 | a0001 | c0001 | t0008 | g0126 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18979 | hp2 | a0001 | c0001 | t0034 | g0066 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18983 | hp2 | a0001 | c0003 | t0003 | g0178 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18992 | hp1 | a0001 | c0001 | t0009 | g0197 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA18994 | hp2 | a0001 | c0003 | t0002 | g0131 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19004 | hp1 | a0001 | c0001 | t0013 | g0249 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19006 | hp1 | a0001 | c0001 | t0009 | g0195 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0246 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19056 | hp1 | a0001 | c0003 | t0002 | g0103 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19065 | hp1 | a0001 | c0001 | t0052 | g0166 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19068 | hp1 | a0001 | c0001 | t0009 | g0201 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19068 | hp2 | a0001 | c0001 | t0051 | g0159 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19084 | hp2 | a0001 | c0001 | t0047 | g0176 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19087 | hp1 | a0001 | c0001 | t0057 | g0208 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19087 | hp2 | a0001 | c0001 | t0059 | g0210 | EAS | JPT | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19240 | hp1 | a0001 | c0001 | t0066 | g0258 | AFR | YRI | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | YRI | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20129 | hp1 | a0001 | c0001 | t0033 | g0022 | AFR | ASW | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20129 | hp2 | a0001 | c0001 | t0030 | g0026 | AFR | ASW | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20752 | hp1 | a0004 | c0005 | t0002 | g0100 | EUR | TSI | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20752 | hp2 | a0001 | c0001 | t0036 | g0083 | EUR | TSI | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | TSI | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0222 | EUR | TSI | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20905 | hp1 | a0001 | c0001 | t0016 | g0257 | SAS | GIH | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20905 | hp2 | a0001 | c0001 | t0010 | g0030 | SAS | GIH | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG01123 | hp2 | a0001 | c0002 | t0024 | g0238 | AMR | CLM | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02109 | hp1 | a0001 | c0001 | t0061 | g0212 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02109 | hp2 | a0001 | c0001 | t0018 | g0209 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02486 | hp1 | a0001 | c0001 | t0060 | g0216 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02486 | hp2 | a0001 | c0001 | t0019 | g0012 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0111 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0250 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG03471 | hp2 | a0001 | c0001 | t0064 | g0247 | AFR | MSL | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | USA | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| HG06807 | hp2 | a0001 | c0001 | t0049 | g0165 | AFR | USA | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA20300 | hp2 | a0001 | c0001 | t0056 | g0196 | AFR | USA | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA21309 | hp1 | a0001 | c0001 | t0012 | g0213 | AFR | LWK | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0067 | g0259 | REF | REF | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0026 | g0004 | REF | REF | BCL11A_chr2_60452194_60558654 | BCL11A | chr2 | 60452194 | 60558654 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:60461625
|
G | T | 1 | a0003 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1287C>A | p.His429Gln | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 1671/6102 | 1287/2508 | 429/835 | chr2 | 60461625 | ||
| chr2:60462139
|
C | T | 1 | a0002 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.773G>A | p.Arg258His | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 1157/6102 | 773/2508 | 258/835 | chr2 | 60462139 | ||
| chr2:60546271
|
C | G | 1 | a0004 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.85G>C | p.Asp29His | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/4 | 469/6102 | 85/2508 | 29/835 | chr2 | 60546271 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:60460824
|
A | G | 6 | a0001c0001a0001c0003a0001c0004others(3): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
synonymous_variant | LOW | c.2088T>C | p.Ser696Ser | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 2472/6102 | 2088/2508 | 696/835 | chr2 | 60460824 | ||
| chr2:60461726
|
G | T | 1 | a0001c0007 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.1186C>A | p.Arg396Arg | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 1570/6102 | 1186/2508 | 396/835 | chr2 | 60461726 | ||
| chr2:60462306
|
T | C | 1 | a0001c0003 | 13 | HG00735.hp2 HG01071.hp2 HG01934.hp2 others(10): Show |
synonymous_variant | LOW | c.606A>G | p.Glu202Glu | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 990/6102 | 606/2508 | 202/835 | chr2 | 60462306 | ||
| chr2:60462372
|
G | C | 1 | a0001c0004 | 2 | HG02965.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.540C>G | p.Thr180Thr | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 924/6102 | 540/2508 | 180/835 | chr2 | 60462372 | ||
| chr2:60462387
|
G | A | 1 | a0001c0009 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.525C>T | p.Cys175Cys | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 909/6102 | 525/2508 | 175/835 | chr2 | 60462387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:60457486
|
C | T | 4 | a0001c0001t0030a0001c0001t0040a0001c0001t0046others(1): Show | 4 | HG02970.hp2 HG03579.hp2 NA20129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2918G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 2918 | chr2 | 60457486 | |||||
| chr2:60457670
|
G | GT | 17 | a0001c0001t0008a0001c0001t0019a0001c0001t0020others(14): Show | 25 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2733dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 2733 | chr2 | 60457670 | |||||
| chr2:60457670
|
GT | G | 12 | a0001c0001t0007a0001c0001t0010a0001c0001t0011others(9): Show | 27 | HG00099.hp1 HG00280.hp2 HG00741.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2733delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 2733 | chr2 | 60457670 | |||||
| chr2:60457695
|
T | C | 1 | a0001c0001t0059 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2709A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 2709 | chr2 | 60457695 | |||||
| chr2:60457777
|
T | A | 1 | a0001c0001t0047 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2627A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 2627 | chr2 | 60457777 | |||||
| chr2:60458431
|
A | T | 1 | a0001c0001t0029 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1973T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 1973 | chr2 | 60458431 | |||||
| chr2:60459047
|
T | C | 1 | a0001c0001t0042 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 1357 | chr2 | 60459047 | |||||
| chr2:60459444
|
C | T | 1 | a0001c0004t0058 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 960 | chr2 | 60459444 | |||||
| chr2:60459493
|
T | TAAAGGAA others(6): Show |
1 | a0001c0001t0048 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*898_*910dupTCATTT others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 910 | chr2 | 60459493 | |||||
| chr2:60459545
|
C | A | 3 | a0001c0001t0021a0001c0001t0032a0001c0001t0064 | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*859G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 859 | chr2 | 60459545 | |||||
| chr2:60459548
|
T | C | 2 | a0001c0001t0049a0001c0001t0061 | 2 | HG02109.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*856A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 856 | chr2 | 60459548 | |||||
| chr2:60459702
|
T | G | 1 | a0001c0001t0036 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*702A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 702 | chr2 | 60459702 | |||||
| chr2:60459950
|
T | C | 1 | a0001c0001t0050 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 454 | chr2 | 60459950 | |||||
| chr2:60460040
|
C | G | 1 | a0001c0002t0028 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 364 | chr2 | 60460040 | |||||
| chr2:60460103
|
GT | G | 4 | a0001c0001t0043a0001c0001t0044a0001c0001t0051others(1): Show | 4 | HG02074.hp2 NA18970.hp1 NA19065.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*300delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 300 | chr2 | 60460103 | |||||
| chr2:60460168
|
G | GA | 13 | a0001c0001t0015a0001c0001t0023a0001c0001t0033others(10): Show | 17 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*235dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 235 | chr2 | 60460168 | |||||
| chr2:60460168
|
GA | G | 8 | a0001c0001t0007a0001c0001t0010a0001c0001t0011others(5): Show | 23 | HG00099.hp1 HG00280.hp2 HG00741.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*235delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 4/4 | 235 | chr2 | 60460168 | |||||
| chr2:60553404
|
C | T | 1 | a0001c0001t0054 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-134G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 134 | chr2 | 60553404 | |||||
| chr2:60553415
|
T | C | 1 | a0001c0001t0034 | 1 | NA18979.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-145A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | chr2 | 60553415 | ||||||
| chr2:60553422
|
A | T | 1 | a0001c0001t0068 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-152T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 152 | chr2 | 60553422 | |||||
| chr2:60553482
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0027 | 1 | HG01943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-223_-213delTTTTTT others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 213 | chr2 | 60553482 | |||||
| chr2:60553508
|
A | AG | 3 | a0001c0001t0017a0001c0001t0019a0001c0002t0017 | 5 | HG01358.hp1 HG02486.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-239_-238insC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 239 | chr2 | 60553508 | |||||
| chr2:60553508
|
A | G | 3 | a0001c0001t0014a0001c0001t0027a0001c0002t0014 | 5 | HG01515.hp1 HG01943.hp2 HG02055.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-238T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 238 | chr2 | 60553508 | |||||
| chr2:60553510
|
A | AGAG | 7 | a0001c0001t0004a0001c0001t0035a0001c0001t0036others(4): Show | 23 | HG00597.hp2 HG00735.hp2 HG01358.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-241_-240insCTC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 241 | chr2 | 60553510 | |||||
| chr2:60553510
|
A | G | 19 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(16): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-240T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 240 | chr2 | 60553510 | |||||
| chr2:60553511
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0066 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCTT others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AAAAAAAA others(5): Show |
2 | a0001c0001t0016a0001c0002t0016 | 4 | HG01361.hp2 HG01975.hp2 HG03098.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCTT others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AAAAAAAA others(4): Show |
3 | a0001c0001t0013a0001c0001t0064a0001c0001t0065 | 7 | HG01167.hp1 HG02818.hp1 HG03139.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCTT others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AAAAAAAG others(3): Show |
5 | a0001c0001t0006a0001c0001t0024a0001c0001t0063others(2): Show | 13 | HG00280.hp1 HG00738.hp1 HG01123.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCTT others(4): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AAAAAAGA others(2): Show |
1 | a0001c0001t0005 | 15 | HG01071.hp1 HG01515.hp2 HG01981.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCTT others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AAAAAGAG others(1): Show |
4 | a0001c0001t0012a0001c0001t0060a0001c0001t0061others(1): Show | 7 | HG00140.hp2 HG02109.hp1 HG02300.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCTT others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AAAAGAGG | 4 | a0001c0001t0018a0001c0001t0057a0001c0001t0059others(1): Show | 6 | HG02027.hp2 HG02109.hp2 HG02965.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCTT others(1): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AAAGAGG | 6 | a0001c0001t0009a0001c0001t0023a0001c0001t0054others(3): Show | 12 | HG00323.hp2 HG00733.hp1 HG01243.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCTT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AAGAGG | 15 | a0001c0001t0003a0001c0001t0011a0001c0001t0015others(12): Show | 51 | HG00597.hp1 HG01168.hp2 HG01169.hp1 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCCTCT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | AGG | 12 | a0001c0001t0001a0001c0001t0010a0001c0001t0020others(9): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-242_-241insCC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 242 | chr2 | 60553511 | |||||
| chr2:60553511
|
A | G | 14 | a0001c0001t0004a0001c0001t0014a0001c0001t0017others(11): Show | 34 | HG00597.hp2 HG00735.hp2 HG01358.hp1 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-241T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 241 | chr2 | 60553511 | |||||
| chr2:60553515
|
G | A | 68 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(65): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
5_prime_UTR_variant | MODIFIER | c.-245C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 245 | chr2 | 60553515 | |||||
| chr2:60553515
|
G | GGAGA | 16 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(13): Show | 57 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-249_-246dupTCTC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/4 | 246 | chr2 | 60553515 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:60462613
|
A | G | 205 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(202): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.488-189T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60462613 | ||||||
| chr2:60462842
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.488-418C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60462842 | ||||||
| chr2:60462965
|
G | A | 2 | a0001c0001t0021g0093a0001c0001t0032g0037 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.488-541C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60462965 | ||||||
| chr2:60463521
|
G | A | 1 | a0001c0003t0002g0143 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.488-1097C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60463521 | ||||||
| chr2:60463682
|
A | AAT | 3 | a0001c0001t0004g0071a0001c0001t0005g0231a0001c0001t0013g0253 | 3 | HG02300.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.488-1260_488-1259d others(4): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60463682 | ||||||
| chr2:60463896
|
G | T | 1 | a0001c0001t0001g0036 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.488-1472C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60463896 | ||||||
| chr2:60463922
|
GA | G | 154 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(151): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.488-1499delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60463922 | ||||||
| chr2:60463984
|
G | A | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.488-1560C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60463984 | ||||||
| chr2:60464710
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.488-2286T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60464710 | ||||||
| chr2:60464840
|
T | C | 4 | a0001c0001t0003g0182a0001c0001t0005g0224a0001c0001t0006g0240others(1): Show | 4 | NA18969.hp1 NA18971.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-2416A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60464840 | ||||||
| chr2:60465115
|
T | C | 2 | a0001c0001t0013g0248a0001c0001t0023g0203 | 2 | HG01167.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.488-2691A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60465115 | ||||||
| chr2:60465156
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.488-2732G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60465156 | ||||||
| chr2:60465350
|
T | G | 2 | a0001c0001t0002g0123a0001c0001t0003g0145 | 2 | NA18988.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.488-2926A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60465350 | ||||||
| chr2:60465587
|
A | G | 1 | a0001c0001t0021g0102 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.487+3145T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60465587 | ||||||
| chr2:60465600
|
C | G | 2 | a0001c0001t0013g0252a0001c0001t0019g0013 | 2 | HG03490.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.487+3132G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60465600 | ||||||
| chr2:60465862
|
C | T | 1 | a0001c0001t0038g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.487+2870G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60465862 | ||||||
| chr2:60466186
|
GACTTTCC others(1): Show |
G | 14 | a0001c0001t0001g0036a0001c0001t0002g0128a0001c0001t0004g0078others(11): Show | 14 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.487+2538_487+2545d others(10): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60466186 | ||||||
| chr2:60466491
|
G | A | 1 | a0001c0001t0008g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.487+2241C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60466491 | ||||||
| chr2:60466534
|
C | T | 1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.487+2198G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60466534 | ||||||
| chr2:60466778
|
C | CT | 5 | a0001c0001t0001g0038a0001c0001t0003g0189a0001c0001t0003g0192others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1953dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60466778 | ||||||
| chr2:60466862
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.487+1870C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60466862 | ||||||
| chr2:60466871
|
T | G | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.487+1861A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60466871 | ||||||
| chr2:60467071
|
A | AGTGGTGG others(44): Show |
1 | a0001c0001t0005g0221 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.487+1610_487+1660d others(53): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467071 | ||||||
| chr2:60467095
|
G | A | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.487+1637C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467095 | ||||||
| chr2:60467096
|
A | G | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.487+1636T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467096 | ||||||
| chr2:60467102
|
G | GTGGTGGT others(422): Show |
1 | a0001c0001t0005g0232 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.487+1629_487+1630i others(431): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467102 | ||||||
| chr2:60467103
|
T | A | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.487+1629A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467103 | ||||||
| chr2:60467110
|
A | G | 1 | a0001c0001t0002g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.487+1622T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467110 | ||||||
| chr2:60467111
|
G | GTGGTGGT others(35): Show |
1 | a0001c0001t0006g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.487+1620_487+1621i others(44): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467111 | ||||||
| chr2:60467111
|
GTGGTGGT others(11): Show |
G | 2 | a0001c0001t0001g0019a0001c0001t0002g0094 | 2 | HG01123.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.487+1603_487+1620d others(20): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467111 | ||||||
| chr2:60467129
|
A | ATGGTGGT others(26): Show |
32 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0002g0141others(29): Show | 32 | HG00423.hp2 HG00544.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.487+1602_487+1603i others(35): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467129 | ||||||
| chr2:60467137
|
G | GGTGGTGG others(17): Show |
3 | a0001c0001t0001g0034a0001c0001t0008g0116a0001c0001t0021g0102 | 3 | HG02572.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.487+1594_487+1595i others(26): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467137 | ||||||
| chr2:60467138
|
T | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0002g0110others(15): Show | 18 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.487+1594A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467138 | ||||||
| chr2:60467138
|
T | TTGGTGGT others(8): Show |
2 | a0001c0001t0038g0069a0001c0001t0063g0234 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.487+1579_487+1593d others(17): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467138 | ||||||
| chr2:60467138
|
T | TTGGTGGT others(14): Show |
2 | a0001c0002t0001g0040a0001c0002t0001g0062 | 2 | HG00099.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.487+1573_487+1593d others(23): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467138 | ||||||
| chr2:60467138
|
T | TTGGTGGT others(5): Show |
1 | a0001c0001t0037g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.487+1593_487+1594i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467138 | ||||||
| chr2:60467147
|
A | ATGGTGGT others(11): Show |
1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.487+1567_487+1584d others(20): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467147 | ||||||
| chr2:60467147
|
A | G | 1 | a0001c0001t0037g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.487+1585T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467147 | ||||||
| chr2:60467147
|
ATGGTGGT others(2): Show |
A | 4 | a0001c0001t0003g0168a0001c0001t0016g0254a0001c0001t0018g0209others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+1576_487+1584d others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467147 | ||||||
| chr2:60467149
|
G | GATGGTGG others(5): Show |
1 | a0001c0003t0004g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.487+1582_487+1583i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467149 | ||||||
| chr2:60467150
|
G | A | 11 | a0001c0001t0002g0110a0001c0001t0002g0144a0001c0001t0006g0239others(8): Show | 11 | HG00280.hp1 HG00642.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+1582C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467150 | ||||||
| chr2:60467159
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.487+1573C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467159 | ||||||
| chr2:60467159
|
G | GTGGTGGT others(98): Show |
1 | a0001c0001t0004g0084 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.487+1572_487+1573i others(107): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467159 | ||||||
| chr2:60467159
|
G | T | 1 | a0001c0003t0004g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.487+1573C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467159 | ||||||
| chr2:60467161
|
G | A | 11 | a0001c0001t0002g0110a0001c0001t0002g0144a0001c0001t0006g0239others(8): Show | 11 | HG00280.hp1 HG00642.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+1571C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467161 | ||||||
| chr2:60467165
|
GTGA | G | 3 | a0001c0001t0004g0082a0001c0001t0033g0022a0001c0001t0065g0251 | 3 | HG02818.hp1 HG04228.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487+1564_487+1566d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467165 | ||||||
| chr2:60467168
|
A | G | 17 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0058others(14): Show | 17 | HG00280.hp1 HG00323.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.487+1564T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467168 | ||||||
| chr2:60467171
|
G | A | 4 | a0001c0001t0009g0204a0001c0001t0009g0205a0001c0001t0010g0057others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1561C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467171 | ||||||
| chr2:60467171
|
G | T | 10 | a0001c0001t0002g0110a0001c0001t0006g0239a0001c0001t0024g0237others(7): Show | 10 | HG00280.hp1 HG02074.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.487+1561C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467171 | ||||||
| chr2:60467177
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.487+1555C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467177 | ||||||
| chr2:60467180
|
G | A | 12 | a0001c0001t0001g0031a0001c0001t0002g0110a0001c0001t0002g0130others(9): Show | 12 | HG00280.hp1 HG01496.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+1552C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467180 | ||||||
| chr2:60467180
|
G | T | 3 | a0001c0001t0009g0204a0001c0001t0009g0205a0001c0001t0012g0215 | 3 | HG00323.hp2 HG02300.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.487+1552C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467180 | ||||||
| chr2:60467182
|
G | A | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.487+1550C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467182 | ||||||
| chr2:60467184
|
T | C | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1548A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467184 | ||||||
| chr2:60467189
|
A | G | 13 | a0001c0001t0001g0031a0001c0001t0002g0110a0001c0001t0002g0144others(10): Show | 13 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.487+1543T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467189 | ||||||
| chr2:60467191
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.487+1541C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467191 | ||||||
| chr2:60467194
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1538C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467194 | ||||||
| chr2:60467195
|
G | C | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1537C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467195 | ||||||
| chr2:60467198
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.487+1534C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467198 | ||||||
| chr2:60467201
|
A | G | 6 | a0001c0001t0002g0124a0001c0001t0009g0204a0001c0001t0009g0205others(3): Show | 6 | HG00323.hp2 HG02300.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+1531T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467201 | ||||||
| chr2:60467201
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.487+1531T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467201 | ||||||
| chr2:60467201
|
ATGGCGG | A | 3 | a0001c0001t0010g0057a0001c0001t0051g0159a0001c0001t0052g0166 | 3 | HG00099.hp1 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.487+1525_487+1530d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467201 | ||||||
| chr2:60467204
|
GCGGTGAT others(11): Show |
G | 8 | a0001c0001t0002g0110a0001c0001t0006g0239a0001c0001t0024g0237others(5): Show | 8 | HG00280.hp1 HG02074.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1510_487+1527d others(20): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467204 | ||||||
| chr2:60467205
|
C | T | 28 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0001g0063others(25): Show | 28 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.487+1527G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467205 | ||||||
| chr2:60467210
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1522T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467210 | ||||||
| chr2:60467210
|
A | T | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487+1522T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467210 | ||||||
| chr2:60467213
|
GTACTGGT others(2): Show |
G | 4 | a0001c0001t0003g0153a0001c0001t0009g0204a0001c0001t0009g0205others(1): Show | 4 | HG00323.hp2 HG02300.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1510_487+1518d others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467213 | ||||||
| chr2:60467215
|
A | AGTGATGG others(17): Show |
1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1516_487+1517i others(26): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467215 | ||||||
| chr2:60467215
|
A | G | 8 | a0001c0001t0001g0031a0001c0001t0002g0144a0001c0001t0010g0050others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1517T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467215 | ||||||
| chr2:60467216
|
C | G | 9 | a0001c0001t0001g0031a0001c0001t0002g0130a0001c0001t0002g0144others(6): Show | 9 | HG00099.hp1 HG00642.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+1516G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467216 | ||||||
| chr2:60467219
|
G | A | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487+1513C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467219 | ||||||
| chr2:60467221
|
G | A | 3 | a0001c0001t0010g0057a0001c0001t0051g0159a0001c0001t0052g0166 | 3 | HG00099.hp1 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.487+1511C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467221 | ||||||
| chr2:60467222
|
A | ATGGTGGT others(191): Show |
1 | a0001c0001t0059g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.487+1509_487+1510i others(200): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467222 | ||||||
| chr2:60467222
|
A | ATGGTGGT others(41): Show |
3 | a0001c0001t0003g0156a0001c0001t0003g0183a0001c0001t0009g0197 | 3 | HG02083.hp2 HG04184.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.487+1462_487+1509d others(50): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467222 | ||||||
| chr2:60467222
|
A | ATGGTGGT others(89): Show |
1 | a0001c0001t0003g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.487+1414_487+1509d others(98): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467222 | ||||||
| chr2:60467222
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0002g0144a0001c0001t0010g0057others(2): Show | 5 | HG00099.hp1 HG00642.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1510T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467222 | ||||||
| chr2:60467226
|
T | C | 2 | a0001c0001t0033g0022a0001c0001t0065g0251 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487+1506A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467226 | ||||||
| chr2:60467231
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0033g0022a0001c0001t0065g0251 | 3 | HG01496.hp2 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487+1501C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467231 | ||||||
| chr2:60467231
|
G | T | 2 | a0001c0001t0051g0159a0001c0001t0052g0166 | 2 | NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.487+1501C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467231 | ||||||
| chr2:60467233
|
G | A | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487+1499C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467233 | ||||||
| chr2:60467236
|
A | AGTGATGG others(68): Show |
1 | a0001c0001t0055g0202 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.487+1421_487+1495d others(77): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467236 | ||||||
| chr2:60467236
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0002g0110a0001c0001t0002g0144others(15): Show | 18 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.487+1496T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467236 | ||||||
| chr2:60467236
|
AGTGATGG others(17): Show |
A | 2 | a0001c0001t0033g0022a0001c0001t0065g0251 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487+1472_487+1495d others(26): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467236 | ||||||
| chr2:60467239
|
GATGGTGG others(5): Show |
G | 1 | a0001c0001t0036g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.487+1481_487+1492d others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467239 | ||||||
| chr2:60467240
|
A | ATGG | 23 | a0001c0001t0003g0149a0001c0001t0007g0092a0001c0001t0007g0095others(20): Show | 24 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.487+1489_487+1491d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467240 | ||||||
| chr2:60467240
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0010g0050 | 2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.487+1492T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467240 | ||||||
| chr2:60467246
|
GTGGTAA | G | 3 | a0001c0001t0010g0057a0001c0001t0051g0159a0001c0001t0052g0166 | 3 | HG00099.hp1 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.487+1480_487+1485d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467246 | ||||||
| chr2:60467251
|
A | G | 14 | a0001c0001t0001g0031a0001c0001t0002g0110a0001c0001t0003g0153others(11): Show | 14 | HG00280.hp1 HG00323.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.487+1481T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467251 | ||||||
| chr2:60467252
|
A | G | 1 | a0001c0001t0002g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.487+1480T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467252 | ||||||
| chr2:60467252
|
ATGGTGGT others(59): Show |
A | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.487+1414_487+1479d others(68): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467252 | ||||||
| chr2:60467255
|
G | T | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.487+1477C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467255 | ||||||
| chr2:60467256
|
T | C | 12 | a0001c0001t0002g0110a0001c0001t0003g0153a0001c0001t0006g0239others(9): Show | 12 | HG00280.hp1 HG00323.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+1476A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467256 | ||||||
| chr2:60467261
|
G | A | 12 | a0001c0001t0002g0110a0001c0001t0003g0153a0001c0001t0006g0239others(9): Show | 12 | HG00280.hp1 HG00323.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+1471C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467261 | ||||||
| chr2:60467261
|
G | C | 2 | a0001c0001t0033g0022a0001c0001t0065g0251 | 2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.487+1471C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467261 | ||||||
| chr2:60467263
|
GGTGATGG others(62): Show |
G | 1 | a0001c0001t0038g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.487+1400_487+1468d others(71): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467263 | ||||||
| chr2:60467264
|
G | A | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.487+1468C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467264 | ||||||
| chr2:60467264
|
G | GTAC | 12 | a0001c0001t0002g0110a0001c0001t0003g0153a0001c0001t0006g0239others(9): Show | 12 | HG00280.hp1 HG00323.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+1467_487+1468i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467264 | ||||||
| chr2:60467267
|
A | G | 15 | a0001c0001t0002g0110a0001c0001t0003g0153a0001c0001t0006g0239others(12): Show | 15 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.487+1465T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467267 | ||||||
| chr2:60467267
|
ATGG | A | 87 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0042others(84): Show | 88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.487+1462_487+1464d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467267 | ||||||
| chr2:60467267
|
ATGGTGGT others(44): Show |
A | 23 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0036others(20): Show | 23 | HG00597.hp1 HG01192.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.487+1414_487+1464d others(53): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467267 | ||||||
| chr2:60467270
|
G | A | 12 | a0001c0001t0002g0110a0001c0001t0003g0153a0001c0001t0006g0239others(9): Show | 12 | HG00280.hp1 HG00323.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+1462C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467270 | ||||||
| chr2:60467270
|
G | GTGGTGGT others(1019): Show |
1 | a0001c0001t0004g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.487+1461_487+1462i others(1028): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467270 | ||||||
| chr2:60467275
|
G | A | 6 | a0001c0001t0007g0099a0001c0001t0007g0112a0001c0001t0007g0113others(3): Show | 6 | HG00733.hp1 HG02615.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1457C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467275 | ||||||
| chr2:60467275
|
GGTGGTGG others(2): Show |
G | 3 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0054g0194 | 3 | HG01243.hp2 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.487+1448_487+1456d others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467275 | ||||||
| chr2:60467276
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1456C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467276 | ||||||
| chr2:60467279
|
G | A | 9 | a0001c0001t0002g0130a0001c0001t0007g0099a0001c0001t0007g0112others(6): Show | 9 | HG00733.hp1 HG00738.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+1453C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467279 | ||||||
| chr2:60467281
|
G | A | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.487+1451C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467281 | ||||||
| chr2:60467282
|
GTAGTGA | G | 6 | a0001c0001t0007g0099a0001c0001t0007g0112a0001c0001t0007g0113others(3): Show | 6 | HG00733.hp1 HG02615.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1444_487+1449d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467282 | ||||||
| chr2:60467284
|
A | G | 8 | a0001c0001t0002g0130a0001c0001t0002g0144a0001c0001t0010g0050others(5): Show | 8 | HG00099.hp1 HG00642.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1448T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467284 | ||||||
| chr2:60467285
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0002g0130a0001c0001t0002g0144others(3): Show | 6 | HG00099.hp1 HG00642.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+1447C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467285 | ||||||
| chr2:60467285
|
G | C | 2 | a0001c0001t0057g0208a0001c0007t0002g0096 | 2 | HG00738.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.487+1447C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467285 | ||||||
| chr2:60467288
|
A | G | 4 | a0001c0001t0002g0130a0001c0001t0015g0185a0001c0001t0057g0208others(1): Show | 4 | HG00738.hp2 HG02280.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1444T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467288 | ||||||
| chr2:60467290
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1442C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467290 | ||||||
| chr2:60467291
|
G | C | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1441C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467291 | ||||||
| chr2:60467294
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0054g0194others(2): Show | 5 | HG00738.hp2 HG01243.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1438C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467294 | ||||||
| chr2:60467294
|
G | GTGATGAT others(5): Show |
1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.487+1437_487+1438i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467294 | ||||||
| chr2:60467299
|
A | G | 7 | a0001c0001t0002g0130a0001c0001t0010g0050a0001c0001t0015g0185others(4): Show | 7 | HG00738.hp2 HG01261.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1433T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467299 | ||||||
| chr2:60467300
|
A | C | 4 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0054g0194others(1): Show | 4 | HG01243.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+1432T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467300 | ||||||
| chr2:60467300
|
A | G | 3 | a0001c0001t0002g0144a0001c0001t0010g0050a0001c0001t0010g0057 | 3 | HG00099.hp1 HG00642.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.487+1432T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467300 | ||||||
| chr2:60467304
|
T | C | 2 | a0001c0001t0051g0159a0001c0001t0052g0166 | 2 | NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.487+1428A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467304 | ||||||
| chr2:60467306
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1426C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467306 | ||||||
| chr2:60467306
|
GTGGTGGT others(2): Show |
G | 5 | a0001c0001t0007g0099a0001c0001t0007g0112a0001c0001t0007g0113others(2): Show | 5 | HG02615.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1417_487+1425d others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467306 | ||||||
| chr2:60467309
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0051g0159others(3): Show | 6 | HG01243.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1423C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467309 | ||||||
| chr2:60467309
|
G | T | 1 | a0001c0001t0002g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.487+1423C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467309 | ||||||
| chr2:60467314
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1418C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467314 | ||||||
| chr2:60467314
|
GATGGTGG others(257): Show |
G | 1 | a0001c0001t0007g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.487+1154_487+1417d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467314 | ||||||
| chr2:60467315
|
A | ATGGTGGT others(200): Show |
1 | a0001c0009t0001g0017 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.487+1416_487+1417i others(209): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467315 | ||||||
| chr2:60467315
|
A | G | 7 | a0001c0001t0002g0144a0001c0001t0010g0050a0001c0001t0010g0057others(4): Show | 7 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+1417T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467315 | ||||||
| chr2:60467315
|
ATGG | A | 6 | a0001c0001t0003g0153a0001c0001t0009g0204a0001c0001t0009g0205others(3): Show | 6 | HG00323.hp2 HG02300.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+1414_487+1416d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467315 | ||||||
| chr2:60467315
|
ATGGTGGT others(590): Show |
A | 1 | a0001c0001t0007g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.487+820_487+1416de others(1): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467315 | ||||||
| chr2:60467318
|
G | A | 6 | a0001c0001t0002g0144a0001c0001t0010g0057a0001c0001t0051g0159others(3): Show | 6 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+1414C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467318 | ||||||
| chr2:60467318
|
G | GTGGTGAT others(248): Show |
3 | a0001c0001t0003g0181a0001c0001t0012g0218a0001c0001t0048g0148 | 3 | HG02080.hp2 HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.487+1413_487+1414i others(257): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467318 | ||||||
| chr2:60467318
|
G | GTGGTGAT others(341): Show |
1 | a0001c0001t0042g0138 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.487+1413_487+1414i others(350): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467318 | ||||||
| chr2:60467318
|
G | GTGGTGAT others(200): Show |
1 | a0001c0001t0001g0045 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.487+1413_487+1414i others(209): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467318 | ||||||
| chr2:60467323
|
GGTGGTGG others(2): Show |
G | 3 | a0001c0001t0012g0213a0001c0001t0045g0114a0001c0002t0001g0061 | 3 | HG01074.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.487+1400_487+1408d others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467323 | ||||||
| chr2:60467324
|
G | A | 75 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0042others(72): Show | 76 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.487+1408C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467324 | ||||||
| chr2:60467327
|
G | A | 80 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0042others(77): Show | 81 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.487+1405C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467327 | ||||||
| chr2:60467327
|
G | T | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.487+1405C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467327 | ||||||
| chr2:60467332
|
A | G | 84 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(81): Show | 85 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.487+1400T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467332 | ||||||
| chr2:60467332
|
AGTGATGG others(122): Show |
A | 2 | a0001c0002t0001g0023a0001c0002t0024g0238 | 2 | HG01123.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.487+1271_487+1399d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467332 | ||||||
| chr2:60467333
|
G | A | 82 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(79): Show | 83 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.487+1399C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467333 | ||||||
| chr2:60467333
|
G | C | 4 | a0001c0001t0034g0066a0001c0001t0047g0176a0001c0001t0057g0208others(1): Show | 4 | HG00738.hp2 NA18979.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1399C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467333 | ||||||
| chr2:60467336
|
A | G | 84 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(81): Show | 85 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.487+1396T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467336 | ||||||
| chr2:60467338
|
G | A | 75 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0042others(72): Show | 76 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.487+1394C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467338 | ||||||
| chr2:60467339
|
G | A | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487+1393C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467339 | ||||||
| chr2:60467339
|
G | C | 75 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0042others(72): Show | 76 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.487+1393C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467339 | ||||||
| chr2:60467341
|
GGTGGTAA others(449): Show |
G | 14 | a0001c0001t0003g0149a0001c0001t0007g0092a0001c0001t0007g0095others(11): Show | 15 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.487+935_487+1390de others(1): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467341 | ||||||
| chr2:60467342
|
G | A | 11 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0012g0213others(8): Show | 11 | HG00738.hp2 HG01074.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+1390C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467342 | ||||||
| chr2:60467347
|
A | G | 81 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0042others(78): Show | 82 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.487+1385T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467347 | ||||||
| chr2:60467348
|
A | C | 11 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0011g0150others(8): Show | 11 | HG00738.hp2 HG01074.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+1384T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467348 | ||||||
| chr2:60467348
|
A | G | 2 | a0001c0001t0010g0057a0001c0009t0001g0017 | 2 | HG00099.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.487+1384T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467348 | ||||||
| chr2:60467351
|
G | A | 2 | a0001c0001t0002g0144a0001c0009t0001g0017 | 2 | HG00642.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.487+1381C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467351 | ||||||
| chr2:60467353
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0010g0050 | 2 | HG01261.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.487+1379C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467353 | ||||||
| chr2:60467354
|
G | A | 76 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0042others(73): Show | 77 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.487+1378C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467354 | ||||||
| chr2:60467354
|
G | C | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1378C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467354 | ||||||
| chr2:60467356
|
G | C | 2 | a0001c0001t0011g0150a0001c0001t0011g0151 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.487+1376C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467356 | ||||||
| chr2:60467357
|
G | A | 11 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0011g0150others(8): Show | 11 | HG00738.hp2 HG01074.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+1375C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467357 | ||||||
| chr2:60467357
|
GTGGTGAT others(179): Show |
G | 1 | a0001c0001t0008g0137 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.487+1189_487+1374d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467357 | ||||||
| chr2:60467360
|
G | A | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.487+1372C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467360 | ||||||
| chr2:60467361
|
T | A | 6 | a0001c0001t0001g0045a0001c0001t0003g0181a0001c0001t0012g0218others(3): Show | 6 | HG02080.hp2 HG02738.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+1371A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467361 | ||||||
| chr2:60467362
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0002g0144a0001c0001t0005g0233others(3): Show | 6 | HG00642.hp1 HG01243.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1370C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467362 | ||||||
| chr2:60467363
|
A | C | 5 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0011g0150others(2): Show | 5 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1369T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467363 | ||||||
| chr2:60467363
|
A | G | 82 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0042others(79): Show | 83 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.487+1369T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467363 | ||||||
| chr2:60467363
|
ATGGTGGT others(542): Show |
A | 5 | a0001c0001t0007g0099a0001c0001t0007g0112a0001c0001t0007g0113others(2): Show | 5 | HG02615.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+820_487+1368de others(1): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467363 | ||||||
| chr2:60467366
|
GTGGTGAT others(47): Show |
G | 2 | a0001c0001t0051g0159a0001c0001t0052g0166 | 2 | NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.487+1312_487+1365d others(56): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467366 | ||||||
| chr2:60467366
|
GTGGTGAT others(176): Show |
G | 3 | a0001c0001t0043g0109a0001c0001t0044g0105a0001c0003t0009g0199 | 3 | HG02074.hp2 NA18970.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.487+1183_487+1365d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467366 | ||||||
| chr2:60467368
|
G | T | 2 | a0001c0001t0011g0150a0001c0001t0011g0151 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.487+1364C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467368 | ||||||
| chr2:60467369
|
GTGATGAT others(74): Show |
G | 16 | a0001c0001t0001g0031a0001c0001t0002g0110a0001c0001t0006g0239others(13): Show | 16 | HG00280.hp1 HG00735.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+1282_487+1362d others(83): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467369 | ||||||
| chr2:60467372
|
A | G | 12 | a0001c0001t0002g0130a0001c0001t0009g0198a0001c0001t0010g0057others(9): Show | 12 | HG00099.hp1 HG00733.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+1360T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467372 | ||||||
| chr2:60467372
|
A | T | 6 | a0001c0001t0001g0045a0001c0001t0003g0181a0001c0001t0012g0218others(3): Show | 6 | HG02080.hp2 HG02738.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+1360T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467372 | ||||||
| chr2:60467374
|
GATGGTGA others(68): Show |
G | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487+1283_487+1357d others(77): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467374 | ||||||
| chr2:60467375
|
A | G | 87 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(84): Show | 88 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.487+1357T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467375 | ||||||
| chr2:60467376
|
T | C | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.487+1356A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467376 | ||||||
| chr2:60467378
|
G | A | 2 | a0001c0001t0057g0208a0001c0007t0002g0096 | 2 | HG00738.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.487+1354C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467378 | ||||||
| chr2:60467381
|
A | G | 7 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0009g0198others(4): Show | 7 | HG00733.hp1 HG00738.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+1351T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467381 | ||||||
| chr2:60467384
|
G | A | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+1348C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467384 | ||||||
| chr2:60467384
|
GTAC | G | 5 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0011g0150others(2): Show | 5 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1345_487+1347d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467384 | ||||||
| chr2:60467386
|
A | G | 8 | a0001c0001t0002g0130a0001c0001t0002g0144a0001c0001t0009g0198others(5): Show | 8 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1346T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467386 | ||||||
| chr2:60467387
|
C | A | 1 | a0001c0003t0002g0107 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.487+1345G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467387 | ||||||
| chr2:60467387
|
C | G | 8 | a0001c0001t0002g0130a0001c0001t0002g0144a0001c0001t0009g0198others(5): Show | 8 | HG00642.hp1 HG00733.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1345G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467387 | ||||||
| chr2:60467390
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0012g0213others(1): Show | 4 | HG01243.hp2 HG02970.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1342C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467390 | ||||||
| chr2:60467390
|
G | GTGGTGAT others(339): Show |
1 | a0001c0001t0048g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.487+1341_487+1342i others(348): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467390 | ||||||
| chr2:60467390
|
GTGGTGAT others(5): Show |
G | 27 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(24): Show | 27 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+1330_487+1341d others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467390 | ||||||
| chr2:60467396
|
A | ATGGTACT others(128): Show |
2 | a0001c0001t0003g0181a0001c0001t0012g0218 | 2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.487+1335_487+1336i others(137): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467396 | ||||||
| chr2:60467396
|
A | ATGGTACT others(329): Show |
1 | a0001c0001t0056g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.487+1335_487+1336i others(338): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467396 | ||||||
| chr2:60467396
|
A | G | 5 | a0001c0001t0002g0130a0001c0001t0002g0144a0001c0001t0034g0066others(2): Show | 5 | HG00642.hp1 HG01978.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1336T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467396 | ||||||
| chr2:60467398
|
GGTGATGG others(158): Show |
G | 1 | a0001c0001t0036g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.487+1169_487+1333d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467398 | ||||||
| chr2:60467399
|
G | A | 3 | a0001c0001t0002g0144a0001c0001t0034g0066a0001c0001t0047g0176 | 3 | HG00642.hp1 NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.487+1333C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467399 | ||||||
| chr2:60467399
|
G | C | 3 | a0001c0001t0002g0130a0001c0001t0057g0208a0001c0007t0002g0096 | 3 | HG00738.hp2 NA19004.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.487+1333C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467399 | ||||||
| chr2:60467399
|
G | GTAC | 8 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(5): Show | 8 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1332_487+1333i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467399 | ||||||
| chr2:60467399
|
G | GTACTGGT others(5): Show |
8 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0004g0067others(5): Show | 8 | HG01261.hp1 HG01934.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1332_487+1333i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467399 | ||||||
| chr2:60467399
|
G | GTACTGGT others(35): Show |
1 | a0001c0001t0001g0045 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.487+1332_487+1333i others(44): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467399 | ||||||
| chr2:60467399
|
G | GTACTGGT others(50): Show |
32 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(29): Show | 33 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.487+1332_487+1333i others(59): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467399 | ||||||
| chr2:60467399
|
GTGA | G | 5 | a0001c0001t0009g0198a0001c0001t0010g0057a0001c0001t0011g0150others(2): Show | 5 | HG00099.hp1 HG00733.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1330_487+1332d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467399 | ||||||
| chr2:60467401
|
G | A | 3 | a0001c0001t0045g0114a0001c0001t0063g0234a0001c0002t0001g0061 | 3 | HG01074.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.487+1331C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467401 | ||||||
| chr2:60467402
|
A | ATGGTGGT others(20): Show |
1 | a0001c0009t0001g0017 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.487+1329_487+1330i others(29): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467402 | ||||||
| chr2:60467402
|
A | ATGGTGGT others(254): Show |
5 | a0001c0001t0002g0141a0001c0001t0003g0156a0001c0001t0003g0158others(2): Show | 5 | HG02083.hp2 HG04184.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1329_487+1330i others(263): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467402 | ||||||
| chr2:60467402
|
A | C | 4 | a0001c0001t0037g0068a0001c0001t0045g0114a0001c0001t0063g0234others(1): Show | 4 | HG01074.hp2 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+1330T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467402 | ||||||
| chr2:60467402
|
A | G | 61 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0042others(58): Show | 62 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.487+1330T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467402 | ||||||
| chr2:60467402
|
ATGGTGAT others(50): Show |
A | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.487+1273_487+1329d others(59): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467402 | ||||||
| chr2:60467402
|
ATGGTGAT others(74): Show |
A | 6 | a0001c0001t0005g0219a0001c0001t0018g0211a0001c0001t0021g0093others(3): Show | 6 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1249_487+1329d others(83): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467402 | ||||||
| chr2:60467403
|
T | C | 2 | a0001c0001t0009g0198a0001c0001t0010g0057 | 2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.487+1329A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467403 | ||||||
| chr2:60467403
|
T | TGGTGGTG others(284): Show |
1 | a0001c0001t0002g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.487+1328_487+1329i others(293): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467403 | ||||||
| chr2:60467405
|
GTGATGGT others(2): Show |
G | 3 | a0001c0001t0045g0114a0001c0001t0063g0234a0001c0002t0001g0061 | 3 | HG01074.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.487+1318_487+1326d others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467405 | ||||||
| chr2:60467405
|
GTGATGGT others(38): Show |
G | 1 | a0001c0001t0038g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.487+1282_487+1326d others(47): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467405 | ||||||
| chr2:60467408
|
A | ATGG | 6 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(3): Show | 6 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1321_487+1323d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467408 | ||||||
| chr2:60467408
|
A | G | 74 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0032others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.487+1324T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467408 | ||||||
| chr2:60467411
|
GTACTGGT others(32): Show |
G | 1 | a0001c0001t0037g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.487+1282_487+1320d others(41): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467411 | ||||||
| chr2:60467413
|
A | G | 81 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0032others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.487+1319T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467413 | ||||||
| chr2:60467414
|
C | A | 13 | a0001c0001t0001g0020a0001c0001t0002g0090a0001c0001t0003g0171others(10): Show | 13 | HG01243.hp2 HG01261.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.487+1318G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467414 | ||||||
| chr2:60467414
|
C | CTGG | 46 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0045others(43): Show | 47 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.487+1315_487+1317d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467414 | ||||||
| chr2:60467414
|
C | G | 68 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0035others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.487+1318G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467414 | ||||||
| chr2:60467417
|
G | C | 3 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0054g0194 | 3 | HG01243.hp2 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.487+1315C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467417 | ||||||
| chr2:60467417
|
GTGATGGT others(119): Show |
G | 2 | a0001c0001t0011g0150a0001c0001t0011g0151 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.487+1189_487+1314d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467417 | ||||||
| chr2:60467419
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0012g0213others(1): Show | 4 | HG01243.hp2 HG02970.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1313C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467419 | ||||||
| chr2:60467420
|
A | C | 4 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0012g0213others(1): Show | 4 | HG01243.hp2 HG02970.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1312T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467420 | ||||||
| chr2:60467420
|
A | G | 30 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(27): Show | 30 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.487+1312T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467420 | ||||||
| chr2:60467423
|
G | A | 29 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(26): Show | 29 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.487+1309C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467423 | ||||||
| chr2:60467423
|
G | GTAC | 11 | a0001c0001t0003g0163a0001c0001t0005g0223a0001c0001t0006g0246others(8): Show | 11 | HG00544.hp2 HG01071.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1308_487+1309i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467423 | ||||||
| chr2:60467426
|
G | A | 7 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(4): Show | 7 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1306C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467426 | ||||||
| chr2:60467428
|
G | A | 2 | a0001c0001t0034g0066a0001c0001t0047g0176 | 2 | NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.487+1304C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467428 | ||||||
| chr2:60467429
|
G | A | 27 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0032others(24): Show | 27 | HG00323.hp2 HG00597.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+1303C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467429 | ||||||
| chr2:60467429
|
G | C | 2 | a0001c0001t0034g0066a0001c0001t0047g0176 | 2 | NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.487+1303C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467429 | ||||||
| chr2:60467431
|
G | A | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.487+1301C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467431 | ||||||
| chr2:60467432
|
G | A | 12 | a0001c0001t0003g0163a0001c0001t0005g0223a0001c0001t0006g0246others(9): Show | 12 | HG00544.hp2 HG01071.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.487+1300C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467432 | ||||||
| chr2:60467434
|
A | G | 56 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(53): Show | 56 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.487+1298T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467434 | ||||||
| chr2:60467434
|
AGTGATG | A | 13 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0002g0097others(10): Show | 13 | HG00597.hp1 HG01192.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+1292_487+1297d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467434 | ||||||
| chr2:60467435
|
G | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0032others(11): Show | 14 | HG00323.hp2 HG01243.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.487+1297C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467435 | ||||||
| chr2:60467437
|
G | A | 11 | a0001c0001t0003g0163a0001c0001t0005g0223a0001c0001t0006g0246others(8): Show | 11 | HG00544.hp2 HG01071.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1295C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467437 | ||||||
| chr2:60467438
|
A | C | 11 | a0001c0001t0003g0163a0001c0001t0005g0223a0001c0001t0006g0246others(8): Show | 11 | HG00544.hp2 HG01071.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1294T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467438 | ||||||
| chr2:60467438
|
A | G | 21 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00323.hp2 HG00735.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.487+1294T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467438 | ||||||
| chr2:60467440
|
G | GCTA | 8 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0004g0067others(5): Show | 8 | HG01261.hp1 HG01934.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1291_487+1292i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467440 | ||||||
| chr2:60467441
|
G | C | 21 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0002g0090others(18): Show | 21 | HG00597.hp1 HG01192.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.487+1291C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467441 | ||||||
| chr2:60467443
|
GGTGGTA | G | 27 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(24): Show | 27 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+1283_487+1288d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467443 | ||||||
| chr2:60467444
|
G | A | 20 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0032others(17): Show | 20 | HG00323.hp2 HG00735.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.487+1288C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467444 | ||||||
| chr2:60467447
|
G | A | 12 | a0001c0001t0003g0163a0001c0001t0005g0223a0001c0001t0006g0246others(9): Show | 12 | HG00544.hp2 HG01071.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.487+1285C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467447 | ||||||
| chr2:60467447
|
G | C | 6 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(3): Show | 6 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1285C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467447 | ||||||
| chr2:60467447
|
GTAA | G | 5 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0009g0198others(2): Show | 5 | HG00733.hp1 HG01243.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1282_487+1284d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467447 | ||||||
| chr2:60467449
|
A | ACTGCTGG others(5): Show |
1 | a0001c0001t0033g0022 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.487+1282_487+1283i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467449 | ||||||
| chr2:60467449
|
A | G | 36 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0002g0090others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.487+1283T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467449 | ||||||
| chr2:60467450
|
A | ATGGTGGT others(20): Show |
1 | a0001c0002t0004g0073 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.487+1281_487+1282i others(29): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467450 | ||||||
| chr2:60467450
|
A | C | 15 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0128others(12): Show | 15 | HG00323.hp2 HG00735.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.487+1282T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467450 | ||||||
| chr2:60467450
|
A | G | 16 | a0001c0001t0003g0163a0001c0001t0005g0223a0001c0001t0006g0246others(13): Show | 16 | HG00544.hp2 HG01071.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+1282T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467450 | ||||||
| chr2:60467453
|
G | A | 2 | a0001c0001t0034g0066a0001c0001t0047g0176 | 2 | NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.487+1279C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467453 | ||||||
| chr2:60467453
|
G | GTAC | 8 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0004g0067others(5): Show | 8 | HG01261.hp1 HG01934.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1278_487+1279i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467453 | ||||||
| chr2:60467453
|
GTGGTGGT others(194): Show |
G | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+1078_487+1278d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467453 | ||||||
| chr2:60467455
|
G | A | 13 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0002g0097others(10): Show | 13 | HG00597.hp1 HG01192.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+1277C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467455 | ||||||
| chr2:60467456
|
G | C | 13 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0002g0097others(10): Show | 13 | HG00597.hp1 HG01192.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+1276C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467456 | ||||||
| chr2:60467456
|
G | GTGA | 8 | a0001c0001t0001g0032a0001c0001t0003g0153a0001c0001t0003g0160others(5): Show | 8 | HG00323.hp2 HG02129.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1275_487+1276i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467456 | ||||||
| chr2:60467456
|
G | T | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487+1276C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467456 | ||||||
| chr2:60467459
|
G | A | 8 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(5): Show | 8 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1273C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467459 | ||||||
| chr2:60467461
|
G | A | 33 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0002g0110others(30): Show | 33 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.487+1271C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGATGG others(11): Show |
1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.487+1270_487+1271i others(20): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGATGG others(14): Show |
24 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0028others(21): Show | 24 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.487+1270_487+1271i others(23): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGATGG others(212): Show |
1 | a0001c0002t0001g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.487+1270_487+1271i others(221): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGATGG others(618): Show |
1 | a0001c0001t0004g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.487+1270_487+1271i others(627): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGATGG others(476): Show |
3 | a0001c0001t0001g0034a0001c0001t0008g0116a0001c0001t0021g0102 | 3 | HG02572.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.487+1270_487+1271i others(485): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGATGG others(62): Show |
24 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(21): Show | 24 | HG00140.hp2 HG00642.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.487+1270_487+1271i others(71): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGATGG others(260): Show |
2 | a0001c0001t0005g0220a0001c0002t0017g0011 | 2 | HG03041.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.487+1270_487+1271i others(269): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGATGG others(110): Show |
1 | a0001c0001t0016g0257 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.487+1270_487+1271i others(119): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467461
|
G | GGTGGTGG others(59): Show |
28 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(25): Show | 29 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.487+1270_487+1271i others(68): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467461 | ||||||
| chr2:60467462
|
G | A | 8 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0004g0067others(5): Show | 8 | HG01261.hp1 HG01934.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1270C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467462 | ||||||
| chr2:60467462
|
GTGA | G | 27 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(24): Show | 27 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+1267_487+1269d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467462 | ||||||
| chr2:60467463
|
T | A | 3 | a0001c0001t0045g0114a0001c0001t0063g0234a0001c0002t0001g0061 | 3 | HG01074.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.487+1269A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467463 | ||||||
| chr2:60467464
|
G | A | 6 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(3): Show | 6 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1268C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467464 | ||||||
| chr2:60467465
|
A | C | 6 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(3): Show | 6 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1267T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467465 | ||||||
| chr2:60467465
|
A | G | 31 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0002g0090others(28): Show | 31 | HG00323.hp2 HG00544.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.487+1267T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467465 | ||||||
| chr2:60467468
|
G | GTGGTGGT others(46): Show |
1 | a0001c0001t0004g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.487+1263_487+1264i others(55): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467468 | ||||||
| chr2:60467468
|
GTGGTGGT others(74): Show |
G | 8 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0004g0082others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1183_487+1263d others(83): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467468 | ||||||
| chr2:60467471
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0043others(32): Show | 35 | HG00323.hp2 HG00597.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.487+1261C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467471 | ||||||
| chr2:60467471
|
GTGGTAA | G | 19 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0002g0097others(16): Show | 19 | HG00597.hp1 HG01168.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.487+1255_487+1260d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467471 | ||||||
| chr2:60467473
|
G | A | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+1259C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467473 | ||||||
| chr2:60467473
|
G | GGTGGTA | 7 | a0001c0001t0001g0045a0001c0001t0002g0091a0001c0001t0002g0119others(4): Show | 7 | HG00544.hp1 HG00738.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1258_487+1259i others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467473 | ||||||
| chr2:60467474
|
G | A | 6 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(3): Show | 6 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1258C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467474 | ||||||
| chr2:60467474
|
G | C | 27 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(24): Show | 27 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+1258C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467474 | ||||||
| chr2:60467474
|
G | T | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.487+1258C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467474 | ||||||
| chr2:60467476
|
A | AGTG | 3 | a0001c0001t0002g0130a0001c0001t0013g0248a0001c0001t0023g0203 | 3 | HG01167.hp1 HG02630.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.487+1255_487+1256i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467476 | ||||||
| chr2:60467476
|
A | G | 27 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0002g0091others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.487+1256T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467476 | ||||||
| chr2:60467477
|
A | C | 30 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(27): Show | 30 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.487+1255T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467477 | ||||||
| chr2:60467477
|
A | G | 16 | a0001c0001t0002g0090a0001c0001t0002g0128a0001c0001t0002g0140others(13): Show | 16 | HG00735.hp1 HG01261.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+1255T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467477 | ||||||
| chr2:60467480
|
G | A | 9 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0004g0067others(6): Show | 9 | HG01261.hp1 HG01934.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.487+1252C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467480 | ||||||
| chr2:60467480
|
GTGGTGGT others(80): Show |
G | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+1165_487+1251d others(89): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467480 | ||||||
| chr2:60467480
|
GTGGTGGT others(155): Show |
G | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.487+1090_487+1251d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467480 | ||||||
| chr2:60467482
|
G | A | 3 | a0001c0001t0002g0140a0001c0001t0063g0234a0001c0002t0001g0061 | 3 | HG01074.hp2 HG02723.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.487+1250C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467482 | ||||||
| chr2:60467483
|
G | C | 2 | a0001c0001t0063g0234a0001c0002t0001g0061 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.487+1249C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467483 | ||||||
| chr2:60467486
|
G | A | 45 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0043others(42): Show | 45 | HG00597.hp1 HG00597.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.487+1246C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467486 | ||||||
| chr2:60467488
|
G | A | 17 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(14): Show | 17 | HG00140.hp1 HG00735.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+1244C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467488 | ||||||
| chr2:60467489
|
G | A | 2 | a0001c0001t0010g0050a0001c0001t0048g0148 | 2 | HG01261.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.487+1243C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467489 | ||||||
| chr2:60467490
|
T | A | 41 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(38): Show | 42 | HG00323.hp1 HG00544.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.487+1242A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467490 | ||||||
| chr2:60467490
|
T | TGATGGTG others(5): Show |
3 | a0001c0001t0004g0078a0001c0001t0013g0253a0001c0007t0002g0096 | 3 | HG00738.hp2 HG01361.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.487+1241_487+1242i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467490 | ||||||
| chr2:60467491
|
G | A | 39 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(36): Show | 39 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(36): Show |
intron_variant | MODIFIER | c.487+1241C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467491 | ||||||
| chr2:60467492
|
A | ATGGTAC | 6 | a0001c0001t0001g0045a0001c0001t0002g0091a0001c0001t0002g0119others(3): Show | 6 | HG00544.hp1 HG01167.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1239_487+1240i others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467492 | ||||||
| chr2:60467492
|
A | C | 30 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(27): Show | 30 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.487+1240T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467492 | ||||||
| chr2:60467492
|
A | G | 21 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0002g0140others(18): Show | 21 | HG00323.hp2 HG00423.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.487+1240T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467492 | ||||||
| chr2:60467495
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0003g0153a0001c0001t0003g0160others(5): Show | 8 | HG00323.hp2 HG02129.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1237C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467495 | ||||||
| chr2:60467495
|
G | GTAC | 3 | a0001c0001t0063g0234a0001c0002t0001g0061a0001c0009t0001g0017 | 3 | HG01074.hp2 HG02723.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.487+1236_487+1237i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467495 | ||||||
| chr2:60467495
|
G | GTGGTGGT others(5): Show |
1 | a0001c0001t0020g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.487+1236_487+1237i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467495 | ||||||
| chr2:60467497
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+1235C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467497 | ||||||
| chr2:60467498
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+1234C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467498 | ||||||
| chr2:60467498
|
G | C | 8 | a0001c0001t0001g0032a0001c0001t0003g0153a0001c0001t0003g0160others(5): Show | 8 | HG00323.hp2 HG02129.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1234C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467498 | ||||||
| chr2:60467500
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0003g0153a0001c0001t0003g0160others(6): Show | 9 | HG00323.hp2 HG02080.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+1232C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467500 | ||||||
| chr2:60467501
|
A | C | 8 | a0001c0001t0001g0032a0001c0001t0003g0153a0001c0001t0003g0160others(5): Show | 8 | HG00323.hp2 HG02129.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1231T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467501 | ||||||
| chr2:60467501
|
A | G | 45 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0065others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.487+1231T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467501 | ||||||
| chr2:60467501
|
A | T | 44 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(41): Show | 45 | HG00323.hp1 HG00544.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.487+1231T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467501 | ||||||
| chr2:60467503
|
G | A | 12 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(9): Show | 12 | HG00735.hp1 HG01168.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.487+1229C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467503 | ||||||
| chr2:60467504
|
A | ATGGTAGT others(11): Show |
1 | a0001c0001t0004g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.487+1227_487+1228i others(20): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467504 | ||||||
| chr2:60467504
|
A | G | 79 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0032others(76): Show | 79 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.487+1228T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467504 | ||||||
| chr2:60467506
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0001t0054g0194 | 3 | HG01243.hp2 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.487+1226C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467506 | ||||||
| chr2:60467510
|
A | G | 59 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(56): Show | 59 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.487+1222T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467510 | ||||||
| chr2:60467510
|
A | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.487+1222T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467510 | ||||||
| chr2:60467513
|
G | C | 13 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0002g0097others(10): Show | 13 | HG00597.hp1 HG01192.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+1219C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467513 | ||||||
| chr2:60467515
|
A | G | 28 | a0001c0001t0001g0020a0001c0001t0002g0090a0001c0001t0002g0128others(25): Show | 28 | HG00735.hp1 HG01074.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.487+1217T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467515 | ||||||
| chr2:60467516
|
C | G | 64 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0043others(61): Show | 64 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.487+1216G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467516 | ||||||
| chr2:60467518
|
G | A | 2 | a0001c0001t0048g0148a0001c0009t0001g0017 | 2 | HG02080.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.487+1214C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467518 | ||||||
| chr2:60467519
|
G | A | 41 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(38): Show | 41 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.487+1213C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467519 | ||||||
| chr2:60467519
|
GTGGTGAT others(17): Show |
G | 4 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0005g0227others(1): Show | 4 | HG02129.hp2 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+1189_487+1212d others(26): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467519 | ||||||
| chr2:60467519
|
GTGGTGAT others(128): Show |
G | 1 | a0001c0001t0037g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.487+1078_487+1212d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467519 | ||||||
| chr2:60467521
|
G | A | 9 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0004g0067others(6): Show | 9 | HG01261.hp1 HG01934.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.487+1211C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467521 | ||||||
| chr2:60467522
|
G | A | 3 | a0001c0001t0002g0140a0001c0001t0048g0148a0001c0009t0001g0017 | 3 | HG02080.hp2 HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.487+1210C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467522 | ||||||
| chr2:60467525
|
A | ATGG | 8 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0004g0067others(5): Show | 8 | HG01261.hp1 HG01934.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1204_487+1206d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467525 | ||||||
| chr2:60467525
|
A | ATGGTACT others(209): Show |
1 | a0001c0003t0002g0107 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.487+1206_487+1207i others(218): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467525 | ||||||
| chr2:60467525
|
A | ATGGTACT others(125): Show |
2 | a0001c0001t0002g0123a0001c0001t0003g0145 | 2 | NA18988.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.487+1206_487+1207i others(134): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467525 | ||||||
| chr2:60467525
|
A | ATGGTACT others(128): Show |
3 | a0001c0001t0003g0173a0001c0001t0008g0132a0001c0001t0056g0196 | 3 | HG04115.hp2 NA19065.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.487+1206_487+1207i others(137): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467525 | ||||||
| chr2:60467525
|
A | G | 52 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(49): Show | 52 | HG00544.hp1 HG00597.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.487+1207T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467525 | ||||||
| chr2:60467525
|
ATGGTGAT others(41): Show |
A | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+1159_487+1206d others(50): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467525 | ||||||
| chr2:60467528
|
G | A | 6 | a0001c0002t0001g0016a0001c0002t0002g0120a0001c0002t0003g0167others(3): Show | 6 | HG01168.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1204C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467528 | ||||||
| chr2:60467528
|
G | C | 2 | a0001c0001t0063g0234a0001c0002t0001g0061 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.487+1204C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467528 | ||||||
| chr2:60467528
|
G | GTACTGGT others(50): Show |
1 | a0001c0001t0001g0042 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.487+1203_487+1204i others(59): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467528 | ||||||
| chr2:60467528
|
G | GTACTGGT others(35): Show |
21 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0055others(18): Show | 22 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.487+1203_487+1204i others(44): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467528 | ||||||
| chr2:60467528
|
G | GTACTGGT others(113): Show |
1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.487+1203_487+1204i others(122): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467528 | ||||||
| chr2:60467530
|
G | A | 69 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0036others(66): Show | 69 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.487+1202C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467530 | ||||||
| chr2:60467531
|
A | ATGGTGGT others(20): Show |
2 | a0001c0001t0004g0078a0001c0007t0002g0096 | 2 | HG00738.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.487+1200_487+1201i others(29): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467531 | ||||||
| chr2:60467531
|
A | ATGGTGGT others(167): Show |
2 | a0001c0002t0001g0024a0004c0005t0002g0100 | 2 | HG01257.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.487+1200_487+1201i others(176): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467531 | ||||||
| chr2:60467531
|
A | ATGGTGGT others(254): Show |
1 | a0001c0002t0004g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.487+1200_487+1201i others(263): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467531 | ||||||
| chr2:60467531
|
A | ATGGTGGT others(98): Show |
1 | a0001c0001t0042g0138 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.487+1200_487+1201i others(107): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467531 | ||||||
| chr2:60467531
|
A | C | 33 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0065others(30): Show | 33 | HG00544.hp2 HG00597.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.487+1201T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467531 | ||||||
| chr2:60467531
|
A | G | 53 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(50): Show | 54 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.487+1201T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467531 | ||||||
| chr2:60467532
|
T | C | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487+1200A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467532 | ||||||
| chr2:60467533
|
G | A | 6 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(3): Show | 6 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1199C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467533 | ||||||
| chr2:60467533
|
G | GGTGGTA | 4 | a0001c0001t0003g0153a0001c0001t0009g0204a0001c0001t0009g0205others(1): Show | 4 | HG00323.hp2 HG02300.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1198_487+1199i others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467533 | ||||||
| chr2:60467533
|
GGTGATGG others(2): Show |
G | 4 | a0001c0001t0021g0093a0001c0001t0032g0037a0001c0001t0064g0247others(1): Show | 4 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+1190_487+1198d others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467533 | ||||||
| chr2:60467534
|
G | GTGGTGGT others(137): Show |
1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.487+1197_487+1198i others(146): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467534 | ||||||
| chr2:60467534
|
GTGA | G | 9 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0005g0223others(6): Show | 9 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.487+1195_487+1197d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467534 | ||||||
| chr2:60467534
|
GTGATGGT others(2): Show |
G | 20 | a0001c0001t0001g0020a0001c0001t0001g0036a0001c0001t0001g0065others(17): Show | 20 | HG00597.hp1 HG01192.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.487+1189_487+1197d others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467534 | ||||||
| chr2:60467536
|
G | A | 1 | a0001c0001t0012g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.487+1196C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467536 | ||||||
| chr2:60467537
|
A | ATGG | 5 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(2): Show | 5 | HG00735.hp1 HG01952.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1192_487+1194d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467537 | ||||||
| chr2:60467537
|
A | G | 63 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0025others(60): Show | 63 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.487+1195T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467537 | ||||||
| chr2:60467540
|
G | A | 1 | a0001c0001t0020g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.487+1192C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467540 | ||||||
| chr2:60467540
|
GTAC | G | 34 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(31): Show | 34 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.487+1189_487+1191d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467540 | ||||||
| chr2:60467542
|
A | G | 49 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0028others(46): Show | 49 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.487+1190T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467542 | ||||||
| chr2:60467543
|
C | A | 10 | a0001c0001t0001g0019a0001c0001t0003g0163a0001c0001t0003g0174others(7): Show | 10 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+1189G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467543 | ||||||
| chr2:60467543
|
C | CTGG | 52 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(49): Show | 53 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.487+1186_487+1188d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467543 | ||||||
| chr2:60467543
|
C | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0002g0128others(37): Show | 40 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.487+1189G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467543 | ||||||
| chr2:60467546
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0068g0260 | 2 | HG03017.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.487+1186C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467546 | ||||||
| chr2:60467548
|
G | A | 4 | a0001c0001t0003g0153a0001c0001t0009g0204a0001c0001t0009g0205others(1): Show | 4 | HG00323.hp2 HG02300.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1184C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467548 | ||||||
| chr2:60467549
|
A | ATGGTGGT others(113): Show |
1 | a0001c0001t0003g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.487+1182_487+1183i others(122): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467549 | ||||||
| chr2:60467549
|
A | G | 38 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(35): Show | 38 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.487+1183T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467549 | ||||||
| chr2:60467549
|
A | T | 1 | a0001c0001t0002g0130 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.487+1183T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467549 | ||||||
| chr2:60467552
|
G | A | 2 | a0001c0001t0002g0130a0001c0001t0027g0005 | 2 | HG01943.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.487+1180C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467552 | ||||||
| chr2:60467554
|
G | A | 21 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.487+1178C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467554 | ||||||
| chr2:60467555
|
G | A | 6 | a0001c0001t0004g0085a0001c0002t0001g0016a0001c0002t0002g0120others(3): Show | 6 | HG01168.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1177C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467555 | ||||||
| chr2:60467555
|
G | C | 21 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.487+1177C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467555 | ||||||
| chr2:60467555
|
G | GTGGAGA | 5 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(2): Show | 5 | HG00735.hp1 HG01952.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1176_487+1177i others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467555 | ||||||
| chr2:60467557
|
G | A | 1 | a0001c0001t0027g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.487+1175C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467557 | ||||||
| chr2:60467558
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0015g0185a0001c0001t0019g0012others(2): Show | 5 | HG01975.hp1 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1174C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467558 | ||||||
| chr2:60467558
|
G | C | 1 | a0001c0001t0027g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.487+1174C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467558 | ||||||
| chr2:60467560
|
GGTA | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.487+1169_487+1171d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467560 | ||||||
| chr2:60467561
|
G | C | 1 | a0001c0003t0002g0108 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.487+1171C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467561 | ||||||
| chr2:60467563
|
A | G | 28 | a0001c0001t0002g0128a0001c0001t0003g0153a0001c0001t0003g0163others(25): Show | 28 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.487+1169T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467563 | ||||||
| chr2:60467564
|
G | C | 4 | a0001c0001t0002g0130a0001c0001t0015g0185a0001c0001t0019g0012others(1): Show | 4 | HG01975.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1168C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467564 | ||||||
| chr2:60467564
|
G | T | 5 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0020g0041others(2): Show | 5 | HG00735.hp1 HG01952.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1168C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467564 | ||||||
| chr2:60467567
|
A | G | 15 | a0001c0001t0002g0130a0001c0001t0003g0153a0001c0001t0009g0204others(12): Show | 15 | HG00323.hp2 HG00423.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.487+1165T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467567 | ||||||
| chr2:60467569
|
G | GCTA | 10 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0005g0223others(7): Show | 10 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+1162_487+1163i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467569 | ||||||
| chr2:60467570
|
G | C | 10 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0005g0223others(7): Show | 10 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.487+1162C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467570 | ||||||
| chr2:60467572
|
G | A | 21 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.487+1160C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467572 | ||||||
| chr2:60467573
|
G | A | 14 | a0001c0001t0002g0128a0001c0001t0002g0130a0001c0001t0005g0222others(11): Show | 14 | HG00735.hp1 HG01168.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.487+1159C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467573 | ||||||
| chr2:60467573
|
G | C | 21 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.487+1159C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467573 | ||||||
| chr2:60467575
|
G | A | 2 | a0001c0001t0020g0047a0001c0001t0036g0083 | 2 | HG00423.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.487+1157C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467575 | ||||||
| chr2:60467578
|
A | AGTG | 4 | a0001c0001t0003g0153a0001c0001t0009g0204a0001c0001t0009g0205others(1): Show | 4 | HG00323.hp2 HG02300.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1153_487+1154i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467578 | ||||||
| chr2:60467578
|
A | G | 71 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0028others(68): Show | 71 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.487+1154T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467578 | ||||||
| chr2:60467579
|
A | C | 14 | a0001c0001t0002g0128a0001c0001t0002g0130a0001c0001t0005g0222others(11): Show | 14 | HG00735.hp1 HG01168.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.487+1153T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467579 | ||||||
| chr2:60467579
|
A | G | 58 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0028others(55): Show | 58 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.487+1153T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467579 | ||||||
| chr2:60467582
|
G | A | 57 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0028others(54): Show | 57 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.487+1150C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467582 | ||||||
| chr2:60467582
|
GTGGTGGT others(65): Show |
G | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.487+1078_487+1149d others(74): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467582 | ||||||
| chr2:60467584
|
G | A | 11 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0005g0223others(8): Show | 11 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1148C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467584 | ||||||
| chr2:60467585
|
G | C | 11 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0005g0223others(8): Show | 11 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1147C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467585 | ||||||
| chr2:60467587
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(32): Show | 35 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.487+1145C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467587 | ||||||
| chr2:60467587
|
G | GATGGTA | 5 | a0001c0002t0001g0016a0001c0002t0002g0120a0001c0002t0003g0167others(2): Show | 5 | HG01168.hp1 HG01358.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1144_487+1145i others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467587 | ||||||
| chr2:60467588
|
G | A | 8 | a0001c0001t0002g0128a0001c0001t0002g0130a0001c0001t0005g0222others(5): Show | 8 | HG00735.hp1 HG01943.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1144C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467588 | ||||||
| chr2:60467588
|
G | C | 40 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(37): Show | 40 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.487+1144C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467588 | ||||||
| chr2:60467591
|
GTGA | G | 10 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0003g0160others(7): Show | 10 | HG01192.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.487+1138_487+1140d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467591 | ||||||
| chr2:60467592
|
T | A | 16 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0002g0090others(13): Show | 16 | HG01243.hp2 HG01261.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+1140A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467592 | ||||||
| chr2:60467594
|
A | ATGGTGGT others(72): Show |
1 | a0001c0001t0056g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.487+1137_487+1138i others(81): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467594 | ||||||
| chr2:60467594
|
A | G | 112 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0028others(109): Show | 113 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.487+1138T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467594 | ||||||
| chr2:60467594
|
ATGG | A | 11 | a0001c0001t0003g0163a0001c0001t0003g0174a0001c0001t0005g0223others(8): Show | 11 | HG00544.hp2 HG01071.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1135_487+1137d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467594 | ||||||
| chr2:60467596
|
G | A | 21 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(18): Show | 21 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.487+1136C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467596 | ||||||
| chr2:60467597
|
G | A | 41 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(38): Show | 41 | HG00544.hp1 HG00597.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.487+1135C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467597 | ||||||
| chr2:60467597
|
G | GTACTGGT others(5): Show |
3 | a0001c0001t0003g0153a0001c0001t0012g0215a0001c0001t0020g0047 | 3 | HG00423.hp1 HG02300.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.487+1134_487+1135i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467597 | ||||||
| chr2:60467597
|
G | GTGGTAGT others(32): Show |
1 | a0001c0001t0059g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.487+1134_487+1135i others(41): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467597 | ||||||
| chr2:60467597
|
G | GTGGTGGT others(257): Show |
1 | a0001c0001t0012g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.487+1134_487+1135i others(266): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467597 | ||||||
| chr2:60467597
|
G | GTGGTGGT others(35): Show |
1 | a0001c0009t0001g0017 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.487+1134_487+1135i others(44): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467597 | ||||||
| chr2:60467597
|
G | GTGGTGGT others(38): Show |
6 | a0001c0001t0002g0094a0001c0001t0003g0173a0001c0001t0004g0078others(3): Show | 6 | HG00738.hp2 HG01123.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1134_487+1135i others(47): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467597 | ||||||
| chr2:60467600
|
G | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(19): Show | 22 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.487+1132C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467600 | ||||||
| chr2:60467600
|
G | GTGTTGA | 8 | a0001c0001t0001g0020a0001c0001t0002g0090a0001c0001t0003g0171others(5): Show | 8 | HG01261.hp1 HG01934.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+1131_487+1132i others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467600 | ||||||
| chr2:60467602
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0061a0004c0005t0002g0100 | 3 | HG01074.hp2 HG01257.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.487+1130C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467602 | ||||||
| chr2:60467603
|
G | T | 7 | a0001c0001t0001g0065a0001c0001t0021g0093a0001c0001t0032g0037others(4): Show | 7 | HG01243.hp2 HG02135.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1129C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467603 | ||||||
| chr2:60467606
|
G | A | 19 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0002g0090others(16): Show | 19 | HG01074.hp2 HG01243.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.487+1126C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467606 | ||||||
| chr2:60467606
|
G | GTAGTGA | 36 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(33): Show | 37 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.487+1125_487+1126i others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467606 | ||||||
| chr2:60467608
|
G | A | 1 | a0001c0001t0008g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.487+1124C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467608 | ||||||
| chr2:60467608
|
GGTA | G | 7 | a0001c0001t0001g0065a0001c0001t0021g0093a0001c0001t0032g0037others(4): Show | 7 | HG01243.hp2 HG02135.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1121_487+1123d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467608 | ||||||
| chr2:60467609
|
G | C | 1 | a0001c0001t0027g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.487+1123C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467609 | ||||||
| chr2:60467609
|
G | GTGATGC | 6 | a0001c0001t0002g0128a0001c0001t0002g0130a0001c0001t0005g0222others(3): Show | 6 | HG00735.hp1 HG01952.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+1122_487+1123i others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467609 | ||||||
| chr2:60467611
|
A | G | 44 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(41): Show | 45 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.487+1121T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467611 | ||||||
| chr2:60467612
|
G | A | 24 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(21): Show | 24 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.487+1120C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467612 | ||||||
| chr2:60467612
|
G | C | 15 | a0001c0001t0001g0020a0001c0001t0002g0090a0001c0001t0002g0128others(12): Show | 15 | HG00735.hp1 HG01261.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.487+1120C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467612 | ||||||
| chr2:60467612
|
G | T | 3 | a0001c0001t0004g0088a0001c0001t0009g0204a0001c0001t0009g0205 | 3 | HG00323.hp2 HG02080.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.487+1120C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467612 | ||||||
| chr2:60467615
|
A | ATGGTGCT others(237): Show |
1 | a0001c0003t0002g0107 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.487+1116_487+1117i others(246): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467615 | ||||||
| chr2:60467615
|
A | C | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+1117T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467615 | ||||||
| chr2:60467615
|
A | G | 77 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(74): Show | 78 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.487+1117T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467615 | ||||||
| chr2:60467617
|
G | A | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+1115C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467617 | ||||||
| chr2:60467618
|
G | C | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+1114C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467618 | ||||||
| chr2:60467620
|
G | A | 7 | a0001c0001t0001g0065a0001c0001t0021g0093a0001c0001t0032g0037others(4): Show | 7 | HG01243.hp2 HG02135.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1112C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467620 | ||||||
| chr2:60467621
|
G | A | 59 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0042others(56): Show | 60 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.487+1111C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467621 | ||||||
| chr2:60467621
|
G | C | 8 | a0001c0001t0001g0065a0001c0001t0010g0057a0001c0001t0021g0093others(5): Show | 8 | HG00099.hp1 HG01243.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1111C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467621 | ||||||
| chr2:60467621
|
GTGGTAAT others(77): Show |
G | 11 | a0001c0001t0001g0032a0001c0001t0001g0049a0001c0001t0001g0058others(8): Show | 11 | HG01256.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+1027_487+1110d others(86): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467621 | ||||||
| chr2:60467624
|
GTAATGGT others(23): Show |
G | 8 | a0001c0001t0001g0065a0001c0001t0010g0057a0001c0001t0021g0093others(5): Show | 8 | HG00099.hp1 HG01243.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1078_487+1107d others(32): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467624 | ||||||
| chr2:60467625
|
T | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(19): Show | 22 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.487+1107A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467625 | ||||||
| chr2:60467626
|
A | G | 26 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0036others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.487+1106T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467626 | ||||||
| chr2:60467627
|
A | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0042others(57): Show | 61 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.487+1105T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467627 | ||||||
| chr2:60467627
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0013g0253 | 2 | HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.487+1105T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467627 | ||||||
| chr2:60467630
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0013g0253 | 2 | HG01192.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.487+1102C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467630 | ||||||
| chr2:60467632
|
G | A | 2 | a0001c0001t0008g0126a0001c0001t0012g0213 | 2 | NA18979.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.487+1100C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467632 | ||||||
| chr2:60467633
|
G | C | 2 | a0001c0001t0008g0126a0001c0001t0012g0213 | 2 | NA18979.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.487+1099C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467633 | ||||||
| chr2:60467636
|
G | A | 60 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0042others(57): Show | 61 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.487+1096C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467636 | ||||||
| chr2:60467636
|
G | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(19): Show | 22 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.487+1096C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467636 | ||||||
| chr2:60467636
|
GTGGTGAT others(32): Show |
G | 2 | a0001c0001t0008g0134a0001c0001t0033g0022 | 2 | HG00544.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.487+1057_487+1095d others(41): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467636 | ||||||
| chr2:60467636
|
GTGGTGAT others(38): Show |
G | 3 | a0001c0001t0003g0163a0001c0001t0006g0246a0001c0003t0002g0108 | 3 | HG01975.hp1 NA18957.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.487+1051_487+1095d others(47): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467636 | ||||||
| chr2:60467639
|
G | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(19): Show | 22 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.487+1093C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467639 | ||||||
| chr2:60467640
|
T | A | 53 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0043others(50): Show | 53 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.487+1092A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467640 | ||||||
| chr2:60467641
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.487+1091C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467641 | ||||||
| chr2:60467642
|
A | C | 1 | a0001c0001t0004g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.487+1090T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467642 | ||||||
| chr2:60467642
|
A | G | 78 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0033others(75): Show | 79 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.487+1090T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467642 | ||||||
| chr2:60467642
|
ATGGTGGT others(263): Show |
A | 3 | a0001c0001t0007g0111a0001c0001t0010g0050a0001c0001t0036g0083 | 3 | HG01261.hp2 HG02559.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.487+820_487+1089de others(1): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467642 | ||||||
| chr2:60467644
|
G | A | 1 | a0001c0001t0004g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.487+1088C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467644 | ||||||
| chr2:60467645
|
G | A | 23 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(20): Show | 23 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.487+1087C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467645 | ||||||
| chr2:60467645
|
GTGGTGAT others(23): Show |
G | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+1057_487+1086d others(32): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467645 | ||||||
| chr2:60467647
|
G | GGTA | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+1084_487+1085i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467647 | ||||||
| chr2:60467648
|
GTGATGAT others(5): Show |
G | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.487+1072_487+1083d others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467648 | ||||||
| chr2:60467650
|
G | A | 72 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0033others(69): Show | 73 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.487+1082C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467650 | ||||||
| chr2:60467650
|
G | GGTGGTGG others(144): Show |
1 | a0001c0009t0001g0017 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.487+1081_487+1082i others(153): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467650 | ||||||
| chr2:60467651
|
A | C | 23 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(20): Show | 23 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.487+1081T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467651 | ||||||
| chr2:60467651
|
A | G | 63 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0042others(60): Show | 64 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.487+1081T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467651 | ||||||
| chr2:60467651
|
A | T | 52 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0043others(49): Show | 52 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.487+1081T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467651 | ||||||
| chr2:60467654
|
A | ATGGTGAT others(8): Show |
47 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(44): Show | 47 | HG00544.hp1 HG00597.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.487+1063_487+1077d others(17): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467654 | ||||||
| chr2:60467654
|
A | G | 40 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(37): Show | 40 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.487+1078T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467654 | ||||||
| chr2:60467656
|
G | A | 3 | a0001c0001t0005g0223a0001c0001t0008g0126a0001c0001t0012g0218 | 3 | HG01071.hp1 HG03831.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.487+1076C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467656 | ||||||
| chr2:60467659
|
G | A | 1 | a0001c0001t0004g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.487+1073C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467659 | ||||||
| chr2:60467659
|
G | C | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.487+1073C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467659 | ||||||
| chr2:60467660
|
A | G | 53 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(50): Show | 54 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.487+1072T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467660 | ||||||
| chr2:60467663
|
G | C | 11 | a0001c0001t0001g0020a0001c0001t0002g0090a0001c0001t0003g0171others(8): Show | 11 | HG00323.hp2 HG01261.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.487+1069C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467663 | ||||||
| chr2:60467665
|
A | G | 8 | a0001c0001t0001g0029a0001c0001t0005g0223a0001c0001t0008g0126others(5): Show | 8 | HG01071.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1067T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467665 | ||||||
| chr2:60467666
|
C | A | 54 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(51): Show | 55 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.487+1066G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467666 | ||||||
| chr2:60467666
|
C | CTGGTGGT others(26): Show |
1 | a0001c0001t0056g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.487+1033_487+1065d others(35): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467666 | ||||||
| chr2:60467666
|
C | G | 5 | a0001c0001t0001g0029a0001c0001t0005g0223a0001c0001t0008g0126others(2): Show | 5 | HG01071.hp1 HG02486.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1066G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467666 | ||||||
| chr2:60467668
|
G | T | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.487+1064C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467668 | ||||||
| chr2:60467671
|
G | A | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+1061C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467671 | ||||||
| chr2:60467672
|
G | C | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+1060C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467672 | ||||||
| chr2:60467675
|
A | ATGGTACT others(41): Show |
1 | a0001c0001t0020g0047 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.487+1056_487+1057i others(50): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467675 | ||||||
| chr2:60467675
|
A | ATGGTACT others(101): Show |
2 | a0001c0001t0002g0094a0001c0001t0003g0173 | 2 | HG01123.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.487+1056_487+1057i others(110): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467675 | ||||||
| chr2:60467675
|
A | ATGGTACT others(161): Show |
1 | a0001c0001t0004g0078 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487+1056_487+1057i others(170): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467675 | ||||||
| chr2:60467675
|
A | ATGGTACT others(41): Show |
1 | a0001c0001t0004g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487+1056_487+1057i others(50): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467675 | ||||||
| chr2:60467675
|
A | ATGGTACT others(47): Show |
7 | a0001c0001t0002g0090a0001c0001t0003g0171a0001c0001t0006g0241others(4): Show | 7 | HG00323.hp2 HG01261.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.487+1056_487+1057i others(56): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467675 | ||||||
| chr2:60467675
|
A | G | 57 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(54): Show | 58 | HG00323.hp1 HG00597.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.487+1057T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467675 | ||||||
| chr2:60467679
|
T | A | 8 | a0001c0001t0002g0097a0001c0001t0002g0125a0001c0001t0003g0146others(5): Show | 8 | HG00597.hp1 HG02027.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1053A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467679 | ||||||
| chr2:60467680
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0001t0005g0233others(2): Show | 5 | HG01071.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1052C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467680 | ||||||
| chr2:60467681
|
A | C | 5 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0001t0005g0233others(2): Show | 5 | HG01071.hp1 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+1051T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467681 | ||||||
| chr2:60467681
|
A | G | 57 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(54): Show | 58 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.487+1051T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467681 | ||||||
| chr2:60467689
|
G | GATGGTGA others(23): Show |
1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.487+1042_487+1043i others(32): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467689 | ||||||
| chr2:60467690
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0001t0005g0233others(1): Show | 4 | HG01071.hp1 HG02970.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1042C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467690 | ||||||
| chr2:60467690
|
G | C | 1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.487+1042C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467690 | ||||||
| chr2:60467690
|
G | T | 8 | a0001c0001t0002g0097a0001c0001t0002g0125a0001c0001t0003g0146others(5): Show | 8 | HG00597.hp1 HG02027.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+1042C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467690 | ||||||
| chr2:60467692
|
GGTGGTGA others(5): Show |
G | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.487+1028_487+1039d others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467692 | ||||||
| chr2:60467693
|
G | A | 9 | a0001c0001t0002g0097a0001c0001t0002g0125a0001c0001t0003g0146others(6): Show | 9 | HG00597.hp1 HG00733.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+1039C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467693 | ||||||
| chr2:60467695
|
G | A | 62 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(59): Show | 63 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.487+1037C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467695 | ||||||
| chr2:60467695
|
G | GGTA | 3 | a0001c0002t0001g0024a0001c0002t0001g0061a0004c0005t0002g0100 | 3 | HG01074.hp2 HG01257.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.487+1036_487+1037i others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467695 | ||||||
| chr2:60467699
|
A | G | 5 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0001t0005g0233others(2): Show | 5 | HG00733.hp1 HG01071.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+1033T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467699 | ||||||
| chr2:60467702
|
G | C | 82 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0028others(79): Show | 82 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.487+1030C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467702 | ||||||
| chr2:60467702
|
GTAC | G | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+1027_487+1029d others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467702 | ||||||
| chr2:60467704
|
A | G | 64 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0054others(61): Show | 65 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.487+1028T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467704 | ||||||
| chr2:60467705
|
C | A | 2 | a0001c0001t0009g0198a0001c0001t0010g0057 | 2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.487+1027G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467705 | ||||||
| chr2:60467705
|
C | CTGGTGGT others(80): Show |
1 | a0001c0001t0006g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.487+1026_487+1027i others(89): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467705 | ||||||
| chr2:60467705
|
C | CTGGTGGT others(74): Show |
1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.487+1026_487+1027i others(83): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467705 | ||||||
| chr2:60467705
|
C | G | 67 | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0042others(64): Show | 68 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.487+1027G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467705 | ||||||
| chr2:60467707
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0061a0004c0005t0002g0100 | 3 | HG01074.hp2 HG01257.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.487+1025C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467707 | ||||||
| chr2:60467708
|
G | A | 4 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0001t0005g0233others(1): Show | 4 | HG01071.hp1 HG02970.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1024C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467708 | ||||||
| chr2:60467709
|
T | C | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+1023A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467709 | ||||||
| chr2:60467713
|
G | A | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+1019C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467713 | ||||||
| chr2:60467714
|
A | G | 4 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0001t0005g0233others(1): Show | 4 | HG01071.hp1 HG02970.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1018T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467714 | ||||||
| chr2:60467719
|
A | G | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+1013T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467719 | ||||||
| chr2:60467720
|
C | A | 4 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0001t0005g0233others(1): Show | 4 | HG01071.hp1 HG02970.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+1012G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467720 | ||||||
| chr2:60467720
|
C | G | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+1012G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467720 | ||||||
| chr2:60467729
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0005g0233a0001c0002t0001g0048 | 3 | HG02970.hp1 HG03710.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.487+1003T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467729 | ||||||
| chr2:60467735
|
G | A | 8 | a0001c0001t0002g0097a0001c0001t0002g0125a0001c0001t0003g0146others(5): Show | 8 | HG00597.hp1 HG02027.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+997C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467735 | ||||||
| chr2:60467738
|
G | A | 1 | a0001c0001t0005g0223 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.487+994C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467738 | ||||||
| chr2:60467743
|
A | G | 13 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0002g0125others(10): Show | 13 | HG00597.hp1 HG01071.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+989T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467743 | ||||||
| chr2:60467746
|
G | A | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+986C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467746 | ||||||
| chr2:60467747
|
A | G | 13 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0002g0125others(10): Show | 13 | HG00597.hp1 HG01071.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+985T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467747 | ||||||
| chr2:60467749
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.487+983C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467749 | ||||||
| chr2:60467750
|
G | A | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+982C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467750 | ||||||
| chr2:60467753
|
G | A | 9 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0002g0125others(6): Show | 9 | HG00597.hp1 HG02027.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.487+979C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467753 | ||||||
| chr2:60467755
|
G | A | 1 | a0001c0001t0005g0223 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.487+977C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467755 | ||||||
| chr2:60467756
|
G | C | 8 | a0001c0001t0002g0097a0001c0001t0002g0125a0001c0001t0003g0146others(5): Show | 8 | HG00597.hp1 HG02027.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+976C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467756 | ||||||
| chr2:60467758
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0005g0223a0001c0001t0009g0198 | 3 | HG00733.hp1 HG01071.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.487+974T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467758 | ||||||
| chr2:60467758
|
AATG | A | 3 | a0001c0002t0001g0027a0001c0002t0002g0121a0001c0002t0003g0169 | 3 | HG02818.hp2 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.487+971_487+973del others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467758 | ||||||
| chr2:60467759
|
A | C | 8 | a0001c0001t0002g0097a0001c0001t0002g0125a0001c0001t0003g0146others(5): Show | 8 | HG00597.hp1 HG02027.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+973T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467759 | ||||||
| chr2:60467759
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0009g0198 | 2 | HG00733.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.487+973T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467759 | ||||||
| chr2:60467767
|
G | A | 1 | a0001c0001t0005g0223 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.487+965C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467767 | ||||||
| chr2:60467768
|
G | A | 13 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0002g0125others(10): Show | 13 | HG00597.hp1 HG02027.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+964C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467768 | ||||||
| chr2:60467768
|
G | GTGGTGGT others(29): Show |
1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.487+963_487+964ins others(36): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467768 | ||||||
| chr2:60467768
|
GTGGAGAT others(47): Show |
G | 13 | a0001c0001t0001g0029a0001c0001t0001g0065a0001c0001t0010g0057others(10): Show | 13 | HG00099.hp1 HG01074.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+910_487+963del others(54): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467768 | ||||||
| chr2:60467768
|
GTGGAGAT others(53): Show |
G | 5 | a0001c0001t0003g0163a0001c0001t0006g0246a0001c0001t0008g0134others(2): Show | 5 | HG00544.hp2 HG01975.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+904_487+963del others(60): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467768 | ||||||
| chr2:60467768
|
GTGGAGAT others(131): Show |
G | 2 | a0001c0001t0005g0219a0001c0001t0018g0211 | 2 | HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.487+826_487+963del | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467768 | ||||||
| chr2:60467771
|
GAGA | G | 5 | a0001c0001t0002g0125a0001c0001t0003g0173a0001c0001t0013g0248others(2): Show | 5 | HG01167.hp1 HG02630.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+958_487+960del others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467771 | ||||||
| chr2:60467771
|
GAGATGGT others(50): Show |
G | 2 | a0001c0001t0012g0213a0001c0001t0045g0114 | 2 | HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.487+904_487+960del others(57): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467771 | ||||||
| chr2:60467772
|
A | T | 94 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(91): Show | 94 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.487+960T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467772 | ||||||
| chr2:60467773
|
G | A | 11 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0003g0146others(8): Show | 11 | HG00597.hp1 HG02027.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+959C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467773 | ||||||
| chr2:60467774
|
A | C | 11 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0003g0146others(8): Show | 11 | HG00597.hp1 HG02027.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.487+958T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467774 | ||||||
| chr2:60467774
|
A | G | 75 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0028others(72): Show | 75 | HG00544.hp1 HG00597.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.487+958T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467774 | ||||||
| chr2:60467776
|
G | A | 2 | a0001c0001t0002g0125a0001c0003t0003g0178 | 2 | NA18983.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.487+956C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467776 | ||||||
| chr2:60467777
|
G | C | 2 | a0001c0001t0002g0125a0001c0003t0003g0178 | 2 | NA18983.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.487+955C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467777 | ||||||
| chr2:60467777
|
G | GTGGTAGT others(2): Show |
27 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0046others(24): Show | 27 | HG00735.hp2 HG00741.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+954_487+955ins others(9): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467777 | ||||||
| chr2:60467777
|
GTGGTGTT others(131): Show |
G | 5 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0004g0082others(2): Show | 5 | HG01256.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+817_487+954del | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467777 | ||||||
| chr2:60467779
|
G | A | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+953C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467779 | ||||||
| chr2:60467780
|
GTGTTGAT others(65): Show |
G | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.487+880_487+951del others(72): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467780 | ||||||
| chr2:60467783
|
T | A | 13 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0003g0146others(10): Show | 13 | HG00597.hp1 HG00733.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+949A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467783 | ||||||
| chr2:60467783
|
T | G | 81 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0028others(78): Show | 81 | HG00544.hp1 HG00597.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.487+949A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467783 | ||||||
| chr2:60467785
|
G | A | 1 | a0001c0001t0004g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487+947C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467785 | ||||||
| chr2:60467786
|
A | ATGGTGAT others(8): Show |
1 | a0001c0001t0003g0170 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.487+931_487+945dup others(15): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467786 | ||||||
| chr2:60467786
|
A | G | 90 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(87): Show | 90 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.487+946T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467786 | ||||||
| chr2:60467788
|
G | A | 49 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0043others(46): Show | 49 | HG00544.hp1 HG00597.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.487+944C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467788 | ||||||
| chr2:60467792
|
A | G | 17 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0002g0125others(14): Show | 17 | HG00597.hp1 HG00733.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+940T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467792 | ||||||
| chr2:60467797
|
A | G | 50 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0042others(47): Show | 50 | HG00544.hp1 HG00597.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.487+935T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467797 | ||||||
| chr2:60467798
|
C | A | 4 | a0001c0001t0002g0125a0001c0001t0004g0067a0001c0001t0009g0198others(1): Show | 4 | HG00733.hp1 NA18945.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+934G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467798 | ||||||
| chr2:60467798
|
C | G | 62 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0036others(59): Show | 62 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.487+934G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467798 | ||||||
| chr2:60467801
|
G | A | 13 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0003g0146others(10): Show | 13 | HG00597.hp1 HG01071.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.487+931C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467801 | ||||||
| chr2:60467803
|
G | GGTA | 5 | a0001c0001t0001g0036a0001c0001t0004g0071a0001c0001t0006g0242others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+928_487+929ins others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467803 | ||||||
| chr2:60467806
|
G | C | 15 | a0001c0001t0001g0042a0001c0001t0003g0149a0001c0001t0007g0092others(12): Show | 16 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+926C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467806 | ||||||
| chr2:60467806
|
GATGGTAC others(53): Show |
G | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+866_487+925del others(60): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467806 | ||||||
| chr2:60467807
|
A | ATGGTGGT others(17): Show |
8 | a0001c0002t0001g0016a0001c0002t0002g0120a0001c0002t0004g0073others(5): Show | 8 | HG00741.hp1 HG01168.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+924_487+925ins others(24): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467807 | ||||||
| chr2:60467807
|
A | ATGGTGGT others(113): Show |
1 | a0001c0002t0003g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.487+924_487+925ins others(120): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467807 | ||||||
| chr2:60467807
|
A | ATGGTGGT others(110): Show |
1 | a0001c0002t0017g0010 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.487+924_487+925ins others(117): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467807 | ||||||
| chr2:60467807
|
A | G | 16 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0002g0125others(13): Show | 16 | HG00597.hp1 HG01071.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+925T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467807 | ||||||
| chr2:60467812
|
A | G | 23 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0036others(20): Show | 23 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.487+920T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467812 | ||||||
| chr2:60467813
|
C | A | 23 | a0001c0001t0001g0020a0001c0001t0002g0097a0001c0001t0003g0146others(20): Show | 23 | HG00597.hp1 HG00741.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.487+919G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467813 | ||||||
| chr2:60467813
|
C | CT | 15 | a0001c0001t0001g0042a0001c0001t0003g0149a0001c0001t0007g0092others(12): Show | 16 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+918dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467813 | ||||||
| chr2:60467813
|
C | G | 23 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0036others(20): Show | 23 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.487+919G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467813 | ||||||
| chr2:60467815
|
G | T | 15 | a0001c0001t0001g0042a0001c0001t0003g0149a0001c0001t0007g0092others(12): Show | 16 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.487+917C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467815 | ||||||
| chr2:60467816
|
G | GTAA | 5 | a0001c0001t0001g0036a0001c0001t0004g0071a0001c0001t0006g0242others(2): Show | 5 | HG00738.hp1 HG00738.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.487+915_487+916ins others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467816 | ||||||
| chr2:60467818
|
G | GGTA | 17 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0046others(14): Show | 17 | HG00735.hp2 HG01071.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.487+913_487+914ins others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467818 | ||||||
| chr2:60467822
|
A | ATGGTGGT others(26): Show |
2 | a0001c0001t0002g0119a0001c0001t0006g0240 | 2 | HG00544.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.487+909_487+910ins others(33): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467822 | ||||||
| chr2:60467822
|
A | ATGGTGGT others(29): Show |
10 | a0001c0001t0001g0063a0001c0001t0002g0106a0001c0001t0002g0118others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.487+909_487+910ins others(36): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467822 | ||||||
| chr2:60467822
|
A | ATGGTGGT others(32): Show |
22 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(19): Show | 22 | HG00597.hp2 HG02056.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.487+909_487+910ins others(39): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467822 | ||||||
| chr2:60467822
|
A | ATGGTGGT others(35): Show |
1 | a0001c0001t0005g0225 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.487+909_487+910ins others(42): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467822 | ||||||
| chr2:60467822
|
A | ATGGTGGT others(447): Show |
1 | a0001c0001t0008g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.487+909_487+910ins others(454): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467822 | ||||||
| chr2:60467822
|
A | ATGGTGGT others(128): Show |
1 | a0001c0002t0004g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.487+909_487+910ins others(135): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467822 | ||||||
| chr2:60467822
|
A | ATGGTGGT others(245): Show |
1 | a0001c0001t0012g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.487+909_487+910ins others(252): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467822 | ||||||
| chr2:60467822
|
A | G | 30 | a0001c0001t0001g0036a0001c0001t0002g0097a0001c0001t0002g0125others(27): Show | 30 | HG00597.hp1 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.487+910T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467822 | ||||||
| chr2:60467824
|
G | GGTGGTGG others(5): Show |
2 | a0001c0001t0003g0173a0001c0001t0003g0177 | 2 | HG02129.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.487+907_487+908ins others(12): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467824 | ||||||
| chr2:60467827
|
G | A | 2 | a0001c0001t0004g0067a0001c0001t0012g0217 | 2 | HG00140.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.487+905C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467827 | ||||||
| chr2:60467827
|
G | GGTGGTA | 17 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0046others(14): Show | 17 | HG00735.hp2 HG01071.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.487+904_487+905ins others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467827 | ||||||
| chr2:60467828
|
A | C | 1 | a0001c0001t0012g0217 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.487+904T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467828 | ||||||
| chr2:60467828
|
A | G | 73 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(70): Show | 73 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.487+904T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467828 | ||||||
| chr2:60467830
|
GGTGGTGG others(188): Show |
G | 7 | a0001c0001t0003g0149a0001c0001t0007g0092a0001c0001t0010g0030others(4): Show | 8 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+707_487+901del | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467830 | ||||||
| chr2:60467831
|
G | A | 1 | a0001c0001t0004g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487+901C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467831 | ||||||
| chr2:60467834
|
G | GTGATGGT others(35): Show |
1 | a0001c0001t0012g0217 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.487+897_487+898ins others(42): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467834 | ||||||
| chr2:60467834
|
G | GTGGTGAT others(32): Show |
1 | a0001c0001t0001g0042 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.487+897_487+898ins others(39): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467834 | ||||||
| chr2:60467836
|
G | A | 2 | a0001c0001t0002g0140a0001c0001t0013g0248 | 2 | HG01167.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.487+896C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467836 | ||||||
| chr2:60467839
|
G | A | 2 | a0001c0001t0003g0173a0001c0001t0003g0177 | 2 | HG02129.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.487+893C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467839 | ||||||
| chr2:60467839
|
GGTGGTGA others(5): Show |
G | 6 | a0001c0001t0010g0015a0001c0001t0011g0188a0001c0001t0015g0193others(3): Show | 6 | HG00280.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+881_487+892del others(12): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467839 | ||||||
| chr2:60467840
|
G | A | 5 | a0001c0001t0002g0140a0001c0001t0003g0173a0001c0001t0003g0177others(2): Show | 5 | HG01081.hp2 HG01167.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.487+892C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467840 | ||||||
| chr2:60467842
|
G | A | 76 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(73): Show | 76 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.487+890C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467842 | ||||||
| chr2:60467842
|
G | GGTA | 12 | a0001c0001t0063g0234a0001c0002t0001g0016a0001c0002t0002g0120others(9): Show | 12 | HG00741.hp1 HG01168.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.487+889_487+890ins others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467842 | ||||||
| chr2:60467842
|
G | GGTGGTGG others(2): Show |
17 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0046others(14): Show | 17 | HG00735.hp2 HG01071.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.487+889_487+890ins others(9): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467842 | ||||||
| chr2:60467845
|
G | A | 2 | a0001c0001t0014g0009a0001c0001t0023g0203 | 2 | HG02630.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.487+887C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467845 | ||||||
| chr2:60467846
|
A | G | 6 | a0001c0001t0001g0042a0001c0001t0002g0140a0001c0001t0003g0173others(3): Show | 6 | HG01081.hp2 HG02129.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+886T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467846 | ||||||
| chr2:60467849
|
C | A | 1 | a0001c0001t0014g0009 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.487+883G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467849 | ||||||
| chr2:60467849
|
C | G | 111 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(108): Show | 111 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.487+883G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467849 | ||||||
| chr2:60467851
|
A | G | 110 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(107): Show | 110 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.487+881T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467851 | ||||||
| chr2:60467852
|
C | A | 9 | a0001c0001t0001g0042a0001c0001t0002g0140a0001c0001t0007g0095others(6): Show | 9 | HG00280.hp2 HG01081.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.487+880G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467852 | ||||||
| chr2:60467852
|
C | CTGGTGGT others(68): Show |
1 | a0001c0001t0056g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.487+879_487+880ins others(75): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467852 | ||||||
| chr2:60467852
|
C | CTGGTGGT others(272): Show |
1 | a0001c0001t0008g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.487+879_487+880ins others(279): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467852 | ||||||
| chr2:60467852
|
C | G | 109 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(106): Show | 109 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.487+880G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467852 | ||||||
| chr2:60467854
|
G | A | 13 | a0001c0001t0045g0114a0001c0001t0063g0234a0001c0002t0001g0016others(10): Show | 13 | HG00741.hp1 HG01168.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.487+878C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467854 | ||||||
| chr2:60467860
|
G | A | 1 | a0001c0001t0013g0248 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.487+872C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467860 | ||||||
| chr2:60467861
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+871T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467861 | ||||||
| chr2:60467866
|
A | G | 3 | a0001c0001t0002g0140a0001c0001t0013g0248a0001c0001t0023g0203 | 3 | HG01167.hp1 HG02630.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.487+866T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467866 | ||||||
| chr2:60467867
|
C | G | 4 | a0001c0001t0002g0140a0001c0001t0009g0198a0001c0001t0013g0248others(1): Show | 4 | HG00733.hp1 HG01167.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+865G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467867 | ||||||
| chr2:60467873
|
G | A | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+859C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467873 | ||||||
| chr2:60467876
|
A | G | 4 | a0001c0001t0002g0140a0001c0001t0003g0171a0001c0001t0004g0067others(1): Show | 4 | HG00733.hp1 HG03017.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.487+856T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467876 | ||||||
| chr2:60467878
|
G | A | 1 | a0001c0001t0004g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487+854C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467878 | ||||||
| chr2:60467878
|
GGTGGTGG others(140): Show |
G | 7 | a0001c0001t0007g0095a0001c0001t0010g0015a0001c0001t0011g0188others(4): Show | 7 | HG00280.hp2 HG01081.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+707_487+853del | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467878 | ||||||
| chr2:60467881
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+851C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467881 | ||||||
| chr2:60467882
|
G | A | 1 | a0001c0001t0004g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487+850C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467882 | ||||||
| chr2:60467885
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+847C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467885 | ||||||
| chr2:60467890
|
A | G | 2 | a0001c0001t0002g0140a0001c0001t0004g0067 | 2 | HG03017.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.487+842T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467890 | ||||||
| chr2:60467893
|
G | A | 1 | a0001c0001t0004g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487+839C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467893 | ||||||
| chr2:60467894
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+838T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467894 | ||||||
| chr2:60467900
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+832C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467900 | ||||||
| chr2:60467905
|
A | G | 2 | a0001c0004t0058g0206a0001c0004t0062g0235 | 2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.487+827T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467905 | ||||||
| chr2:60467906
|
A | ATGG | 19 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0045others(16): Show | 19 | HG00544.hp1 HG00738.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.487+823_487+825dup others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467906 | ||||||
| chr2:60467906
|
A | ATGGTGG | 48 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0055others(45): Show | 49 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.487+820_487+825dup others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467906 | ||||||
| chr2:60467906
|
A | ATGGTGGT others(188): Show |
1 | a0001c0001t0002g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.487+825_487+826ins others(195): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467906 | ||||||
| chr2:60467906
|
A | ATGGTGGT others(89): Show |
1 | a0001c0001t0002g0094 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.487+825_487+826ins others(96): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467906 | ||||||
| chr2:60467906
|
A | ATGGTGGT others(86): Show |
1 | a0001c0001t0012g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.487+825_487+826ins others(93): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467906 | ||||||
| chr2:60467906
|
A | ATGGTGGT others(59): Show |
8 | a0001c0001t0002g0128a0001c0001t0005g0222a0001c0001t0009g0204others(5): Show | 8 | HG00323.hp2 HG00735.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.487+825_487+826ins others(66): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467906 | ||||||
| chr2:60467906
|
A | ATGGTGGT others(149): Show |
1 | a0001c0009t0001g0017 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.487+825_487+826ins others(156): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467906 | ||||||
| chr2:60467906
|
A | C | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+826T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467906 | ||||||
| chr2:60467908
|
GGTGGTGG others(173): Show |
G | 1 | a0001c0001t0005g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.487+644_487+823del | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467908 | ||||||
| chr2:60467912
|
G | A | 3 | a0001c0001t0004g0067a0001c0001t0005g0219a0001c0001t0018g0211 | 3 | HG03130.hp1 HG03540.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.487+820C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467912 | ||||||
| chr2:60467912
|
G | GTGGTGGT others(2): Show |
77 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(74): Show | 77 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.487+819_487+820ins others(9): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467912 | ||||||
| chr2:60467912
|
G | GTGGTGGT others(89): Show |
1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.487+819_487+820ins others(96): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467912 | ||||||
| chr2:60467915
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+817C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467915 | ||||||
| chr2:60467918
|
GTGGTGGT others(83): Show |
G | 3 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250 | 3 | HG02630.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.487+724_487+813del others(90): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467918 | ||||||
| chr2:60467921
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0009g0198 | 2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.487+811C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467921 | ||||||
| chr2:60467921
|
G | GTGGTGGT others(641): Show |
1 | a0001c0002t0001g0024 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.487+810_487+811ins others(648): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467921 | ||||||
| chr2:60467929
|
A | G | 1 | a0001c0002t0016g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.487+803T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467929 | ||||||
| chr2:60467933
|
A | G | 1 | a0001c0002t0016g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.487+799T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467933 | ||||||
| chr2:60467936
|
G | A | 1 | a0001c0002t0016g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.487+796C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467936 | ||||||
| chr2:60467939
|
G | C | 95 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(92): Show | 95 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.487+793C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467939 | ||||||
| chr2:60467944
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0002g0140a0001c0001t0009g0198 | 3 | HG00733.hp1 HG03017.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.487+788C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467944 | ||||||
| chr2:60467945
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+787C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467945 | ||||||
| chr2:60467947
|
G | A | 1 | a0001c0002t0016g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.487+785C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467947 | ||||||
| chr2:60467947
|
G | C | 91 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(88): Show | 91 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.487+785C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467947 | ||||||
| chr2:60467948
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+784T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467948 | ||||||
| chr2:60467953
|
A | G | 4 | a0001c0001t0001g0029a0001c0001t0002g0140a0001c0001t0009g0198others(1): Show | 4 | HG00733.hp1 HG01361.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+779T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467953 | ||||||
| chr2:60467954
|
C | CT | 95 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(92): Show | 95 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.487+777dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467954 | ||||||
| chr2:60467954
|
C | G | 2 | a0001c0001t0002g0140a0001c0002t0016g0255 | 2 | HG01361.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.487+778G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467954 | ||||||
| chr2:60467956
|
G | T | 95 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(92): Show | 95 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.487+776C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467956 | ||||||
| chr2:60467960
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+772C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467960 | ||||||
| chr2:60467962
|
G | C | 2 | a0001c0001t0001g0029a0001c0001t0009g0198 | 2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.487+770C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467962 | ||||||
| chr2:60467963
|
A | G | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.487+769T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467963 | ||||||
| chr2:60467968
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0009g0198 | 2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.487+764C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467968 | ||||||
| chr2:60467969
|
G | A | 95 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(92): Show | 95 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.487+763C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467969 | ||||||
| chr2:60467969
|
G | C | 2 | a0001c0001t0001g0029a0001c0001t0009g0198 | 2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.487+763C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467969 | ||||||
| chr2:60467974
|
G | T | 2 | a0001c0001t0001g0029a0001c0001t0009g0198 | 2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.487+758C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467974 | ||||||
| chr2:60467975
|
G | GTGGTAGT others(33): Show |
1 | a0001c0002t0016g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.487+756_487+757ins others(40): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467975 | ||||||
| chr2:60467977
|
A | G | 98 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(95): Show | 98 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.487+755T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467977 | ||||||
| chr2:60467987
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0009g0198 | 2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.487+745C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467987 | ||||||
| chr2:60467987
|
GTGGTAA | G | 3 | a0001c0001t0005g0219a0001c0001t0018g0211a0001c0001t0019g0012 | 3 | HG02486.hp2 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.487+739_487+744del others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467987 | ||||||
| chr2:60467989
|
GGTA | G | 8 | a0001c0001t0007g0099a0001c0001t0007g0111a0001c0001t0007g0112others(5): Show | 8 | HG01261.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+740_487+742del others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467989 | ||||||
| chr2:60467990
|
GTAA | G | 70 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(67): Show | 70 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.487+739_487+741del others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467990 | ||||||
| chr2:60467992
|
A | G | 16 | a0001c0001t0001g0058a0001c0001t0004g0082a0001c0001t0005g0223others(13): Show | 16 | HG00099.hp1 HG00733.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+740T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467992 | ||||||
| chr2:60467993
|
A | G | 15 | a0001c0001t0001g0058a0001c0001t0004g0082a0001c0001t0005g0223others(12): Show | 15 | HG00099.hp1 HG00733.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.487+739T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467993 | ||||||
| chr2:60467998
|
G | A | 8 | a0001c0001t0007g0099a0001c0001t0007g0111a0001c0001t0007g0112others(5): Show | 8 | HG01261.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+734C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467998 | ||||||
| chr2:60467999
|
G | A | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+733C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467999 | ||||||
| chr2:60467999
|
G | C | 8 | a0001c0001t0007g0099a0001c0001t0007g0111a0001c0001t0007g0112others(5): Show | 8 | HG01261.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+733C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60467999 | ||||||
| chr2:60468002
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+730C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468002 | ||||||
| chr2:60468004
|
G | A | 12 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0004g0082others(9): Show | 12 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+728C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468004 | ||||||
| chr2:60468008
|
A | G | 106 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(103): Show | 107 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.487+724T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468008 | ||||||
| chr2:60468010
|
G | A | 84 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(81): Show | 84 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.487+722C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468010 | ||||||
| chr2:60468010
|
GGTGGTGG others(8): Show |
G | 8 | a0001c0001t0007g0099a0001c0001t0007g0111a0001c0001t0007g0112others(5): Show | 8 | HG01261.hp2 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.487+707_487+721del others(15): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468010 | ||||||
| chr2:60468011
|
G | A | 12 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0004g0082others(9): Show | 12 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+721C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468011 | ||||||
| chr2:60468013
|
G | A | 4 | a0001c0001t0005g0219a0001c0001t0009g0198a0001c0001t0018g0211others(1): Show | 4 | HG00733.hp1 HG02486.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+719C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468013 | ||||||
| chr2:60468014
|
G | A | 72 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(69): Show | 72 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.487+718C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468014 | ||||||
| chr2:60468014
|
G | C | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+718C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468014 | ||||||
| chr2:60468016
|
G | A | 74 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(71): Show | 74 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.487+716C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468016 | ||||||
| chr2:60468017
|
G | A | 75 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(72): Show | 75 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.487+715C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468017 | ||||||
| chr2:60468017
|
G | GTAGTGAT others(177): Show |
22 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0055others(19): Show | 23 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.487+714_487+715ins others(184): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468017 | ||||||
| chr2:60468017
|
G | GTGATGGT others(174): Show |
1 | a0001c0001t0055g0202 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.487+714_487+715ins others(181): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468017 | ||||||
| chr2:60468017
|
G | GTGGTAGT others(180): Show |
4 | a0001c0001t0002g0123a0001c0001t0003g0145a0001c0001t0004g0085others(1): Show | 4 | HG01943.hp2 HG04228.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+714_487+715ins others(187): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468017 | ||||||
| chr2:60468017
|
G | GTGGTAGT others(270): Show |
2 | a0001c0001t0003g0181a0001c0001t0005g0232 | 2 | HG02738.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.487+714_487+715ins others(277): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468017 | ||||||
| chr2:60468019
|
G | A | 3 | a0001c0001t0005g0219a0001c0001t0018g0211a0001c0001t0019g0012 | 3 | HG02486.hp2 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.487+713C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468019 | ||||||
| chr2:60468019
|
GGTGGTA | G | 12 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0004g0082others(9): Show | 12 | HG00099.hp1 HG01256.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.487+707_487+712del others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468019 | ||||||
| chr2:60468020
|
G | A | 3 | a0001c0001t0005g0219a0001c0001t0018g0211a0001c0001t0019g0012 | 3 | HG02486.hp2 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.487+712C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468020 | ||||||
| chr2:60468023
|
G | A | 1 | a0001c0001t0009g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.487+709C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468023 | ||||||
| chr2:60468025
|
A | AGTGATGG others(93): Show |
1 | a0001c0001t0004g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.487+706_487+707ins others(100): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(84): Show |
12 | a0001c0001t0002g0122a0001c0002t0001g0024a0001c0002t0002g0120others(9): Show | 12 | HG01123.hp2 HG01257.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.487+706_487+707ins others(91): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(87): Show |
65 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0036others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.487+706_487+707ins others(94): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(545): Show |
3 | a0001c0001t0001g0034a0001c0001t0008g0116a0001c0001t0021g0102 | 3 | HG02572.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.487+706_487+707ins others(552): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(90): Show |
2 | a0001c0002t0001g0016a0001c0002t0008g0115 | 2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.487+706_487+707ins others(97): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(600): Show |
1 | a0001c0001t0003g0152 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.487+706_487+707ins others(607): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(420): Show |
1 | a0001c0001t0018g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.487+706_487+707ins others(427): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(270): Show |
1 | a0001c0001t0003g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.487+706_487+707ins others(277): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(273): Show |
17 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(14): Show | 17 | HG00140.hp2 HG01515.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.487+706_487+707ins others(280): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(279): Show |
6 | a0001c0002t0001g0040a0001c0002t0001g0051a0001c0002t0001g0052others(3): Show | 6 | HG00140.hp1 HG01081.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+706_487+707ins others(286): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(462): Show |
1 | a0001c0001t0006g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.487+706_487+707ins others(469): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(276): Show |
1 | a0001c0002t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.487+706_487+707ins others(283): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | AGTGATGG others(559): Show |
2 | a0001c0002t0001g0018a0001c0002t0031g0053 | 2 | HG01192.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.487+706_487+707ins others(566): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468025
|
A | G | 107 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0028others(104): Show | 108 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.487+707T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468025 | ||||||
| chr2:60468028
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+704C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468028 | ||||||
| chr2:60468029
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(1): Show | 4 | HG02630.hp2 HG03471.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+703C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468029 | ||||||
| chr2:60468032
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+700C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468032 | ||||||
| chr2:60468034
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.487+698C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468034 | ||||||
| chr2:60468035
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(1): Show | 4 | HG02630.hp2 HG03471.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+697T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468035 | ||||||
| chr2:60468037
|
G | A | 1 | a0001c0002t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+695C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468037 | ||||||
| chr2:60468076
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.487+656C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468076 | ||||||
| chr2:60468088
|
T | G | 1 | a0001c0002t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+644A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468088 | ||||||
| chr2:60468093
|
T | C | 1 | a0001c0001t0008g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.487+639A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468093 | ||||||
| chr2:60468104
|
A | G | 1 | a0001c0002t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+628T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468104 | ||||||
| chr2:60468111
|
C | T | 1 | a0001c0002t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+621G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468111 | ||||||
| chr2:60468116
|
G | A | 1 | a0001c0002t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+616C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468116 | ||||||
| chr2:60468121
|
T | G | 1 | a0001c0002t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+611A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468121 | ||||||
| chr2:60468276
|
C | A | 1 | a0001c0001t0012g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.487+456G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468276 | ||||||
| chr2:60468532
|
G | A | 3 | a0001c0001t0003g0163a0001c0001t0009g0195a0001c0001t0059g0210 | 3 | NA18957.hp2 NA19006.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.487+200C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468532 | ||||||
| chr2:60468588
|
G | A | 1 | a0001c0001t0005g0232 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.487+144C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468588 | ||||||
| chr2:60468613
|
T | C | 1 | a0001c0002t0017g0010 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.487+119A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 3/3 | chr2 | 60468613 | ||||||
| chr2:60469048
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.386-215C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60469048 | ||||||
| chr2:60469150
|
G | A | 4 | a0001c0001t0015g0185a0001c0001t0033g0022a0001c0001t0037g0068others(1): Show | 4 | HG02280.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-317C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60469150 | ||||||
| chr2:60469393
|
T | C | 1 | a0001c0001t0005g0233 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.386-560A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60469393 | ||||||
| chr2:60469425
|
G | T | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.386-592C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60469425 | ||||||
| chr2:60469501
|
A | G | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-668T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60469501 | ||||||
| chr2:60470089
|
T | G | 1 | a0001c0001t0006g0243 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.386-1256A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60470089 | ||||||
| chr2:60470329
|
A | C | 28 | a0001c0001t0003g0149a0001c0001t0007g0092a0001c0001t0007g0095others(25): Show | 29 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.386-1496T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60470329 | ||||||
| chr2:60470330
|
C | T | 259 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(256): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.386-1497G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60470330 | ||||||
| chr2:60470341
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.386-1508A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60470341 | ||||||
| chr2:60470519
|
C | A | 127 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0032others(124): Show | 128 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.386-1686G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60470519 | ||||||
| chr2:60470743
|
G | A | 3 | a0001c0001t0021g0093a0001c0001t0032g0037a0001c0001t0064g0247 | 3 | HG02572.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.386-1910C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60470743 | ||||||
| chr2:60470801
|
T | A | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.386-1968A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60470801 | ||||||
| chr2:60470934
|
T | A | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-2101A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60470934 | ||||||
| chr2:60471037
|
T | C | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-2204A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60471037 | ||||||
| chr2:60471115
|
C | CTTTCGAA others(4): Show |
1 | a0001c0001t0016g0257 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.386-2283_386-2282i others(13): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60471115 | ||||||
| chr2:60471118
|
T | C | 1 | a0001c0001t0016g0257 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.386-2285A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60471118 | ||||||
| chr2:60471152
|
C | T | 95 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0033others(92): Show | 96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.386-2319G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60471152 | ||||||
| chr2:60471262
|
A | C | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(127): Show | 131 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.386-2429T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60471262 | ||||||
| chr2:60471326
|
C | T | 127 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(124): Show | 128 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.386-2493G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60471326 | ||||||
| chr2:60471819
|
G | T | 2 | a0001c0001t0013g0252a0001c0001t0019g0013 | 2 | HG03490.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.386-2986C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60471819 | ||||||
| chr2:60472044
|
T | C | 1 | a0001c0001t0004g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.386-3211A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60472044 | ||||||
| chr2:60472282
|
C | A | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-3449G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60472282 | ||||||
| chr2:60472522
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0003g0189 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.386-3689C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60472522 | ||||||
| chr2:60472523
|
C | G | 1 | a0001c0001t0002g0097 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.386-3690G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60472523 | ||||||
| chr2:60472545
|
T | C | 2 | a0001c0001t0038g0069a0001c0001t0063g0234 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.386-3712A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60472545 | ||||||
| chr2:60472733
|
C | G | 1 | a0001c0002t0016g0255 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.386-3900G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60472733 | ||||||
| chr2:60472902
|
G | C | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-4069C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60472902 | ||||||
| chr2:60472999
|
AAGCATTT others(45): Show |
A | 13 | a0001c0001t0001g0036a0001c0001t0002g0128a0001c0001t0003g0149others(10): Show | 13 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-4218_386-4167d others(54): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60472999 | ||||||
| chr2:60473007
|
A | G | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-4174T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473007 | ||||||
| chr2:60473029
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.386-4196C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473029 | ||||||
| chr2:60473096
|
A | G | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-4263T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473096 | ||||||
| chr2:60473116
|
A | G | 1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.386-4283T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473116 | ||||||
| chr2:60473139
|
C | T | 4 | a0001c0001t0045g0114a0001c0002t0001g0023a0001c0002t0004g0077others(1): Show | 4 | HG01358.hp1 HG02145.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-4306G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473139 | ||||||
| chr2:60473240
|
GT | G | 131 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(128): Show | 132 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.386-4408delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473240 | ||||||
| chr2:60473297
|
A | C | 1 | a0001c0001t0003g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.386-4464T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473297 | ||||||
| chr2:60473432
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.386-4599C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473432 | ||||||
| chr2:60473488
|
C | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-4655G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473488 | ||||||
| chr2:60473668
|
A | G | 1 | a0001c0001t0004g0088 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.386-4835T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473668 | ||||||
| chr2:60473752
|
A | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-4919T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473752 | ||||||
| chr2:60473936
|
TA | T | 4 | a0001c0001t0001g0038a0001c0001t0003g0189a0001c0001t0003g0192others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-5104delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60473936 | ||||||
| chr2:60474033
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.386-5200A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60474033 | ||||||
| chr2:60474181
|
T | G | 1 | a0001c0001t0005g0223 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.386-5348A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60474181 | ||||||
| chr2:60474200
|
T | C | 124 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(121): Show | 125 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.386-5367A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60474200 | ||||||
| chr2:60474211
|
G | A | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-5378C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60474211 | ||||||
| chr2:60474310
|
C | CA | 15 | a0001c0001t0001g0036a0001c0001t0002g0128a0001c0001t0003g0149others(12): Show | 15 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.386-5478dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60474310 | ||||||
| chr2:60474588
|
G | A | 2 | a0001c0001t0015g0190a0001c0001t0053g0191 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.386-5755C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60474588 | ||||||
| chr2:60474756
|
A | G | 3 | a0001c0002t0001g0023a0001c0002t0004g0077a0001c0002t0017g0010 | 3 | HG01358.hp1 HG02145.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.386-5923T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60474756 | ||||||
| chr2:60475045
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250 | 3 | HG02630.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.386-6212C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60475045 | ||||||
| chr2:60475199
|
C | T | 1 | a0001c0001t0027g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.386-6366G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60475199 | ||||||
| chr2:60475631
|
T | C | 14 | a0001c0001t0001g0036a0001c0001t0002g0128a0001c0001t0003g0149others(11): Show | 14 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.386-6798A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60475631 | ||||||
| chr2:60475697
|
T | C | 5 | a0001c0001t0015g0185a0001c0001t0016g0254a0001c0001t0033g0022others(2): Show | 5 | HG02280.hp1 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.386-6864A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60475697 | ||||||
| chr2:60475845
|
T | C | 1 | a0001c0001t0003g0181 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.386-7012A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60475845 | ||||||
| chr2:60475911
|
A | T | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-7078T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60475911 | ||||||
| chr2:60476138
|
C | T | 1 | a0001c0001t0004g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.386-7305G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60476138 | ||||||
| chr2:60476194
|
G | T | 1 | a0001c0001t0015g0193 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.386-7361C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60476194 | ||||||
| chr2:60476376
|
A | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.386-7543T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60476376 | ||||||
| chr2:60476591
|
A | G | 14 | a0001c0001t0001g0036a0001c0001t0002g0128a0001c0001t0003g0149others(11): Show | 14 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.386-7758T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60476591 | ||||||
| chr2:60476742
|
C | T | 1 | a0001c0001t0061g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.386-7909G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60476742 | ||||||
| chr2:60477267
|
C | T | 1 | a0001c0001t0005g0232 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.386-8434G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477267 | ||||||
| chr2:60477342
|
C | T | 2 | a0001c0001t0021g0093a0001c0001t0032g0037 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.386-8509G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477342 | ||||||
| chr2:60477349
|
T | A | 140 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0029others(137): Show | 141 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.386-8516A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477349 | ||||||
| chr2:60477404
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.386-8571G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477404 | ||||||
| chr2:60477600
|
T | TAAAG | 7 | a0001c0001t0001g0019a0001c0001t0005g0219a0001c0001t0009g0198others(4): Show | 7 | HG00733.hp1 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-8768_386-8767i others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477600 | ||||||
| chr2:60477600
|
T | TAAAGAAA others(1): Show |
61 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0063others(58): Show | 61 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.386-8768_386-8767i others(10): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477600 | ||||||
| chr2:60477600
|
T | TAAAGAAA others(5): Show |
27 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0046others(24): Show | 28 | HG00597.hp1 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.386-8768_386-8767i others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477600 | ||||||
| chr2:60477600
|
T | TAAAGAAA others(9): Show |
4 | a0001c0001t0001g0029a0001c0001t0020g0047a0001c0001t0045g0114others(1): Show | 4 | HG00099.hp2 HG00423.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-8768_386-8767i others(18): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477600 | ||||||
| chr2:60477600
|
T | TGAAAG | 30 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(27): Show | 30 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.386-8768_386-8767i others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477600 | ||||||
| chr2:60477600
|
T | TGAAAGAA others(2): Show |
3 | a0001c0001t0002g0136a0001c0001t0006g0236a0001c0002t0001g0052 | 3 | HG02683.hp2 HG03490.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.386-8768_386-8767i others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477600 | ||||||
| chr2:60477604
|
T | G | 145 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0029others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.386-8771A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477604 | ||||||
| chr2:60477608
|
G | T | 12 | a0001c0001t0001g0036a0001c0001t0003g0149a0001c0001t0004g0078others(9): Show | 12 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.386-8775C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477608 | ||||||
| chr2:60477731
|
G | T | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.386-8898C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477731 | ||||||
| chr2:60477763
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.386-8930G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477763 | ||||||
| chr2:60477798
|
A | T | 180 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(177): Show | 181 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.386-8965T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477798 | ||||||
| chr2:60477888
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.386-9055G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477888 | ||||||
| chr2:60477958
|
C | CT | 15 | a0001c0001t0001g0065a0001c0001t0002g0091a0001c0001t0005g0219others(12): Show | 15 | HG02074.hp1 HG02109.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.386-9126dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477958 | ||||||
| chr2:60477958
|
CT | C | 7 | a0001c0001t0002g0106a0001c0001t0002g0118a0001c0001t0003g0156others(4): Show | 7 | HG01167.hp2 HG01169.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-9126delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477958 | ||||||
| chr2:60477962
|
T | A | 20 | a0001c0001t0001g0031a0001c0001t0003g0152a0001c0001t0006g0242others(17): Show | 21 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.386-9129A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60477962 | ||||||
| chr2:60478097
|
G | A | 33 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(30): Show | 33 | HG00140.hp1 HG00741.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.386-9264C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478097 | ||||||
| chr2:60478412
|
A | G | 1 | a0001c0002t0028g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.386-9579T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478412 | ||||||
| chr2:60478473
|
C | G | 29 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0003g0152others(26): Show | 30 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.386-9640G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478473 | ||||||
| chr2:60478658
|
A | C | 3 | a0001c0001t0038g0069a0001c0001t0049g0165a0001c0001t0061g0212 | 3 | HG02109.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.386-9825T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478658 | ||||||
| chr2:60478678
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.386-9845T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478678 | ||||||
| chr2:60478720
|
C | T | 1 | a0001c0001t0013g0249 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.386-9887G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478720 | ||||||
| chr2:60478930
|
C | T | 1 | a0001c0003t0002g0107 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.386-10097G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478930 | ||||||
| chr2:60478942
|
C | T | 2 | a0001c0001t0002g0106a0001c0001t0002g0118 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.386-10109G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478942 | ||||||
| chr2:60478968
|
G | GT | 38 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.386-10136dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478968 | ||||||
| chr2:60478968
|
GT | G | 18 | a0001c0001t0001g0031a0001c0001t0003g0152a0001c0001t0006g0242others(15): Show | 19 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.386-10136delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478968 | ||||||
| chr2:60478975
|
T | G | 4 | a0001c0001t0010g0015a0001c0001t0015g0190a0001c0001t0053g0191others(1): Show | 4 | HG02055.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-10142A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60478975 | ||||||
| chr2:60479094
|
T | C | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-10261A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60479094 | ||||||
| chr2:60479124
|
T | G | 20 | a0001c0001t0001g0031a0001c0001t0002g0110a0001c0001t0003g0152others(17): Show | 21 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.386-10291A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60479124 | ||||||
| chr2:60479134
|
G | A | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-10301C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60479134 | ||||||
| chr2:60479263
|
G | A | 1 | a0001c0002t0004g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.386-10430C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60479263 | ||||||
| chr2:60479859
|
C | A | 1 | a0001c0001t0006g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.386-11026G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60479859 | ||||||
| chr2:60479903
|
C | A | 19 | a0001c0001t0001g0031a0001c0001t0003g0152a0001c0001t0006g0242others(16): Show | 20 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.386-11070G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60479903 | ||||||
| chr2:60480027
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.386-11194C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480027 | ||||||
| chr2:60480047
|
G | A | 19 | a0001c0001t0001g0031a0001c0001t0003g0152a0001c0001t0006g0242others(16): Show | 20 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.386-11214C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480047 | ||||||
| chr2:60480062
|
G | A | 1 | a0001c0001t0007g0112 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.386-11229C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480062 | ||||||
| chr2:60480384
|
C | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-11551G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480384 | ||||||
| chr2:60480453
|
A | G | 49 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0038others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.386-11620T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480453 | ||||||
| chr2:60480511
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0002g0001 | 3 | HG00733.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.386-11678C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480511 | ||||||
| chr2:60480759
|
G | A | 78 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0035others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.386-11926C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480759 | ||||||
| chr2:60480806
|
C | G | 19 | a0001c0001t0001g0031a0001c0001t0003g0152a0001c0001t0006g0242others(16): Show | 20 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.386-11973G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480806 | ||||||
| chr2:60480860
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.386-12027G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480860 | ||||||
| chr2:60480874
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0009g0204a0001c0001t0009g0205others(1): Show | 4 | HG00323.hp2 HG01192.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-12041A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480874 | ||||||
| chr2:60480976
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0004g0074 | 3 | HG01884.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.386-12143T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60480976 | ||||||
| chr2:60481220
|
C | A | 1 | a0001c0001t0022g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.386-12387G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481220 | ||||||
| chr2:60481267
|
G | A | 11 | a0001c0001t0001g0036a0001c0001t0003g0149a0001c0001t0004g0078others(8): Show | 11 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.386-12434C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481267 | ||||||
| chr2:60481363
|
C | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-12530G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481363 | ||||||
| chr2:60481422
|
C | T | 1 | a0001c0001t0005g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.386-12589G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481422 | ||||||
| chr2:60481462
|
C | T | 103 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(100): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-12629G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481462 | ||||||
| chr2:60481570
|
G | A | 2 | a0001c0001t0049g0165a0001c0001t0061g0212 | 2 | HG02109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.386-12737C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481570 | ||||||
| chr2:60481756
|
T | A | 6 | a0001c0001t0003g0168a0001c0001t0003g0170a0001c0001t0004g0076others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-12923A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481756 | ||||||
| chr2:60481864
|
G | A | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.386-13031C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481864 | ||||||
| chr2:60481954
|
C | T | 27 | a0001c0001t0002g0106a0001c0001t0002g0118a0001c0001t0002g0141others(24): Show | 27 | HG00544.hp2 HG00735.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.386-13121G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60481954 | ||||||
| chr2:60482053
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.386-13220T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60482053 | ||||||
| chr2:60482108
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0068g0260 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.386-13275C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60482108 | ||||||
| chr2:60482147
|
A | G | 1 | a0001c0001t0003g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.386-13314T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60482147 | ||||||
| chr2:60482170
|
A | G | 6 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-13337T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60482170 | ||||||
| chr2:60482589
|
G | A | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-13756C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60482589 | ||||||
| chr2:60482765
|
C | T | 1 | a0001c0001t0037g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.386-13932G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60482765 | ||||||
| chr2:60483139
|
T | C | 3 | a0001c0001t0038g0069a0001c0001t0049g0165a0001c0001t0061g0212 | 3 | HG02109.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.386-14306A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483139 | ||||||
| chr2:60483153
|
T | C | 2 | a0001c0001t0003g0192a0001c0001t0014g0006 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.386-14320A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483153 | ||||||
| chr2:60483431
|
T | C | 1 | a0001c0001t0054g0194 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.386-14598A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483431 | ||||||
| chr2:60483436
|
G | A | 78 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(75): Show | 79 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.386-14603C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483436 | ||||||
| chr2:60483441
|
T | A | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.386-14608A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483441 | ||||||
| chr2:60483603
|
G | A | 113 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.386-14770C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483603 | ||||||
| chr2:60483637
|
C | T | 257 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.386-14804G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483637 | ||||||
| chr2:60483892
|
CT | C | 113 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.386-15060delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483892 | ||||||
| chr2:60483965
|
TTGTTAGA others(5): Show |
T | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.386-15144_386-1513 others(16): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60483965 | ||||||
| chr2:60484096
|
T | C | 1 | a0001c0001t0002g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.386-15263A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60484096 | ||||||
| chr2:60484324
|
T | C | 7 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0002g0144others(4): Show | 7 | HG00642.hp1 HG01256.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.386-15491A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60484324 | ||||||
| chr2:60484430
|
T | A | 1 | a0001c0001t0007g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.386-15597A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60484430 | ||||||
| chr2:60484730
|
C | T | 2 | a0001c0001t0009g0198a0001c0001t0014g0009 | 2 | HG00733.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.386-15897G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60484730 | ||||||
| chr2:60484963
|
T | TA | 13 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0002g0122others(10): Show | 13 | HG02486.hp2 HG02738.hp2 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-16131dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60484963 | ||||||
| chr2:60484963
|
TA | T | 14 | a0001c0001t0001g0020a0001c0001t0004g0071a0001c0001t0006g0240others(11): Show | 14 | HG00738.hp1 HG01167.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.386-16131delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60484963 | ||||||
| chr2:60484990
|
C | A | 1 | a0001c0001t0004g0084 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.386-16157G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60484990 | ||||||
| chr2:60485228
|
A | G | 1 | a0001c0001t0005g0221 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.386-16395T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60485228 | ||||||
| chr2:60485286
|
C | T | 10 | a0001c0001t0001g0036a0001c0001t0003g0149a0001c0001t0004g0078others(7): Show | 10 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-16453G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60485286 | ||||||
| chr2:60485385
|
C | T | 1 | a0001c0001t0054g0194 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.386-16552G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60485385 | ||||||
| chr2:60485449
|
C | A | 20 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0063others(17): Show | 20 | HG01243.hp1 HG02074.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-16616G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60485449 | ||||||
| chr2:60485555
|
T | A | 1 | a0001c0001t0006g0245 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.386-16722A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60485555 | ||||||
| chr2:60485717
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0005g0227a0001c0001t0022g0180 | 3 | HG02056.hp1 HG02129.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.386-16884C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60485717 | ||||||
| chr2:60485749
|
A | C | 1 | a0001c0002t0001g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.386-16916T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60485749 | ||||||
| chr2:60485908
|
A | C | 1 | a0001c0001t0017g0014 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.386-17075T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60485908 | ||||||
| chr2:60486014
|
C | CA | 15 | a0001c0001t0001g0036a0001c0001t0003g0149a0001c0001t0004g0078others(12): Show | 15 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.386-17182dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60486014 | ||||||
| chr2:60486100
|
A | G | 121 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0035others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.386-17267T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60486100 | ||||||
| chr2:60486359
|
G | T | 1 | a0001c0001t0054g0194 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.386-17526C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60486359 | ||||||
| chr2:60486697
|
C | T | 1 | a0001c0002t0001g0016 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.386-17864G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60486697 | ||||||
| chr2:60486934
|
C | T | 1 | a0001c0001t0002g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.386-18101G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60486934 | ||||||
| chr2:60487040
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.386-18207T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487040 | ||||||
| chr2:60487378
|
G | C | 1 | a0001c0001t0054g0194 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.386-18545C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487378 | ||||||
| chr2:60487408
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.386-18575A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487408 | ||||||
| chr2:60487450
|
A | C | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-18617T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487450 | ||||||
| chr2:60487479
|
G | A | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-18646C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487479 | ||||||
| chr2:60487566
|
T | A | 1 | a0001c0001t0066g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.386-18733A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487566 | ||||||
| chr2:60487641
|
C | G | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-18808G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487641 | ||||||
| chr2:60487672
|
G | A | 1 | a0001c0002t0001g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.386-18839C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487672 | ||||||
| chr2:60487726
|
A | C | 136 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0035others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.386-18893T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487726 | ||||||
| chr2:60487754
|
G | A | 1 | a0001c0001t0014g0006 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.386-18921C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487754 | ||||||
| chr2:60487830
|
G | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0020g0047others(1): Show | 4 | HG00423.hp1 HG02056.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-18997C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60487830 | ||||||
| chr2:60488044
|
C | T | 133 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0035others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.386-19211G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488044 | ||||||
| chr2:60488048
|
G | T | 4 | a0001c0001t0012g0213a0001c0001t0013g0248a0001c0001t0013g0253others(1): Show | 4 | HG01167.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-19215C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488048 | ||||||
| chr2:60488049
|
C | T | 4 | a0001c0001t0012g0213a0001c0001t0013g0248a0001c0001t0013g0253others(1): Show | 4 | HG01167.hp1 HG03139.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-19216G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488049 | ||||||
| chr2:60488183
|
G | A | 1 | a0001c0001t0004g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.386-19350C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488183 | ||||||
| chr2:60488314
|
G | A | 3 | a0001c0001t0016g0254a0001c0001t0037g0068a0001c0001t0065g0251 | 3 | HG02809.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.386-19481C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488314 | ||||||
| chr2:60488462
|
G | C | 1 | a0001c0001t0049g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.386-19629C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488462 | ||||||
| chr2:60488634
|
T | C | 1 | a0001c0001t0003g0157 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.386-19801A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488634 | ||||||
| chr2:60488736
|
T | TTTTG | 4 | a0001c0001t0001g0029a0001c0001t0005g0219a0001c0002t0001g0024others(1): Show | 4 | HG01123.hp2 HG01257.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-19907_386-1990 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488736 | ||||||
| chr2:60488736
|
TTTTG | T | 7 | a0001c0001t0001g0028a0001c0001t0002g0097a0001c0001t0003g0187others(4): Show | 7 | HG00597.hp2 HG01884.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-19907_386-1990 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488736 | ||||||
| chr2:60488802
|
CG | C | 10 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(7): Show | 10 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-19970delC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488802 | ||||||
| chr2:60488812
|
TGCAATGG others(1): Show |
T | 3 | a0001c0001t0038g0069a0001c0001t0049g0165a0001c0001t0061g0212 | 3 | HG02109.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.386-19987_386-1998 others(12): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488812 | ||||||
| chr2:60488918
|
C | A | 2 | a0001c0001t0018g0211a0001c0001t0019g0012 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.386-20085G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488918 | ||||||
| chr2:60488966
|
G | A | 1 | a0001c0001t0035g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.386-20133C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60488966 | ||||||
| chr2:60489118
|
T | A | 1 | a0001c0001t0003g0172 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.386-20285A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60489118 | ||||||
| chr2:60489173
|
G | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0003g0152others(19): Show | 23 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.386-20340C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60489173 | ||||||
| chr2:60489245
|
C | T | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-20412G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60489245 | ||||||
| chr2:60489723
|
G | A | 1 | a0001c0001t0036g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.386-20890C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60489723 | ||||||
| chr2:60489836
|
C | T | 2 | a0001c0001t0006g0239a0001c0009t0001g0017 | 2 | HG00280.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.386-21003G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60489836 | ||||||
| chr2:60490264
|
G | T | 20 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0003g0152others(17): Show | 21 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.386-21431C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490264 | ||||||
| chr2:60490281
|
C | T | 1 | a0001c0002t0002g0121 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.386-21448G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490281 | ||||||
| chr2:60490350
|
T | C | 1 | a0001c0001t0004g0072 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.386-21517A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490350 | ||||||
| chr2:60490424
|
C | T | 1 | a0001c0001t0013g0248 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.386-21591G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490424 | ||||||
| chr2:60490542
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.386-21709T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490542 | ||||||
| chr2:60490543
|
T | G | 1 | a0001c0002t0028g0044 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.386-21710A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490543 | ||||||
| chr2:60490570
|
G | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21737C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490570 | ||||||
| chr2:60490582
|
T | A | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21749A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490582 | ||||||
| chr2:60490641
|
A | G | 10 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(7): Show | 10 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-21808T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490641 | ||||||
| chr2:60490674
|
C | A | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21841G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490674 | ||||||
| chr2:60490684
|
T | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21851A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490684 | ||||||
| chr2:60490688
|
G | T | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21855C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490688 | ||||||
| chr2:60490691
|
T | A | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21858A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490691 | ||||||
| chr2:60490695
|
C | A | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21862G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490695 | ||||||
| chr2:60490697
|
A | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21864T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490697 | ||||||
| chr2:60490697
|
A | G | 1 | a0001c0003t0003g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.386-21864T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490697 | ||||||
| chr2:60490701
|
G | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21868C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490701 | ||||||
| chr2:60490702
|
T | G | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21869A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490702 | ||||||
| chr2:60490710
|
A | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21877T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490710 | ||||||
| chr2:60490715
|
G | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21882C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490715 | ||||||
| chr2:60490746
|
T | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21913A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490746 | ||||||
| chr2:60490751
|
A | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21918T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490751 | ||||||
| chr2:60490774
|
T | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21941A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490774 | ||||||
| chr2:60490775
|
G | T | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21942C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490775 | ||||||
| chr2:60490785
|
T | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21952A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490785 | ||||||
| chr2:60490790
|
T | C | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21957A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490790 | ||||||
| chr2:60490807
|
G | T | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21974C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490807 | ||||||
| chr2:60490821
|
G | GACAAATA others(15): Show |
1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-21989_386-2198 others(26): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490821 | ||||||
| chr2:60490846
|
A | T | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-22013T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490846 | ||||||
| chr2:60490908
|
T | G | 198 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.386-22075A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490908 | ||||||
| chr2:60490940
|
TA | T | 6 | a0001c0001t0009g0198a0001c0001t0013g0252a0001c0001t0014g0009others(3): Show | 6 | HG00733.hp1 HG01358.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-22108delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60490940 | ||||||
| chr2:60491109
|
A | T | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-22276T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491109 | ||||||
| chr2:60491110
|
T | A | 1 | a0001c0001t0057g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.386-22277A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491110 | ||||||
| chr2:60491142
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.386-22309G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491142 | ||||||
| chr2:60491143
|
G | A | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-22310C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491143 | ||||||
| chr2:60491212
|
C | T | 120 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0035others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.386-22379G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491212 | ||||||
| chr2:60491277
|
T | C | 1 | a0001c0001t0004g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.386-22444A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491277 | ||||||
| chr2:60491420
|
C | T | 1 | a0001c0002t0004g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.386-22587G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491420 | ||||||
| chr2:60491434
|
A | G | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-22601T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491434 | ||||||
| chr2:60491515
|
A | G | 1 | a0001c0001t0012g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.386-22682T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491515 | ||||||
| chr2:60491573
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.386-22740C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491573 | ||||||
| chr2:60491586
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.386-22753C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491586 | ||||||
| chr2:60491689
|
G | GA | 118 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0035others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.386-22857dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491689 | ||||||
| chr2:60491713
|
G | T | 31 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(28): Show | 32 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.386-22880C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491713 | ||||||
| chr2:60491939
|
C | T | 107 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.386-23106G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60491939 | ||||||
| chr2:60492195
|
G | T | 1 | a0001c0001t0003g0187 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.386-23362C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492195 | ||||||
| chr2:60492368
|
A | AAAAC | 33 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.386-23539_386-2353 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492368 | ||||||
| chr2:60492479
|
T | C | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-23646A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492479 | ||||||
| chr2:60492615
|
C | CCT | 44 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0038others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.386-23784_386-2378 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492615 | ||||||
| chr2:60492615
|
C | CCTCT | 4 | a0001c0001t0013g0248a0001c0001t0013g0253a0001c0001t0015g0193others(1): Show | 4 | HG01167.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-23786_386-2378 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492615 | ||||||
| chr2:60492615
|
CCT | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0012g0213 | 3 | HG02083.hp1 NA18983.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.386-23784_386-2378 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492615 | ||||||
| chr2:60492783
|
A | G | 14 | a0001c0001t0001g0034a0001c0001t0002g0110a0001c0001t0006g0239others(11): Show | 14 | HG00280.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.386-23950T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492783 | ||||||
| chr2:60492835
|
C | A | 193 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(190): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.386-24002G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492835 | ||||||
| chr2:60492852
|
G | A | 1 | a0001c0003t0003g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.386-24019C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492852 | ||||||
| chr2:60492968
|
C | G | 3 | a0001c0001t0016g0254a0001c0001t0037g0068a0001c0001t0065g0251 | 3 | HG02809.hp1 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.386-24135G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60492968 | ||||||
| chr2:60493073
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.386-24240C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493073 | ||||||
| chr2:60493111
|
C | T | 108 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.386-24278G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493111 | ||||||
| chr2:60493183
|
GT | G | 107 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.386-24351delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493183 | ||||||
| chr2:60493450
|
C | T | 1 | a0001c0001t0007g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.386-24617G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493450 | ||||||
| chr2:60493454
|
A | G | 107 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.386-24621T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493454 | ||||||
| chr2:60493612
|
G | A | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.386-24779C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493612 | ||||||
| chr2:60493622
|
G | A | 107 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.386-24789C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493622 | ||||||
| chr2:60493634
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-24801C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493634 | ||||||
| chr2:60493816
|
A | G | 194 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.386-24983T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493816 | ||||||
| chr2:60493997
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.386-25164G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60493997 | ||||||
| chr2:60494172
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0002g0140 | 2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.386-25339C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494172 | ||||||
| chr2:60494176
|
A | G | 107 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.386-25343T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494176 | ||||||
| chr2:60494212
|
G | A | 107 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(104): Show | 108 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.386-25379C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494212 | ||||||
| chr2:60494343
|
C | A | 1 | a0001c0004t0058g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.386-25510G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494343 | ||||||
| chr2:60494369
|
T | C | 1 | a0001c0001t0064g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.386-25536A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494369 | ||||||
| chr2:60494614
|
G | T | 1 | a0001c0003t0002g0103 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.386-25781C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494614 | ||||||
| chr2:60494905
|
C | T | 63 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(60): Show | 64 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.386-26072G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494905 | ||||||
| chr2:60494938
|
A | T | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.386-26105T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494938 | ||||||
| chr2:60494985
|
T | C | 1 | a0001c0002t0001g0016 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.386-26152A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60494985 | ||||||
| chr2:60495106
|
A | G | 42 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0031others(39): Show | 43 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.386-26273T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495106 | ||||||
| chr2:60495150
|
C | T | 1 | a0001c0001t0048g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.386-26317G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495150 | ||||||
| chr2:60495223
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-26390G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495223 | ||||||
| chr2:60495330
|
G | A | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-26497C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495330 | ||||||
| chr2:60495595
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.386-26762G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495595 | ||||||
| chr2:60495608
|
T | G | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-26775A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495608 | ||||||
| chr2:60495765
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.386-26932T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495765 | ||||||
| chr2:60495836
|
C | A | 9 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-27003G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495836 | ||||||
| chr2:60495851
|
G | C | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.386-27018C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495851 | ||||||
| chr2:60495899
|
T | TA | 9 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-27067dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495899 | ||||||
| chr2:60495961
|
C | CA | 194 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.386-27129_386-2712 others(5): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495961 | ||||||
| chr2:60495965
|
T | A | 1 | a0001c0001t0006g0242 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.386-27132A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495965 | ||||||
| chr2:60495970
|
A | T | 1 | a0001c0001t0006g0242 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.386-27137T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495970 | ||||||
| chr2:60495973
|
AC | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(49): Show | 53 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.386-27141delG | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495973 | ||||||
| chr2:60495974
|
C | A | 1 | a0001c0001t0006g0242 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.386-27141G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60495974 | ||||||
| chr2:60496038
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-27205C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496038 | ||||||
| chr2:60496131
|
G | A | 32 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.386-27298C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496131 | ||||||
| chr2:60496172
|
C | A | 1 | a0001c0001t0065g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.386-27339G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496172 | ||||||
| chr2:60496440
|
A | G | 2 | a0001c0001t0016g0254a0001c0001t0065g0251 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.386-27607T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496440 | ||||||
| chr2:60496496
|
T | C | 6 | a0001c0001t0001g0032a0001c0001t0003g0160a0001c0001t0013g0250others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-27663A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496496 | ||||||
| chr2:60496537
|
T | C | 131 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0035others(128): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.386-27704A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496537 | ||||||
| chr2:60496603
|
G | C | 1 | a0001c0001t0004g0071 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.386-27770C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496603 | ||||||
| chr2:60496694
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-27861G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496694 | ||||||
| chr2:60496770
|
G | A | 10 | a0001c0001t0001g0036a0001c0001t0003g0149a0001c0001t0004g0078others(7): Show | 10 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-27937C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496770 | ||||||
| chr2:60496774
|
G | GCT | 117 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0035others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.386-27943_386-2794 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496774 | ||||||
| chr2:60496774
|
G | GCTCT | 3 | a0001c0001t0002g0101a0001c0002t0001g0052a0001c0002t0003g0169 | 3 | HG00323.hp1 HG02683.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.386-27945_386-2794 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496774 | ||||||
| chr2:60496880
|
C | T | 2 | a0001c0001t0008g0126a0001c0001t0047g0176 | 2 | NA18979.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.386-28047G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496880 | ||||||
| chr2:60496951
|
T | C | 194 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.386-28118A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496951 | ||||||
| chr2:60496952
|
G | T | 194 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.386-28119C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60496952 | ||||||
| chr2:60497072
|
G | A | 1 | a0001c0001t0007g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-28239C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60497072 | ||||||
| chr2:60497628
|
GATA | G | 257 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.386-28798_386-2879 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60497628 | ||||||
| chr2:60497683
|
T | C | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.386-28850A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60497683 | ||||||
| chr2:60497832
|
A | G | 3 | a0001c0001t0049g0165a0001c0001t0061g0212a0001c0001t0063g0234 | 3 | HG02109.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.386-28999T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60497832 | ||||||
| chr2:60497908
|
G | C | 2 | a0001c0001t0003g0149a0001c0001t0004g0078 | 2 | HG01361.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.386-29075C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60497908 | ||||||
| chr2:60498076
|
G | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-29243C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60498076 | ||||||
| chr2:60498316
|
G | C | 74 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(71): Show | 75 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.386-29483C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60498316 | ||||||
| chr2:60498321
|
G | A | 1 | a0001c0001t0006g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.386-29488C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60498321 | ||||||
| chr2:60498364
|
C | T | 1 | a0001c0001t0008g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.386-29531G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60498364 | ||||||
| chr2:60498677
|
G | A | 1 | a0001c0001t0044g0105 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.386-29844C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60498677 | ||||||
| chr2:60498993
|
T | C | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-30160A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60498993 | ||||||
| chr2:60499193
|
C | T | 1 | a0001c0001t0067g0259 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.386-30360G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60499193 | ||||||
| chr2:60499256
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-30423G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60499256 | ||||||
| chr2:60499292
|
C | T | 40 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(37): Show | 41 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.386-30459G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60499292 | ||||||
| chr2:60499390
|
A | T | 1 | a0001c0001t0004g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.386-30557T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60499390 | ||||||
| chr2:60499594
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.386-30761G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60499594 | ||||||
| chr2:60500230
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.386-31397A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500230 | ||||||
| chr2:60500281
|
G | A | 29 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.386-31448C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500281 | ||||||
| chr2:60500291
|
C | G | 1 | a0001c0001t0023g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-31458G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500291 | ||||||
| chr2:60500354
|
C | G | 1 | a0001c0001t0008g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.386-31521G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500354 | ||||||
| chr2:60500494
|
G | A | 55 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0031others(52): Show | 56 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.386-31661C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500494 | ||||||
| chr2:60500712
|
A | G | 3 | a0001c0001t0003g0152a0001c0001t0011g0150a0001c0001t0011g0151 | 3 | HG01256.hp1 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.386-31879T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500712 | ||||||
| chr2:60500785
|
G | A | 4 | a0001c0001t0010g0015a0001c0001t0015g0190a0001c0001t0053g0191others(1): Show | 4 | HG02055.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-31952C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500785 | ||||||
| chr2:60500787
|
G | T | 1 | a0001c0002t0014g0008 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386-31954C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500787 | ||||||
| chr2:60500858
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-32025G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60500858 | ||||||
| chr2:60501009
|
G | A | 1 | a0001c0001t0003g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.386-32176C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501009 | ||||||
| chr2:60501014
|
C | T | 2 | a0001c0002t0003g0169a0001c0002t0017g0011 | 2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.386-32181G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501014 | ||||||
| chr2:60501021
|
C | G | 13 | a0001c0001t0001g0034a0001c0001t0002g0110a0001c0001t0007g0099others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.386-32188G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501021 | ||||||
| chr2:60501051
|
C | T | 1 | a0001c0001t0023g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-32218G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501051 | ||||||
| chr2:60501369
|
C | T | 1 | a0001c0001t0046g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.386-32536G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501369 | ||||||
| chr2:60501374
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG00642.hp2 HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.386-32541C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501374 | ||||||
| chr2:60501436
|
A | G | 6 | a0001c0001t0002g0001a0001c0001t0003g0149a0001c0001t0007g0092others(3): Show | 8 | HG00733.hp1 HG00741.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-32603T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501436 | ||||||
| chr2:60501448
|
G | A | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.386-32615C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501448 | ||||||
| chr2:60501496
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.386-32663G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501496 | ||||||
| chr2:60501505
|
C | CT | 17 | a0001c0001t0002g0101a0001c0001t0002g0119a0001c0001t0003g0153others(14): Show | 17 | HG00323.hp1 HG00544.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.386-32673dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501505 | ||||||
| chr2:60501505
|
CT | C | 48 | a0001c0001t0001g0021a0001c0001t0001g0028a0001c0001t0001g0049others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.386-32673delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501505 | ||||||
| chr2:60501505
|
CTT | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(14): Show | 17 | HG02055.hp2 HG02083.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.386-32674_386-3267 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501505 | ||||||
| chr2:60501567
|
T | C | 1 | a0001c0001t0003g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.386-32734A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501567 | ||||||
| chr2:60501786
|
G | A | 2 | a0001c0001t0002g0123a0001c0001t0003g0145 | 2 | NA18988.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.386-32953C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60501786 | ||||||
| chr2:60502038
|
G | A | 8 | a0001c0001t0001g0028a0001c0001t0003g0187a0001c0001t0004g0074others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-33205C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60502038 | ||||||
| chr2:60502159
|
G | A | 115 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.386-33326C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60502159 | ||||||
| chr2:60502269
|
T | G | 1 | a0001c0001t0005g0220 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.386-33436A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60502269 | ||||||
| chr2:60502460
|
C | T | 1 | a0001c0003t0003g0184 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.386-33627G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60502460 | ||||||
| chr2:60502567
|
A | G | 18 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0029others(15): Show | 18 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.386-33734T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60502567 | ||||||
| chr2:60502801
|
C | A | 1 | a0001c0001t0016g0257 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.386-33968G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60502801 | ||||||
| chr2:60503062
|
C | T | 1 | a0001c0001t0022g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.386-34229G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60503062 | ||||||
| chr2:60503277
|
C | G | 3 | a0001c0002t0001g0023a0001c0002t0004g0077a0001c0002t0017g0010 | 3 | HG01358.hp1 HG02145.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.386-34444G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60503277 | ||||||
| chr2:60503487
|
C | A | 2 | a0001c0001t0001g0059a0001c0001t0007g0095 | 2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.386-34654G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60503487 | ||||||
| chr2:60503493
|
G | T | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.386-34660C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60503493 | ||||||
| chr2:60503523
|
T | G | 1 | a0001c0001t0021g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.386-34690A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60503523 | ||||||
| chr2:60503987
|
A | G | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-35154T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60503987 | ||||||
| chr2:60504078
|
G | T | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.386-35245C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504078 | ||||||
| chr2:60504204
|
G | C | 20 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0003g0152others(17): Show | 20 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.386-35371C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504204 | ||||||
| chr2:60504228
|
C | G | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-35395G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504228 | ||||||
| chr2:60504259
|
C | T | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-35426G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504259 | ||||||
| chr2:60504532
|
CA | C | 35 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(32): Show | 35 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.386-35700delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504532 | ||||||
| chr2:60504547
|
A | G | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-35714T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504547 | ||||||
| chr2:60504622
|
C | G | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.386-35789G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504622 | ||||||
| chr2:60504631
|
C | T | 5 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(2): Show | 5 | HG02055.hp1 HG03540.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-35798G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504631 | ||||||
| chr2:60504643
|
G | C | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-35810C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504643 | ||||||
| chr2:60504801
|
A | C | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.386-35968T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504801 | ||||||
| chr2:60504964
|
G | A | 7 | a0001c0001t0001g0034a0001c0001t0003g0170a0001c0001t0013g0253others(4): Show | 7 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.386-36131C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60504964 | ||||||
| chr2:60505010
|
G | A | 6 | a0001c0001t0001g0031a0001c0001t0003g0152a0001c0001t0004g0078others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-36177C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505010 | ||||||
| chr2:60505073
|
T | C | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-36240A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505073 | ||||||
| chr2:60505081
|
G | C | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-36248C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505081 | ||||||
| chr2:60505136
|
G | C | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-36303C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505136 | ||||||
| chr2:60505145
|
C | CA | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-36313dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505145 | ||||||
| chr2:60505181
|
C | T | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-36348G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505181 | ||||||
| chr2:60505267
|
G | A | 1 | a0001c0001t0010g0057 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.386-36434C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505267 | ||||||
| chr2:60505296
|
C | T | 5 | a0001c0001t0002g0127a0001c0001t0002g0130a0001c0001t0003g0163others(2): Show | 5 | NA18957.hp2 NA18973.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-36463G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505296 | ||||||
| chr2:60505350
|
C | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.386-36517G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505350 | ||||||
| chr2:60505555
|
A | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-36722T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505555 | ||||||
| chr2:60505854
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0065others(1): Show | 4 | HG02080.hp1 HG02135.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-37021C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505854 | ||||||
| chr2:60505901
|
G | A | 1 | a0001c0001t0005g0224 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.386-37068C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60505901 | ||||||
| chr2:60506108
|
C | CT | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-37276dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60506108 | ||||||
| chr2:60506434
|
C | T | 1 | a0001c0001t0046g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.386-37601G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60506434 | ||||||
| chr2:60506452
|
G | A | 1 | a0002c0006t0012g0214 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.386-37619C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60506452 | ||||||
| chr2:60506709
|
G | A | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.386-37876C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60506709 | ||||||
| chr2:60506772
|
T | A | 1 | a0001c0001t0046g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.386-37939A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60506772 | ||||||
| chr2:60507213
|
AGGAAGGA others(41): Show |
A | 1 | a0001c0001t0001g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.386-38428_386-3838 others(52): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507213 | ||||||
| chr2:60507213
|
AGGAAGGA others(46): Show |
A | 7 | a0001c0001t0001g0035a0001c0001t0001g0058a0001c0001t0004g0072others(4): Show | 7 | HG00597.hp2 HG03654.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.386-38433_386-3838 others(57): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507213 | ||||||
| chr2:60507213
|
AGGAAGGA others(51): Show |
A | 9 | a0001c0001t0001g0039a0001c0001t0002g0144a0001c0001t0004g0081others(6): Show | 9 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-38438_386-3838 others(62): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507213 | ||||||
| chr2:60507213
|
AGGAAGGA others(56): Show |
A | 9 | a0001c0001t0001g0049a0001c0001t0003g0168a0001c0001t0042g0138others(6): Show | 9 | HG00738.hp2 HG01256.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-38443_386-3838 others(67): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507213 | ||||||
| chr2:60507213
|
AGGAAGGA others(61): Show |
A | 23 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0063others(20): Show | 23 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.386-38448_386-3838 others(72): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507213 | ||||||
| chr2:60507213
|
AGGAAGGA others(66): Show |
A | 6 | a0001c0001t0001g0042a0001c0001t0004g0085a0001c0001t0006g0246others(3): Show | 6 | HG02698.hp1 HG03688.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-38453_386-3838 others(77): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507213 | ||||||
| chr2:60507213
|
AGGAAGGA others(71): Show |
A | 4 | a0001c0001t0001g0065a0001c0001t0002g0122a0001c0001t0003g0158others(1): Show | 4 | HG02080.hp1 HG02135.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-38458_386-3838 others(82): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507213 | ||||||
| chr2:60507213
|
AGGAAGGA others(76): Show |
A | 1 | a0001c0001t0008g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.386-38463_386-3838 others(87): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507213 | ||||||
| chr2:60507214
|
GGAA | G | 26 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0183others(23): Show | 26 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.386-38384_386-3838 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507214 | ||||||
| chr2:60507214
|
GGAAGGAA | G | 4 | a0001c0001t0003g0170a0001c0001t0019g0012a0001c0001t0038g0069others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-38388_386-3838 others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507214 | ||||||
| chr2:60507217
|
A | G | 1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.386-38384T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507217 | ||||||
| chr2:60507221
|
A | G | 1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386-38388T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507221 | ||||||
| chr2:60507223
|
GAA | G | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0183others(24): Show | 27 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.386-38392_386-3839 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507223 | ||||||
| chr2:60507226
|
GGAA | G | 4 | a0001c0001t0003g0170a0001c0001t0019g0012a0001c0001t0038g0069others(1): Show | 4 | HG02145.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-38396_386-3839 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507226 | ||||||
| chr2:60507227
|
G | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0183others(24): Show | 27 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.386-38394C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507227 | ||||||
| chr2:60507229
|
A | G | 28 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0183others(25): Show | 28 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.386-38396T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507229 | ||||||
| chr2:60507232
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0020g0047 | 3 | HG00423.hp1 HG02083.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.386-38399T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507232 | ||||||
| chr2:60507232
|
AAGGG | A | 2 | a0001c0001t0002g0124a0001c0001t0002g0128 | 2 | HG01952.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.386-38403_386-3840 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507232 | ||||||
| chr2:60507236
|
G | A | 5 | a0001c0001t0006g0239a0001c0001t0022g0180a0001c0002t0001g0051others(2): Show | 5 | HG00140.hp1 HG00280.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.386-38403C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507236 | ||||||
| chr2:60507237
|
A | AAG | 3 | a0001c0001t0053g0191a0001c0001t0061g0212a0001c0001t0063g0234 | 3 | HG02055.hp2 HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.386-38405_386-3840 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507237 | ||||||
| chr2:60507237
|
AGGG | A | 28 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0170others(25): Show | 28 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.386-38407_386-3840 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507237 | ||||||
| chr2:60507237
|
AGGGAGGG others(7): Show |
A | 2 | a0001c0001t0001g0043a0001c0001t0020g0047 | 2 | HG00423.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.386-38418_386-3840 others(18): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507237 | ||||||
| chr2:60507237
|
AGGGAGGG others(12): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.386-38423_386-3840 others(23): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507237 | ||||||
| chr2:60507238
|
G | A | 1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.386-38405C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507238 | ||||||
| chr2:60507240
|
G | A | 4 | a0001c0001t0006g0239a0001c0001t0053g0191a0001c0001t0061g0212others(1): Show | 4 | HG00280.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-38407C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507240 | ||||||
| chr2:60507241
|
A | AGGGGAGG others(4): Show |
1 | a0001c0001t0001g0045 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.386-38409_386-3840 others(15): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507241 | ||||||
| chr2:60507241
|
AGGGAG | A | 22 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0054others(19): Show | 22 | HG00642.hp2 HG01123.hp2 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.386-38413_386-3840 others(9): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507241 | ||||||
| chr2:60507241
|
AGGGAGGG others(3): Show |
A | 51 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0033others(48): Show | 51 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.386-38418_386-3840 others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507241 | ||||||
| chr2:60507241
|
AGGGAGGG others(8): Show |
A | 48 | a0001c0001t0001g0034a0001c0001t0001g0059a0001c0001t0001g0064others(45): Show | 49 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.386-38423_386-3840 others(19): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507241 | ||||||
| chr2:60507241
|
AGGGAGGG others(13): Show |
A | 15 | a0001c0001t0002g0097a0001c0001t0002g0101a0001c0001t0005g0227others(12): Show | 16 | HG00323.hp1 HG00741.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.386-38428_386-3840 others(24): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507241 | ||||||
| chr2:60507241
|
AGGGAGGG others(18): Show |
A | 3 | a0001c0001t0003g0153a0001c0001t0010g0030a0001c0001t0044g0105 | 3 | NA18970.hp1 NA18994.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.386-38433_386-3840 others(29): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507241 | ||||||
| chr2:60507245
|
AGGGGAGG others(4): Show |
A | 1 | a0001c0002t0001g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.386-38423_386-3841 others(15): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507245 | ||||||
| chr2:60507245
|
AGGGGAGG others(9): Show |
A | 1 | a0001c0001t0022g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.386-38428_386-3841 others(20): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507245 | ||||||
| chr2:60507246
|
G | A | 31 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0170others(28): Show | 31 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.386-38413C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507246 | ||||||
| chr2:60507246
|
G | GGGA | 4 | a0001c0001t0006g0239a0001c0002t0001g0023a0001c0002t0004g0077others(1): Show | 4 | HG00280.hp1 HG01358.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-38414_386-3841 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507246 | ||||||
| chr2:60507251
|
G | A | 30 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0170others(27): Show | 30 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.386-38418C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507251 | ||||||
| chr2:60507256
|
G | A | 26 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0003g0183others(23): Show | 26 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.386-38423C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507256 | ||||||
| chr2:60507258
|
G | C | 7 | a0001c0001t0001g0028a0001c0001t0003g0187a0001c0001t0004g0074others(4): Show | 7 | HG01884.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-38425C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507258 | ||||||
| chr2:60507261
|
G | A | 17 | a0001c0001t0001g0029a0001c0001t0003g0183a0001c0001t0003g0192others(14): Show | 17 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.386-38428C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507261 | ||||||
| chr2:60507266
|
G | A | 15 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0003g0183others(12): Show | 15 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.386-38433C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507266 | ||||||
| chr2:60507271
|
G | A | 17 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0038others(14): Show | 17 | HG00597.hp2 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.386-38438C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507271 | ||||||
| chr2:60507276
|
G | A | 21 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(18): Show | 21 | HG00099.hp1 HG00597.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.386-38443C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507276 | ||||||
| chr2:60507281
|
G | A | 30 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(27): Show | 30 | HG00099.hp1 HG00597.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.386-38448C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507281 | ||||||
| chr2:60507286
|
G | A | 52 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0035others(49): Show | 52 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.386-38453C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507286 | ||||||
| chr2:60507291
|
G | A | 57 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0035others(54): Show | 57 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.386-38458C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507291 | ||||||
| chr2:60507296
|
G | A | 60 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0035others(57): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.386-38463C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507296 | ||||||
| chr2:60507296
|
GGGGAGGG others(18): Show |
G | 1 | a0001c0001t0014g0009 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.386-38488_386-3846 others(29): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507296 | ||||||
| chr2:60507301
|
G | A | 61 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0035others(58): Show | 61 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.386-38468C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507301 | ||||||
| chr2:60507301
|
G | GGGGAAGG others(3): Show |
1 | a0001c0001t0066g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.386-38469_386-3846 others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507301 | ||||||
| chr2:60507301
|
GGGGAGGG others(13): Show |
G | 2 | a0001c0001t0002g0125a0001c0002t0001g0027 | 2 | HG03942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.386-38488_386-3846 others(24): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507301 | ||||||
| chr2:60507306
|
G | A | 48 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(45): Show | 48 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.386-38473C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507306 | ||||||
| chr2:60507311
|
G | A | 65 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0038others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.386-38478C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507311 | ||||||
| chr2:60507315
|
AG | A | 19 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0003g0152others(16): Show | 19 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.386-38483delC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507315 | ||||||
| chr2:60507316
|
G | A | 142 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.386-38483C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507316 | ||||||
| chr2:60507316
|
G | GGGGAA | 28 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0055others(25): Show | 28 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.386-38488_386-3848 others(9): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507316 | ||||||
| chr2:60507316
|
G | GGGGAAGG others(3): Show |
4 | a0001c0001t0005g0227a0001c0001t0007g0098a0001c0001t0023g0203others(1): Show | 4 | HG02129.hp2 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-38493_386-3848 others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507316 | ||||||
| chr2:60507316
|
G | GGGGAAGG others(8): Show |
1 | a0001c0001t0001g0064 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.386-38498_386-3848 others(19): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507316 | ||||||
| chr2:60507316
|
G | GGGGAAGG others(13): Show |
4 | a0001c0001t0035g0080a0001c0001t0039g0142a0001c0001t0060g0216others(1): Show | 4 | HG01981.hp2 HG02258.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-38503_386-3848 others(24): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507316 | ||||||
| chr2:60507316
|
G | GGGGAAGG others(23): Show |
2 | a0001c0002t0001g0023a0001c0002t0004g0077 | 2 | HG02145.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.386-38513_386-3848 others(34): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507316 | ||||||
| chr2:60507316
|
G | GGGGAGGG others(18): Show |
1 | a0001c0002t0017g0010 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.386-38484_386-3848 others(29): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507316 | ||||||
| chr2:60507316
|
GGGGAAGG others(57): Show |
G | 2 | a0001c0001t0003g0170a0001c0001t0015g0185 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386-38547_386-3848 others(68): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507316 | ||||||
| chr2:60507319
|
GA | G | 14 | a0001c0001t0001g0029a0001c0001t0003g0183a0001c0001t0003g0192others(11): Show | 14 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.386-38487delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507319 | ||||||
| chr2:60507321
|
A | G | 16 | a0001c0001t0001g0028a0001c0001t0003g0187a0001c0001t0004g0074others(13): Show | 16 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.386-38488T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507321 | ||||||
| chr2:60507325
|
A | G | 14 | a0001c0001t0001g0029a0001c0001t0003g0183a0001c0001t0003g0192others(11): Show | 14 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.386-38492T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507325 | ||||||
| chr2:60507325
|
AAGGGAAG others(47): Show |
A | 2 | a0001c0001t0010g0015a0001c0001t0037g0068 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.386-38546_386-3849 others(58): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507325 | ||||||
| chr2:60507326
|
A | G | 14 | a0001c0001t0001g0028a0001c0001t0003g0187a0001c0001t0004g0074others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.386-38493T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507326 | ||||||
| chr2:60507330
|
A | G | 14 | a0001c0001t0001g0029a0001c0001t0003g0183a0001c0001t0003g0192others(11): Show | 14 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.386-38497T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507330 | ||||||
| chr2:60507330
|
AAGGGAAG others(42): Show |
A | 6 | a0001c0001t0001g0028a0001c0001t0003g0187a0001c0001t0004g0074others(3): Show | 6 | HG01243.hp2 HG01884.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-38546_386-3849 others(53): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507330 | ||||||
| chr2:60507331
|
A | G | 8 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0019g0012others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-38498T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507331 | ||||||
| chr2:60507335
|
A | G | 13 | a0001c0001t0001g0029a0001c0001t0003g0183a0001c0001t0003g0192others(10): Show | 13 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-38502T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507335 | ||||||
| chr2:60507336
|
A | G | 8 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0019g0012others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-38503T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507336 | ||||||
| chr2:60507340
|
A | G | 10 | a0001c0001t0001g0029a0001c0001t0003g0183a0001c0001t0003g0192others(7): Show | 10 | HG02055.hp1 HG02055.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-38507T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507340 | ||||||
| chr2:60507340
|
AAG | A | 19 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0003g0152others(16): Show | 19 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.386-38509_386-3850 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507340 | ||||||
| chr2:60507340
|
AAGGGAAG others(36): Show |
A | 1 | a0001c0001t0004g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.386-38550_386-3850 others(47): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507340 | ||||||
| chr2:60507341
|
A | G | 8 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0019g0012others(5): Show | 8 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-38508T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507341 | ||||||
| chr2:60507345
|
A | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0058others(10): Show | 13 | HG00642.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.386-38512T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507345 | ||||||
| chr2:60507345
|
AAGGGAAG others(27): Show |
A | 3 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0045g0114 | 3 | HG03098.hp1 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.386-38546_386-3851 others(38): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507345 | ||||||
| chr2:60507345
|
AAGGGAAG others(31): Show |
A | 3 | a0001c0001t0005g0233a0001c0001t0013g0248a0001c0001t0056g0196 | 3 | HG01167.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.386-38550_386-3851 others(42): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507345 | ||||||
| chr2:60507346
|
A | G | 6 | a0001c0001t0019g0012a0001c0001t0038g0069a0001c0001t0061g0212others(3): Show | 6 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-38513T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507346 | ||||||
| chr2:60507350
|
A | G | 5 | a0001c0001t0001g0029a0001c0001t0012g0213a0001c0001t0015g0190others(2): Show | 5 | HG02055.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-38517T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507350 | ||||||
| chr2:60507350
|
AAG | A | 7 | a0001c0001t0001g0031a0001c0001t0003g0152a0001c0001t0004g0078others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-38519_386-3851 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507350 | ||||||
| chr2:60507350
|
AAGGGAAG others(26): Show |
A | 1 | a0001c0001t0003g0183 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.386-38550_386-3851 others(37): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507350 | ||||||
| chr2:60507351
|
A | G | 23 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0058others(20): Show | 23 | HG00323.hp2 HG00642.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.386-38518T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507351 | ||||||
| chr2:60507352
|
G | GGA | 17 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0058others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.386-38520_386-3851 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507352 | ||||||
| chr2:60507355
|
A | G | 49 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0035others(46): Show | 49 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.386-38522T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507355 | ||||||
| chr2:60507355
|
AAGGGAAG others(17): Show |
A | 1 | a0001c0001t0065g0251 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.386-38546_386-3852 others(28): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507355 | ||||||
| chr2:60507355
|
AAGGGAAG others(21): Show |
A | 4 | a0001c0001t0001g0029a0001c0001t0003g0192a0001c0001t0014g0006others(1): Show | 4 | HG02055.hp1 HG03540.hp1 NA20905.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-38550_386-3852 others(32): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507355 | ||||||
| chr2:60507356
|
A | G | 5 | a0001c0001t0019g0012a0001c0001t0038g0069a0001c0001t0061g0212others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-38523T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507356 | ||||||
| chr2:60507360
|
A | G | 4 | a0001c0001t0012g0213a0001c0001t0015g0190a0001c0001t0015g0193others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-38527T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507360 | ||||||
| chr2:60507360
|
AAG | A | 15 | a0001c0001t0001g0031a0001c0001t0001g0038a0001c0001t0001g0039others(12): Show | 15 | HG00642.hp1 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.386-38529_386-3852 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507360 | ||||||
| chr2:60507361
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0049others(32): Show | 35 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.386-38528T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507361 | ||||||
| chr2:60507362
|
G | GGA | 30 | a0001c0001t0001g0021a0001c0001t0001g0035a0001c0001t0001g0049others(27): Show | 30 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.386-38530_386-3852 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507362 | ||||||
| chr2:60507365
|
A | G | 49 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0035others(46): Show | 49 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.386-38532T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507365 | ||||||
| chr2:60507365
|
AAGGGAAG others(7): Show |
A | 1 | a0001c0004t0062g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.386-38546_386-3853 others(18): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507365 | ||||||
| chr2:60507366
|
A | G | 4 | a0001c0001t0019g0012a0001c0001t0038g0069a0001c0001t0061g0212others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-38533T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507366 | ||||||
| chr2:60507370
|
A | G | 4 | a0001c0001t0012g0213a0001c0001t0015g0190a0001c0001t0015g0193others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-38537T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507370 | ||||||
| chr2:60507370
|
AAG | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0038others(23): Show | 26 | HG00323.hp2 HG00642.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.386-38539_386-3853 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507370 | ||||||
| chr2:60507371
|
A | G | 22 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0002g0122others(19): Show | 22 | HG00099.hp1 HG00738.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.386-38538T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507371 | ||||||
| chr2:60507372
|
G | GGA | 19 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0002g0122others(16): Show | 19 | HG00099.hp1 HG00738.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.386-38540_386-3853 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507372 | ||||||
| chr2:60507375
|
A | G | 45 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0035others(42): Show | 45 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.386-38542T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507375 | ||||||
| chr2:60507376
|
A | G | 3 | a0001c0001t0038g0069a0001c0001t0061g0212a0001c0001t0063g0234 | 3 | HG02109.hp1 HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.386-38543T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507376 | ||||||
| chr2:60507379
|
G | A | 3 | a0001c0001t0038g0069a0001c0001t0061g0212a0001c0001t0063g0234 | 3 | HG02109.hp1 HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.386-38546C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507379 | ||||||
| chr2:60507380
|
A | G | 13 | a0001c0001t0001g0028a0001c0001t0003g0187a0001c0001t0004g0074others(10): Show | 13 | HG01243.hp2 HG01884.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-38547T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507380 | ||||||
| chr2:60507380
|
AGGG | A | 4 | a0001c0001t0012g0213a0001c0001t0015g0190a0001c0001t0015g0193others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-38550_386-3854 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507380 | ||||||
| chr2:60507448
|
A | G | 36 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0003g0170others(33): Show | 36 | HG00323.hp2 HG01123.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.385+38523T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507448 | ||||||
| chr2:60507501
|
C | A | 1 | a0001c0001t0030g0026 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.385+38470G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507501 | ||||||
| chr2:60507649
|
C | G | 8 | a0001c0001t0001g0028a0001c0001t0003g0187a0001c0001t0004g0074others(5): Show | 8 | HG01243.hp2 HG01884.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+38322G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507649 | ||||||
| chr2:60507654
|
C | T | 1 | a0001c0001t0008g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.385+38317G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507654 | ||||||
| chr2:60507670
|
G | A | 1 | a0001c0001t0059g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.385+38301C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507670 | ||||||
| chr2:60507769
|
G | C | 1 | a0001c0001t0017g0014 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.385+38202C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507769 | ||||||
| chr2:60507833
|
C | T | 6 | a0001c0001t0003g0170a0001c0001t0013g0253a0001c0001t0016g0254others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+38138G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507833 | ||||||
| chr2:60507866
|
A | T | 1 | a0001c0003t0004g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.385+38105T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60507866 | ||||||
| chr2:60508036
|
C | A | 6 | a0001c0001t0001g0031a0001c0001t0003g0152a0001c0001t0004g0078others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.385+37935G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60508036 | ||||||
| chr2:60508159
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.385+37812T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60508159 | ||||||
| chr2:60508354
|
G | T | 1 | a0001c0002t0017g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.385+37617C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60508354 | ||||||
| chr2:60508741
|
A | G | 1 | a0001c0001t0059g0210 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.385+37230T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60508741 | ||||||
| chr2:60508764
|
G | A | 1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+37207C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60508764 | ||||||
| chr2:60508958
|
T | C | 3 | a0001c0001t0009g0204a0001c0001t0009g0205a0001c0001t0012g0215 | 3 | HG00323.hp2 HG02300.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.385+37013A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60508958 | ||||||
| chr2:60509357
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0003g0187others(3): Show | 6 | HG01884.hp2 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.385+36614G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60509357 | ||||||
| chr2:60509394
|
G | A | 22 | a0001c0001t0001g0029a0001c0001t0003g0152a0001c0001t0003g0183others(19): Show | 22 | HG01167.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.385+36577C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60509394 | ||||||
| chr2:60509622
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.385+36349G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60509622 | ||||||
| chr2:60509702
|
C | T | 70 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.385+36269G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60509702 | ||||||
| chr2:60509717
|
G | A | 13 | a0001c0001t0001g0029a0001c0001t0003g0183a0001c0001t0003g0192others(10): Show | 13 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.385+36254C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60509717 | ||||||
| chr2:60509759
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.385+36212G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60509759 | ||||||
| chr2:60509850
|
T | G | 77 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): Show |
intron_variant | MODIFIER | c.385+36121A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60509850 | ||||||
| chr2:60509969
|
C | A | 2 | a0001c0001t0015g0185a0001c0001t0054g0194 | 2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.385+36002G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60509969 | ||||||
| chr2:60510019
|
G | A | 1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+35952C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510019 | ||||||
| chr2:60510025
|
C | A | 65 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.385+35946G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510025 | ||||||
| chr2:60510138
|
T | C | 1 | a0001c0001t0003g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.385+35833A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510138 | ||||||
| chr2:60510179
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG01884.hp2 HG02615.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+35792G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510179 | ||||||
| chr2:60510266
|
C | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(6): Show | 9 | HG01243.hp2 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.385+35705G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510266 | ||||||
| chr2:60510350
|
A | G | 15 | a0001c0001t0001g0031a0001c0001t0004g0070a0001c0001t0004g0078others(12): Show | 15 | HG00323.hp2 HG01361.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+35621T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510350 | ||||||
| chr2:60510450
|
A | G | 15 | a0001c0001t0001g0031a0001c0001t0004g0070a0001c0001t0004g0078others(12): Show | 15 | HG00323.hp2 HG01361.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+35521T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510450 | ||||||
| chr2:60510637
|
T | C | 1 | a0001c0001t0008g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.385+35334A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510637 | ||||||
| chr2:60510666
|
C | T | 13 | a0001c0001t0003g0183a0001c0001t0003g0192a0001c0001t0004g0076others(10): Show | 13 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.385+35305G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510666 | ||||||
| chr2:60510671
|
C | T | 1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+35300G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510671 | ||||||
| chr2:60510743
|
G | A | 1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+35228C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510743 | ||||||
| chr2:60510842
|
A | G | 15 | a0001c0001t0001g0031a0001c0001t0004g0070a0001c0001t0004g0078others(12): Show | 15 | HG00323.hp2 HG01361.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+35129T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510842 | ||||||
| chr2:60510946
|
A | G | 1 | a0001c0002t0003g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.385+35025T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60510946 | ||||||
| chr2:60511092
|
C | T | 147 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.385+34879G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511092 | ||||||
| chr2:60511148
|
G | T | 1 | a0001c0001t0010g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.385+34823C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511148 | ||||||
| chr2:60511177
|
G | C | 15 | a0001c0001t0001g0031a0001c0001t0004g0070a0001c0001t0004g0078others(12): Show | 15 | HG00323.hp2 HG01361.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+34794C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511177 | ||||||
| chr2:60511224
|
G | A | 15 | a0001c0001t0001g0031a0001c0001t0004g0070a0001c0001t0004g0078others(12): Show | 15 | HG00323.hp2 HG01361.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+34747C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511224 | ||||||
| chr2:60511373
|
A | G | 2 | a0001c0001t0003g0156a0001c0003t0002g0104 | 2 | HG02132.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.385+34598T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511373 | ||||||
| chr2:60511462
|
G | A | 1 | a0001c0001t0006g0243 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.385+34509C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511462 | ||||||
| chr2:60511532
|
T | G | 72 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.385+34439A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511532 | ||||||
| chr2:60511582
|
G | A | 1 | a0001c0001t0042g0138 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.385+34389C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511582 | ||||||
| chr2:60511851
|
A | G | 71 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.385+34120T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511851 | ||||||
| chr2:60511908
|
G | A | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.385+34063C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511908 | ||||||
| chr2:60511926
|
T | A | 71 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.385+34045A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60511926 | ||||||
| chr2:60512006
|
G | A | 1 | a0001c0001t0021g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.385+33965C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60512006 | ||||||
| chr2:60512681
|
T | C | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.385+33290A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60512681 | ||||||
| chr2:60512796
|
C | G | 5 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0037g0068others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+33175G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60512796 | ||||||
| chr2:60512946
|
C | T | 1 | a0001c0001t0047g0176 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.385+33025G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60512946 | ||||||
| chr2:60513033
|
C | T | 1 | a0001c0001t0054g0194 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.385+32938G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513033 | ||||||
| chr2:60513046
|
G | A | 1 | a0001c0002t0004g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.385+32925C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513046 | ||||||
| chr2:60513084
|
G | A | 2 | a0001c0001t0004g0076a0001c0001t0056g0196 | 2 | NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.385+32887C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513084 | ||||||
| chr2:60513153
|
G | A | 1 | a0001c0001t0061g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.385+32818C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513153 | ||||||
| chr2:60513188
|
G | A | 75 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.385+32783C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513188 | ||||||
| chr2:60513356
|
C | T | 54 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.385+32615G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513356 | ||||||
| chr2:60513389
|
T | C | 13 | a0001c0001t0001g0031a0001c0001t0004g0070a0001c0001t0004g0078others(10): Show | 13 | HG00323.hp2 HG01123.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.385+32582A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513389 | ||||||
| chr2:60513393
|
G | A | 1 | a0001c0001t0061g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.385+32578C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513393 | ||||||
| chr2:60513487
|
G | A | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+32484C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513487 | ||||||
| chr2:60513702
|
G | T | 1 | a0001c0004t0062g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.385+32269C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513702 | ||||||
| chr2:60513825
|
T | G | 2 | a0001c0001t0038g0069a0001c0001t0061g0212 | 2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.385+32146A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513825 | ||||||
| chr2:60513893
|
G | C | 3 | a0001c0001t0021g0102a0001c0001t0032g0037a0001c0001t0064g0247 | 3 | HG02572.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.385+32078C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513893 | ||||||
| chr2:60513927
|
C | A | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.385+32044G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60513927 | ||||||
| chr2:60514285
|
C | T | 1 | a0001c0002t0017g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.385+31686G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514285 | ||||||
| chr2:60514347
|
A | G | 3 | a0001c0001t0035g0080a0001c0001t0039g0142a0001c0001t0060g0216 | 3 | HG01981.hp2 HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.385+31624T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514347 | ||||||
| chr2:60514385
|
G | A | 21 | a0001c0001t0005g0223a0001c0001t0010g0050a0001c0001t0010g0057others(18): Show | 21 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.385+31586C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514385 | ||||||
| chr2:60514428
|
G | A | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+31543C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514428 | ||||||
| chr2:60514495
|
T | TA | 6 | a0001c0001t0009g0204a0001c0001t0012g0215a0001c0001t0037g0068others(3): Show | 6 | HG01358.hp1 HG02080.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+31475dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514495 | ||||||
| chr2:60514495
|
TA | T | 5 | a0001c0001t0001g0028a0001c0001t0004g0074a0001c0001t0005g0228others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+31475delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514495 | ||||||
| chr2:60514495
|
TAAA | T | 48 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.385+31473_385+3147 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514495 | ||||||
| chr2:60514495
|
TAAAA | T | 5 | a0001c0001t0002g0136a0001c0001t0011g0150a0001c0001t0055g0202others(2): Show | 5 | HG01074.hp2 HG01256.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+31472_385+3147 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514495 | ||||||
| chr2:60514599
|
C | T | 1 | a0001c0001t0005g0231 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.385+31372G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514599 | ||||||
| chr2:60514851
|
A | T | 1 | a0001c0001t0002g0144 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.385+31120T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514851 | ||||||
| chr2:60514873
|
G | GA | 50 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.385+31097dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514873 | ||||||
| chr2:60514881
|
A | G | 5 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0037g0068others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+31090T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514881 | ||||||
| chr2:60514992
|
G | A | 1 | a0001c0001t0006g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.385+30979C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60514992 | ||||||
| chr2:60515039
|
T | A | 5 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0037g0068others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+30932A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515039 | ||||||
| chr2:60515110
|
C | T | 5 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(2): Show | 5 | HG02055.hp1 HG03540.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+30861G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515110 | ||||||
| chr2:60515126
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.385+30845G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515126 | ||||||
| chr2:60515290
|
C | T | 54 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.385+30681G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515290 | ||||||
| chr2:60515354
|
G | A | 3 | a0001c0001t0003g0152a0001c0001t0011g0150a0001c0001t0011g0151 | 3 | HG01256.hp1 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.385+30617C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515354 | ||||||
| chr2:60515437
|
C | T | 54 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.385+30534G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515437 | ||||||
| chr2:60515451
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0004g0088 | 2 | HG02080.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.385+30520C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515451 | ||||||
| chr2:60515570
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.385+30401C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515570 | ||||||
| chr2:60515869
|
G | A | 1 | a0001c0001t0005g0228 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.385+30102C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515869 | ||||||
| chr2:60515915
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0007g0095 | 2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.385+30056C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515915 | ||||||
| chr2:60515961
|
C | T | 1 | a0001c0001t0003g0172 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.385+30010G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60515961 | ||||||
| chr2:60516024
|
C | A | 1 | a0001c0001t0002g0119 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.385+29947G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516024 | ||||||
| chr2:60516092
|
T | A | 1 | a0001c0001t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.385+29879A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516092 | ||||||
| chr2:60516131
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.385+29840C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516131 | ||||||
| chr2:60516470
|
A | G | 10 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(7): Show | 10 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+29501T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516470 | ||||||
| chr2:60516491
|
G | A | 4 | a0001c0001t0012g0213a0001c0001t0015g0190a0001c0001t0015g0193others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+29480C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516491 | ||||||
| chr2:60516540
|
T | A | 54 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.385+29431A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516540 | ||||||
| chr2:60516545
|
G | A | 1 | a0001c0001t0003g0173 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.385+29426C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516545 | ||||||
| chr2:60516625
|
A | G | 1 | a0001c0001t0005g0228 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.385+29346T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516625 | ||||||
| chr2:60516788
|
G | A | 1 | a0001c0001t0004g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.385+29183C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516788 | ||||||
| chr2:60516898
|
C | A | 2 | a0001c0001t0003g0173a0001c0001t0003g0177 | 2 | HG02129.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.385+29073G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516898 | ||||||
| chr2:60516907
|
G | C | 1 | a0001c0001t0011g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.385+29064C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516907 | ||||||
| chr2:60516987
|
G | T | 5 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0037g0068others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+28984C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516987 | ||||||
| chr2:60516988
|
T | TATTTA | 5 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0037g0068others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+28982_385+2898 others(9): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60516988 | ||||||
| chr2:60517143
|
G | T | 1 | a0001c0001t0009g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.385+28828C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517143 | ||||||
| chr2:60517179
|
A | G | 1 | a0001c0001t0054g0194 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.385+28792T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517179 | ||||||
| chr2:60517196
|
A | G | 149 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0038others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.385+28775T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517196 | ||||||
| chr2:60517323
|
C | A | 1 | a0001c0001t0006g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.385+28648G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517323 | ||||||
| chr2:60517461
|
G | A | 1 | a0001c0001t0008g0132 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385+28510C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517461 | ||||||
| chr2:60517498
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.385+28473G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517498 | ||||||
| chr2:60517737
|
T | G | 152 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0035others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.385+28234A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517737 | ||||||
| chr2:60517861
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0002g0144others(1): Show | 4 | HG00642.hp1 HG01256.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+28110C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517861 | ||||||
| chr2:60517937
|
A | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG01884.hp2 HG02083.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+28034T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517937 | ||||||
| chr2:60517939
|
A | C | 12 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG01884.hp2 HG02083.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+28032T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517939 | ||||||
| chr2:60517941
|
C | CATGCATG others(169): Show |
12 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(9): Show | 12 | HG01884.hp2 HG02083.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+28029_385+2803 others(180): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60517941 | ||||||
| chr2:60518058
|
A | T | 1 | a0001c0002t0008g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.385+27913T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518058 | ||||||
| chr2:60518157
|
T | G | 1 | a0001c0002t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.385+27814A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518157 | ||||||
| chr2:60518217
|
T | A | 1 | a0001c0003t0004g0079 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.385+27754A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518217 | ||||||
| chr2:60518237
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0003g0160 | 2 | HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.385+27734T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518237 | ||||||
| chr2:60518261
|
C | T | 56 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.385+27710G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518261 | ||||||
| chr2:60518337
|
G | A | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385+27634C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518337 | ||||||
| chr2:60518344
|
A | C | 1 | a0001c0002t0017g0011 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.385+27627T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518344 | ||||||
| chr2:60518931
|
G | A | 5 | a0001c0001t0013g0253a0001c0001t0016g0254a0001c0001t0037g0068others(2): Show | 5 | HG02809.hp1 HG02818.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+27040C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518931 | ||||||
| chr2:60518967
|
C | A | 1 | a0001c0001t0034g0066 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.385+27004G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60518967 | ||||||
| chr2:60519076
|
C | A | 2 | a0001c0001t0003g0192a0001c0001t0014g0006 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.385+26895G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519076 | ||||||
| chr2:60519374
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.385+26597T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519374 | ||||||
| chr2:60519539
|
T | TTGCC | 124 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.385+26428_385+2643 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519539 | ||||||
| chr2:60519539
|
T | TTGCCTGC others(5): Show |
5 | a0001c0001t0004g0084a0001c0001t0004g0087a0001c0001t0025g0003others(2): Show | 5 | HG00280.hp2 HG01943.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+26420_385+2643 others(16): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519539 | ||||||
| chr2:60519539
|
T | TTGCCTGC others(9): Show |
9 | a0001c0001t0002g0001a0001c0001t0003g0149a0001c0001t0004g0086others(6): Show | 11 | HG00733.hp1 HG00741.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.385+26416_385+2643 others(20): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519539 | ||||||
| chr2:60519539
|
TTGCC | T | 10 | a0001c0001t0003g0183a0001c0001t0009g0197a0001c0001t0012g0218others(7): Show | 10 | HG02083.hp2 HG02809.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.385+26428_385+2643 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519539 | ||||||
| chr2:60519539
|
TTGCCTGC others(1): Show |
T | 2 | a0001c0001t0019g0012a0001c0001t0063g0234 | 2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.385+26424_385+2643 others(12): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519539 | ||||||
| chr2:60519539
|
TTGCCTGC others(5): Show |
T | 1 | a0001c0002t0001g0023 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.385+26420_385+2643 others(16): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519539 | ||||||
| chr2:60519772
|
C | T | 2 | a0001c0001t0002g0094a0001c0001t0006g0245 | 2 | HG01123.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.385+26199G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519772 | ||||||
| chr2:60519984
|
T | C | 3 | a0001c0001t0003g0158a0001c0001t0015g0162a0001c0001t0057g0208 | 3 | NA18962.hp1 NA18990.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.385+25987A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60519984 | ||||||
| chr2:60520057
|
T | C | 158 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.385+25914A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60520057 | ||||||
| chr2:60520414
|
T | C | 1 | a0001c0001t0004g0070 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.385+25557A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60520414 | ||||||
| chr2:60520527
|
G | A | 1 | a0001c0001t0020g0041 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.385+25444C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60520527 | ||||||
| chr2:60520528
|
C | A | 55 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.385+25443G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60520528 | ||||||
| chr2:60520608
|
T | C | 151 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0038others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.385+25363A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60520608 | ||||||
| chr2:60520756
|
G | T | 1 | a0001c0001t0018g0211 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+25215C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60520756 | ||||||
| chr2:60520830
|
C | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385+25141G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60520830 | ||||||
| chr2:60520856
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.385+25115G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60520856 | ||||||
| chr2:60521003
|
T | A | 1 | a0001c0001t0004g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.385+24968A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521003 | ||||||
| chr2:60521041
|
G | A | 3 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0018g0207 | 3 | HG00597.hp1 HG02027.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.385+24930C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521041 | ||||||
| chr2:60521067
|
G | GCA | 12 | a0001c0001t0001g0043a0001c0001t0003g0182a0001c0001t0003g0183others(9): Show | 12 | HG01167.hp1 HG01243.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.385+24902_385+2490 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521067 | ||||||
| chr2:60521067
|
G | GCACA | 6 | a0001c0001t0012g0213a0001c0001t0015g0185a0001c0001t0015g0190others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+24900_385+2490 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521067 | ||||||
| chr2:60521067
|
G | GCACACA | 4 | a0001c0001t0003g0187a0001c0001t0011g0188a0001c0001t0012g0218others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+24898_385+2490 others(10): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521067 | ||||||
| chr2:60521067
|
G | GCACACAC others(3): Show |
2 | a0001c0001t0001g0029a0001c0001t0004g0074 | 2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.385+24894_385+2490 others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521067 | ||||||
| chr2:60521067
|
GCA | G | 7 | a0001c0001t0006g0239a0001c0001t0013g0253a0001c0001t0019g0012others(4): Show | 7 | HG00280.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+24902_385+2490 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521067 | ||||||
| chr2:60521067
|
GCACA | G | 13 | a0001c0001t0001g0031a0001c0001t0004g0078a0001c0001t0005g0219others(10): Show | 13 | HG01123.hp2 HG01361.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.385+24900_385+2490 others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521067 | ||||||
| chr2:60521067
|
GCACACA | G | 4 | a0001c0001t0002g0101a0001c0001t0009g0204a0001c0001t0009g0205others(1): Show | 4 | HG00323.hp1 HG00323.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+24898_385+2490 others(10): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521067 | ||||||
| chr2:60521069
|
A | G | 1 | a0001c0001t0005g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.385+24902T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521069 | ||||||
| chr2:60521093
|
A | T | 4 | a0001c0001t0001g0059a0001c0001t0002g0123a0001c0001t0003g0147others(1): Show | 4 | HG00733.hp2 HG02293.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+24878T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521093 | ||||||
| chr2:60521095
|
A | T | 118 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0035others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.385+24876T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521095 | ||||||
| chr2:60521097
|
A | T | 16 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0002g0001others(13): Show | 18 | HG00423.hp2 HG00733.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.385+24874T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521097 | ||||||
| chr2:60521098
|
CACTCACA | C | 3 | a0001c0001t0002g0123a0001c0001t0003g0147a0001c0001t0005g0226 | 3 | HG02293.hp2 NA18988.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.385+24866_385+2487 others(11): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521098 | ||||||
| chr2:60521099
|
A | T | 1 | a0001c0001t0004g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.385+24872T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521099 | ||||||
| chr2:60521100
|
CTCACA | C | 118 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0035others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.385+24866_385+2487 others(9): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521100 | ||||||
| chr2:60521101
|
T | A | 18 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0059others(15): Show | 20 | HG00423.hp2 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.385+24870A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521101 | ||||||
| chr2:60521102
|
CACA | C | 16 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0002g0001others(13): Show | 18 | HG00423.hp2 HG00733.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.385+24866_385+2486 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521102 | ||||||
| chr2:60521105
|
A | AC | 11 | a0001c0001t0003g0152a0001c0001t0003g0192a0001c0001t0005g0233others(8): Show | 11 | HG01167.hp1 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.385+24865dupG | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521105 | ||||||
| chr2:60521105
|
A | T | 2 | a0001c0001t0038g0069a0001c0001t0061g0212 | 2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.385+24866T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521105 | ||||||
| chr2:60521113
|
A | T | 1 | a0001c0001t0001g0059 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.385+24858T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521113 | ||||||
| chr2:60521123
|
A | T | 1 | a0001c0001t0002g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.385+24848T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521123 | ||||||
| chr2:60521156
|
T | C | 1 | a0001c0001t0061g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.385+24815A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521156 | ||||||
| chr2:60521352
|
G | A | 2 | a0001c0001t0003g0192a0001c0001t0014g0006 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.385+24619C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521352 | ||||||
| chr2:60521357
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.385+24614G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521357 | ||||||
| chr2:60521396
|
T | C | 4 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0002g0144others(1): Show | 4 | HG00642.hp1 HG01256.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+24575A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521396 | ||||||
| chr2:60521434
|
G | C | 1 | a0001c0001t0008g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.385+24537C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521434 | ||||||
| chr2:60521477
|
C | T | 3 | a0001c0001t0003g0152a0001c0001t0011g0150a0001c0001t0011g0151 | 3 | HG01256.hp1 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.385+24494G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521477 | ||||||
| chr2:60521623
|
A | G | 142 | a0001c0001t0001g0025a0001c0001t0001g0033a0001c0001t0001g0035others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.385+24348T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521623 | ||||||
| chr2:60521810
|
T | C | 169 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(166): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.385+24161A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521810 | ||||||
| chr2:60521943
|
T | G | 158 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.385+24028A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521943 | ||||||
| chr2:60521974
|
T | C | 158 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.385+23997A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60521974 | ||||||
| chr2:60522027
|
G | T | 1 | a0001c0001t0010g0050 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.385+23944C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522027 | ||||||
| chr2:60522306
|
T | C | 2 | a0001c0001t0003g0181a0001c0001t0008g0132 | 2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.385+23665A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522306 | ||||||
| chr2:60522313
|
T | C | 1 | a0001c0001t0013g0249 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.385+23658A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522313 | ||||||
| chr2:60522323
|
T | C | 1 | a0001c0001t0061g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.385+23648A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522323 | ||||||
| chr2:60522386
|
A | C | 12 | a0001c0001t0001g0034a0001c0001t0002g0110a0001c0001t0007g0099others(9): Show | 12 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+23585T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522386 | ||||||
| chr2:60522491
|
TCAAGACT others(8): Show |
T | 3 | a0001c0001t0038g0069a0001c0001t0054g0194a0001c0001t0061g0212 | 3 | HG01243.hp2 HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.385+23465_385+2347 others(19): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522491 | ||||||
| chr2:60522698
|
T | C | 1 | a0001c0001t0063g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+23273A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522698 | ||||||
| chr2:60522837
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.385+23134G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522837 | ||||||
| chr2:60522843
|
A | C | 2 | a0001c0001t0015g0185a0001c0001t0056g0196 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.385+23128T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60522843 | ||||||
| chr2:60523020
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385+22951A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523020 | ||||||
| chr2:60523168
|
C | T | 9 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(6): Show | 9 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.385+22803G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523168 | ||||||
| chr2:60523190
|
G | C | 3 | a0001c0001t0021g0102a0001c0001t0032g0037a0001c0001t0064g0247 | 3 | HG02572.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.385+22781C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523190 | ||||||
| chr2:60523425
|
T | A | 1 | a0001c0001t0037g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.385+22546A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523425 | ||||||
| chr2:60523425
|
T | C | 165 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.385+22546A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523425 | ||||||
| chr2:60523651
|
AT | A | 35 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.385+22319delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523651 | ||||||
| chr2:60523771
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.385+22200C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523771 | ||||||
| chr2:60523847
|
C | T | 3 | a0001c0001t0016g0254a0001c0001t0065g0251a0001c0004t0062g0235 | 3 | HG02818.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.385+22124G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523847 | ||||||
| chr2:60523898
|
A | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 8 | HG01884.hp2 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.385+22073T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60523898 | ||||||
| chr2:60524015
|
CA | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG01884.hp2 HG02615.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+21955delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60524015 | ||||||
| chr2:60524333
|
A | G | 1 | a0001c0002t0001g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.385+21638T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60524333 | ||||||
| chr2:60524390
|
G | A | 1 | a0001c0001t0048g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.385+21581C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60524390 | ||||||
| chr2:60524445
|
A | T | 1 | a0001c0001t0015g0193 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.385+21526T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60524445 | ||||||
| chr2:60524534
|
C | T | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+21437G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60524534 | ||||||
| chr2:60524560
|
TG | T | 53 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.385+21410delC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60524560 | ||||||
| chr2:60525571
|
G | C | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+20400C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60525571 | ||||||
| chr2:60525968
|
T | C | 5 | a0001c0001t0004g0084a0001c0001t0004g0086a0001c0001t0004g0087others(2): Show | 5 | HG01358.hp2 HG01943.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+20003A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60525968 | ||||||
| chr2:60525980
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.385+19991A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60525980 | ||||||
| chr2:60526138
|
C | A | 1 | a0001c0001t0003g0145 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.385+19833G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60526138 | ||||||
| chr2:60526458
|
C | G | 159 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0028others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.385+19513G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60526458 | ||||||
| chr2:60526644
|
C | T | 2 | a0001c0001t0038g0069a0001c0001t0061g0212 | 2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.385+19327G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60526644 | ||||||
| chr2:60526758
|
G | A | 2 | a0001c0001t0003g0183a0001c0001t0012g0218 | 2 | HG02083.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.385+19213C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60526758 | ||||||
| chr2:60526820
|
T | C | 2 | a0001c0002t0001g0023a0001c0002t0004g0077 | 2 | HG02145.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.385+19151A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60526820 | ||||||
| chr2:60527112
|
C | A | 1 | a0001c0001t0010g0030 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.385+18859G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60527112 | ||||||
| chr2:60527257
|
C | G | 1 | a0001c0001t0003g0175 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.385+18714G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60527257 | ||||||
| chr2:60527971
|
G | A | 2 | a0001c0001t0005g0227a0001c0001t0022g0180 | 2 | HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.385+18000C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60527971 | ||||||
| chr2:60528078
|
G | C | 6 | a0001c0001t0002g0106a0001c0001t0002g0118a0001c0003t0002g0107others(3): Show | 6 | HG01167.hp2 HG01169.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+17893C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528078 | ||||||
| chr2:60528099
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.385+17872C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528099 | ||||||
| chr2:60528130
|
T | C | 1 | a0001c0001t0006g0246 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.385+17841A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528130 | ||||||
| chr2:60528149
|
C | T | 1 | a0001c0001t0003g0157 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.385+17822G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528149 | ||||||
| chr2:60528295
|
G | A | 2 | a0001c0002t0001g0023a0001c0002t0004g0077 | 2 | HG02145.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.385+17676C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528295 | ||||||
| chr2:60528513
|
T | C | 1 | a0001c0002t0004g0075 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.385+17458A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528513 | ||||||
| chr2:60528529
|
T | C | 1 | a0001c0001t0005g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.385+17442A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528529 | ||||||
| chr2:60528627
|
C | T | 11 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(8): Show | 11 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.385+17344G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528627 | ||||||
| chr2:60528628
|
G | A | 31 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(28): Show | 31 | HG00323.hp2 HG01123.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.385+17343C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528628 | ||||||
| chr2:60528632
|
T | C | 1 | a0001c0001t0021g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.385+17339A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528632 | ||||||
| chr2:60528663
|
C | T | 10 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(7): Show | 10 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+17308G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528663 | ||||||
| chr2:60528808
|
GTAA | G | 11 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(8): Show | 11 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.385+17160_385+1716 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528808 | ||||||
| chr2:60528830
|
T | C | 1 | a0001c0001t0012g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.385+17141A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60528830 | ||||||
| chr2:60529048
|
C | T | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.385+16923G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529048 | ||||||
| chr2:60529080
|
G | A | 1 | a0001c0001t0049g0165 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.385+16891C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529080 | ||||||
| chr2:60529345
|
T | C | 250 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.385+16626A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529345 | ||||||
| chr2:60529369
|
C | T | 10 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(7): Show | 10 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+16602G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529369 | ||||||
| chr2:60529537
|
T | C | 2 | a0001c0001t0010g0015a0001c0001t0054g0194 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385+16434A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529537 | ||||||
| chr2:60529620
|
C | G | 10 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(7): Show | 10 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+16351G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529620 | ||||||
| chr2:60529926
|
T | C | 1 | a0001c0001t0003g0175 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.385+16045A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529926 | ||||||
| chr2:60529975
|
C | T | 1 | a0001c0001t0004g0081 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.385+15996G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529975 | ||||||
| chr2:60529995
|
A | C | 9 | a0001c0001t0003g0192a0001c0001t0004g0076a0001c0001t0005g0233others(6): Show | 9 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.385+15976T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60529995 | ||||||
| chr2:60530284
|
C | T | 137 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0038others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.385+15687G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530284 | ||||||
| chr2:60530307
|
T | A | 1 | a0001c0001t0011g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.385+15664A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530307 | ||||||
| chr2:60530332
|
T | TA | 114 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0038others(111): Show | 116 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.385+15638dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530332 | ||||||
| chr2:60530332
|
T | TAA | 15 | a0001c0001t0005g0229a0001c0001t0006g0242a0001c0001t0006g0245others(12): Show | 15 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+15637_385+1563 others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530332 | ||||||
| chr2:60530332
|
T | TAAA | 21 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0004g0070others(18): Show | 21 | HG00323.hp2 HG01123.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.385+15636_385+1563 others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530332 | ||||||
| chr2:60530332
|
TA | T | 5 | a0001c0001t0002g0118a0001c0001t0011g0150a0001c0001t0019g0012others(2): Show | 5 | HG01169.hp2 HG01256.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+15638delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530332 | ||||||
| chr2:60530422
|
C | T | 1 | a0001c0003t0003g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.385+15549G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530422 | ||||||
| chr2:60530640
|
A | C | 5 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0005g0224others(2): Show | 5 | HG00597.hp1 HG02027.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+15331T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530640 | ||||||
| chr2:60530654
|
GATGTACA others(10): Show |
G | 1 | a0001c0002t0014g0007 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.385+15300_385+1531 others(21): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530654 | ||||||
| chr2:60530667
|
C | G | 12 | a0001c0001t0001g0029a0001c0001t0003g0187a0001c0001t0003g0192others(9): Show | 12 | HG01167.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+15304G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530667 | ||||||
| chr2:60530900
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.385+15071G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530900 | ||||||
| chr2:60530948
|
C | T | 1 | a0001c0002t0001g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.385+15023G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60530948 | ||||||
| chr2:60531032
|
T | C | 2 | a0001c0001t0003g0183a0001c0001t0012g0218 | 2 | HG02083.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.385+14939A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60531032 | ||||||
| chr2:60531038
|
T | C | 1 | a0001c0001t0043g0109 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.385+14933A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60531038 | ||||||
| chr2:60531169
|
A | G | 3 | a0001c0001t0003g0152a0001c0001t0011g0150a0001c0001t0011g0151 | 3 | HG01256.hp1 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.385+14802T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60531169 | ||||||
| chr2:60531292
|
C | T | 1 | a0001c0001t0009g0197 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.385+14679G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60531292 | ||||||
| chr2:60531624
|
T | C | 4 | a0001c0001t0015g0185a0001c0001t0019g0012a0001c0001t0038g0069others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+14347A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60531624 | ||||||
| chr2:60531895
|
T | C | 1 | a0001c0001t0038g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.385+14076A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60531895 | ||||||
| chr2:60531908
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.385+14063G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60531908 | ||||||
| chr2:60532113
|
C | G | 1 | a0001c0001t0003g0175 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.385+13858G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60532113 | ||||||
| chr2:60532328
|
GT | G | 14 | a0001c0001t0003g0152a0001c0001t0003g0192a0001c0001t0004g0076others(11): Show | 14 | HG01167.hp1 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.385+13642delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60532328 | ||||||
| chr2:60532565
|
G | A | 1 | a0001c0002t0002g0120 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.385+13406C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60532565 | ||||||
| chr2:60532612
|
G | T | 197 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.385+13359C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60532612 | ||||||
| chr2:60532656
|
T | C | 1 | a0001c0004t0058g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.385+13315A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60532656 | ||||||
| chr2:60532741
|
G | A | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+13230C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60532741 | ||||||
| chr2:60532897
|
C | A | 186 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.385+13074G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60532897 | ||||||
| chr2:60532974
|
T | C | 1 | a0001c0001t0003g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.385+12997A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60532974 | ||||||
| chr2:60533028
|
A | G | 2 | a0001c0001t0001g0045a0001c0002t0004g0073 | 2 | HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.385+12943T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60533028 | ||||||
| chr2:60533377
|
C | G | 1 | a0001c0003t0002g0108 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.385+12594G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60533377 | ||||||
| chr2:60533502
|
G | A | 186 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.385+12469C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60533502 | ||||||
| chr2:60533606
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.385+12365G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60533606 | ||||||
| chr2:60534351
|
C | T | 3 | a0001c0001t0003g0181a0001c0001t0008g0129a0001c0001t0008g0132 | 3 | HG02738.hp1 HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.385+11620G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60534351 | ||||||
| chr2:60534424
|
G | A | 2 | a0001c0001t0038g0069a0001c0001t0066g0258 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.385+11547C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60534424 | ||||||
| chr2:60534864
|
T | C | 1 | a0001c0001t0009g0197 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.385+11107A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60534864 | ||||||
| chr2:60534920
|
A | T | 1 | a0001c0001t0018g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.385+11051T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60534920 | ||||||
| chr2:60535028
|
C | T | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385+10943G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60535028 | ||||||
| chr2:60535367
|
T | G | 188 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.385+10604A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60535367 | ||||||
| chr2:60535420
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.385+10551A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60535420 | ||||||
| chr2:60535445
|
A | G | 2 | a0001c0001t0011g0150a0001c0001t0011g0151 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.385+10526T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60535445 | ||||||
| chr2:60535967
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.385+10004C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60535967 | ||||||
| chr2:60536032
|
T | C | 2 | a0001c0001t0038g0069a0001c0001t0066g0258 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.385+9939A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60536032 | ||||||
| chr2:60536034
|
T | C | 2 | a0001c0001t0038g0069a0001c0001t0066g0258 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.385+9937A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60536034 | ||||||
| chr2:60536603
|
A | G | 2 | a0001c0001t0002g0097a0001c0001t0002g0122 | 2 | NA18944.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.385+9368T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60536603 | ||||||
| chr2:60537176
|
TTAACA | T | 132 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(129): Show | 134 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.385+8790_385+8794d others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60537176 | ||||||
| chr2:60537199
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(7): Show | 10 | HG01257.hp1 HG01358.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+8772C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60537199 | ||||||
| chr2:60537474
|
G | C | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+8497C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60537474 | ||||||
| chr2:60537541
|
G | A | 1 | a0001c0001t0007g0113 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.385+8430C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60537541 | ||||||
| chr2:60537806
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(7): Show | 10 | HG01257.hp1 HG01358.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+8165C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60537806 | ||||||
| chr2:60537909
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.385+8062G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60537909 | ||||||
| chr2:60538158
|
G | C | 1 | a0001c0001t0002g0127 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.385+7813C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538158 | ||||||
| chr2:60538230
|
T | C | 2 | a0001c0001t0030g0026a0001c0002t0004g0075 | 2 | HG03688.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385+7741A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538230 | ||||||
| chr2:60538298
|
C | T | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+7673G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538298 | ||||||
| chr2:60538380
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.385+7591G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538380 | ||||||
| chr2:60538719
|
GTC | G | 10 | a0001c0001t0001g0025a0001c0001t0003g0181a0001c0001t0005g0233others(7): Show | 10 | HG00735.hp2 HG01167.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.385+7250_385+7251d others(4): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538719 | ||||||
| chr2:60538719
|
GTCTC | G | 8 | a0001c0001t0003g0192a0001c0001t0004g0085a0001c0001t0011g0150others(5): Show | 8 | HG01256.hp1 HG01258.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+7248_385+7251d others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538719 | ||||||
| chr2:60538733
|
CTCTCTCT others(1): Show |
C | 4 | a0001c0001t0003g0187a0001c0001t0004g0074a0001c0001t0011g0188others(1): Show | 4 | HG01884.hp2 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+7230_385+7237d others(10): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538733 | ||||||
| chr2:60538735
|
CTCTCTG | C | 6 | a0001c0001t0003g0152a0001c0001t0012g0218a0001c0001t0014g0006others(3): Show | 6 | HG00099.hp2 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+7230_385+7235d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538735 | ||||||
| chr2:60538735
|
CTCTCTGT others(5): Show |
C | 1 | a0001c0003t0009g0199 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.385+7224_385+7235d others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538735 | ||||||
| chr2:60538737
|
C | G | 3 | a0001c0001t0004g0076a0001c0001t0053g0191a0001c0004t0058g0206 | 3 | HG02055.hp2 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.385+7234G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538737 | ||||||
| chr2:60538737
|
CTCTG | C | 12 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0063others(9): Show | 12 | HG00733.hp1 HG01168.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+7230_385+7233d others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538737 | ||||||
| chr2:60538737
|
CTCTGTG | C | 93 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(90): Show | 95 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.385+7228_385+7233d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538737 | ||||||
| chr2:60538737
|
CTCTGTGT others(1): Show |
C | 11 | a0001c0001t0001g0033a0001c0001t0002g0127a0001c0001t0008g0116others(8): Show | 11 | HG00423.hp2 HG01074.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.385+7226_385+7233d others(10): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538737 | ||||||
| chr2:60538737
|
CTCTGTGT others(3): Show |
C | 3 | a0001c0001t0005g0228a0001c0002t0002g0121a0001c0003t0041g0135 | 3 | HG01071.hp2 HG02897.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.385+7224_385+7233d others(12): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538737 | ||||||
| chr2:60538737
|
CTCTGTGT others(5): Show |
C | 1 | a0003c0008t0003g0154 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.385+7222_385+7233d others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538737 | ||||||
| chr2:60538737
|
CTCTGTGT others(13): Show |
C | 1 | a0001c0001t0047g0176 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.385+7214_385+7233d others(22): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538737 | ||||||
| chr2:60538739
|
C | G | 9 | a0001c0001t0003g0156a0001c0001t0004g0076a0001c0001t0005g0233others(6): Show | 9 | HG01361.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.385+7232G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538739 | ||||||
| chr2:60538739
|
CTG | C | 22 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0002g0090others(19): Show | 22 | HG00741.hp1 HG01071.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.385+7230_385+7231d others(4): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538739 | ||||||
| chr2:60538739
|
CTGTG | C | 31 | a0001c0001t0001g0045a0001c0001t0001g0059a0001c0001t0002g0106others(28): Show | 31 | HG00544.hp1 HG00733.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.385+7228_385+7231d others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538739 | ||||||
| chr2:60538739
|
CTGTGTG | C | 16 | a0001c0001t0002g0101a0001c0001t0002g0110a0001c0001t0003g0175others(13): Show | 16 | HG00323.hp1 HG01081.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.385+7226_385+7231d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538739 | ||||||
| chr2:60538739
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0048g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.385+7220_385+7231d others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538739 | ||||||
| chr2:60538741
|
G | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0036others(12): Show | 15 | HG00323.hp2 HG01123.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+7230C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538741 | ||||||
| chr2:60538743
|
G | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0003g0189others(8): Show | 11 | HG01071.hp1 HG01257.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.385+7228C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538743 | ||||||
| chr2:60538745
|
G | C | 5 | a0001c0001t0004g0078a0001c0001t0005g0219a0001c0001t0013g0252others(2): Show | 5 | HG01361.hp1 HG03130.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+7226C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538745 | ||||||
| chr2:60538747
|
G | C | 1 | a0001c0001t0066g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385+7224C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538747 | ||||||
| chr2:60538791
|
G | A | 1 | a0001c0001t0022g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.385+7180C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538791 | ||||||
| chr2:60538826
|
CACTGTAC others(27): Show |
C | 1 | a0001c0003t0009g0199 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.385+7111_385+7144d others(36): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538826 | ||||||
| chr2:60538829
|
T | C | 2 | a0001c0001t0015g0190a0001c0001t0053g0191 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.385+7142A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538829 | ||||||
| chr2:60538983
|
GAATTGGG others(126): Show |
G | 1 | a0001c0003t0009g0199 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.385+6855_385+6987d others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60538983 | ||||||
| chr2:60539093
|
G | A | 2 | a0001c0001t0051g0159a0001c0001t0052g0166 | 2 | NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.385+6878C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539093 | ||||||
| chr2:60539125
|
T | G | 1 | a0001c0003t0009g0199 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.385+6846A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539125 | ||||||
| chr2:60539250
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.385+6721G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539250 | ||||||
| chr2:60539285
|
G | A | 2 | a0001c0001t0005g0221a0001c0001t0005g0222 | 2 | HG01515.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.385+6686C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539285 | ||||||
| chr2:60539366
|
C | G | 1 | a0001c0001t0018g0209 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.385+6605G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539366 | ||||||
| chr2:60539420
|
G | A | 1 | a0001c0001t0006g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.385+6551C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539420 | ||||||
| chr2:60539552
|
C | T | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385+6419G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539552 | ||||||
| chr2:60539569
|
C | T | 3 | a0001c0001t0003g0192a0001c0001t0014g0006a0001c0001t0015g0193 | 3 | HG02055.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.385+6402G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539569 | ||||||
| chr2:60539824
|
G | A | 1 | a0001c0002t0014g0008 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.385+6147C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60539824 | ||||||
| chr2:60540203
|
A | C | 1 | a0001c0001t0045g0114 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.385+5768T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540203 | ||||||
| chr2:60540212
|
C | A | 1 | a0001c0001t0015g0185 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385+5759G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540212 | ||||||
| chr2:60540287
|
T | G | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+5684A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540287 | ||||||
| chr2:60540437
|
G | A | 1 | a0001c0001t0012g0218 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.385+5534C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540437 | ||||||
| chr2:60540487
|
C | A | 1 | a0001c0001t0004g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.385+5484G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540487 | ||||||
| chr2:60540690
|
G | T | 1 | a0001c0001t0011g0002 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.385+5281C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540690 | ||||||
| chr2:60540843
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.385+5128G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540843 | ||||||
| chr2:60540943
|
GT | G | 3 | a0001c0001t0002g0090a0001c0001t0002g0144a0001c0009t0001g0017 | 3 | HG00642.hp1 HG02004.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.385+5027delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540943 | ||||||
| chr2:60540946
|
T | TG | 3 | a0001c0001t0001g0029a0001c0001t0002g0091a0001c0001t0012g0213 | 3 | HG02135.hp1 NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.385+5024_385+5025i others(3): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TGTGTG | 4 | a0001c0001t0005g0228a0001c0001t0008g0132a0001c0001t0022g0179others(1): Show | 4 | HG02056.hp2 HG03704.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+5024_385+5025i others(7): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TGTGTGTG others(4): Show |
1 | a0001c0002t0002g0133 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.385+5024_385+5025i others(13): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TTG | 30 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0025others(27): Show | 30 | HG00323.hp1 HG01167.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.385+5023_385+5024d others(4): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TTGTG | 42 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0054others(39): Show | 43 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.385+5021_385+5024d others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TTGTGTG | 31 | a0001c0001t0002g0106a0001c0001t0002g0118a0001c0001t0002g0119others(28): Show | 31 | HG00423.hp1 HG00544.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.385+5019_385+5024d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0007g0098a0001c0001t0052g0166a0001c0002t0004g0073others(3): Show | 6 | HG01934.hp2 HG02698.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+5017_385+5024d others(10): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TTGTGTGT others(3): Show |
2 | a0001c0001t0001g0045a0001c0001t0003g0152 | 2 | HG03927.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.385+5015_385+5024d others(12): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0009g0195a0001c0001t0020g0041a0001c0003t0002g0107 | 3 | HG00735.hp1 HG01978.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.385+5013_385+5024d others(14): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TTGTGTGT others(7): Show |
2 | a0001c0001t0008g0129a0001c0001t0056g0196 | 2 | HG03688.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.385+5011_385+5024d others(16): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
T | TTGTGTGT others(9): Show |
1 | a0001c0003t0002g0108 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.385+5009_385+5024d others(18): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
TTG | T | 52 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0046others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.385+5023_385+5024d others(4): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
TTGTG | T | 44 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0038others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.385+5021_385+5024d others(6): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540946
|
TTGTGTG | T | 5 | a0001c0001t0001g0042a0001c0001t0004g0067a0001c0001t0015g0190others(2): Show | 5 | HG02055.hp2 HG03453.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+5019_385+5024d others(8): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540946 | ||||||
| chr2:60540965
|
T | A | 1 | a0001c0001t0054g0194 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.385+5006A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60540965 | ||||||
| chr2:60541001
|
G | C | 1 | a0001c0001t0055g0202 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.385+4970C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60541001 | ||||||
| chr2:60541002
|
T | G | 1 | a0001c0001t0046g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.385+4969A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60541002 | ||||||
| chr2:60541107
|
A | G | 3 | a0001c0001t0003g0152a0001c0001t0011g0150a0001c0001t0011g0151 | 3 | HG01256.hp1 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.385+4864T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60541107 | ||||||
| chr2:60541229
|
TA | T | 133 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.385+4741delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60541229 | ||||||
| chr2:60541647
|
A | G | 2 | a0001c0001t0020g0041a0001c0002t0001g0040 | 2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.385+4324T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60541647 | ||||||
| chr2:60541843
|
G | A | 133 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.385+4128C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60541843 | ||||||
| chr2:60542025
|
T | C | 1 | a0001c0002t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.385+3946A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60542025 | ||||||
| chr2:60542250
|
A | T | 1 | a0001c0001t0043g0109 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.385+3721T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60542250 | ||||||
| chr2:60542320
|
G | A | 69 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(66): Show | 69 | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.385+3651C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60542320 | ||||||
| chr2:60542430
|
C | G | 1 | a0001c0001t0054g0194 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.385+3541G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60542430 | ||||||
| chr2:60542510
|
C | T | 1 | a0001c0001t0003g0183 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.385+3461G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60542510 | ||||||
| chr2:60542937
|
G | A | 1 | a0001c0001t0003g0183 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.385+3034C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60542937 | ||||||
| chr2:60542945
|
G | A | 29 | a0001c0001t0001g0035a0001c0001t0001g0058a0001c0001t0001g0059others(26): Show | 29 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.385+3026C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60542945 | ||||||
| chr2:60543029
|
T | TA | 77 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0038others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.385+2941dupT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543029 | ||||||
| chr2:60543029
|
TA | T | 5 | a0001c0001t0002g0101a0001c0001t0010g0030a0001c0001t0054g0194others(2): Show | 5 | HG00323.hp1 HG01243.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+2941delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543029 | ||||||
| chr2:60543319
|
C | T | 188 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.385+2652G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543319 | ||||||
| chr2:60543344
|
A | C | 2 | a0001c0001t0015g0185a0001c0001t0056g0196 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.385+2627T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543344 | ||||||
| chr2:60543507
|
A | C | 5 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0005g0224others(2): Show | 5 | HG00597.hp1 HG02027.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+2464T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543507 | ||||||
| chr2:60543518
|
C | G | 3 | a0001c0001t0003g0187a0001c0001t0004g0074a0001c0001t0011g0188 | 3 | HG01884.hp2 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.385+2453G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543518 | ||||||
| chr2:60543519
|
C | T | 1 | a0001c0003t0003g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.385+2452G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543519 | ||||||
| chr2:60543760
|
C | T | 4 | a0001c0001t0003g0187a0001c0001t0004g0074a0001c0001t0011g0188others(1): Show | 4 | HG01884.hp2 HG02615.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+2211G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543760 | ||||||
| chr2:60543805
|
T | C | 1 | a0001c0001t0008g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.385+2166A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543805 | ||||||
| chr2:60543852
|
T | C | 5 | a0001c0001t0003g0192a0001c0001t0014g0006a0001c0001t0015g0190others(2): Show | 5 | HG02055.hp1 HG02055.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+2119A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543852 | ||||||
| chr2:60543876
|
A | G | 1 | a0001c0001t0037g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.385+2095T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543876 | ||||||
| chr2:60543924
|
C | T | 1 | a0001c0001t0056g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.385+2047G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60543924 | ||||||
| chr2:60544264
|
G | T | 1 | a0001c0001t0006g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.385+1707C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60544264 | ||||||
| chr2:60544372
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.385+1599T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60544372 | ||||||
| chr2:60544449
|
G | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0032g0037 | 3 | HG01884.hp1 HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.385+1522C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60544449 | ||||||
| chr2:60544594
|
G | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 11 | HG01257.hp1 HG01358.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.385+1377C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60544594 | ||||||
| chr2:60544597
|
G | C | 1 | a0001c0001t0001g0034 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.385+1374C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60544597 | ||||||
| chr2:60545008
|
A | G | 1 | a0001c0001t0066g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385+963T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545008 | ||||||
| chr2:60545054
|
T | C | 1 | a0001c0001t0002g0119 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.385+917A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545054 | ||||||
| chr2:60545281
|
T | C | 1 | a0001c0004t0058g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.385+690A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545281 | ||||||
| chr2:60545402
|
C | T | 1 | a0001c0001t0061g0212 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.385+569G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545402 | ||||||
| chr2:60545404
|
T | C | 1 | a0001c0001t0064g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.385+567A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545404 | ||||||
| chr2:60545407
|
G | A | 1 | a0001c0003t0041g0135 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.385+564C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545407 | ||||||
| chr2:60545516
|
G | A | 1 | a0001c0001t0002g0136 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.385+455C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545516 | ||||||
| chr2:60545702
|
A | G | 1 | a0001c0001t0038g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.385+269T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545702 | ||||||
| chr2:60545744
|
T | G | 1 | a0001c0001t0066g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385+227A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545744 | ||||||
| chr2:60545844
|
G | C | 5 | a0001c0001t0001g0025a0001c0001t0003g0187a0001c0001t0004g0074others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+127C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545844 | ||||||
| chr2:60545900
|
T | G | 1 | a0001c0002t0001g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.385+71A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | 60545900 | ||||||
| chr2:60546552
|
AAC | A | 133 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.56-254_56-253delGT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60546552 | ||||||
| chr2:60546802
|
T | C | 1 | a0001c0001t0018g0207 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.56-502A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60546802 | ||||||
| chr2:60546930
|
G | A | 1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.56-630C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60546930 | ||||||
| chr2:60547232
|
T | G | 1 | a0001c0001t0007g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.56-932A>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60547232 | ||||||
| chr2:60547255
|
G | A | 1 | a0001c0001t0004g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.56-955C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60547255 | ||||||
| chr2:60547356
|
G | T | 1 | a0001c0001t0046g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.56-1056C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60547356 | ||||||
| chr2:60547509
|
AT | A | 11 | a0001c0001t0001g0036a0001c0001t0004g0078a0001c0001t0005g0223others(8): Show | 11 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-1210delA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60547509 | ||||||
| chr2:60547511
|
CA | C | 42 | a0001c0001t0001g0028a0001c0001t0003g0152a0001c0001t0003g0187others(39): Show | 42 | HG00099.hp2 HG00738.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.56-1212delT | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60547511 | ||||||
| chr2:60547512
|
A | C | 11 | a0001c0001t0001g0036a0001c0001t0004g0078a0001c0001t0005g0223others(8): Show | 11 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.56-1212T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60547512 | ||||||
| chr2:60547638
|
T | C | 190 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.56-1338A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60547638 | ||||||
| chr2:60547771
|
C | T | 1 | a0001c0001t0007g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.56-1471G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60547771 | ||||||
| chr2:60548278
|
G | A | 1 | a0001c0002t0004g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.56-1978C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548278 | ||||||
| chr2:60548305
|
A | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0013g0253others(2): Show | 5 | HG02809.hp1 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-2005T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548305 | ||||||
| chr2:60548306
|
T | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG00423.hp2 HG01257.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.56-2006A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548306 | ||||||
| chr2:60548330
|
C | CT | 36 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0038others(33): Show | 36 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.56-2031dupA | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548330 | ||||||
| chr2:60548330
|
C | CTT | 22 | a0001c0001t0003g0152a0001c0001t0003g0192a0001c0001t0004g0074others(19): Show | 22 | HG00099.hp2 HG00738.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.56-2032_56-2031dup others(2): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548330 | ||||||
| chr2:60548528
|
G | A | 1 | a0001c0001t0042g0138 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.56-2228C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548528 | ||||||
| chr2:60548617
|
T | C | 1 | a0001c0001t0007g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.56-2317A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548617 | ||||||
| chr2:60548685
|
T | C | 258 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.56-2385A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548685 | ||||||
| chr2:60548920
|
T | C | 1 | a0001c0002t0001g0024 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.56-2620A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548920 | ||||||
| chr2:60548950
|
A | C | 1 | a0001c0001t0019g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.56-2650T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548950 | ||||||
| chr2:60548990
|
T | C | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.56-2690A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60548990 | ||||||
| chr2:60549102
|
T | A | 1 | a0001c0001t0002g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.56-2802A>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60549102 | ||||||
| chr2:60549104
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.56-2804T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60549104 | ||||||
| chr2:60549404
|
A | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.56-3104T>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60549404 | ||||||
| chr2:60549627
|
G | A | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.56-3327C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60549627 | ||||||
| chr2:60549920
|
G | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.55+3296C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60549920 | ||||||
| chr2:60550081
|
G | A | 7 | a0001c0001t0003g0192a0001c0001t0005g0233a0001c0001t0010g0015others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.55+3135C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60550081 | ||||||
| chr2:60550363
|
G | C | 70 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0036others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.55+2853C>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60550363 | ||||||
| chr2:60550597
|
C | T | 1 | a0001c0002t0001g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.55+2619G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60550597 | ||||||
| chr2:60550628
|
C | G | 31 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(28): Show | 33 | HG00741.hp2 HG01081.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.55+2588G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60550628 | ||||||
| chr2:60550688
|
A | AG | 14 | a0001c0001t0002g0091a0001c0001t0002g0094a0001c0001t0002g0141others(11): Show | 14 | HG00741.hp2 HG01123.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.55+2527dupC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60550688 | ||||||
| chr2:60550901
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.55+2315G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60550901 | ||||||
| chr2:60551112
|
A | G | 1 | a0001c0001t0013g0249 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.55+2104T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60551112 | ||||||
| chr2:60551302
|
G | A | 1 | a0001c0002t0001g0062 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.55+1914C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60551302 | ||||||
| chr2:60551458
|
G | T | 1 | a0001c0001t0002g0090 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.55+1758C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60551458 | ||||||
| chr2:60551839
|
G | A | 1 | a0001c0001t0013g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.55+1377C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60551839 | ||||||
| chr2:60552343
|
A | C | 138 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.55+873T>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552343 | ||||||
| chr2:60552351
|
G | A | 5 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 5 | HG02080.hp1 HG02135.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+865C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552351 | ||||||
| chr2:60552569
|
C | A | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.55+647G>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552569 | ||||||
| chr2:60552626
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.55+590T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552626 | ||||||
| chr2:60552705
|
A | G | 142 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.55+511T>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552705 | ||||||
| chr2:60552818
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.55+398C>T | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552818 | ||||||
| chr2:60552887
|
CG | C | 135 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.55+328delC | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552887 | ||||||
| chr2:60552891
|
GC | G | 3 | a0001c0001t0064g0247a0001c0001t0066g0258a0001c0004t0058g0206 | 3 | HG02965.hp2 HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.55+324delG | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552891 | ||||||
| chr2:60552892
|
C | G | 2 | a0001c0001t0010g0015a0001c0001t0037g0068 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.55+324G>C | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552892 | ||||||
| chr2:60552894
|
G | T | 1 | a0001c0001t0004g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.55+322C>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60552894 | ||||||
| chr2:60553060
|
C | T | 1 | a0001c0001t0068g0260 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.55+156G>A | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60553060 | ||||||
| chr2:60553085
|
T | C | 1 | a0001c0001t0004g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.55+131A>G | BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 1/3 | chr2 | 60553085 |