Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 607 |
| ensemblid | ENSG00000116128.12 |
| hgncid | 1008 |
| symbol | BCL9 |
| name | BCL9 transcription coactivator |
| refseq_nuc | NM_004326.4 |
| refseq_prot | NP_004317.2 |
| ensembl_nuc | ENST00000234739.8 |
| ensembl_prot | ENSP00000234739.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 147541501 |
| end | 147626216 |
| strand | + |
| ver | v1.2 |
| region | chr1:147541501-147626216 |
| region5000 | chr1:147536501-147631216 |
| regionname0 | BCL9_chr1_147541501_147626216 |
| regionname5000 | BCL9_chr1_147536501_147631216 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1426 | 271 | 81 | 37 | 126 | 7 | 18 | 95 | BCL9_chr1_147536501_147631216 | BCL9 | MHSSN others(1421): Show |
chr1 | 147536501 | 147631216 |
| a0002 | 0/0 | 1426 | 38 | 3 | 9 | 10 | 9 | 7 | 7 | BCL9_chr1_147536501_147631216 | BCL9 | MHSSN others(1421): Show |
chr1 | 147536501 | 147631216 |
| a0003 | 0/0 | 1426 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | MHSSN others(1421): Show |
chr1 | 147536501 | 147631216 |
| a0004 | 0/0 | 1426 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | MHSSN others(1421): Show |
chr1 | 147536501 | 147631216 |
| a0005 | 0/0 | 1426 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | MHSSN others(1421): Show |
chr1 | 147536501 | 147631216 |
| a0006 | 0/0 | 1426 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | MHSSN others(1421): Show |
chr1 | 147536501 | 147631216 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4278 | 267 | 80 | 35 | 126 | 6 | 18 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0001c0006 | 0/0 | 4278 | 2 | 0 | 1 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0001c0007 | 0/0 | 4278 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0001c0010 | 0/0 | 4278 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0002c0002 | 0/0 | 4278 | 34 | 3 | 7 | 10 | 8 | 6 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0002c0003 | 0/0 | 4278 | 4 | 0 | 2 | 0 | 1 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0003c0004 | 0/0 | 4278 | 3 | 0 | 2 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0004c0005 | 0/0 | 4278 | 2 | 0 | 2 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0005c0009 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 | ||
| a0006c0008 | 0/0 | 4278 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | ATGCA others(4273): Show |
chr1 | 147536501 | 147631216 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6189 | 34 | 1 | 6 | 24 | 0 | 2 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0002 | 0/0 | 6189 | 31 | 7 | 4 | 17 | 1 | 2 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0003 | 0/0 | 6189 | 38 | 4 | 3 | 31 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0004 | 0/0 | 6189 | 36 | 0 | 4 | 29 | 1 | 2 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0005 | 0/0 | 6189 | 27 | 1 | 8 | 17 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0006 | 0/0 | 6189 | 21 | 20 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0007 | 0/0 | 6189 | 13 | 5 | 4 | 0 | 2 | 2 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0008 | 0/0 | 6189 | 14 | 14 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0009 | 0/0 | 6189 | 13 | 11 | 2 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0010 | 0/0 | 6189 | 6 | 1 | 1 | 4 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0011 | 0/0 | 6189 | 6 | 2 | 0 | 0 | 1 | 3 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0012 | 0/1 | 6189 | 5 | 1 | 1 | 0 | 0 | 2 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0013 | 0/0 | 6189 | 3 | 0 | 0 | 3 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0014 | 0/0 | 6189 | 3 | 3 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0015 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0016 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0017 | 0/0 | 6189 | 2 | 0 | 0 | 0 | 1 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0019 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0020 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0021 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0022 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0023 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0024 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0025 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0026 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0027 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0028 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0001t0029 | 0/0 | 6189 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0006t0010 | 0/0 | 6189 | 2 | 0 | 1 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0007t0009 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0001c0010t0003 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0002c0002t0001 | 0/0 | 6189 | 22 | 1 | 5 | 6 | 7 | 3 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0002c0002t0002 | 0/0 | 6189 | 9 | 1 | 2 | 4 | 1 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0002c0002t0005 | 0/0 | 6189 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0002c0002t0007 | 0/0 | 6189 | 2 | 0 | 0 | 0 | 0 | 2 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0002c0003t0001 | 0/0 | 6189 | 4 | 0 | 2 | 0 | 1 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0003c0004t0001 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0003c0004t0002 | 0/0 | 6189 | 2 | 0 | 1 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0004c0005t0001 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0004c0005t0018 | 0/0 | 6189 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0005c0009t0005 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| a0006c0008t0001 | 0/0 | 6189 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | AGACC others(6184): Show |
chr1 | 147536501 | 147631216 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0010g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0010g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0010g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0010g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0011g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0011g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0012g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0012g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0012g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0012g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0013g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0013g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0013g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0014g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0014g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0015g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0015g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0016g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0017g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0017g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0019g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0020g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0021g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0022g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0023g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0024g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0025g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0026g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0027g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0028g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0001t0029g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0006t0010g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0006t0010g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0007t0009g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0001c0010t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0002t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0003t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0003c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0003c0004t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0003c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0004c0005t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0004c0005t0018g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0005c0009t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| a0006c0008t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0006 | t0010 | g0171 | EUR | GBR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0106 | EUR | GBR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0083 | EUR | GBR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0093 | EUR | GBR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0094 | EUR | FIN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0097 | EUR | FIN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00323 | hp1 | a0001 | c0001 | t0011 | g0146 | EUR | FIN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0134 | EUR | FIN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00544 | hp1 | a0005 | c0009 | t0005 | g0032 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00597 | hp2 | a0006 | c0008 | t0001 | g0038 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0246 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01071 | hp1 | a0003 | c0004 | t0001 | g0123 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0153 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01074 | hp2 | a0004 | c0005 | t0018 | g0277 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01081 | hp2 | a0001 | c0001 | t0019 | g0274 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0127 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01168 | hp2 | a0001 | c0006 | t0010 | g0172 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0077 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01175 | hp1 | a0004 | c0005 | t0001 | g0147 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01192 | hp2 | a0003 | c0004 | t0002 | g0019 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0073 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0151 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0011 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0219 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0011 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | IBS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0091 | EUR | IBS | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01884 | hp2 | a0001 | c0001 | t0021 | g0220 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0275 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01934 | hp1 | a0001 | c0001 | t0012 | g0242 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0084 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01952 | hp1 | a0001 | c0010 | t0003 | g0263 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01952 | hp2 | a0001 | c0001 | t0010 | g0283 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0154 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0155 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0198 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0213 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0217 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02273 | hp1 | a0001 | c0001 | t0007 | g0072 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02280 | hp1 | a0001 | c0001 | t0014 | g0195 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0229 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | KHV | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0158 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0207 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02602 | hp1 | a0002 | c0002 | t0007 | g0086 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0279 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0130 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0238 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02630 | hp2 | a0001 | c0001 | t0023 | g0208 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0284 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0055 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0120 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0203 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0193 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0209 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02735 | hp1 | a0001 | c0001 | t0017 | g0244 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02738 | hp1 | a0002 | c0002 | t0007 | g0103 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02738 | hp2 | a0001 | c0001 | t0020 | g0245 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0218 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0139 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0200 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0214 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0278 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0211 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0191 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0122 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0227 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0197 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0231 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03209 | hp1 | a0001 | c0001 | t0026 | g0057 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03209 | hp2 | a0001 | c0007 | t0009 | g0273 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0270 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03225 | hp2 | a0001 | c0001 | t0024 | g0194 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0224 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0202 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0282 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0272 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | MSL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03710 | hp1 | a0001 | c0001 | t0028 | g0089 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0149 | SAS | PJL | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0148 | SAS | BEB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03834 | hp1 | a0001 | c0001 | t0012 | g0204 | SAS | BEB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0126 | SAS | BEB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | BEB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03927 | hp2 | a0001 | c0001 | t0011 | g0070 | SAS | BEB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0095 | SAS | BEB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG03942 | hp2 | a0001 | c0001 | t0029 | g0135 | SAS | BEB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG04115 | hp1 | a0001 | c0001 | t0012 | g0174 | SAS | STU | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG04115 | hp2 | a0003 | c0004 | t0002 | g0236 | SAS | STU | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | YRI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0223 | AFR | YRI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0099 | AFR | YRI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0265 | AFR | YRI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18945 | hp2 | a0001 | c0001 | t0027 | g0012 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18954 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18977 | hp2 | a0001 | c0001 | t0013 | g0169 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18983 | hp1 | a0001 | c0001 | t0010 | g0254 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18986 | hp1 | a0001 | c0001 | t0010 | g0016 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18997 | hp1 | a0001 | c0001 | t0013 | g0168 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0016 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0226 | AFR | LWK | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19030 | hp2 | a0001 | c0001 | t0022 | g0212 | AFR | LWK | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19043 | hp1 | a0001 | c0001 | t0016 | g0266 | AFR | LWK | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | LWK | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19070 | hp1 | a0001 | c0001 | t0010 | g0199 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19081 | hp2 | a0001 | c0001 | t0013 | g0167 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0235 | AFR | YRI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | YRI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0280 | AFR | ASW | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0069 | AFR | ASW | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20752 | hp1 | a0001 | c0001 | t0017 | g0087 | EUR | TSI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0044 | EUR | TSI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0141 | EUR | TSI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0247 | EUR | TSI | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0145 | SAS | GIH | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | GIH | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0186 | AMR | CLM | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0210 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0215 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG02559 | hp2 | a0002 | c0002 | t0005 | g0082 | AFR | ACB | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0222 | AFR | USA | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0240 | AFR | USA | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0128 | EAS | JPT | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | USA | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0228 | AFR | USA | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0232 | AFR | LWK | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| NA21309 | hp2 | a0001 | c0001 | t0025 | g0239 | AFR | LWK | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0012 | g0252 | REF | REF | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0039 | REF | REF | BCL9_chr1_147536501_147631216 | BCL9 | chr1 | 147536501 | 147631216 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147604909 | A | G | 2 | a0001 a0002 |
69 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(66): Show |
splice_region_variant | LOW | c.-345A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/10 | chr1 | 147604909 | |||||||
| chr1:147619060 | G | A | 1 | a0003 | 3 | HG01071.hp1 HG01192.hp2 HG04115.hp2 |
missense_variant | MODERATE | c.905G>A | p.Gly302Asp | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/10 | 1556/6189 | 905/4281 | 302/1426 | chr1 | 147619060 | |||
| chr1:147620166 | C | T | 1 | a0002 | 38 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(35): Show |
missense_variant | MODERATE | c.2011C>T | p.Pro671Ser | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/10 | 2662/6189 | 2011/4281 | 671/1426 | chr1 | 147620166 | |||
| chr1:147624225 | C | G | 1 | a0005 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3547C>G | p.Leu1183Val | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 4198/6189 | 3547/4281 | 1183/1426 | chr1 | 147624225 | |||
| chr1:147624311 | G | A | 1 | a0004 | 2 | HG01074.hp2 HG01175.hp1 |
missense_variant | MODERATE | c.3633G>A | p.Met1211Ile | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 4284/6189 | 3633/4281 | 1211/1426 | chr1 | 147624311 | |||
| chr1:147624699 | A | G | 1 | a0006 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.4021A>G | p.Met1341Val | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 4672/6189 | 4021/4281 | 1341/1426 | chr1 | 147624699 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147619883 | G | A | 1 | a0002c0003 | 4 | HG01358.hp2 HG01433.hp2 HG03942.hp1 others(1): Show |
synonymous_variant | LOW | c.1728G>A | p.Pro576Pro | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/10 | 2379/6189 | 1728/4281 | 576/1426 | chr1 | 147619883 | |||
| chr1:147620189 | T | A | 1 | a0001c0007 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2034T>A | p.Pro678Pro | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/10 | 2685/6189 | 2034/4281 | 678/1426 | chr1 | 147620189 | |||
| chr1:147620906 | A | C | 1 | a0001c0010 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.2751A>C | p.Ser917Ser | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/10 | 3402/6189 | 2751/4281 | 917/1426 | chr1 | 147620906 | |||
| chr1:147624704 | C | T | 1 | a0001c0006 | 2 | HG00099.hp1 HG01168.hp2 |
synonymous_variant | LOW | c.4026C>T | p.Pro1342Pro | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 4677/6189 | 4026/4281 | 1342/1426 | chr1 | 147624704 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147541592 | G | A | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(21): Show |
160 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(157): Show |
5_prime_UTR_variant | MODIFIER | c.-560G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/10 | 70245 | chr1 | 147541592 | ||||||
| chr1:147604799 | C | T | 1 | a0001c0001t0025 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-455C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/10 | 7038 | chr1 | 147604799 | ||||||
| chr1:147606805 | G | T | 4 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0020 others(1): Show |
8 | HG01934.hp1 HG02486.hp2 HG02735.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-321G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/10 | 5032 | chr1 | 147606805 | ||||||
| chr1:147624993 | G | A | 7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(4): Show |
62 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*34G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 34 | chr1 | 147624993 | ||||||
| chr1:147625027 | G | C | 3 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0026 |
17 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*68G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 68 | chr1 | 147625027 | ||||||
| chr1:147625077 | G | A | 1 | a0001c0001t0021 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 118 | chr1 | 147625077 | ||||||
| chr1:147625105 | C | T | 1 | a0001c0001t0023 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 146 | chr1 | 147625105 | ||||||
| chr1:147625454 | T | C | 1 | a0001c0001t0016 | 2 | HG03453.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*495T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 495 | chr1 | 147625454 | ||||||
| chr1:147625465 | T | C | 14 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(11): Show |
110 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*506T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 506 | chr1 | 147625465 | ||||||
| chr1:147625540 | G | A | 1 | a0004c0005t0018 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*581G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 581 | chr1 | 147625540 | ||||||
| chr1:147625834 | T | C | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(8): Show |
70 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*875T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 875 | chr1 | 147625834 | ||||||
| chr1:147625887 | C | T | 1 | a0001c0001t0019 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*928C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 10/10 | 928 | chr1 | 147625887 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147541737 | G | A | 14 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0003g0003 others(11): Show |
17 | HG00423.hp2 HG00544.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-478+63G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147541737 | |||||||
| chr1:147541818 | C | G | 1 | a0001c0001t0006g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-478+144C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147541818 | |||||||
| chr1:147542050 | A | G | 1 | a0001c0001t0010g0283 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-478+376A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542050 | |||||||
| chr1:147542066 | A | C | 98 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(95): Show |
108 | HG00609.hp1 HG00639.hp1 HG00738.hp2 others(105): Show |
intron_variant | MODIFIER | c.-478+392A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542066 | |||||||
| chr1:147542142 | G | T | 1 | a0001c0001t0006g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-478+468G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542142 | |||||||
| chr1:147542476 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-478+802G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542476 | |||||||
| chr1:147542550 | C | G | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+876C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542550 | |||||||
| chr1:147542720 | G | T | 1 | a0001c0001t0002g0281 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-478+1046G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542720 | |||||||
| chr1:147542808 | G | A | 2 | a0001c0001t0008g0196 a0001c0001t0014g0195 |
2 | HG02280.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-478+1134G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542808 | |||||||
| chr1:147542811 | A | G | 1 | a0001c0001t0009g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-478+1137A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542811 | |||||||
| chr1:147542973 | G | C | 2 | a0001c0001t0009g0197 a0001c0001t0015g0198 |
2 | HG02055.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-478+1299G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147542973 | |||||||
| chr1:147543409 | C | T | 152 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(149): Show |
166 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-478+1735C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147543409 | |||||||
| chr1:147543424 | T | A | 1 | a0001c0001t0010g0199 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-478+1750T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147543424 | |||||||
| chr1:147543772 | T | G | 89 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(86): Show |
97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-478+2098T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147543772 | |||||||
| chr1:147543803 | G | C | 7 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0006g0237 others(4): Show |
7 | HG02630.hp1 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-478+2129G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147543803 | |||||||
| chr1:147543848 | A | G | 1 | a0002c0002t0001g0156 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-478+2174A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147543848 | |||||||
| chr1:147543883 | C | A | 12 | a0001c0001t0002g0281 a0001c0001t0003g0159 a0001c0001t0003g0160 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-478+2209C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147543883 | |||||||
| chr1:147543993 | T | G | 1 | a0001c0001t0005g0036 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-478+2319T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147543993 | |||||||
| chr1:147544009 | C | T | 5 | a0001c0001t0003g0159 a0001c0001t0003g0160 a0001c0001t0003g0161 others(2): Show |
5 | HG01891.hp1 HG02145.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-478+2335C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544009 | |||||||
| chr1:147544163 | A | C | 56 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(53): Show |
61 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-478+2489A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544163 | |||||||
| chr1:147544332 | A | G | 151 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(148): Show |
165 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-478+2658A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544332 | |||||||
| chr1:147544405 | CCTCT | C | 28 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0281 others(25): Show |
31 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.-478+2735_-478+273 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147544405 | ||||||
| chr1:147544564 | G | T | 8 | a0001c0001t0001g0015 a0001c0001t0004g0154 a0001c0001t0005g0036 others(5): Show |
9 | HG01071.hp2 HG01081.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-478+2890G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544564 | |||||||
| chr1:147544575 | C | T | 1 | a0002c0002t0002g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-478+2901C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544575 | |||||||
| chr1:147544639 | C | T | 6 | a0001c0001t0002g0221 a0001c0001t0006g0222 a0001c0001t0009g0218 others(3): Show |
6 | HG01433.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-478+2965C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544639 | |||||||
| chr1:147544645 | C | T | 1 | a0001c0001t0007g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-478+2971C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544645 | |||||||
| chr1:147544678 | T | G | 57 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(54): Show |
62 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-478+3004T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544678 | |||||||
| chr1:147544836 | T | C | 2 | a0001c0001t0009g0197 a0001c0001t0015g0198 |
2 | HG02055.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-478+3162T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544836 | |||||||
| chr1:147544838 | C | T | 1 | a0001c0001t0006g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-478+3164C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544838 | |||||||
| chr1:147544859 | C | T | 28 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0281 others(25): Show |
31 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.-478+3185C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147544859 | |||||||
| chr1:147545166 | C | A | 55 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(52): Show |
60 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-478+3492C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545166 | |||||||
| chr1:147545178 | A | T | 1 | a0002c0002t0002g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-478+3504A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545178 | |||||||
| chr1:147545348 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-478+3674T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545348 | |||||||
| chr1:147545370 | T | C | 39 | a0001c0001t0002g0019 a0001c0001t0002g0233 a0001c0001t0002g0234 others(36): Show |
40 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.-478+3696T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545370 | |||||||
| chr1:147545672 | C | T | 1 | a0001c0001t0010g0016 | 2 | NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-478+3998C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545672 | |||||||
| chr1:147545678 | C | T | 1 | a0001c0001t0011g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-478+4004C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545678 | |||||||
| chr1:147545754 | A | C | 28 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0281 others(25): Show |
31 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.-478+4080A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545754 | |||||||
| chr1:147545829 | T | C | 1 | a0006c0008t0001g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-478+4155T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545829 | |||||||
| chr1:147545872 | A | G | 1 | a0001c0001t0006g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-478+4198A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545872 | |||||||
| chr1:147545944 | T | A | 21 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0006g0216 others(18): Show |
23 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.-478+4270T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545944 | |||||||
| chr1:147545987 | C | T | 1 | a0002c0002t0002g0022 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-478+4313C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147545987 | |||||||
| chr1:147546154 | G | T | 1 | a0001c0001t0006g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-478+4480G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546154 | |||||||
| chr1:147546248 | G | A | 44 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(41): Show |
48 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-478+4574G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546248 | |||||||
| chr1:147546263 | A | G | 87 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(84): Show |
95 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-478+4589A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546263 | |||||||
| chr1:147546342 | A | T | 2 | a0001c0001t0009g0197 a0001c0001t0015g0198 |
2 | HG02055.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-478+4668A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546342 | |||||||
| chr1:147546345 | T | A | 9 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0006g0237 others(6): Show |
9 | HG02630.hp1 HG02723.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-478+4671T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546345 | |||||||
| chr1:147546461 | T | A | 8 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(5): Show |
13 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-478+4787T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546461 | |||||||
| chr1:147546591 | G | A | 74 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(71): Show |
81 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-478+4917G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546591 | |||||||
| chr1:147546759 | G | C | 46 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(43): Show |
50 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-478+5085G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546759 | |||||||
| chr1:147546944 | G | A | 4 | a0001c0001t0006g0271 a0001c0001t0006g0272 a0001c0001t0009g0270 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+5270G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147546944 | |||||||
| chr1:147547002 | G | GT | 226 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(223): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.-478+5337dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147547002 | ||||||
| chr1:147547011 | T | TA | 57 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(54): Show |
62 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-478+5338dupA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147547011 | ||||||
| chr1:147547020 | C | T | 7 | a0001c0001t0002g0281 a0001c0001t0006g0201 a0001c0001t0006g0203 others(4): Show |
8 | HG02486.hp1 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-478+5346C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147547020 | |||||||
| chr1:147547114 | A | G | 28 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0281 others(25): Show |
31 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.-478+5440A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147547114 | |||||||
| chr1:147547266 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0005g0040 a0001c0001t0005g0042 |
3 | HG02027.hp1 HG02074.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-478+5592T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147547266 | |||||||
| chr1:147547342 | T | C | 1 | a0001c0001t0004g0043 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-478+5668T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147547342 | |||||||
| chr1:147547392 | C | T | 150 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(147): Show |
164 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.-478+5718C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147547392 | |||||||
| chr1:147547909 | T | C | 1 | a0001c0001t0019g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-478+6235T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147547909 | |||||||
| chr1:147547931 | T | C | 1 | a0002c0003t0001g0044 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-478+6257T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147547931 | |||||||
| chr1:147547988 | G | A | 1 | a0001c0001t0006g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-478+6314G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147547988 | |||||||
| chr1:147548029 | T | C | 7 | a0001c0001t0002g0281 a0001c0001t0006g0201 a0001c0001t0006g0203 others(4): Show |
8 | HG02486.hp1 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-478+6355T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147548029 | |||||||
| chr1:147548172 | G | T | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+6498G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147548172 | |||||||
| chr1:147548328 | C | T | 28 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0281 others(25): Show |
31 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.-478+6654C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147548328 | |||||||
| chr1:147548685 | A | G | 54 | a0001c0001t0002g0019 a0001c0001t0002g0233 a0001c0001t0002g0234 others(51): Show |
56 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.-478+7011A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147548685 | |||||||
| chr1:147548839 | C | A | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-478+7165C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147548839 | |||||||
| chr1:147548867 | A | T | 44 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(41): Show |
48 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-478+7193A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147548867 | |||||||
| chr1:147548979 | C | CT | 44 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(41): Show |
48 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-478+7322dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147548979 | ||||||
| chr1:147548979 | C | CTT | 6 | a0001c0001t0003g0243 a0001c0001t0006g0192 a0001c0001t0006g0275 others(3): Show |
6 | HG01256.hp2 HG01891.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-478+7321_-478+732 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147548979 | ||||||
| chr1:147548979 | C | CTTT | 84 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(81): Show |
91 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-478+7320_-478+732 others(7): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147548979 | ||||||
| chr1:147548979 | CTT | C | 21 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0006g0216 others(18): Show |
23 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.-478+7321_-478+732 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147548979 | ||||||
| chr1:147549037 | T | C | 1 | a0001c0001t0012g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-478+7363T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147549037 | |||||||
| chr1:147549045 | C | T | 1 | a0001c0001t0019g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-478+7371C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147549045 | |||||||
| chr1:147549083 | T | C | 11 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(8): Show |
11 | HG00597.hp2 HG00673.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.-478+7409T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147549083 | |||||||
| chr1:147549177 | G | A | 28 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0281 others(25): Show |
31 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.-478+7503G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147549177 | |||||||
| chr1:147549375 | C | T | 21 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0006g0216 others(18): Show |
23 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.-478+7701C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147549375 | |||||||
| chr1:147549648 | G | C | 30 | a0001c0001t0002g0019 a0001c0001t0002g0248 a0001c0001t0002g0249 others(27): Show |
31 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-478+7974G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147549648 | |||||||
| chr1:147549679 | C | A | 19 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0276 others(16): Show |
19 | HG01074.hp2 HG01891.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.-478+8005C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147549679 | |||||||
| chr1:147549744 | A | G | 1 | a0001c0001t0029g0135 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-478+8070A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147549744 | |||||||
| chr1:147550117 | C | CT | 8 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(5): Show |
13 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-478+8447dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147550117 | ||||||
| chr1:147550285 | G | T | 3 | a0001c0001t0011g0146 a0002c0002t0001g0014 a0004c0005t0001g0147 |
4 | HG00323.hp1 HG01175.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+8611G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147550285 | |||||||
| chr1:147550327 | A | G | 2 | a0001c0001t0006g0237 a0001c0001t0006g0238 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-478+8653A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147550327 | |||||||
| chr1:147550425 | G | A | 1 | a0001c0001t0006g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-478+8751G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147550425 | |||||||
| chr1:147550532 | C | G | 27 | a0001c0001t0002g0019 a0001c0001t0002g0248 a0001c0001t0002g0249 others(24): Show |
28 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-478+8858C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147550532 | |||||||
| chr1:147550555 | G | A | 1 | a0001c0001t0019g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-478+8881G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147550555 | |||||||
| chr1:147550805 | G | A | 2 | a0001c0001t0001g0045 a0006c0008t0001g0038 |
2 | HG00597.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-478+9131G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147550805 | |||||||
| chr1:147550857 | G | A | 1 | a0001c0001t0006g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-478+9183G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147550857 | |||||||
| chr1:147550923 | T | C | 57 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(54): Show |
62 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-478+9249T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147550923 | |||||||
| chr1:147551019 | G | T | 1 | a0001c0001t0004g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-478+9345G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551019 | |||||||
| chr1:147551021 | A | G | 5 | a0001c0001t0006g0018 a0001c0001t0006g0230 a0001c0001t0009g0231 others(2): Show |
6 | HG01175.hp2 HG02280.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-478+9347A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551021 | |||||||
| chr1:147551031 | C | CCTTATAA others(4): Show |
1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+9359_-478+936 others(15): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147551031 | ||||||
| chr1:147551073 | T | C | 1 | a0001c0001t0003g0009 | 2 | HG00423.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.-478+9399T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551073 | |||||||
| chr1:147551123 | A | C | 1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-478+9449A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551123 | |||||||
| chr1:147551237 | A | G | 1 | a0001c0001t0004g0145 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-478+9563A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551237 | |||||||
| chr1:147551252 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-478+9578G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551252 | |||||||
| chr1:147551494 | C | T | 13 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(10): Show |
18 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-478+9820C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551494 | |||||||
| chr1:147551661 | G | A | 1 | a0001c0001t0004g0189 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-478+9987G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551661 | |||||||
| chr1:147551783 | A | G | 1 | a0001c0001t0008g0215 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-478+10109A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551783 | |||||||
| chr1:147551864 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-478+10190G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551864 | |||||||
| chr1:147551959 | G | A | 9 | a0001c0001t0002g0221 a0001c0001t0006g0222 a0001c0001t0009g0218 others(6): Show |
9 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-478+10285G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147551959 | |||||||
| chr1:147552120 | C | T | 53 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(50): Show |
58 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-478+10446C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552120 | |||||||
| chr1:147552273 | G | A | 53 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(50): Show |
58 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-478+10599G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552273 | |||||||
| chr1:147552301 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-478+10627T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552301 | |||||||
| chr1:147552381 | G | T | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+10707G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552381 | |||||||
| chr1:147552382 | T | G | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+10708T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552382 | |||||||
| chr1:147552384 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+10710G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552384 | |||||||
| chr1:147552443 | T | TA | 11 | a0001c0001t0002g0221 a0001c0001t0006g0216 a0001c0001t0006g0222 others(8): Show |
11 | HG01433.hp1 HG01884.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+10775dupA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147552443 | ||||||
| chr1:147552466 | C | T | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+10792C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552466 | |||||||
| chr1:147552792 | C | T | 2 | a0001c0001t0002g0221 a0001c0001t0006g0222 |
2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-478+11118C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552792 | |||||||
| chr1:147552868 | A | G | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+11194A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147552868 | |||||||
| chr1:147552975 | A | AT | 254 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(251): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-478+11314dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147552975 | ||||||
| chr1:147552975 | A | ATT | 11 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(8): Show |
16 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-478+11313_-478+11 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147552975 | ||||||
| chr1:147553022 | T | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+11348T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553022 | |||||||
| chr1:147553100 | T | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+11426T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553100 | |||||||
| chr1:147553127 | T | C | 50 | a0001c0001t0002g0206 a0001c0001t0002g0233 a0001c0001t0002g0234 others(47): Show |
53 | HG01074.hp2 HG01175.hp2 HG02055.hp1 others(50): Show |
intron_variant | MODIFIER | c.-478+11453T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553127 | |||||||
| chr1:147553144 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-478+11470C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553144 | |||||||
| chr1:147553230 | C | G | 1 | a0001c0001t0005g0155 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-478+11556C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553230 | |||||||
| chr1:147553245 | T | A | 1 | a0001c0001t0009g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-478+11571T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553245 | |||||||
| chr1:147553543 | C | T | 56 | a0001c0001t0002g0206 a0001c0001t0002g0233 a0001c0001t0002g0234 others(53): Show |
60 | HG01074.hp2 HG01175.hp2 HG01891.hp2 others(57): Show |
intron_variant | MODIFIER | c.-478+11869C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553543 | |||||||
| chr1:147553603 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-478+11929C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553603 | |||||||
| chr1:147553619 | G | C | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+11945G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553619 | |||||||
| chr1:147553620 | C | G | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+11946C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553620 | |||||||
| chr1:147553717 | C | G | 56 | a0001c0001t0002g0206 a0001c0001t0002g0233 a0001c0001t0002g0234 others(53): Show |
60 | HG01074.hp2 HG01175.hp2 HG01891.hp2 others(57): Show |
intron_variant | MODIFIER | c.-478+12043C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553717 | |||||||
| chr1:147553745 | A | C | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+12071A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553745 | |||||||
| chr1:147553836 | A | C | 5 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(2): Show |
10 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-478+12162A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553836 | |||||||
| chr1:147553923 | T | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+12249T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147553923 | |||||||
| chr1:147554277 | A | G | 1 | a0001c0001t0002g0256 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-478+12603A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554277 | |||||||
| chr1:147554304 | T | C | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+12630T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554304 | |||||||
| chr1:147554348 | G | A | 17 | a0001c0001t0002g0019 a0001c0001t0002g0248 a0001c0001t0002g0249 others(14): Show |
17 | HG00639.hp1 HG00738.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.-478+12674G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554348 | |||||||
| chr1:147554350 | C | G | 56 | a0001c0001t0002g0206 a0001c0001t0002g0233 a0001c0001t0002g0234 others(53): Show |
60 | HG01074.hp2 HG01175.hp2 HG01891.hp2 others(57): Show |
intron_variant | MODIFIER | c.-478+12676C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554350 | |||||||
| chr1:147554369 | G | T | 4 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+12695G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554369 | |||||||
| chr1:147554412 | C | T | 152 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(149): Show |
166 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-478+12738C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554412 | |||||||
| chr1:147554531 | C | A | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-478+12857C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554531 | |||||||
| chr1:147554555 | T | C | 60 | a0001c0001t0002g0206 a0001c0001t0002g0233 a0001c0001t0002g0234 others(57): Show |
64 | HG01074.hp2 HG01175.hp2 HG01891.hp2 others(61): Show |
intron_variant | MODIFIER | c.-478+12881T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554555 | |||||||
| chr1:147554594 | A | C | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+12920A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554594 | |||||||
| chr1:147554688 | G | A | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+13014G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554688 | |||||||
| chr1:147554737 | T | C | 1 | a0001c0001t0004g0060 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-478+13063T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554737 | |||||||
| chr1:147554882 | G | C | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+13208G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554882 | |||||||
| chr1:147554935 | A | C | 1 | a0001c0001t0006g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-478+13261A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554935 | |||||||
| chr1:147554947 | T | C | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(5): Show |
8 | HG00438.hp1 HG00544.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-478+13273T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147554947 | |||||||
| chr1:147555222 | T | C | 1 | a0001c0001t0019g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-478+13548T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555222 | |||||||
| chr1:147555448 | C | T | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+13774C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555448 | |||||||
| chr1:147555531 | G | T | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+13857G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555531 | |||||||
| chr1:147555580 | T | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+13906T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555580 | |||||||
| chr1:147555593 | T | C | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+13919T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555593 | |||||||
| chr1:147555594 | C | T | 2 | a0001c0001t0005g0128 a0001c0001t0005g0129 |
2 | NA18955.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-478+13920C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555594 | |||||||
| chr1:147555691 | C | T | 4 | a0001c0001t0002g0253 a0001c0001t0002g0264 a0001c0001t0003g0255 others(1): Show |
4 | HG02080.hp1 NA18983.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-478+14017C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555691 | |||||||
| chr1:147555713 | C | T | 3 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 |
3 | HG02145.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-478+14039C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555713 | |||||||
| chr1:147555803 | A | G | 1 | a0004c0005t0001g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-478+14129A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147555803 | |||||||
| chr1:147556092 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+14418A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147556092 | |||||||
| chr1:147556267 | C | T | 4 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+14593C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147556267 | |||||||
| chr1:147556284 | A | AT | 273 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(270): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-478+14622dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147556284 | ||||||
| chr1:147556284 | A | ATT | 9 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(6): Show |
14 | HG00609.hp1 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-478+14621_-478+14 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147556284 | ||||||
| chr1:147556326 | A | G | 1 | a0001c0001t0019g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-478+14652A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147556326 | |||||||
| chr1:147556416 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-478+14742G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147556416 | |||||||
| chr1:147556442 | ATTATTTT others(5): Show |
A | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+14783_-478+14 others(18): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147556442 | ||||||
| chr1:147556486 | C | G | 1 | a0001c0001t0006g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-478+14812C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147556486 | |||||||
| chr1:147556713 | G | A | 4 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0014g0235 others(1): Show |
4 | HG02818.hp1 NA19043.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+15039G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147556713 | |||||||
| chr1:147556878 | T | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+15204T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147556878 | |||||||
| chr1:147556953 | C | T | 1 | a0001c0001t0010g0283 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-478+15279C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147556953 | |||||||
| chr1:147557143 | G | A | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+15469G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557143 | |||||||
| chr1:147557180 | T | C | 1 | a0001c0001t0004g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-478+15506T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557180 | |||||||
| chr1:147557185 | T | A | 3 | a0001c0001t0011g0146 a0002c0002t0001g0014 a0004c0005t0001g0147 |
4 | HG00323.hp1 HG01175.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+15511T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557185 | |||||||
| chr1:147557235 | A | G | 1 | a0001c0001t0021g0220 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-478+15561A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557235 | |||||||
| chr1:147557403 | A | G | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+15729A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557403 | |||||||
| chr1:147557509 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-478+15835G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557509 | |||||||
| chr1:147557594 | C | T | 1 | a0002c0002t0001g0014 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-478+15920C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557594 | |||||||
| chr1:147557613 | G | A | 1 | a0001c0001t0016g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-478+15939G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557613 | |||||||
| chr1:147557666 | C | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+15992C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557666 | |||||||
| chr1:147557683 | G | A | 1 | a0001c0001t0010g0283 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-478+16009G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557683 | |||||||
| chr1:147557698 | G | A | 151 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(148): Show |
165 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-478+16024G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557698 | |||||||
| chr1:147557789 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-478+16115A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557789 | |||||||
| chr1:147557790 | T | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+16116T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557790 | |||||||
| chr1:147557960 | TG | T | 3 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 |
3 | HG02145.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-478+16287delG | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147557960 | |||||||
| chr1:147558140 | C | T | 9 | a0001c0001t0002g0281 a0001c0001t0006g0271 a0001c0001t0006g0272 others(6): Show |
9 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-478+16466C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147558140 | |||||||
| chr1:147558153 | T | C | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+16479T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147558153 | |||||||
| chr1:147558455 | G | A | 1 | a0001c0001t0004g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-478+16781G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147558455 | |||||||
| chr1:147558576 | A | T | 60 | a0001c0001t0002g0206 a0001c0001t0002g0233 a0001c0001t0002g0234 others(57): Show |
64 | HG01074.hp2 HG01175.hp2 HG01891.hp2 others(61): Show |
intron_variant | MODIFIER | c.-478+16902A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147558576 | |||||||
| chr1:147558633 | C | T | 1 | a0001c0001t0011g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-478+16959C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147558633 | |||||||
| chr1:147558681 | G | A | 41 | a0001c0001t0001g0015 a0001c0001t0001g0074 a0001c0001t0001g0088 others(38): Show |
45 | HG00140.hp1 HG01071.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-478+17007G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147558681 | |||||||
| chr1:147558848 | C | T | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+17174C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147558848 | |||||||
| chr1:147559118 | C | G | 1 | a0001c0001t0014g0229 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-478+17444C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147559118 | |||||||
| chr1:147559126 | TTC | T | 8 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0006g0275 others(5): Show |
9 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-478+17454_-478+17 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147559126 | ||||||
| chr1:147559128 | C | CT | 184 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(181): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-478+17466dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147559128 | ||||||
| chr1:147559545 | A | G | 9 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(6): Show |
14 | HG00609.hp1 HG01081.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-478+17871A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147559545 | |||||||
| chr1:147559775 | G | A | 1 | a0001c0001t0003g0165 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-478+18101G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147559775 | |||||||
| chr1:147559832 | T | A | 4 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+18158T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147559832 | |||||||
| chr1:147559905 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-478+18231T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147559905 | |||||||
| chr1:147559951 | G | A | 4 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+18277G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147559951 | |||||||
| chr1:147560171 | G | A | 1 | a0001c0001t0011g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-478+18497G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147560171 | |||||||
| chr1:147560230 | C | T | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+18556C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147560230 | |||||||
| chr1:147560312 | G | A | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+18638G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147560312 | |||||||
| chr1:147560417 | C | G | 1 | a0001c0001t0025g0239 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-478+18743C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147560417 | |||||||
| chr1:147560535 | A | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+18861A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147560535 | |||||||
| chr1:147560715 | C | G | 1 | a0001c0001t0003g0187 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-478+19041C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147560715 | |||||||
| chr1:147560802 | G | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+19128G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147560802 | |||||||
| chr1:147560859 | A | T | 2 | a0001c0001t0004g0001 a0001c0001t0004g0125 |
5 | NA18942.hp2 NA18960.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+19185A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147560859 | |||||||
| chr1:147561000 | G | A | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
3 | HG01099.hp2 HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-478+19326G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147561000 | |||||||
| chr1:147561442 | T | C | 1 | a0001c0001t0006g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-478+19768T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147561442 | |||||||
| chr1:147561529 | C | A | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+19855C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147561529 | |||||||
| chr1:147561577 | A | G | 1 | a0001c0001t0008g0158 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-478+19903A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147561577 | |||||||
| chr1:147561794 | A | G | 72 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0206 others(69): Show |
81 | HG00609.hp1 HG01074.hp2 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.-478+20120A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147561794 | |||||||
| chr1:147561804 | C | G | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+20130C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147561804 | |||||||
| chr1:147562011 | G | C | 2 | a0001c0001t0011g0070 a0001c0001t0011g0148 |
2 | HG03831.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-478+20337G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562011 | |||||||
| chr1:147562068 | C | T | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+20394C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562068 | |||||||
| chr1:147562093 | C | G | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+20419C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562093 | |||||||
| chr1:147562119 | G | A | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+20445G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562119 | |||||||
| chr1:147562176 | A | G | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+20502A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562176 | |||||||
| chr1:147562317 | G | A | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+20643G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562317 | |||||||
| chr1:147562331 | A | AAAATAAA others(1): Show |
6 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-478+20673_-478+20 others(14): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147562331 | ||||||
| chr1:147562383 | G | A | 27 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0281 others(24): Show |
27 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(24): Show |
intron_variant | MODIFIER | c.-478+20709G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562383 | |||||||
| chr1:147562399 | T | C | 6 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-478+20725T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562399 | |||||||
| chr1:147562670 | G | A | 6 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-478+20996G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562670 | |||||||
| chr1:147562713 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-478+21039T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562713 | |||||||
| chr1:147562724 | A | G | 1 | a0001c0001t0016g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-478+21050A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562724 | |||||||
| chr1:147562825 | T | C | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-478+21151T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147562825 | |||||||
| chr1:147563004 | T | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+21330T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563004 | |||||||
| chr1:147563188 | T | C | 5 | a0001c0001t0002g0276 a0001c0001t0006g0192 a0001c0001t0006g0282 others(2): Show |
5 | HG01074.hp2 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+21514T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563188 | |||||||
| chr1:147563277 | C | T | 2 | a0001c0001t0006g0237 a0001c0001t0006g0238 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-478+21603C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563277 | |||||||
| chr1:147563330 | A | G | 1 | a0001c0001t0010g0016 | 2 | NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-478+21656A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563330 | |||||||
| chr1:147563341 | A | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+21667A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563341 | |||||||
| chr1:147563357 | C | A | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-478+21683C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563357 | |||||||
| chr1:147563382 | A | T | 1 | a0001c0001t0014g0229 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-478+21708A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563382 | |||||||
| chr1:147563473 | T | A | 2 | a0001c0001t0017g0244 a0001c0001t0020g0245 |
2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-478+21799T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563473 | |||||||
| chr1:147563505 | A | G | 1 | a0001c0001t0014g0229 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-478+21831A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563505 | |||||||
| chr1:147563716 | C | T | 1 | a0001c0001t0006g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-478+22042C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563716 | |||||||
| chr1:147563796 | A | G | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+22122A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563796 | |||||||
| chr1:147563798 | C | T | 72 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0206 others(69): Show |
81 | HG00609.hp1 HG01074.hp2 HG01081.hp2 others(78): Show |
intron_variant | MODIFIER | c.-478+22124C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563798 | |||||||
| chr1:147563934 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-478+22260C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147563934 | |||||||
| chr1:147564069 | C | T | 6 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-478+22395C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564069 | |||||||
| chr1:147564257 | C | T | 1 | a0001c0001t0006g0272 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-478+22583C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564257 | |||||||
| chr1:147564283 | C | A | 3 | a0001c0001t0012g0242 a0001c0001t0019g0274 a0001c0001t0024g0194 |
3 | HG01081.hp2 HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-478+22609C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564283 | |||||||
| chr1:147564300 | G | A | 1 | a0001c0001t0003g0023 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-478+22626G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564300 | |||||||
| chr1:147564355 | CT | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+22684delT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147564355 | ||||||
| chr1:147564441 | G | T | 1 | a0001c0001t0029g0135 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-478+22767G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564441 | |||||||
| chr1:147564455 | C | A | 1 | a0001c0001t0028g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-478+22781C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564455 | |||||||
| chr1:147564456 | T | G | 1 | a0001c0001t0005g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-478+22782T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564456 | |||||||
| chr1:147564479 | T | C | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+22805T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564479 | |||||||
| chr1:147564673 | A | G | 1 | a0001c0001t0005g0155 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-478+22999A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564673 | |||||||
| chr1:147564683 | G | C | 1 | a0001c0001t0006g0275 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-478+23009G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564683 | |||||||
| chr1:147564918 | T | A | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+23244T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564918 | |||||||
| chr1:147564923 | A | G | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+23249A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564923 | |||||||
| chr1:147564980 | T | C | 1 | a0001c0001t0006g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-478+23306T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564980 | |||||||
| chr1:147564988 | T | TGAGTACA others(14): Show |
1 | a0001c0001t0004g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-478+23315_-478+23 others(27): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147564988 | ||||||
| chr1:147564988 | T | TTTCGAGT others(17): Show |
1 | a0001c0001t0004g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-478+23314_-478+23 others(30): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564988 | |||||||
| chr1:147564992 | A | G | 2 | a0001c0001t0004g0090 a0001c0001t0004g0124 |
2 | HG02071.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-478+23318A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147564992 | |||||||
| chr1:147565378 | A | T | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+23704A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147565378 | |||||||
| chr1:147565690 | A | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+24016A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147565690 | |||||||
| chr1:147565767 | C | T | 6 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-478+24093C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147565767 | |||||||
| chr1:147565790 | T | C | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-478+24116T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147565790 | |||||||
| chr1:147565816 | A | G | 3 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 |
3 | HG02145.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-478+24142A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147565816 | |||||||
| chr1:147565825 | T | C | 57 | a0001c0001t0002g0206 a0001c0001t0002g0233 a0001c0001t0002g0234 others(54): Show |
61 | HG01074.hp2 HG01175.hp2 HG01891.hp2 others(58): Show |
intron_variant | MODIFIER | c.-478+24151T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147565825 | |||||||
| chr1:147565866 | T | C | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+24192T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147565866 | |||||||
| chr1:147565928 | T | G | 1 | a0001c0001t0014g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-478+24254T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147565928 | |||||||
| chr1:147566049 | G | A | 8 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(5): Show |
13 | HG00609.hp1 HG01081.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-478+24375G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566049 | |||||||
| chr1:147566111 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-478+24437T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566111 | |||||||
| chr1:147566157 | A | G | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-478+24483A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566157 | |||||||
| chr1:147566175 | G | A | 4 | a0001c0001t0013g0167 a0001c0001t0013g0168 a0001c0001t0013g0169 others(1): Show |
4 | NA18977.hp2 NA18997.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-478+24501G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566175 | |||||||
| chr1:147566346 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+24672G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566346 | |||||||
| chr1:147566347 | A | G | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+24673A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566347 | |||||||
| chr1:147566450 | C | T | 82 | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0034 others(79): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-478+24776C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566450 | |||||||
| chr1:147566532 | G | T | 82 | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0034 others(79): Show |
87 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-478+24858G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566532 | |||||||
| chr1:147566608 | T | A | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-478+24934T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566608 | |||||||
| chr1:147566613 | G | A | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+24939G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566613 | |||||||
| chr1:147566656 | C | T | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-478+24982C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566656 | |||||||
| chr1:147566736 | G | T | 1 | a0001c0001t0006g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-478+25062G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566736 | |||||||
| chr1:147566756 | CAAAAAAA others(3): Show |
C | 83 | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0034 others(80): Show |
88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-478+25096_-478+25 others(16): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147566756 | ||||||
| chr1:147566766 | G | GA | 194 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(191): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.-478+25101dupA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147566766 | ||||||
| chr1:147566769 | AAAAAAAG | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+25099_-478+25 others(13): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147566769 | ||||||
| chr1:147566900 | G | A | 1 | a0001c0001t0006g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-478+25226G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566900 | |||||||
| chr1:147566942 | C | G | 85 | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0034 others(82): Show |
90 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-478+25268C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147566942 | |||||||
| chr1:147567153 | G | C | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-478+25479G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147567153 | |||||||
| chr1:147567200 | C | A | 1 | a0001c0001t0003g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-478+25526C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147567200 | |||||||
| chr1:147567326 | C | G | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-478+25652C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147567326 | |||||||
| chr1:147567474 | T | C | 3 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 |
3 | HG02145.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-478+25800T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147567474 | |||||||
| chr1:147567641 | C | A | 1 | a0001c0001t0016g0266 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-478+25967C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147567641 | |||||||
| chr1:147567650 | A | C | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+25976A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147567650 | |||||||
| chr1:147567724 | G | C | 2 | a0001c0001t0007g0072 a0001c0001t0007g0149 |
2 | HG02273.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-478+26050G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147567724 | |||||||
| chr1:147567975 | C | T | 2 | a0001c0001t0004g0134 a0001c0001t0007g0120 |
2 | HG00323.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-478+26301C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147567975 | |||||||
| chr1:147568003 | C | T | 1 | a0003c0004t0001g0123 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-478+26329C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568003 | |||||||
| chr1:147568016 | C | T | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+26342C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568016 | |||||||
| chr1:147568064 | G | C | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-478+26390G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568064 | |||||||
| chr1:147568174 | G | C | 1 | a0001c0001t0008g0193 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-478+26500G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568174 | |||||||
| chr1:147568214 | T | A | 53 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(50): Show |
58 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-478+26540T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568214 | |||||||
| chr1:147568295 | A | T | 154 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(151): Show |
168 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.-478+26621A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568295 | |||||||
| chr1:147568475 | C | CAA | 8 | a0002c0002t0001g0091 a0002c0002t0001g0092 a0002c0002t0001g0093 others(5): Show |
9 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-478+26806_-478+26 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147568475 | ||||||
| chr1:147568482 | G | A | 8 | a0002c0002t0001g0091 a0002c0002t0001g0092 a0002c0002t0001g0093 others(5): Show |
9 | HG00140.hp2 HG00280.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-478+26808G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568482 | |||||||
| chr1:147568482 | G | GA | 78 | a0001c0001t0002g0019 a0001c0001t0002g0031 a0001c0001t0002g0034 others(75): Show |
83 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-478+26818dupA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147568482 | ||||||
| chr1:147568482 | G | GAA | 194 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(191): Show |
218 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.-478+26817_-478+26 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147568482 | ||||||
| chr1:147568521 | C | G | 1 | a0004c0005t0018g0277 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-478+26847C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568521 | |||||||
| chr1:147568648 | A | C | 3 | a0001c0001t0011g0146 a0002c0002t0001g0014 a0004c0005t0001g0147 |
4 | HG00323.hp1 HG01175.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-478+26974A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568648 | |||||||
| chr1:147568731 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-478+27057A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568731 | |||||||
| chr1:147568819 | G | A | 1 | a0001c0001t0004g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-478+27145G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568819 | |||||||
| chr1:147568828 | T | G | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-478+27154T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568828 | |||||||
| chr1:147568930 | C | T | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-478+27256C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147568930 | |||||||
| chr1:147569111 | G | A | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-478+27437G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569111 | |||||||
| chr1:147569144 | C | T | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+27470C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569144 | |||||||
| chr1:147569158 | T | A | 154 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(151): Show |
168 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.-478+27484T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569158 | |||||||
| chr1:147569235 | T | G | 1 | a0001c0001t0005g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-478+27561T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569235 | |||||||
| chr1:147569348 | C | G | 9 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(6): Show |
14 | HG00609.hp1 HG01081.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-478+27674C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569348 | |||||||
| chr1:147569468 | A | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+27794A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569468 | |||||||
| chr1:147569473 | C | CAA | 185 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0037 others(182): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-478+27813_-478+27 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147569473 | ||||||
| chr1:147569473 | C | CAAA | 89 | a0001c0001t0001g0015 a0001c0001t0002g0019 a0001c0001t0002g0031 others(86): Show |
95 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-478+27812_-478+27 others(9): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147569473 | ||||||
| chr1:147569488 | A | AAAAG | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+27814_-478+27 others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569488 | |||||||
| chr1:147569489 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+27815G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569489 | |||||||
| chr1:147569493 | G | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+27819G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569493 | |||||||
| chr1:147569502 | C | T | 150 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(147): Show |
164 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.-478+27828C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569502 | |||||||
| chr1:147569526 | C | T | 11 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0003g0003 others(8): Show |
14 | HG00423.hp2 HG00544.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.-478+27852C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569526 | |||||||
| chr1:147569645 | G | A | 1 | a0001c0001t0009g0202 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-478+27971G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569645 | |||||||
| chr1:147569781 | T | C | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+28107T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147569781 | |||||||
| chr1:147570183 | A | G | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+28509A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570183 | |||||||
| chr1:147570366 | T | C | 3 | a0001c0001t0010g0283 a0001c0001t0012g0204 a0001c0001t0012g0205 |
3 | HG01952.hp2 HG02486.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-478+28692T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570366 | |||||||
| chr1:147570390 | G | C | 57 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(54): Show |
62 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-478+28716G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570390 | |||||||
| chr1:147570551 | G | A | 2 | a0001c0001t0011g0146 a0004c0005t0001g0147 |
2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-478+28877G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570551 | |||||||
| chr1:147570584 | G | GC | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+28916dupC | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147570584 | ||||||
| chr1:147570631 | T | TTTTC | 70 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0037 others(67): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-478+28960_-478+28 others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147570631 | ||||||
| chr1:147570632 | T | TTTC | 84 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0045 others(81): Show |
88 | HG00140.hp1 HG00673.hp2 HG01071.hp2 others(85): Show |
intron_variant | MODIFIER | c.-478+28960_-478+28 others(9): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147570632 | ||||||
| chr1:147570633 | T | TTC | 39 | a0001c0001t0001g0074 a0001c0001t0002g0206 a0001c0001t0002g0276 others(36): Show |
43 | HG01074.hp2 HG01175.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.-478+28960_-478+28 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147570633 | ||||||
| chr1:147570634 | T | TC | 86 | a0001c0001t0001g0098 a0001c0001t0002g0002 a0001c0001t0002g0019 others(83): Show |
96 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-478+28960_-478+28 others(7): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570634 | |||||||
| chr1:147570635 | T | C | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+28961T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570635 | |||||||
| chr1:147570639 | C | T | 198 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(195): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.-478+28965C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570639 | |||||||
| chr1:147570644 | T | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+28970T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570644 | |||||||
| chr1:147570653 | T | TG | 57 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(54): Show |
62 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-478+28979_-478+28 others(7): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570653 | |||||||
| chr1:147570653 | T | TTG | 21 | a0001c0001t0001g0098 a0001c0001t0002g0019 a0001c0001t0002g0248 others(18): Show |
21 | HG00639.hp1 HG00738.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-478+28979_-478+28 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570653 | |||||||
| chr1:147570716 | A | T | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+29042A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570716 | |||||||
| chr1:147570792 | C | T | 1 | a0001c0001t0005g0186 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-478+29118C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570792 | |||||||
| chr1:147570814 | C | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+29140C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570814 | |||||||
| chr1:147570815 | A | C | 1 | a0002c0002t0001g0051 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-478+29141A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570815 | |||||||
| chr1:147570826 | GGTTTCTC others(1938): Show |
G | 1 | a0001c0001t0005g0073 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-478+29158_-478+31 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147570826 | ||||||
| chr1:147570862 | T | C | 155 | a0001c0001t0001g0098 a0001c0001t0002g0002 a0001c0001t0002g0019 others(152): Show |
169 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-478+29188T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570862 | |||||||
| chr1:147570923 | C | T | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+29249C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570923 | |||||||
| chr1:147570936 | A | G | 1 | a0001c0001t0004g0145 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-478+29262A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147570936 | |||||||
| chr1:147571163 | T | C | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-478+29489T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571163 | |||||||
| chr1:147571229 | G | A | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-478+29555G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571229 | |||||||
| chr1:147571379 | A | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+29705A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571379 | |||||||
| chr1:147571392 | C | T | 1 | a0001c0001t0009g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-478+29718C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571392 | |||||||
| chr1:147571426 | G | A | 1 | a0001c0001t0012g0204 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-478+29752G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571426 | |||||||
| chr1:147571474 | C | G | 61 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0233 others(58): Show |
65 | HG01074.hp2 HG01175.hp2 HG01433.hp1 others(62): Show |
intron_variant | MODIFIER | c.-478+29800C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571474 | |||||||
| chr1:147571492 | G | A | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-478+29818G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571492 | |||||||
| chr1:147571519 | A | T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(6): Show |
14 | HG00609.hp1 HG01081.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-478+29845A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571519 | |||||||
| chr1:147571754 | G | A | 78 | a0001c0001t0001g0098 a0001c0001t0002g0019 a0001c0001t0002g0031 others(75): Show |
83 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-478+30080G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571754 | |||||||
| chr1:147571906 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-478+30232C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571906 | |||||||
| chr1:147571991 | G | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0112 others(5): Show |
9 | HG02132.hp2 NA18951.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.-478+30317G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147571991 | |||||||
| chr1:147572002 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-478+30328C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572002 | |||||||
| chr1:147572007 | G | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+30333G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572007 | |||||||
| chr1:147572056 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-478+30382G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572056 | |||||||
| chr1:147572067 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-478+30393G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572067 | |||||||
| chr1:147572083 | C | CAA | 211 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(208): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.-478+30417_-478+30 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147572083 | ||||||
| chr1:147572083 | C | CAAA | 65 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0233 others(62): Show |
69 | HG01074.hp2 HG01081.hp2 HG01175.hp2 others(66): Show |
intron_variant | MODIFIER | c.-478+30416_-478+30 others(9): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147572083 | ||||||
| chr1:147572083 | C | CAAAA | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(3): Show |
11 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-478+30415_-478+30 others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147572083 | ||||||
| chr1:147572103 | G | A | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-478+30429G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572103 | |||||||
| chr1:147572131 | A | G | 2 | a0001c0001t0006g0237 a0001c0001t0006g0238 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-478+30457A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572131 | |||||||
| chr1:147572217 | G | A | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-478+30543G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572217 | |||||||
| chr1:147572220 | CA | C | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+30548delA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147572220 | ||||||
| chr1:147572244 | AAAAAAC | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(4): Show |
12 | HG00609.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-478+30593_-478+30 others(12): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147572244 | ||||||
| chr1:147572278 | A | G | 1 | a0001c0001t0028g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-478+30604A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572278 | |||||||
| chr1:147572384 | A | T | 1 | a0001c0001t0005g0129 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-478+30710A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572384 | |||||||
| chr1:147572890 | G | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0170 |
2 | HG02074.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-478+31216G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572890 | |||||||
| chr1:147572957 | G | A | 1 | a0001c0001t0029g0135 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-478+31283G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147572957 | |||||||
| chr1:147573064 | G | T | 8 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0268 others(5): Show |
13 | HG00609.hp1 HG01081.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-478+31390G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147573064 | |||||||
| chr1:147573127 | A | G | 1 | a0001c0001t0004g0145 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-478+31453A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147573127 | |||||||
| chr1:147573233 | C | G | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-477-31544C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147573233 | |||||||
| chr1:147573240 | C | T | 2 | a0001c0001t0008g0211 a0001c0001t0022g0212 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-477-31537C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147573240 | |||||||
| chr1:147573444 | ACT | A | 52 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(49): Show |
57 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.-477-31330_-477-31 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147573444 | ||||||
| chr1:147573641 | A | G | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-477-31136A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147573641 | |||||||
| chr1:147573993 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-477-30784T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147573993 | |||||||
| chr1:147574039 | A | G | 1 | a0001c0001t0019g0274 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-477-30738A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147574039 | |||||||
| chr1:147574084 | C | G | 19 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0046 others(16): Show |
19 | HG00597.hp2 HG00673.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.-477-30693C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147574084 | |||||||
| chr1:147574303 | C | T | 1 | a0001c0001t0017g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-477-30474C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147574303 | |||||||
| chr1:147575009 | G | T | 1 | a0001c0001t0002g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-477-29768G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147575009 | |||||||
| chr1:147575033 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-477-29744G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147575033 | |||||||
| chr1:147575502 | A | G | 2 | a0001c0001t0007g0058 a0001c0001t0007g0059 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-477-29275A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147575502 | |||||||
| chr1:147575759 | T | C | 3 | a0001c0001t0012g0242 a0001c0001t0019g0274 a0001c0001t0024g0194 |
3 | HG01081.hp2 HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-477-29018T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147575759 | |||||||
| chr1:147575799 | A | G | 11 | a0001c0001t0002g0281 a0001c0001t0006g0271 a0001c0001t0006g0272 others(8): Show |
11 | HG02055.hp1 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-477-28978A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147575799 | |||||||
| chr1:147575881 | C | CA | 155 | a0001c0001t0001g0098 a0001c0001t0002g0002 a0001c0001t0002g0019 others(152): Show |
169 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-477-28894dupA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147575881 | ||||||
| chr1:147576058 | C | A | 1 | a0001c0001t0003g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-477-28719C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576058 | |||||||
| chr1:147576210 | A | G | 1 | a0005c0009t0005g0032 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-477-28567A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576210 | |||||||
| chr1:147576307 | G | C | 57 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(54): Show |
62 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-477-28470G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576307 | |||||||
| chr1:147576319 | G | T | 31 | a0001c0001t0002g0221 a0001c0001t0002g0233 a0001c0001t0002g0234 others(28): Show |
31 | HG01433.hp1 HG01884.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.-477-28458G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576319 | |||||||
| chr1:147576361 | C | T | 6 | a0001c0001t0002g0019 a0001c0001t0002g0248 a0001c0001t0002g0249 others(3): Show |
6 | HG00738.hp2 HG01192.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-477-28416C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576361 | |||||||
| chr1:147576437 | T | C | 3 | a0001c0001t0012g0242 a0001c0001t0019g0274 a0001c0001t0024g0194 |
3 | HG01081.hp2 HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-477-28340T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576437 | |||||||
| chr1:147576459 | G | A | 4 | a0001c0001t0004g0060 a0001c0001t0004g0121 a0001c0001t0004g0122 others(1): Show |
4 | HG01071.hp1 HG01192.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-477-28318G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576459 | |||||||
| chr1:147576573 | A | G | 3 | a0001c0001t0012g0242 a0001c0001t0019g0274 a0001c0001t0024g0194 |
3 | HG01081.hp2 HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-477-28204A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576573 | |||||||
| chr1:147576808 | G | A | 155 | a0001c0001t0001g0098 a0001c0001t0002g0002 a0001c0001t0002g0019 others(152): Show |
169 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-477-27969G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576808 | |||||||
| chr1:147576861 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-477-27916A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147576861 | |||||||
| chr1:147577053 | T | A | 3 | a0001c0001t0012g0242 a0001c0001t0019g0274 a0001c0001t0024g0194 |
3 | HG01081.hp2 HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-477-27724T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147577053 | |||||||
| chr1:147577165 | C | T | 9 | a0001c0001t0002g0276 a0001c0001t0006g0282 a0001c0001t0007g0058 others(6): Show |
9 | HG01074.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-477-27612C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147577165 | |||||||
| chr1:147577213 | C | T | 1 | a0001c0001t0008g0210 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-477-27564C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147577213 | |||||||
| chr1:147577243 | T | G | 1 | a0001c0001t0005g0077 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-477-27534T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147577243 | |||||||
| chr1:147577381 | T | A | 1 | a0001c0001t0010g0199 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-477-27396T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147577381 | |||||||
| chr1:147577392 | G | A | 2 | a0001c0001t0002g0281 a0001c0001t0006g0272 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-477-27385G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147577392 | |||||||
| chr1:147577834 | A | ATG | 20 | a0001c0001t0001g0045 a0001c0001t0001g0074 a0001c0001t0001g0088 others(17): Show |
23 | HG00609.hp2 HG00621.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.-477-26907_-477-26 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTG | 36 | a0001c0001t0001g0098 a0001c0001t0002g0019 a0001c0001t0002g0221 others(33): Show |
37 | HG00738.hp2 HG01071.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.-477-26909_-477-26 others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTGTG | 75 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0034 others(72): Show |
84 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.-477-26911_-477-26 others(12): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTGTGT others(1): Show |
17 | a0001c0001t0002g0234 a0001c0001t0002g0276 a0001c0001t0003g0159 others(14): Show |
17 | HG00323.hp1 HG01074.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-477-26913_-477-26 others(14): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTGTGT others(3): Show |
20 | a0001c0001t0002g0031 a0001c0001t0002g0259 a0001c0001t0003g0003 others(17): Show |
23 | HG00544.hp1 HG01081.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.-477-26915_-477-26 others(16): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTGTGT others(5): Show |
6 | a0001c0001t0002g0176 a0001c0001t0003g0023 a0001c0001t0003g0165 others(3): Show |
6 | HG02056.hp1 HG02523.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.-477-26917_-477-26 others(18): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTGTGT others(7): Show |
18 | a0001c0001t0002g0179 a0001c0001t0002g0188 a0001c0001t0003g0024 others(15): Show |
19 | HG00438.hp2 HG00558.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.-477-26919_-477-26 others(20): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTGTGT others(9): Show |
2 | a0001c0001t0002g0183 a0001c0001t0013g0168 |
2 | NA18997.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-477-26921_-477-26 others(22): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTGTGT others(11): Show |
1 | a0001c0001t0003g0026 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-477-26923_-477-26 others(24): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | A | ATGTGTGT others(13): Show |
1 | a0001c0001t0013g0169 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-477-26925_-477-26 others(26): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147577834 | ATGTG | A | 4 | a0001c0001t0004g0065 a0001c0001t0010g0283 a0001c0001t0012g0204 others(1): Show |
4 | HG00544.hp2 HG01952.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-477-26909_-477-26 others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147577834 | ||||||
| chr1:147578078 | C | T | 56 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0176 others(53): Show |
61 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-477-26699C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147578078 | |||||||
| chr1:147578197 | A | G | 40 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0131 others(37): Show |
43 | HG00140.hp1 HG01071.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.-477-26580A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147578197 | |||||||
| chr1:147578558 | C | T | 1 | a0001c0001t0010g0283 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-477-26219C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147578558 | |||||||
| chr1:147578721 | A | G | 1 | a0001c0001t0012g0242 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-477-26056A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147578721 | |||||||
| chr1:147578758 | G | A | 2 | a0001c0001t0012g0242 a0001c0001t0019g0274 |
2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-477-26019G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147578758 | |||||||
| chr1:147578797 | T | C | 121 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0098 others(118): Show |
129 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.-477-25980T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147578797 | |||||||
| chr1:147578865 | C | CTT | 62 | a0001c0001t0002g0206 a0001c0001t0002g0221 a0001c0001t0002g0233 others(59): Show |
66 | HG01175.hp2 HG01433.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.-477-25904_-477-25 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147578865 | ||||||
| chr1:147579016 | C | A | 2 | a0001c0001t0007g0010 a0001c0001t0007g0069 |
3 | HG01099.hp2 HG01346.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-477-25761C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579016 | |||||||
| chr1:147579220 | A | C | 2 | a0001c0001t0006g0237 a0001c0001t0006g0238 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-477-25557A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579220 | |||||||
| chr1:147579258 | G | A | 62 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0131 others(59): Show |
68 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-477-25519G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579258 | |||||||
| chr1:147579408 | A | G | 1 | a0001c0001t0012g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-477-25369A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579408 | |||||||
| chr1:147579502 | C | T | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-477-25275C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579502 | |||||||
| chr1:147579573 | A | C | 1 | a0001c0001t0004g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-477-25204A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579573 | |||||||
| chr1:147579693 | C | T | 28 | a0001c0001t0001g0074 a0001c0001t0004g0068 a0001c0001t0005g0036 others(25): Show |
30 | HG00140.hp1 HG01071.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-477-25084C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579693 | |||||||
| chr1:147579755 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-477-25022C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579755 | |||||||
| chr1:147579846 | G | A | 1 | a0001c0001t0008g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-477-24931G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579846 | |||||||
| chr1:147579946 | T | G | 2 | a0001c0001t0004g0043 a0001c0001t0004g0066 |
2 | HG02071.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-477-24831T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147579946 | |||||||
| chr1:147580090 | T | C | 4 | a0001c0001t0001g0056 a0001c0001t0007g0099 a0001c0001t0025g0239 others(1): Show |
4 | HG02109.hp1 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-477-24687T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147580090 | |||||||
| chr1:147580092 | C | T | 1 | a0001c0001t0014g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-477-24685C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147580092 | |||||||
| chr1:147580272 | T | C | 2 | a0001c0001t0007g0083 a0001c0001t0019g0274 |
2 | HG00140.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-477-24505T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147580272 | |||||||
| chr1:147580402 | C | T | 1 | a0001c0001t0010g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-477-24375C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147580402 | |||||||
| chr1:147580555 | C | T | 1 | a0001c0001t0012g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-477-24222C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147580555 | |||||||
| chr1:147580784 | A | C | 1 | a0001c0001t0009g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-477-23993A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147580784 | |||||||
| chr1:147580855 | G | C | 24 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0216 others(21): Show |
25 | HG01175.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-477-23922G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147580855 | |||||||
| chr1:147580985 | TTGA | T | 3 | a0001c0001t0004g0063 a0001c0001t0004g0065 a0001c0001t0004g0068 |
3 | HG00544.hp2 HG02132.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-477-23787_-477-23 others(9): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147580985 | ||||||
| chr1:147581000 | G | A | 24 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0216 others(21): Show |
25 | HG01175.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-477-23777G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147581000 | |||||||
| chr1:147581540 | G | A | 94 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(91): Show |
102 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-477-23237G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147581540 | |||||||
| chr1:147581629 | C | T | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-477-23148C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147581629 | |||||||
| chr1:147581640 | T | G | 261 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(258): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-477-23137T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147581640 | |||||||
| chr1:147581874 | T | C | 4 | a0001c0001t0006g0284 a0001c0001t0007g0191 a0001c0001t0009g0218 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-477-22903T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147581874 | |||||||
| chr1:147581875 | A | G | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-22902A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147581875 | |||||||
| chr1:147582206 | C | T | 1 | a0001c0006t0010g0172 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-477-22571C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147582206 | |||||||
| chr1:147582273 | A | T | 120 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(117): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-477-22504A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147582273 | |||||||
| chr1:147582308 | T | C | 2 | a0001c0001t0006g0203 a0001c0001t0011g0130 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-477-22469T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147582308 | |||||||
| chr1:147582433 | A | G | 124 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(121): Show |
133 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.-477-22344A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147582433 | |||||||
| chr1:147582520 | T | C | 6 | a0001c0001t0007g0058 a0001c0001t0007g0059 a0001c0001t0009g0197 others(3): Show |
6 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-477-22257T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147582520 | |||||||
| chr1:147582555 | G | A | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-477-22222G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147582555 | |||||||
| chr1:147582746 | T | A | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-477-22031T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147582746 | |||||||
| chr1:147583057 | A | G | 121 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(118): Show |
135 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-477-21720A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147583057 | |||||||
| chr1:147583261 | A | G | 1 | a0002c0002t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-477-21516A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147583261 | |||||||
| chr1:147583361 | T | A | 1 | a0001c0001t0011g0126 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-477-21416T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147583361 | |||||||
| chr1:147583507 | G | A | 3 | a0001c0001t0006g0223 a0001c0001t0009g0267 a0001c0001t0021g0220 |
3 | HG01884.hp2 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-477-21270G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147583507 | |||||||
| chr1:147583588 | G | A | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-477-21189G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147583588 | |||||||
| chr1:147583674 | C | A | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-477-21103C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147583674 | |||||||
| chr1:147583910 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-477-20867G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147583910 | |||||||
| chr1:147584092 | G | A | 1 | a0001c0001t0004g0100 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-477-20685G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584092 | |||||||
| chr1:147584140 | C | T | 94 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(91): Show |
102 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-477-20637C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584140 | |||||||
| chr1:147584336 | C | T | 1 | a0002c0002t0007g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-477-20441C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584336 | |||||||
| chr1:147584347 | G | A | 1 | a0001c0001t0006g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-477-20430G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584347 | |||||||
| chr1:147584386 | C | CT | 123 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(120): Show |
132 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.-477-20383dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147584386 | ||||||
| chr1:147584428 | T | A | 1 | a0001c0001t0003g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-477-20349T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584428 | |||||||
| chr1:147584436 | A | G | 1 | a0001c0001t0004g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-477-20341A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584436 | |||||||
| chr1:147584478 | A | C | 128 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(125): Show |
137 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-477-20299A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584478 | |||||||
| chr1:147584481 | T | A | 155 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(152): Show |
170 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-477-20296T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584481 | |||||||
| chr1:147584684 | G | T | 2 | a0001c0001t0003g0177 a0001c0001t0005g0081 |
2 | HG02523.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-477-20093G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584684 | |||||||
| chr1:147584806 | C | A | 23 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0138 others(20): Show |
29 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.-477-19971C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584806 | |||||||
| chr1:147584832 | C | T | 1 | a0002c0003t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-477-19945C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584832 | |||||||
| chr1:147584957 | G | A | 1 | a0001c0001t0011g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-477-19820G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147584957 | |||||||
| chr1:147585086 | G | C | 1 | a0001c0001t0023g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-477-19691G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147585086 | |||||||
| chr1:147585154 | C | T | 1 | a0001c0001t0015g0217 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-477-19623C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147585154 | |||||||
| chr1:147585422 | T | G | 92 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(89): Show |
100 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-477-19355T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147585422 | |||||||
| chr1:147585587 | C | T | 1 | a0001c0001t0006g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-477-19190C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147585587 | |||||||
| chr1:147586050 | T | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0107 others(2): Show |
5 | HG00597.hp2 NA18977.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.-477-18727T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147586050 | |||||||
| chr1:147586316 | C | A | 29 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0216 others(26): Show |
30 | HG01175.hp2 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.-477-18461C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147586316 | |||||||
| chr1:147586520 | A | C | 1 | a0001c0001t0006g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-477-18257A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147586520 | |||||||
| chr1:147586773 | A | T | 121 | a0001c0001t0001g0047 a0001c0001t0002g0176 a0001c0001t0002g0179 others(118): Show |
130 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-477-18004A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147586773 | |||||||
| chr1:147586857 | A | C | 2 | a0001c0001t0006g0237 a0001c0001t0006g0238 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-477-17920A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147586857 | |||||||
| chr1:147586995 | T | G | 147 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(144): Show |
162 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-477-17782T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147586995 | |||||||
| chr1:147587024 | T | TTCTC | 254 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(251): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-477-17743_-477-17 others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587024 | ||||||
| chr1:147587036 | C | CTCTA | 18 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0138 others(15): Show |
23 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-477-17740_-477-17 others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587036 | ||||||
| chr1:147587038 | A | C | 120 | a0001c0001t0001g0047 a0001c0001t0002g0176 a0001c0001t0002g0179 others(117): Show |
129 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-477-17739A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587038 | |||||||
| chr1:147587095 | C | T | 1 | a0001c0001t0007g0149 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-477-17682C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587095 | |||||||
| chr1:147587208 | T | G | 1 | a0001c0001t0004g0124 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-477-17569T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587208 | |||||||
| chr1:147587268 | GT | G | 117 | a0001c0001t0001g0047 a0001c0001t0002g0176 a0001c0001t0002g0179 others(114): Show |
126 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-477-17506delT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587268 | ||||||
| chr1:147587326 | C | G | 117 | a0001c0001t0001g0047 a0001c0001t0002g0176 a0001c0001t0002g0179 others(114): Show |
126 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-477-17451C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587326 | |||||||
| chr1:147587606 | A | G | 94 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(91): Show |
102 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-477-17171A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587606 | |||||||
| chr1:147587756 | C | CTG | 16 | a0001c0001t0001g0041 a0001c0001t0001g0056 a0001c0001t0001g0061 others(13): Show |
17 | HG00099.hp2 HG00140.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.-477-16982_-477-16 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587756 | ||||||
| chr1:147587756 | C | CTGTGTG | 3 | a0002c0002t0001g0114 a0002c0002t0002g0260 a0002c0002t0002g0261 |
3 | NA18981.hp2 NA19003.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-477-16986_-477-16 others(12): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587756 | ||||||
| chr1:147587756 | CTG | C | 3 | a0001c0001t0002g0221 a0001c0001t0007g0149 a0001c0001t0008g0158 |
3 | HG02572.hp1 HG02965.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-477-16982_-477-16 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587756 | ||||||
| chr1:147587756 | CTGTG | C | 26 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0138 others(23): Show |
31 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.-477-16984_-477-16 others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587756 | ||||||
| chr1:147587756 | CTGTGTG | C | 88 | a0001c0001t0001g0047 a0001c0001t0002g0176 a0001c0001t0002g0179 others(85): Show |
97 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-477-16986_-477-16 others(12): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587756 | ||||||
| chr1:147587756 | CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0006g0216 a0001c0001t0006g0237 a0001c0001t0006g0238 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-477-16990_-477-16 others(16): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587756 | ||||||
| chr1:147587756 | CTGTGTGT others(5): Show |
C | 26 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0222 others(23): Show |
27 | HG01175.hp2 HG01884.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.-477-16992_-477-16 others(18): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587756 | ||||||
| chr1:147587756 | CTGTGTGT others(7): Show |
C | 4 | a0001c0001t0006g0284 a0001c0001t0009g0218 a0001c0001t0014g0195 others(1): Show |
4 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-477-16994_-477-16 others(20): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147587756 | ||||||
| chr1:147587779 | T | G | 1 | a0002c0002t0007g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-477-16998T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587779 | |||||||
| chr1:147587852 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-477-16925C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587852 | |||||||
| chr1:147587881 | G | A | 3 | a0001c0001t0006g0216 a0001c0001t0006g0237 a0001c0001t0006g0238 |
3 | HG02630.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-477-16896G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587881 | |||||||
| chr1:147587971 | A | G | 149 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(146): Show |
164 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.-477-16806A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147587971 | |||||||
| chr1:147588091 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-16686G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147588091 | |||||||
| chr1:147588103 | T | A | 2 | a0001c0001t0006g0237 a0001c0001t0006g0238 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-477-16674T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147588103 | |||||||
| chr1:147588292 | T | C | 154 | a0001c0001t0001g0047 a0001c0001t0001g0056 a0001c0001t0001g0062 others(151): Show |
169 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-477-16485T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147588292 | |||||||
| chr1:147588435 | C | T | 121 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(118): Show |
135 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-477-16342C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147588435 | |||||||
| chr1:147588546 | G | A | 97 | a0001c0001t0001g0047 a0001c0001t0001g0131 a0001c0001t0002g0176 others(94): Show |
105 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-477-16231G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147588546 | |||||||
| chr1:147588715 | T | C | 150 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(147): Show |
165 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-477-16062T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147588715 | |||||||
| chr1:147588989 | T | C | 3 | a0001c0001t0006g0284 a0001c0001t0009g0218 a0001c0001t0014g0195 |
3 | HG02280.hp1 HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-477-15788T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147588989 | |||||||
| chr1:147589132 | A | C | 24 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0216 others(21): Show |
25 | HG01175.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-477-15645A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147589132 | |||||||
| chr1:147589154 | C | T | 24 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0216 others(21): Show |
25 | HG01175.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-477-15623C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147589154 | |||||||
| chr1:147589217 | C | T | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-15560C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147589217 | |||||||
| chr1:147589237 | T | G | 5 | a0001c0001t0004g0080 a0001c0001t0005g0004 a0001c0001t0005g0075 others(2): Show |
7 | NA18971.hp1 NA18974.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.-477-15540T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147589237 | |||||||
| chr1:147589399 | C | T | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-15378C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147589399 | |||||||
| chr1:147589413 | G | C | 3 | a0001c0001t0006g0018 a0001c0001t0006g0230 a0001c0001t0006g0278 |
4 | HG01175.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-477-15364G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147589413 | |||||||
| chr1:147589979 | T | C | 1 | a0001c0001t0007g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-477-14798T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147589979 | |||||||
| chr1:147590325 | C | T | 1 | a0001c0001t0003g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-477-14452C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147590325 | |||||||
| chr1:147590607 | CCACTCAT others(3): Show |
C | 133 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(130): Show |
147 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.-477-14166_-477-14 others(16): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147590607 | ||||||
| chr1:147590766 | C | T | 1 | a0006c0008t0001g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-477-14011C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147590766 | |||||||
| chr1:147590781 | A | C | 1 | a0006c0008t0001g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-477-13996A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147590781 | |||||||
| chr1:147590782 | T | C | 151 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(148): Show |
166 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-477-13995T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147590782 | |||||||
| chr1:147590948 | A | G | 12 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0006g0275 others(9): Show |
13 | HG01891.hp2 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-477-13829A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147590948 | |||||||
| chr1:147591139 | A | G | 3 | a0001c0001t0006g0284 a0001c0001t0009g0218 a0001c0001t0014g0195 |
3 | HG02280.hp1 HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-477-13638A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147591139 | |||||||
| chr1:147591543 | C | G | 3 | a0001c0001t0007g0083 a0001c0001t0015g0217 a0001c0001t0025g0239 |
3 | HG00140.hp1 HG02145.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-477-13234C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147591543 | |||||||
| chr1:147591852 | A | G | 1 | a0001c0001t0014g0229 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-477-12925A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147591852 | |||||||
| chr1:147592113 | A | G | 2 | a0001c0001t0003g0025 a0001c0001t0003g0182 |
2 | NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-477-12664A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147592113 | |||||||
| chr1:147592385 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0249 others(1): Show |
4 | HG00738.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-477-12392G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147592385 | |||||||
| chr1:147592494 | A | T | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-477-12283A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147592494 | |||||||
| chr1:147592510 | C | G | 116 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(113): Show |
130 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.-477-12267C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147592510 | |||||||
| chr1:147592519 | C | A | 1 | a0001c0001t0014g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-477-12258C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147592519 | |||||||
| chr1:147592626 | G | A | 1 | a0001c0001t0009g0202 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-477-12151G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147592626 | |||||||
| chr1:147593410 | G | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0046 others(8): Show |
13 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.-477-11367G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147593410 | |||||||
| chr1:147593472 | A | G | 1 | a0001c0001t0003g0030 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-477-11305A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147593472 | |||||||
| chr1:147593512 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-477-11265T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147593512 | |||||||
| chr1:147593726 | C | T | 4 | a0001c0001t0006g0284 a0001c0001t0007g0083 a0001c0001t0009g0218 others(1): Show |
4 | HG00140.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-477-11051C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147593726 | |||||||
| chr1:147593864 | G | A | 1 | a0001c0001t0020g0245 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-477-10913G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147593864 | |||||||
| chr1:147593895 | A | G | 4 | a0001c0001t0006g0284 a0001c0001t0007g0083 a0001c0001t0009g0218 others(1): Show |
4 | HG00140.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-477-10882A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147593895 | |||||||
| chr1:147594234 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-477-10543G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147594234 | |||||||
| chr1:147594395 | G | A | 3 | a0001c0001t0006g0284 a0001c0001t0009g0218 a0001c0001t0014g0195 |
3 | HG02280.hp1 HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-477-10382G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147594395 | |||||||
| chr1:147594459 | C | G | 1 | a0002c0002t0001g0092 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-477-10318C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147594459 | |||||||
| chr1:147594483 | T | C | 12 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0138 others(9): Show |
17 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-477-10294T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147594483 | |||||||
| chr1:147594540 | C | G | 1 | a0001c0001t0002g0031 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-477-10237C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147594540 | |||||||
| chr1:147594570 | A | T | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-477-10207A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147594570 | |||||||
| chr1:147595037 | T | C | 1 | a0001c0001t0006g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-477-9740T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147595037 | |||||||
| chr1:147595263 | C | T | 1 | a0001c0001t0010g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-477-9514C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147595263 | |||||||
| chr1:147595264 | G | A | 13 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0138 others(10): Show |
18 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-477-9513G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147595264 | |||||||
| chr1:147595529 | G | A | 103 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(100): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-477-9248G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147595529 | |||||||
| chr1:147595602 | C | A | 6 | a0001c0001t0005g0036 a0001c0001t0005g0150 a0001c0001t0005g0151 others(3): Show |
6 | HG01071.hp2 HG01081.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-477-9175C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147595602 | |||||||
| chr1:147595713 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-477-9064A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147595713 | |||||||
| chr1:147595859 | T | G | 2 | a0001c0006t0010g0171 a0001c0006t0010g0172 |
2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.-477-8918T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147595859 | |||||||
| chr1:147596402 | C | CTT | 281 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(278): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.-477-8368_-477-836 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147596402 | ||||||
| chr1:147596413 | T | TTC | 22 | a0001c0001t0002g0176 a0001c0001t0004g0080 a0001c0001t0004g0132 others(19): Show |
23 | HG00544.hp1 HG00597.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-477-8363_-477-836 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147596413 | ||||||
| chr1:147596414 | T | TC | 259 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(256): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-477-8363_-477-836 others(5): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147596414 | |||||||
| chr1:147596415 | T | C | 2 | a0001c0001t0002g0206 a0001c0001t0003g0173 |
2 | HG02886.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-477-8362T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147596415 | |||||||
| chr1:147596446 | C | T | 103 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(100): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-477-8331C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147596446 | |||||||
| chr1:147596462 | G | A | 1 | a0001c0001t0011g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-477-8315G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147596462 | |||||||
| chr1:147596499 | C | T | 1 | a0001c0001t0004g0054 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-477-8278C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147596499 | |||||||
| chr1:147596604 | G | A | 35 | a0001c0001t0001g0047 a0001c0001t0002g0176 a0001c0001t0002g0179 others(32): Show |
37 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.-477-8173G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147596604 | |||||||
| chr1:147596757 | A | G | 9 | a0001c0001t0006g0192 a0001c0001t0006g0282 a0001c0001t0007g0058 others(6): Show |
9 | HG02055.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-477-8020A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147596757 | |||||||
| chr1:147596911 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-7866G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147596911 | |||||||
| chr1:147597095 | T | G | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-477-7682T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597095 | |||||||
| chr1:147597199 | T | G | 151 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(148): Show |
166 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-477-7578T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597199 | |||||||
| chr1:147597301 | T | C | 147 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(144): Show |
162 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-477-7476T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597301 | |||||||
| chr1:147597314 | A | G | 3 | a0001c0001t0006g0284 a0001c0001t0009g0218 a0001c0001t0014g0195 |
3 | HG02280.hp1 HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-477-7463A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597314 | |||||||
| chr1:147597320 | G | A | 3 | a0002c0003t0001g0011 a0002c0003t0001g0044 a0002c0003t0001g0095 |
4 | HG01358.hp2 HG01433.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-477-7457G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597320 | |||||||
| chr1:147597360 | T | A | 3 | a0001c0001t0006g0284 a0001c0001t0009g0218 a0001c0001t0014g0195 |
3 | HG02280.hp1 HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-477-7417T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597360 | |||||||
| chr1:147597406 | A | G | 1 | a0001c0001t0025g0239 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-477-7371A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597406 | |||||||
| chr1:147597420 | G | A | 2 | a0001c0001t0006g0192 a0001c0001t0006g0282 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-477-7357G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597420 | |||||||
| chr1:147597436 | T | A | 4 | a0001c0001t0001g0047 a0001c0001t0002g0259 a0001c0001t0003g0262 others(1): Show |
4 | HG02080.hp2 NA18960.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-477-7341T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597436 | |||||||
| chr1:147597669 | G | A | 2 | a0001c0001t0006g0271 a0001c0001t0006g0272 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-477-7108G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597669 | |||||||
| chr1:147597790 | G | C | 15 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0006g0275 others(12): Show |
16 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-477-6987G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597790 | |||||||
| chr1:147597797 | A | G | 2 | a0001c0001t0017g0244 a0001c0001t0020g0245 |
2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-477-6980A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597797 | |||||||
| chr1:147597932 | T | G | 1 | a0001c0001t0006g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-477-6845T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597932 | |||||||
| chr1:147597938 | T | C | 12 | a0001c0001t0002g0206 a0001c0001t0008g0008 a0001c0001t0008g0193 others(9): Show |
14 | HG02055.hp2 HG02109.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-477-6839T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147597938 | |||||||
| chr1:147598121 | G | C | 18 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0006g0275 others(15): Show |
19 | HG00140.hp1 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-477-6656G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598121 | |||||||
| chr1:147598139 | T | C | 1 | a0001c0001t0009g0202 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-477-6638T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598139 | |||||||
| chr1:147598161 | G | A | 1 | a0001c0001t0004g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-477-6616G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598161 | |||||||
| chr1:147598206 | T | A | 1 | a0001c0001t0004g0065 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-477-6571T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598206 | |||||||
| chr1:147598543 | G | T | 1 | a0001c0001t0004g0122 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-477-6234G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598543 | |||||||
| chr1:147598663 | C | T | 29 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0216 others(26): Show |
30 | HG01175.hp2 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.-477-6114C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598663 | |||||||
| chr1:147598751 | C | T | 1 | a0001c0001t0003g0255 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-477-6026C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598751 | |||||||
| chr1:147598816 | C | T | 155 | a0001c0001t0001g0047 a0001c0001t0001g0056 a0001c0001t0001g0062 others(152): Show |
170 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.-477-5961C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598816 | |||||||
| chr1:147598831 | A | C | 1 | a0001c0001t0008g0207 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-477-5946A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598831 | |||||||
| chr1:147598854 | T | C | 1 | a0001c0001t0006g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-477-5923T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598854 | |||||||
| chr1:147598907 | G | C | 1 | a0001c0001t0009g0270 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-477-5870G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598907 | |||||||
| chr1:147598928 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-477-5849C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598928 | |||||||
| chr1:147598934 | C | T | 1 | a0001c0001t0012g0242 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-477-5843C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147598934 | |||||||
| chr1:147599276 | C | T | 9 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0006g0275 others(6): Show |
10 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-477-5501C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599276 | |||||||
| chr1:147599346 | T | G | 1 | a0001c0001t0028g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-477-5431T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599346 | |||||||
| chr1:147599430 | T | C | 1 | a0001c0001t0011g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-477-5347T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599430 | |||||||
| chr1:147599475 | G | T | 2 | a0001c0001t0004g0005 a0001c0001t0004g0101 |
4 | NA18944.hp2 NA19010.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.-477-5302G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599475 | |||||||
| chr1:147599487 | G | GC | 11 | a0001c0001t0006g0223 a0001c0001t0006g0282 a0001c0001t0009g0267 others(8): Show |
11 | HG02055.hp1 HG02602.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-477-5284dupC | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147599487 | ||||||
| chr1:147599490 | C | G | 104 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(101): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-477-5287C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599490 | |||||||
| chr1:147599493 | CG | C | 105 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(102): Show |
118 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-477-5283delG | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599493 | |||||||
| chr1:147599494 | G | C | 46 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0201 others(43): Show |
48 | HG01175.hp2 HG01884.hp2 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.-477-5283G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599494 | |||||||
| chr1:147599495 | C | CA | 17 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0006g0275 others(14): Show |
18 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.-477-5282_-477-528 others(5): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599495 | |||||||
| chr1:147599497 | C | A | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-5280C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599497 | |||||||
| chr1:147599498 | C | G | 104 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(101): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-477-5279C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599498 | |||||||
| chr1:147599516 | A | G | 156 | a0001c0001t0001g0047 a0001c0001t0001g0056 a0001c0001t0001g0062 others(153): Show |
171 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.-477-5261A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599516 | |||||||
| chr1:147599601 | C | A | 1 | a0001c0001t0006g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-477-5176C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599601 | |||||||
| chr1:147599817 | C | A | 1 | a0001c0001t0002g0249 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-477-4960C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599817 | |||||||
| chr1:147599818 | C | G | 1 | a0001c0001t0002g0249 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-477-4959C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599818 | |||||||
| chr1:147599819 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-477-4958C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599819 | |||||||
| chr1:147599904 | A | G | 17 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0006g0275 others(14): Show |
18 | HG00140.hp1 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-477-4873A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599904 | |||||||
| chr1:147599911 | A | G | 1 | a0001c0001t0004g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-477-4866A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599911 | |||||||
| chr1:147599927 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-477-4850G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599927 | |||||||
| chr1:147599943 | G | A | 1 | a0001c0001t0029g0135 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-477-4834G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147599943 | |||||||
| chr1:147600068 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-4709G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147600068 | |||||||
| chr1:147600144 | C | T | 2 | a0001c0001t0009g0231 a0003c0004t0001g0123 |
2 | HG01071.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-477-4633C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147600144 | |||||||
| chr1:147600383 | G | T | 1 | a0002c0002t0007g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-477-4394G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147600383 | |||||||
| chr1:147600532 | G | C | 1 | a0001c0001t0004g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-477-4245G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147600532 | |||||||
| chr1:147600566 | G | T | 1 | a0001c0001t0003g0187 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-477-4211G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147600566 | |||||||
| chr1:147600611 | G | C | 1 | a0001c0001t0006g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-477-4166G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147600611 | |||||||
| chr1:147600639 | G | A | 23 | a0001c0001t0006g0192 a0001c0001t0006g0222 a0001c0001t0006g0223 others(20): Show |
23 | HG01884.hp2 HG02055.hp1 HG02602.hp1 others(20): Show |
intron_variant | MODIFIER | c.-477-4138G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147600639 | |||||||
| chr1:147600930 | C | T | 1 | a0001c0001t0004g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-477-3847C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147600930 | |||||||
| chr1:147601171 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0002g0034 a0006c0008t0001g0038 |
3 | HG00597.hp2 NA18989.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-477-3606G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601171 | |||||||
| chr1:147601562 | A | C | 12 | a0001c0001t0001g0062 a0001c0001t0001g0074 a0001c0001t0001g0138 others(9): Show |
17 | HG00438.hp1 HG01081.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-477-3215A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601562 | |||||||
| chr1:147601584 | CAT | C | 104 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(101): Show |
117 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-477-3192_-477-319 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601584 | |||||||
| chr1:147601590 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-477-3187G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601590 | |||||||
| chr1:147601613 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-477-3164G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601613 | |||||||
| chr1:147601618 | A | T | 1 | a0002c0002t0001g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-477-3159A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601618 | |||||||
| chr1:147601705 | G | C | 2 | a0002c0002t0001g0091 a0002c0002t0001g0092 |
2 | HG01257.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-477-3072G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601705 | |||||||
| chr1:147601739 | T | C | 1 | a0001c0001t0009g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-477-3038T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601739 | |||||||
| chr1:147601900 | TTTTA | T | 9 | a0001c0001t0006g0201 a0001c0001t0006g0203 a0001c0001t0006g0275 others(6): Show |
10 | HG01891.hp2 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-477-2873_-477-287 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147601900 | ||||||
| chr1:147601931 | C | T | 1 | a0002c0002t0007g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-477-2846C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601931 | |||||||
| chr1:147601965 | A | G | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-2812A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601965 | |||||||
| chr1:147601986 | C | T | 103 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(100): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-477-2791C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147601986 | |||||||
| chr1:147602182 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-2595G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602182 | |||||||
| chr1:147602225 | T | G | 1 | a0001c0001t0005g0078 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-477-2552T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602225 | |||||||
| chr1:147602225 | T | TTG | 3 | a0001c0001t0001g0104 a0001c0001t0002g0264 a0001c0001t0006g0222 |
3 | HG03831.hp1 HG06807.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-477-2552_-477-255 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602225 | |||||||
| chr1:147602240 | T | A | 103 | a0001c0001t0001g0047 a0001c0001t0001g0062 a0001c0001t0001g0074 others(100): Show |
116 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.-477-2537T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602240 | |||||||
| chr1:147602245 | A | G | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-477-2532A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602245 | |||||||
| chr1:147602276 | A | G | 158 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0056 others(155): Show |
174 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.-477-2501A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602276 | |||||||
| chr1:147602326 | C | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0183 |
2 | HG02056.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-477-2451C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602326 | |||||||
| chr1:147602704 | AAG | A | 3 | a0001c0001t0003g0159 a0001c0001t0003g0162 a0001c0001t0009g0228 |
3 | HG01891.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-477-2071_-477-207 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147602704 | ||||||
| chr1:147602744 | G | A | 3 | a0001c0001t0002g0188 a0001c0001t0002g0253 a0001c0001t0002g0264 |
3 | HG02080.hp1 NA18954.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-477-2033G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602744 | |||||||
| chr1:147602865 | A | G | 3 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0005g0105 |
3 | HG00621.hp1 NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-477-1912A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147602865 | |||||||
| chr1:147603020 | C | T | 3 | a0001c0001t0007g0072 a0001c0001t0007g0149 a0001c0001t0011g0146 |
3 | HG00323.hp1 HG02273.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-477-1757C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147603020 | |||||||
| chr1:147603052 | A | G | 2 | a0001c0001t0015g0217 a0001c0001t0025g0239 |
2 | HG02145.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-477-1725A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147603052 | |||||||
| chr1:147603388 | G | A | 272 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(269): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.-477-1389G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147603388 | |||||||
| chr1:147603897 | A | G | 1 | a0001c0001t0011g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-477-880A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147603897 | |||||||
| chr1:147604154 | C | T | 1 | a0001c0001t0003g0030 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-477-623C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147604154 | |||||||
| chr1:147604173 | A | C | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-477-604A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147604173 | |||||||
| chr1:147604462 | G | T | 45 | a0001c0001t0006g0018 a0001c0001t0006g0192 a0001c0001t0006g0222 others(42): Show |
47 | HG00140.hp1 HG00323.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.-477-315G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147604462 | |||||||
| chr1:147604513 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-477-264C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147604513 | |||||||
| chr1:147604649 | C | T | 3 | a0001c0001t0006g0216 a0001c0001t0006g0237 a0001c0001t0006g0238 |
3 | HG02630.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-477-128C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147604649 | |||||||
| chr1:147604649 | CCTAA | C | 54 | a0001c0001t0003g0020 a0001c0001t0003g0025 a0001c0001t0003g0181 others(51): Show |
58 | HG00323.hp1 HG01099.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.-477-125_-477-122d others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 147604649 | ||||||
| chr1:147604678 | C | T | 1 | a0001c0001t0003g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-477-99C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 1/9 | chr1 | 147604678 | |||||||
| chr1:147604923 | T | C | 272 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(269): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.-343+12T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147604923 | |||||||
| chr1:147604987 | A | G | 1 | a0001c0001t0007g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-343+76A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147604987 | |||||||
| chr1:147605011 | C | T | 1 | a0001c0001t0008g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-343+100C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605011 | |||||||
| chr1:147605130 | A | AG | 3 | a0001c0001t0001g0045 a0001c0001t0002g0034 a0006c0008t0001g0038 |
3 | HG00597.hp2 NA18989.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-343+222dupG | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 147605130 | ||||||
| chr1:147605211 | T | C | 1 | a0001c0001t0002g0248 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-343+300T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605211 | |||||||
| chr1:147605221 | C | G | 7 | a0001c0001t0006g0216 a0001c0001t0006g0237 a0001c0001t0006g0238 others(4): Show |
7 | HG02145.hp1 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-343+310C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605221 | |||||||
| chr1:147605222 | A | G | 10 | a0001c0001t0006g0203 a0001c0001t0009g0017 a0001c0001t0009g0200 others(7): Show |
11 | HG02280.hp2 HG02615.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-343+311A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605222 | |||||||
| chr1:147605490 | G | A | 123 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0041 others(120): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-343+579G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605490 | |||||||
| chr1:147605581 | G | A | 1 | a0001c0001t0011g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-343+670G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605581 | |||||||
| chr1:147605728 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-343+817C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605728 | |||||||
| chr1:147605903 | G | C | 1 | a0001c0001t0002g0259 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-342-881G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605903 | |||||||
| chr1:147605948 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-342-836G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605948 | |||||||
| chr1:147605992 | T | C | 1 | a0001c0001t0017g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-342-792T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147605992 | |||||||
| chr1:147606212 | G | A | 1 | a0001c0001t0006g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-342-572G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147606212 | |||||||
| chr1:147606478 | C | T | 1 | a0001c0001t0003g0180 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-342-306C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147606478 | |||||||
| chr1:147606632 | G | A | 1 | a0001c0001t0023g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-342-152G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147606632 | |||||||
| chr1:147606674 | T | C | 3 | a0001c0001t0006g0216 a0001c0001t0006g0237 a0001c0001t0006g0238 |
3 | HG02630.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-342-110T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 2/9 | chr1 | 147606674 | |||||||
| chr1:147607091 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-260+225G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147607091 | |||||||
| chr1:147607192 | T | C | 1 | a0001c0001t0024g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-260+326T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147607192 | |||||||
| chr1:147607358 | A | G | 2 | a0001c0001t0016g0224 a0001c0001t0016g0266 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-260+492A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147607358 | |||||||
| chr1:147607717 | G | A | 1 | a0002c0002t0001g0097 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-260+851G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147607717 | |||||||
| chr1:147608330 | C | CTT | 7 | a0001c0001t0001g0046 a0001c0001t0002g0251 a0001c0001t0002g0276 others(4): Show |
7 | HG02886.hp2 HG03453.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.-260+1483_-260+148 others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 147608330 | ||||||
| chr1:147608330 | C | CTTTT | 100 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0112 others(97): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-260+1481_-260+148 others(8): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 147608330 | ||||||
| chr1:147608330 | C | CTTTTT | 9 | a0001c0001t0002g0258 a0001c0001t0003g0160 a0001c0001t0008g0213 others(6): Show |
9 | HG01074.hp1 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-260+1480_-260+148 others(9): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 147608330 | ||||||
| chr1:147608330 | CTTT | C | 12 | a0001c0001t0003g0181 a0001c0001t0004g0001 a0001c0001t0004g0012 others(9): Show |
15 | HG00558.hp1 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.-260+1482_-260+148 others(7): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 147608330 | ||||||
| chr1:147608383 | C | T | 98 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0002g0183 others(95): Show |
105 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-260+1517C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147608383 | |||||||
| chr1:147608594 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-260+1728G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147608594 | |||||||
| chr1:147608946 | T | G | 1 | a0001c0001t0005g0096 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-260+2080T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147608946 | |||||||
| chr1:147608966 | C | T | 1 | a0002c0002t0002g0022 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-260+2100C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147608966 | |||||||
| chr1:147609125 | G | A | 1 | a0001c0001t0023g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-260+2259G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147609125 | |||||||
| chr1:147609390 | A | G | 213 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0112 others(210): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-259-2188A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147609390 | |||||||
| chr1:147609517 | C | G | 4 | a0001c0001t0001g0056 a0001c0001t0007g0099 a0001c0001t0009g0231 others(1): Show |
4 | HG02109.hp1 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-259-2061C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147609517 | |||||||
| chr1:147609851 | T | C | 1 | a0001c0001t0011g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-259-1727T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147609851 | |||||||
| chr1:147609944 | A | G | 1 | a0002c0002t0001g0094 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-259-1634A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147609944 | |||||||
| chr1:147610172 | A | T | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-259-1406A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147610172 | |||||||
| chr1:147610227 | G | A | 102 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0002g0183 others(99): Show |
109 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-259-1351G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147610227 | |||||||
| chr1:147610333 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-259-1245G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147610333 | |||||||
| chr1:147610486 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-259-1092C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147610486 | |||||||
| chr1:147610739 | T | C | 4 | a0001c0001t0008g0158 a0001c0001t0008g0196 a0001c0001t0008g0227 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-259-839T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147610739 | |||||||
| chr1:147611014 | T | G | 1 | a0001c0001t0023g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-259-564T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147611014 | |||||||
| chr1:147611063 | C | T | 4 | a0001c0001t0001g0098 a0001c0001t0002g0188 a0001c0001t0002g0253 others(1): Show |
4 | HG02080.hp1 NA18954.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.-259-515C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147611063 | |||||||
| chr1:147611100 | A | G | 1 | a0001c0001t0005g0128 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-259-478A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147611100 | |||||||
| chr1:147611195 | G | C | 1 | a0001c0001t0003g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-259-383G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147611195 | |||||||
| chr1:147611315 | T | C | 208 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0112 others(205): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-259-263T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147611315 | |||||||
| chr1:147611481 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-259-97G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 3/9 | chr1 | 147611481 | |||||||
| chr1:147611945 | T | C | 205 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0112 others(202): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.53+56T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 4/9 | chr1 | 147611945 | |||||||
| chr1:147612160 | A | G | 1 | a0001c0001t0023g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53+271A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 4/9 | chr1 | 147612160 | |||||||
| chr1:147612288 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.53+399C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 4/9 | chr1 | 147612288 | |||||||
| chr1:147612438 | C | T | 2 | a0001c0001t0004g0090 a0001c0001t0004g0124 |
2 | HG02071.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.54-445C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 4/9 | chr1 | 147612438 | |||||||
| chr1:147612592 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.54-291A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 4/9 | chr1 | 147612592 | |||||||
| chr1:147612708 | A | G | 4 | a0001c0001t0005g0036 a0001c0001t0005g0150 a0001c0001t0005g0151 others(1): Show |
4 | HG01071.hp2 HG01081.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-175A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 4/9 | chr1 | 147612708 | |||||||
| chr1:147612724 | CAG | C | 6 | a0001c0001t0001g0056 a0001c0001t0007g0099 a0001c0001t0009g0218 others(3): Show |
6 | HG02083.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-158_54-157delAG | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 4/9 | chr1 | 147612724 | |||||||
| chr1:147612733 | C | T | 2 | a0001c0001t0016g0224 a0001c0001t0016g0266 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.54-150C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 4/9 | chr1 | 147612733 | |||||||
| chr1:147613267 | G | A | 75 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0002g0183 others(72): Show |
81 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.370+68G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 5/9 | chr1 | 147613267 | |||||||
| chr1:147613413 | C | G | 67 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0002g0183 others(64): Show |
73 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.370+214C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 5/9 | chr1 | 147613413 | |||||||
| chr1:147613532 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.370+333T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 5/9 | chr1 | 147613532 | |||||||
| chr1:147613541 | C | G | 3 | a0002c0003t0001g0011 a0002c0003t0001g0044 a0002c0003t0001g0095 |
4 | HG01358.hp2 HG01433.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+342C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 5/9 | chr1 | 147613541 | |||||||
| chr1:147613552 | C | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0170 |
2 | HG02074.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.370+353C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 5/9 | chr1 | 147613552 | |||||||
| chr1:147613860 | A | G | 2 | a0001c0001t0006g0275 a0001c0001t0023g0208 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.371-567A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 5/9 | chr1 | 147613860 | |||||||
| chr1:147614223 | G | A | 3 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0006g0157 |
3 | HG02145.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.371-204G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 5/9 | chr1 | 147614223 | |||||||
| chr1:147614359 | A | T | 5 | a0001c0001t0004g0090 a0001c0001t0004g0100 a0001c0001t0004g0109 others(2): Show |
5 | HG02056.hp2 HG02071.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.371-68A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 5/9 | chr1 | 147614359 | |||||||
| chr1:147614705 | A | C | 115 | a0001c0001t0001g0056 a0001c0001t0002g0176 a0001c0001t0002g0179 others(112): Show |
122 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.560+89A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | chr1 | 147614705 | |||||||
| chr1:147614780 | C | T | 1 | a0001c0001t0006g0282 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.560+164C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | chr1 | 147614780 | |||||||
| chr1:147614844 | C | CT | 279 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(276): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.560+241dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 147614844 | ||||||
| chr1:147615112 | A | T | 1 | a0001c0001t0023g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.560+496A>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | chr1 | 147615112 | |||||||
| chr1:147615167 | G | A | 103 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0002g0183 others(100): Show |
110 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.560+551G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | chr1 | 147615167 | |||||||
| chr1:147615211 | TTTTCTAA others(3): Show |
T | 1 | a0002c0002t0002g0166 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.561-591_561-582del others(10): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | chr1 | 147615211 | |||||||
| chr1:147615536 | A | G | 106 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0002g0183 others(103): Show |
113 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.561-267A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | chr1 | 147615536 | |||||||
| chr1:147615633 | A | G | 1 | a0001c0001t0009g0202 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.561-170A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | chr1 | 147615633 | |||||||
| chr1:147615772 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.561-31C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 6/9 | chr1 | 147615772 | |||||||
| chr1:147615921 | T | A | 75 | a0001c0001t0001g0013 a0001c0001t0001g0112 a0001c0001t0001g0119 others(72): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.660+19T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147615921 | |||||||
| chr1:147616044 | T | C | 2 | a0001c0001t0003g0024 a0001c0001t0003g0026 |
2 | NA18944.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.660+142T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616044 | |||||||
| chr1:147616069 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.660+167A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616069 | |||||||
| chr1:147616083 | C | T | 1 | a0001c0001t0009g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.660+181C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616083 | |||||||
| chr1:147616157 | T | G | 1 | a0001c0001t0023g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.660+255T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616157 | |||||||
| chr1:147616226 | T | A | 197 | a0001c0001t0001g0013 a0001c0001t0001g0112 a0001c0001t0001g0119 others(194): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.660+324T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616226 | |||||||
| chr1:147616333 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.660+431C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616333 | |||||||
| chr1:147616436 | A | G | 10 | a0001c0001t0001g0056 a0001c0001t0006g0216 a0001c0001t0006g0237 others(7): Show |
10 | HG02083.hp1 HG02109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.660+534A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616436 | |||||||
| chr1:147616490 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.660+588G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616490 | |||||||
| chr1:147616573 | C | G | 2 | a0001c0001t0016g0224 a0001c0001t0016g0266 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.660+671C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616573 | |||||||
| chr1:147616624 | G | A | 1 | a0002c0002t0001g0110 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.660+722G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616624 | |||||||
| chr1:147616772 | C | CA | 181 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(178): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.660+881dupA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 147616772 | ||||||
| chr1:147616834 | A | G | 2 | a0001c0001t0006g0203 a0001c0001t0011g0130 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.660+932A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147616834 | |||||||
| chr1:147617106 | T | C | 213 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0112 others(210): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.660+1204T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617106 | |||||||
| chr1:147617313 | G | A | 1 | a0001c0001t0004g0053 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.660+1411G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617313 | |||||||
| chr1:147617456 | C | T | 7 | a0001c0001t0001g0056 a0001c0001t0007g0099 a0001c0001t0009g0218 others(4): Show |
7 | HG02083.hp1 HG02109.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.661-1360C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617456 | |||||||
| chr1:147617517 | C | T | 93 | a0001c0001t0001g0013 a0001c0001t0001g0112 a0001c0001t0001g0119 others(90): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.661-1299C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617517 | |||||||
| chr1:147617529 | C | CGTAA | 93 | a0001c0001t0001g0013 a0001c0001t0001g0112 a0001c0001t0001g0119 others(90): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.661-1287_661-1286i others(6): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617529 | |||||||
| chr1:147617540 | C | T | 6 | a0001c0001t0006g0018 a0001c0001t0006g0230 a0001c0001t0006g0271 others(3): Show |
7 | HG01175.hp2 HG02615.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.661-1276C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617540 | |||||||
| chr1:147617541 | T | G | 208 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0112 others(205): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.661-1275T>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617541 | |||||||
| chr1:147617542 | T | A | 208 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0112 others(205): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.661-1274T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617542 | |||||||
| chr1:147617606 | A | G | 2 | a0001c0001t0014g0195 a0001c0001t0014g0229 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.661-1210A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617606 | |||||||
| chr1:147617633 | T | A | 2 | a0002c0002t0001g0111 a0002c0002t0001g0113 |
2 | HG01884.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.661-1183T>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147617633 | |||||||
| chr1:147618468 | C | T | 1 | a0002c0002t0002g0166 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.661-348C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147618468 | |||||||
| chr1:147618520 | A | G | 1 | a0001c0001t0014g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.661-296A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147618520 | |||||||
| chr1:147618635 | T | TA | 281 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(278): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.661-168dupA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 147618635 | ||||||
| chr1:147618776 | C | T | 2 | a0001c0001t0014g0235 a0001c0001t0015g0198 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.661-40C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 7/9 | chr1 | 147618776 | |||||||
| chr1:147621075 | C | T | 4 | a0002c0002t0001g0091 a0002c0002t0001g0092 a0002c0002t0001g0094 others(1): Show |
4 | HG00280.hp1 HG01257.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2902+18C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147621075 | |||||||
| chr1:147621161 | G | T | 1 | a0001c0001t0006g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2902+104G>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147621161 | |||||||
| chr1:147621273 | TAAAAG | T | 55 | a0001c0001t0004g0001 a0001c0001t0004g0005 a0001c0001t0004g0012 others(52): Show |
63 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.2902+217_2902+221d others(7): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147621273 | |||||||
| chr1:147621545 | TCA | T | 3 | a0002c0002t0001g0097 a0002c0002t0002g0247 a0002c0002t0005g0082 |
3 | HG00280.hp2 HG02559.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2902+491_2902+492d others(4): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 147621545 | ||||||
| chr1:147621577 | T | C | 24 | a0001c0001t0003g0159 a0001c0001t0006g0018 a0001c0001t0006g0192 others(21): Show |
25 | HG01175.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.2902+520T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147621577 | |||||||
| chr1:147621733 | A | G | 2 | a0001c0001t0016g0224 a0001c0001t0016g0266 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2903-538A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147621733 | |||||||
| chr1:147621788 | C | T | 1 | a0001c0001t0006g0240 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2903-483C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147621788 | |||||||
| chr1:147621873 | A | G | 101 | a0001c0001t0002g0176 a0001c0001t0002g0179 a0001c0001t0002g0183 others(98): Show |
108 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.2903-398A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147621873 | |||||||
| chr1:147621911 | C | T | 2 | a0001c0001t0016g0224 a0001c0001t0016g0266 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2903-360C>T | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147621911 | |||||||
| chr1:147622026 | C | A | 2 | a0001c0001t0016g0224 a0001c0001t0016g0266 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2903-245C>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147622026 | |||||||
| chr1:147622076 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2903-195A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147622076 | |||||||
| chr1:147622086 | A | G | 213 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0112 others(210): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2903-185A>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147622086 | |||||||
| chr1:147622110 | G | C | 1 | a0001c0001t0004g0043 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2903-161G>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 8/9 | chr1 | 147622110 | |||||||
| chr1:147622594 | G | A | 2 | a0001c0001t0010g0209 a0002c0002t0007g0086 |
2 | HG02602.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3163+63G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147622594 | |||||||
| chr1:147622741 | AG | A | 6 | a0001c0001t0005g0004 a0001c0001t0005g0071 a0001c0001t0005g0075 others(3): Show |
8 | NA18954.hp1 NA18955.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.3163+211delG | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147622741 | |||||||
| chr1:147622968 | C | CT | 283 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(280): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.3163+448dupT | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 147622968 | ||||||
| chr1:147623031 | T | C | 1 | a0002c0002t0007g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3163+500T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147623031 | |||||||
| chr1:147623262 | CA | C | 209 | a0001c0001t0001g0056 a0001c0001t0002g0176 a0001c0001t0002g0179 others(206): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.3164-578delA | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 147623262 | ||||||
| chr1:147623280 | C | G | 8 | a0001c0001t0012g0174 a0001c0001t0012g0204 a0001c0001t0012g0205 others(5): Show |
8 | HG01934.hp1 HG02486.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.3164-562C>G | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147623280 | |||||||
| chr1:147623311 | G | A | 1 | a0001c0001t0007g0191 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3164-531G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147623311 | |||||||
| chr1:147623397 | A | C | 1 | a0001c0001t0003g0029 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3164-445A>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147623397 | |||||||
| chr1:147623538 | T | C | 10 | a0001c0001t0001g0015 a0001c0001t0007g0010 a0001c0001t0007g0072 others(7): Show |
12 | HG01074.hp2 HG01099.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3164-304T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147623538 | |||||||
| chr1:147623585 | T | C | 1 | a0001c0001t0010g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3164-257T>C | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147623585 | |||||||
| chr1:147623653 | G | A | 1 | a0001c0001t0023g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3164-189G>A | BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 9/9 | chr1 | 147623653 |