Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 604 |
| ensemblid | ENSG00000113916.18 |
| hgncid | 1001 |
| symbol | BCL6 |
| name | BCL6 transcription repressor |
| refseq_nuc | NM_001706.5 |
| refseq_prot | NP_001697.2 |
| ensembl_nuc | ENST00000406870.7 |
| ensembl_prot | ENSP00000384371.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 187721381 |
| end | 187745468 |
| strand | - |
| ver | v1.2 |
| region | chr3:187721381-187745468 |
| region5000 | chr3:187716381-187750468 |
| regionname0 | BCL6_chr3_187721381_187745468 |
| regionname5000 | BCL6_chr3_187716381_187750468 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 706 | 332 | 49 | 70 | 164 | 14 | 34 | 121 | BCL6_chr3_187716381_187750468 | BCL6 | MASPA others(701): Show |
chr3 | 187716381 | 187750468 |
| a0002 | 0/1 | 706 | 67 | 38 | 3 | 21 | 2 | 2 | 17 | BCL6_chr3_187716381_187750468 | BCL6 | MASPA others(701): Show |
chr3 | 187716381 | 187750468 |
| a0003 | 0/0 | 706 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | MASPA others(701): Show |
chr3 | 187716381 | 187750468 |
| a0004 | 0/0 | 706 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | MASPA others(701): Show |
chr3 | 187716381 | 187750468 |
| a0005 | 0/0 | 706 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | MASPA others(701): Show |
chr3 | 187716381 | 187750468 |
| a0006 | 0/0 | 706 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | MASPA others(701): Show |
chr3 | 187716381 | 187750468 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2118 | 233 | 8 | 51 | 137 | 9 | 28 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0001c0002 | 1/0 | 2118 | 66 | 35 | 13 | 11 | 2 | 4 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0001c0004 | 0/0 | 2118 | 30 | 6 | 5 | 15 | 3 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0001c0009 | 0/0 | 2118 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0001c0011 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0001c0013 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0002c0003 | 0/1 | 2118 | 62 | 33 | 3 | 21 | 2 | 2 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0002c0005 | 0/0 | 2118 | 4 | 4 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0002c0012 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0003c0006 | 0/0 | 2118 | 2 | 0 | 2 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0004c0010 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0005c0007 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 | ||
| a0006c0008 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | ATGGC others(2113): Show |
chr3 | 187716381 | 187750468 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3306 | 47 | 4 | 12 | 25 | 3 | 3 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0001c0001t0002 | 0/0 | 3308 | 177 | 4 | 34 | 110 | 6 | 23 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0001c0001t0003 | 0/0 | 3308 | 4 | 0 | 3 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0001c0001t0005 | 0/0 | 3308 | 2 | 0 | 2 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0001c0001t0006 | 0/0 | 3308 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0001c0001t0007 | 0/0 | 3308 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0001c0001t0009 | 0/0 | 3308 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0001c0002t0001 | 1/0 | 3306 | 64 | 33 | 13 | 11 | 2 | 4 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0001c0002t0002 | 0/0 | 3308 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0001c0002t0008 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0001c0004t0001 | 0/0 | 3306 | 30 | 6 | 5 | 15 | 3 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0001c0009t0001 | 0/0 | 3306 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0001c0011t0002 | 0/0 | 3308 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0001c0013t0002 | 0/0 | 3308 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0002c0003t0001 | 0/0 | 3306 | 60 | 33 | 3 | 21 | 2 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0002c0003t0004 | 0/1 | 3306 | 2 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0002c0005t0001 | 0/0 | 3306 | 4 | 4 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0002c0012t0001 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0003c0006t0001 | 0/0 | 3306 | 2 | 0 | 2 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0004c0010t0002 | 0/0 | 3308 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3303): Show |
chr3 | 187716381 | 187750468 |
| a0005c0007t0001 | 0/0 | 3306 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| a0006c0008t0001 | 0/0 | 3306 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | AGAAC others(3301): Show |
chr3 | 187716381 | 187750468 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0007g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0001t0009g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0301 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0002t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0004t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0009t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0011t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0001c0013t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0004g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0003t0004g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0005t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0005t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0002c0012t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0003c0006t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0003c0006t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0004c0010t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0005c0007t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| a0006c0008t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0265 | EUR | GBR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0299 | EUR | GBR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0026 | EUR | GBR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0198 | EUR | GBR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0277 | EUR | FIN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0326 | EUR | FIN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | FIN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0139 | EUR | FIN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00408 | hp1 | a0004 | c0010 | t0002 | g0105 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0201 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0108 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0307 | EAS | CHS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0306 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0208 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01074 | hp2 | a0003 | c0006 | t0001 | g0290 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01081 | hp1 | a0001 | c0004 | t0001 | g0032 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0074 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0032 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0239 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0088 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0042 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0332 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0322 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0077 | EUR | IBS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | IBS | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0342 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0197 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0352 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01952 | hp1 | a0005 | c0007 | t0001 | g0114 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0357 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01981 | hp1 | a0001 | c0013 | t0002 | g0125 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0220 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0161 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0118 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02055 | hp1 | a0002 | c0003 | t0001 | g0046 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0150 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02056 | hp1 | a0002 | c0003 | t0001 | g0200 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0351 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0232 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CDX | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | CDX | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CDX | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0174 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0149 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0350 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0300 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0162 | EAS | KHV | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0167 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02622 | hp1 | a0002 | c0012 | t0001 | g0337 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0356 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0230 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02647 | hp1 | a0002 | c0005 | t0001 | g0040 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0354 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0339 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0353 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0235 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0194 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0344 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02896 | hp1 | a0002 | c0005 | t0001 | g0024 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0346 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02897 | hp1 | a0002 | c0005 | t0001 | g0024 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0237 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0257 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0348 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0231 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03017 | hp1 | a0002 | c0003 | t0004 | g0359 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03017 | hp2 | a0001 | c0009 | t0001 | g0333 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0207 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03041 | hp2 | a0001 | c0002 | t0008 | g0187 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03130 | hp1 | a0002 | c0005 | t0001 | g0177 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0202 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0206 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03209 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0309 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0094 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0196 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0355 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | ESN | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0349 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0347 | AFR | GWD | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03579 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | STU | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0305 | SAS | PJL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0336 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0343 | SAS | STU | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0143 | AFR | YRI | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0151 | AFR | YRI | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18941 | hp1 | a0001 | c0004 | t0001 | g0076 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18944 | hp2 | a0001 | c0004 | t0001 | g0160 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18948 | hp2 | a0001 | c0004 | t0001 | g0341 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18951 | hp2 | a0001 | c0004 | t0001 | g0331 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0313 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0263 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0178 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0303 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0107 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18970 | hp1 | a0002 | c0003 | t0001 | g0062 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18977 | hp2 | a0001 | c0011 | t0002 | g0259 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0071 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18986 | hp2 | a0002 | c0003 | t0001 | g0308 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0141 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18998 | hp1 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18998 | hp2 | a0001 | c0004 | t0001 | g0340 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0360 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19005 | hp2 | a0001 | c0004 | t0001 | g0258 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | LWK | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0188 | AFR | LWK | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0058 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19074 | hp1 | a0001 | c0004 | t0001 | g0159 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0119 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0304 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19091 | hp1 | a0001 | c0004 | t0001 | g0148 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | YRI | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | ASW | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | ASW | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA20752 | hp1 | a0001 | c0004 | t0001 | g0314 | EUR | TSI | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0203 | EUR | TSI | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0323 | EUR | TSI | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | TSI | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | GIH | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | GIH | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01123 | hp1 | a0003 | c0006 | t0001 | g0145 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0069 | AMR | CLM | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0229 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0358 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0243 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | ACB | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03471 | hp1 | a0006 | c0008 | t0001 | g0225 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | MSL | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | USA | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0233 | AFR | USA | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18955 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA18955 | hp2 | a0001 | c0001 | t0009 | g0327 | EAS | JPT | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0195 | AFR | LWK | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0193 | AFR | LWK | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0004 | g0153 | REF | REF | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0301 | REF | REF | BCL6_chr3_187716381_187750468 | BCL6 | chr3 | 187716381 | 187750468 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:187728423 | C | T | 2 | a0002 a0003 |
68 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(65): Show |
missense_variant | MODERATE | c.1477G>A | p.Ala493Thr | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/10 | 1585/3306 | 1477/2121 | 493/706 | chr3 | 187728423 | |||
| chr3:187729057 | C | T | 1 | a0004 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.1348G>A | p.Val450Ile | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/10 | 1456/3306 | 1348/2121 | 450/706 | chr3 | 187729057 | |||
| chr3:187729913 | C | A | 1 | a0003 | 2 | HG01074.hp2 HG01123.hp1 |
missense_variant | MODERATE | c.492G>T | p.Glu164Asp | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/10 | 600/3306 | 492/2121 | 164/706 | chr3 | 187729913 | |||
| chr3:187730012 | C | G | 1 | a0006 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.393G>C | p.Glu131Asp | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/10 | 501/3306 | 393/2121 | 131/706 | chr3 | 187730012 | |||
| chr3:187733575 | C | T | 1 | a0005 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.119G>A | p.Arg40His | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/10 | 227/3306 | 119/2121 | 40/706 | chr3 | 187733575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:187725517 | G | A | 1 | a0001c0013 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.1821C>T | p.Cys607Cys | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/10 | 1929/3306 | 1821/2121 | 607/706 | chr3 | 187725517 | |||
| chr3:187725526 | G | A | 1 | a0001c0004 | 30 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(27): Show |
synonymous_variant | LOW | c.1812C>T | p.Cys604Cys | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/10 | 1920/3306 | 1812/2121 | 604/706 | chr3 | 187725526 | |||
| chr3:187728484 | G | T | 1 | a0001c0009 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1416C>A | p.Pro472Pro | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/10 | 1524/3306 | 1416/2121 | 472/706 | chr3 | 187728484 | |||
| chr3:187729244 | G | A | 5 | a0001c0001 a0001c0011 a0001c0013 others(2): Show |
237 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(234): Show |
synonymous_variant | LOW | c.1161C>T | p.Asn387Asn | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/10 | 1269/3306 | 1161/2121 | 387/706 | chr3 | 187729244 | |||
| chr3:187729712 | T | G | 1 | a0001c0011 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.693A>C | p.Pro231Pro | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/10 | 801/3306 | 693/2121 | 231/706 | chr3 | 187729712 | |||
| chr3:187729778 | G | A | 1 | a0002c0012 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.627C>T | p.Ser209Ser | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/10 | 735/3306 | 627/2121 | 209/706 | chr3 | 187729778 | |||
| chr3:187729817 | G | A | 1 | a0001c0013 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.588C>T | p.Ser196Ser | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/10 | 696/3306 | 588/2121 | 196/706 | chr3 | 187729817 | |||
| chr3:187733550 | C | T | 1 | a0002c0005 | 4 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.144G>A | p.Thr48Thr | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/10 | 252/3306 | 144/2121 | 48/706 | chr3 | 187733550 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:187721435 | G | A | 1 | a0002c0003t0004 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1023C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 1023 | chr3 | 187721435 | ||||||
| chr3:187721814 | C | T | 1 | a0001c0002t0008 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 644 | chr3 | 187721814 | ||||||
| chr3:187721823 | T | A | 1 | a0001c0001t0003 | 4 | HG00642.hp1 HG01346.hp1 HG01993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*635A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 635 | chr3 | 187721823 | ||||||
| chr3:187721958 | T | TTA | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(7): Show |
190 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*498_*499dupTA | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 499 | chr3 | 187721958 | ||||||
| chr3:187722061 | C | T | 1 | a0001c0001t0007 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*397G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 397 | chr3 | 187722061 | ||||||
| chr3:187722207 | A | G | 1 | a0001c0001t0006 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*251T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 251 | chr3 | 187722207 | ||||||
| chr3:187722309 | G | A | 1 | a0001c0001t0009 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 149 | chr3 | 187722309 | ||||||
| chr3:187722323 | C | A | 1 | a0001c0001t0005 | 2 | HG01192.hp2 HG01433.hp1 |
3_prime_UTR_variant | MODIFIER | c.*135G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 135 | chr3 | 187722323 | ||||||
| chr3:187722435 | C | T | 1 | a0001c0001t0003 | 4 | HG00642.hp1 HG01346.hp1 HG01993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 10/10 | 23 | chr3 | 187722435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:187722718 | C | A | 175 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(172): Show |
190 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1978-117G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187722718 | |||||||
| chr3:187722760 | G | A | 2 | a0001c0002t0001g0028 a0001c0002t0001g0186 |
3 | HG01358.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1978-159C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187722760 | |||||||
| chr3:187722784 | A | G | 22 | a0001c0001t0002g0008 a0001c0001t0002g0020 a0001c0001t0002g0038 others(19): Show |
25 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.1978-183T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187722784 | |||||||
| chr3:187722830 | C | A | 3 | a0002c0003t0001g0188 a0003c0006t0001g0145 a0003c0006t0001g0290 |
3 | HG01074.hp2 HG01123.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1978-229G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187722830 | |||||||
| chr3:187722974 | G | C | 3 | a0002c0003t0001g0188 a0003c0006t0001g0145 a0003c0006t0001g0290 |
3 | HG01074.hp2 HG01123.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1978-373C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187722974 | |||||||
| chr3:187722993 | C | T | 2 | a0001c0001t0002g0240 a0001c0001t0002g0289 |
2 | HG03942.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1978-392G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187722993 | |||||||
| chr3:187723165 | C | T | 1 | a0001c0004t0001g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1978-564G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187723165 | |||||||
| chr3:187723199 | A | G | 1 | a0002c0003t0001g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1978-598T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187723199 | |||||||
| chr3:187723301 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1978-700C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187723301 | |||||||
| chr3:187723322 | A | G | 1 | a0001c0002t0001g0278 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1978-721T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187723322 | |||||||
| chr3:187723622 | T | C | 1 | a0001c0002t0001g0246 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1978-1021A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187723622 | |||||||
| chr3:187723768 | C | G | 1 | a0001c0002t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1978-1167G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187723768 | |||||||
| chr3:187724028 | A | C | 68 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0023 others(65): Show |
72 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1977+913T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724028 | |||||||
| chr3:187724100 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1977+841G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724100 | |||||||
| chr3:187724161 | C | T | 32 | a0001c0002t0001g0023 a0001c0002t0001g0063 a0001c0002t0001g0124 others(29): Show |
33 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1977+780G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724161 | |||||||
| chr3:187724206 | C | T | 1 | a0002c0012t0001g0337 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1977+735G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724206 | |||||||
| chr3:187724213 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1977+728C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724213 | |||||||
| chr3:187724380 | T | C | 357 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(354): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.1977+561A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724380 | |||||||
| chr3:187724411 | G | A | 6 | a0001c0002t0001g0028 a0001c0002t0001g0185 a0001c0002t0001g0186 others(3): Show |
7 | HG01081.hp2 HG01358.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1977+530C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724411 | |||||||
| chr3:187724468 | T | A | 2 | a0001c0002t0001g0232 a0001c0002t0001g0300 |
2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1977+473A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724468 | |||||||
| chr3:187724507 | T | G | 1 | a0001c0001t0001g0255 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1977+434A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724507 | |||||||
| chr3:187724593 | G | A | 1 | a0001c0002t0001g0237 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1977+348C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724593 | |||||||
| chr3:187724739 | C | A | 129 | a0001c0001t0001g0133 a0001c0001t0002g0008 a0001c0001t0002g0009 others(126): Show |
137 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1977+202G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724739 | |||||||
| chr3:187724799 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1977+142A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724799 | |||||||
| chr3:187724847 | G | C | 1 | a0002c0003t0001g0305 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1977+94C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724847 | |||||||
| chr3:187724873 | C | T | 6 | a0001c0002t0001g0028 a0001c0002t0001g0185 a0001c0002t0001g0186 others(3): Show |
7 | HG01081.hp2 HG01358.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1977+68G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724873 | |||||||
| chr3:187724874 | G | GCTCCACC others(12): Show |
39 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(36): Show |
47 | HG00323.hp1 HG00741.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.1977+48_1977+66dup others(19): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 9/9 | chr3 | 187724874 | |||||||
| chr3:187725091 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1840-13C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725091 | |||||||
| chr3:187725159 | T | C | 8 | a0002c0003t0001g0143 a0002c0003t0001g0206 a0002c0003t0001g0207 others(5): Show |
8 | HG01074.hp1 HG02630.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1840-81A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725159 | |||||||
| chr3:187725164 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0315 |
2 | HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1840-86C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725164 | |||||||
| chr3:187725278 | A | G | 1 | a0002c0003t0001g0200 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1840-200T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725278 | |||||||
| chr3:187725278 | ACCCGCTC others(10): Show |
A | 1 | a0001c0001t0002g0132 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1839+204_1840-201d others(19): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725278 | |||||||
| chr3:187725315 | C | T | 12 | a0001c0002t0001g0027 a0001c0002t0001g0146 a0001c0002t0001g0154 others(9): Show |
13 | HG01167.hp1 HG01169.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1839+184G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725315 | |||||||
| chr3:187725316 | G | A | 1 | a0002c0003t0001g0351 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1839+183C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725316 | |||||||
| chr3:187725402 | ACTTGCCT others(13): Show |
A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0092 |
2 | NA18964.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1839+77_1839+96del others(20): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725402 | |||||||
| chr3:187725417 | CCTCCGCT others(30): Show |
C | 1 | a0001c0002t0001g0350 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1839+45_1839+81del others(37): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725417 | |||||||
| chr3:187725425 | T | C | 40 | a0001c0001t0002g0293 a0001c0002t0001g0014 a0001c0002t0001g0021 others(37): Show |
43 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.1839+74A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725425 | |||||||
| chr3:187725437 | CCTCCGCT others(10): Show |
C | 46 | a0001c0001t0002g0293 a0001c0002t0001g0014 a0001c0002t0001g0021 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1839+45_1839+61del others(17): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725437 | |||||||
| chr3:187725453 | C | A | 1 | a0002c0005t0001g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1839+46G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725453 | |||||||
| chr3:187725453 | C | T | 12 | a0001c0002t0001g0027 a0001c0002t0001g0146 a0001c0002t0001g0154 others(9): Show |
13 | HG01167.hp1 HG01169.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1839+46G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725453 | |||||||
| chr3:187725454 | G | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0092 |
2 | NA18964.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1839+45C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725454 | |||||||
| chr3:187725479 | C | T | 40 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0023 others(37): Show |
43 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.1839+20G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725479 | |||||||
| chr3:187725480 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1839+19C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 8/9 | chr3 | 187725480 | |||||||
| chr3:187725727 | G | A | 1 | a0001c0001t0002g0353 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1709-98C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187725727 | |||||||
| chr3:187725765 | G | A | 1 | a0001c0002t0001g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1709-136C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187725765 | |||||||
| chr3:187725790 | C | A | 2 | a0001c0001t0002g0036 a0001c0001t0002g0269 |
2 | HG02027.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1709-161G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187725790 | |||||||
| chr3:187725816 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1709-187G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187725816 | |||||||
| chr3:187725934 | C | A | 40 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0023 others(37): Show |
43 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.1709-305G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187725934 | |||||||
| chr3:187726079 | T | C | 2 | a0001c0001t0002g0101 a0001c0001t0002g0130 |
2 | HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1709-450A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187726079 | |||||||
| chr3:187726106 | G | C | 1 | a0001c0001t0002g0121 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1709-477C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187726106 | |||||||
| chr3:187726111 | A | T | 1 | a0001c0001t0002g0121 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1709-482T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187726111 | |||||||
| chr3:187726239 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0294 a0001c0001t0001g0296 |
4 | NA18962.hp1 NA18987.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1708+492A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187726239 | |||||||
| chr3:187726422 | T | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(268): Show |
306 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.1708+309A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 7/9 | chr3 | 187726422 | |||||||
| chr3:187727023 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1541-125G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727023 | |||||||
| chr3:187727111 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0334 |
2 | NA18960.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1541-213C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727111 | |||||||
| chr3:187727209 | C | T | 2 | a0002c0005t0001g0177 a0002c0012t0001g0337 |
2 | HG02622.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1541-311G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727209 | |||||||
| chr3:187727265 | A | G | 53 | a0002c0003t0001g0001 a0002c0003t0001g0004 a0002c0003t0001g0005 others(50): Show |
65 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1541-367T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727265 | |||||||
| chr3:187727296 | C | T | 1 | a0001c0002t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1541-398G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727296 | |||||||
| chr3:187727333 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1541-435T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727333 | |||||||
| chr3:187727409 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(212): Show |
238 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1541-511T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727409 | |||||||
| chr3:187727418 | T | C | 56 | a0002c0003t0001g0001 a0002c0003t0001g0004 a0002c0003t0001g0005 others(53): Show |
68 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1541-520A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727418 | |||||||
| chr3:187727422 | G | A | 29 | a0001c0004t0001g0032 a0001c0004t0001g0042 a0001c0004t0001g0058 others(26): Show |
30 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1541-524C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727422 | |||||||
| chr3:187727469 | C | T | 54 | a0002c0003t0001g0001 a0002c0003t0001g0004 a0002c0003t0001g0005 others(51): Show |
66 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.1541-571G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727469 | |||||||
| chr3:187727538 | G | C | 1 | a0001c0001t0001g0296 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1541-640C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727538 | |||||||
| chr3:187727541 | C | T | 176 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0008 others(173): Show |
191 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1541-643G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727541 | |||||||
| chr3:187727638 | C | T | 2 | a0003c0006t0001g0145 a0003c0006t0001g0290 |
2 | HG01074.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1540+722G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727638 | |||||||
| chr3:187727699 | A | AT | 4 | a0002c0003t0001g0004 a0002c0003t0001g0174 a0002c0003t0001g0230 others(1): Show |
6 | HG02109.hp1 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540+660dupA | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727699 | |||||||
| chr3:187727740 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1540+620C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727740 | |||||||
| chr3:187727775 | A | G | 1 | a0001c0001t0002g0325 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1540+585T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727775 | |||||||
| chr3:187727918 | C | T | 3 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0209 |
3 | HG02735.hp2 HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1540+442G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727918 | |||||||
| chr3:187727973 | T | C | 1 | a0002c0003t0001g0167 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1540+387A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187727973 | |||||||
| chr3:187728021 | A | G | 56 | a0002c0003t0001g0001 a0002c0003t0001g0004 a0002c0003t0001g0005 others(53): Show |
68 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1540+339T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187728021 | |||||||
| chr3:187728044 | A | G | 3 | a0002c0003t0001g0001 a0002c0003t0001g0005 a0002c0003t0001g0025 |
9 | HG01884.hp2 HG02451.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1540+316T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187728044 | |||||||
| chr3:187728054 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1540+306C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187728054 | |||||||
| chr3:187728104 | A | G | 359 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(356): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.1540+256T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187728104 | |||||||
| chr3:187728247 | A | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0224 |
2 | HG00323.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1540+113T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187728247 | |||||||
| chr3:187728258 | C | T | 1 | a0001c0002t0008g0187 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1540+102G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187728258 | |||||||
| chr3:187728271 | C | T | 29 | a0001c0004t0001g0032 a0001c0004t0001g0042 a0001c0004t0001g0058 others(26): Show |
30 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1540+89G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 6/9 | chr3 | 187728271 | |||||||
| chr3:187728590 | C | G | 1 | a0001c0004t0001g0314 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1356-46G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/9 | chr3 | 187728590 | |||||||
| chr3:187728602 | C | G | 28 | a0001c0004t0001g0032 a0001c0004t0001g0042 a0001c0004t0001g0058 others(25): Show |
29 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1356-58G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/9 | chr3 | 187728602 | |||||||
| chr3:187728705 | A | G | 360 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(357): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1356-161T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/9 | chr3 | 187728705 | |||||||
| chr3:187728943 | T | C | 54 | a0002c0003t0001g0001 a0002c0003t0001g0004 a0002c0003t0001g0005 others(51): Show |
66 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.1355+107A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 5/9 | chr3 | 187728943 | |||||||
| chr3:187730098 | T | C | 2 | a0001c0001t0002g0057 a0001c0001t0002g0260 |
2 | HG00597.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.384-77A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730098 | |||||||
| chr3:187730138 | C | T | 176 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0008 others(173): Show |
191 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.384-117G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730138 | |||||||
| chr3:187730221 | T | G | 360 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(357): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.384-200A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730221 | |||||||
| chr3:187730243 | T | A | 38 | a0001c0002t0001g0014 a0001c0002t0001g0021 a0001c0002t0001g0034 others(35): Show |
40 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.384-222A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730243 | |||||||
| chr3:187730261 | T | C | 1 | a0001c0001t0006g0313 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.384-240A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730261 | |||||||
| chr3:187730274 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.384-253A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730274 | |||||||
| chr3:187730466 | C | T | 43 | a0001c0002t0001g0023 a0001c0002t0001g0027 a0001c0002t0001g0146 others(40): Show |
46 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.384-445G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730466 | |||||||
| chr3:187730504 | C | T | 1 | a0002c0003t0001g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384-483G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730504 | |||||||
| chr3:187730581 | G | A | 9 | a0001c0001t0002g0008 a0001c0001t0002g0038 a0001c0001t0002g0047 others(6): Show |
11 | HG01106.hp2 HG01934.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.384-560C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730581 | |||||||
| chr3:187730737 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.384-716G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187730737 | |||||||
| chr3:187731040 | G | A | 2 | a0001c0001t0002g0109 a0001c0001t0002g0315 |
2 | HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.383+669C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731040 | |||||||
| chr3:187731162 | T | C | 9 | a0001c0002t0001g0023 a0001c0002t0001g0027 a0001c0002t0001g0146 others(6): Show |
11 | HG01167.hp1 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.383+547A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731162 | |||||||
| chr3:187731209 | G | A | 51 | a0002c0003t0001g0004 a0002c0003t0001g0007 a0002c0003t0001g0019 others(48): Show |
57 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.383+500C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731209 | |||||||
| chr3:187731302 | T | A | 2 | a0002c0003t0001g0141 a0002c0003t0001g0178 |
2 | NA18961.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.383+407A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731302 | |||||||
| chr3:187731452 | G | A | 1 | a0002c0003t0001g0207 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.383+257C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731452 | |||||||
| chr3:187731462 | G | A | 8 | a0001c0002t0001g0028 a0001c0002t0001g0185 a0001c0002t0001g0186 others(5): Show |
9 | HG01081.hp2 HG01358.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.383+247C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731462 | |||||||
| chr3:187731555 | G | A | 4 | a0001c0001t0003g0085 a0001c0001t0003g0129 a0001c0001t0003g0318 others(1): Show |
4 | HG00642.hp1 HG01346.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+154C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731555 | |||||||
| chr3:187731659 | C | T | 1 | a0001c0001t0002g0323 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.383+50G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731659 | |||||||
| chr3:187731681 | C | T | 3 | a0001c0001t0002g0065 a0001c0001t0002g0284 a0001c0001t0002g0363 |
3 | NA18946.hp2 NA18994.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.383+28G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 4/9 | chr3 | 187731681 | |||||||
| chr3:187732134 | G | C | 351 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(348): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.162-204C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732134 | |||||||
| chr3:187732155 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(46): Show |
58 | HG00323.hp1 HG00741.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.162-225G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732155 | |||||||
| chr3:187732279 | T | C | 33 | a0001c0002t0001g0021 a0001c0002t0001g0164 a0001c0002t0001g0348 others(30): Show |
35 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.162-349A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732279 | |||||||
| chr3:187732340 | C | T | 169 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(166): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.162-410G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732340 | |||||||
| chr3:187732482 | C | G | 57 | a0001c0001t0001g0147 a0001c0001t0001g0205 a0001c0002t0001g0028 others(54): Show |
69 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.162-552G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732482 | |||||||
| chr3:187732546 | A | G | 2 | a0001c0001t0002g0234 a0001c0002t0002g0202 |
2 | HG00735.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.162-616T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732546 | |||||||
| chr3:187732566 | T | A | 32 | a0001c0002t0001g0021 a0001c0002t0001g0164 a0001c0002t0001g0348 others(29): Show |
34 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.162-636A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732566 | |||||||
| chr3:187732630 | AGCTAT | A | 3 | a0001c0001t0002g0136 a0001c0001t0002g0240 a0001c0001t0002g0289 |
3 | HG03490.hp1 HG03942.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.162-705_162-701del others(5): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732630 | |||||||
| chr3:187732744 | A | G | 1 | a0001c0002t0001g0039 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.161+789T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732744 | |||||||
| chr3:187732869 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.161+664A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187732869 | |||||||
| chr3:187733109 | T | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0296 |
3 | NA18962.hp1 NA18987.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.161+424A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187733109 | |||||||
| chr3:187733121 | T | A | 1 | a0001c0002t0001g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.161+412A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187733121 | |||||||
| chr3:187733325 | G | A | 351 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(348): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.161+208C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187733325 | |||||||
| chr3:187733383 | C | G | 1 | a0006c0008t0001g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161+150G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187733383 | |||||||
| chr3:187733428 | A | G | 1 | a0002c0012t0001g0337 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161+105T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187733428 | |||||||
| chr3:187733525 | T | A | 3 | a0002c0003t0001g0019 a0002c0003t0001g0201 a0002c0003t0001g0307 |
4 | HG00544.hp2 HG00673.hp2 NA19002.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.161+8A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 3/9 | chr3 | 187733525 | |||||||
| chr3:187733784 | G | T | 1 | a0002c0005t0001g0024 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-10-81C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187733784 | |||||||
| chr3:187733821 | A | G | 351 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(348): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.-10-118T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187733821 | |||||||
| chr3:187733913 | T | C | 173 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0008 others(170): Show |
188 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.-10-210A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187733913 | |||||||
| chr3:187733921 | C | T | 173 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0008 others(170): Show |
188 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.-10-218G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187733921 | |||||||
| chr3:187734123 | T | C | 8 | a0002c0003t0001g0143 a0002c0003t0001g0206 a0002c0003t0001g0207 others(5): Show |
8 | HG01074.hp1 HG02630.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-420A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734123 | |||||||
| chr3:187734172 | C | G | 1 | a0001c0002t0001g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-10-469G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734172 | |||||||
| chr3:187734192 | C | A | 43 | a0001c0002t0001g0014 a0001c0002t0001g0034 a0001c0002t0001g0039 others(40): Show |
45 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-10-489G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734192 | |||||||
| chr3:187734193 | A | C | 43 | a0001c0002t0001g0014 a0001c0002t0001g0034 a0001c0002t0001g0039 others(40): Show |
45 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-10-490T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734193 | |||||||
| chr3:187734331 | C | T | 6 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 others(3): Show |
6 | HG01256.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+538G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734331 | |||||||
| chr3:187734334 | G | A | 1 | a0001c0002t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+535C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734334 | |||||||
| chr3:187734407 | G | A | 2 | a0002c0003t0001g0203 a0002c0003t0004g0359 |
2 | HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-11+462C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734407 | |||||||
| chr3:187734448 | T | C | 4 | a0001c0002t0001g0021 a0001c0002t0001g0164 a0001c0002t0001g0348 others(1): Show |
5 | HG02622.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+421A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734448 | |||||||
| chr3:187734460 | T | G | 1 | a0002c0003t0001g0347 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-11+409A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734460 | |||||||
| chr3:187734525 | T | C | 1 | a0001c0002t0001g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-11+344A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734525 | |||||||
| chr3:187734694 | G | T | 57 | a0001c0001t0001g0147 a0001c0001t0001g0205 a0001c0002t0001g0028 others(54): Show |
69 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-11+175C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734694 | |||||||
| chr3:187734800 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-11+69G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 2/9 | chr3 | 187734800 | |||||||
| chr3:187735122 | A | G | 351 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(348): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.-49-215T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735122 | |||||||
| chr3:187735279 | G | A | 8 | a0002c0003t0001g0143 a0002c0003t0001g0206 a0002c0003t0001g0207 others(5): Show |
8 | HG01074.hp1 HG02630.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-372C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735279 | |||||||
| chr3:187735310 | C | T | 1 | a0001c0004t0001g0220 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-49-403G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735310 | |||||||
| chr3:187735318 | A | C | 1 | a0001c0002t0001g0204 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-49-411T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735318 | |||||||
| chr3:187735357 | C | T | 173 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0008 others(170): Show |
188 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.-49-450G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735357 | |||||||
| chr3:187735358 | G | A | 2 | a0002c0003t0001g0094 a0002c0003t0001g0235 |
2 | HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-49-451C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735358 | |||||||
| chr3:187735386 | C | T | 32 | a0001c0002t0001g0021 a0001c0002t0001g0164 a0001c0002t0001g0348 others(29): Show |
34 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.-49-479G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735386 | |||||||
| chr3:187735436 | T | C | 7 | a0001c0001t0001g0147 a0001c0001t0001g0205 a0001c0002t0001g0028 others(4): Show |
8 | HG01081.hp2 HG01358.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49-529A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735436 | |||||||
| chr3:187735470 | T | A | 1 | a0001c0001t0002g0282 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-49-563A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735470 | |||||||
| chr3:187735513 | T | C | 1 | a0002c0003t0001g0303 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-49-606A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735513 | |||||||
| chr3:187735529 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0002g0098 |
2 | NA18990.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-49-622G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735529 | |||||||
| chr3:187735582 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-49-675T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735582 | |||||||
| chr3:187735613 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0002g0128 a0001c0013t0002g0125 |
3 | HG01243.hp2 HG01978.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-49-706G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735613 | |||||||
| chr3:187735787 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-880A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735787 | |||||||
| chr3:187735823 | T | G | 33 | a0001c0002t0001g0021 a0001c0002t0001g0164 a0001c0002t0001g0348 others(30): Show |
35 | HG00099.hp2 HG00621.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.-49-916A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735823 | |||||||
| chr3:187735833 | C | A | 1 | a0001c0001t0001g0254 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-926G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735833 | |||||||
| chr3:187735837 | T | TA | 7 | a0001c0001t0002g0189 a0001c0001t0002g0266 a0001c0001t0002g0332 others(4): Show |
8 | HG01257.hp2 HG01261.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49-931dupT | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735837 | |||||||
| chr3:187735837 | TA | T | 9 | a0001c0001t0002g0009 a0001c0001t0002g0083 a0001c0001t0002g0093 others(6): Show |
10 | HG02135.hp2 NA18941.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-931delT | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735837 | |||||||
| chr3:187735922 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-1015C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735922 | |||||||
| chr3:187735924 | T | G | 1 | a0001c0001t0001g0254 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-1017A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735924 | |||||||
| chr3:187735926 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-1019C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187735926 | |||||||
| chr3:187736134 | A | C | 1 | a0001c0002t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-49-1227T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187736134 | |||||||
| chr3:187736413 | T | C | 1 | a0002c0003t0001g0235 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-49-1506A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187736413 | |||||||
| chr3:187736581 | C | G | 1 | a0001c0001t0002g0102 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-49-1674G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187736581 | |||||||
| chr3:187736747 | GC | G | 38 | a0002c0003t0001g0001 a0002c0003t0001g0004 a0002c0003t0001g0005 others(35): Show |
49 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-49-1841delG | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187736747 | |||||||
| chr3:187736887 | A | C | 351 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(348): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.-49-1980T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187736887 | |||||||
| chr3:187736943 | C | G | 171 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0008 others(168): Show |
186 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-49-2036G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187736943 | |||||||
| chr3:187736961 | C | A | 1 | a0001c0001t0001g0254 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-2054G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187736961 | |||||||
| chr3:187737040 | CAA | C | 6 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 others(3): Show |
6 | HG01256.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-2135_-49-2134d others(4): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737040 | |||||||
| chr3:187737171 | G | A | 2 | a0001c0002t0001g0023 a0001c0002t0001g0245 |
3 | HG02895.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-49-2264C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737171 | |||||||
| chr3:187737239 | A | G | 2 | a0002c0003t0001g0203 a0002c0003t0004g0359 |
2 | HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-49-2332T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737239 | |||||||
| chr3:187737347 | C | CAG | 17 | a0001c0001t0002g0033 a0001c0001t0002g0064 a0001c0001t0002g0086 others(14): Show |
17 | HG00621.hp1 HG00735.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.-49-2442_-49-2441d others(4): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | C | CAGAG | 11 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0183 others(8): Show |
13 | HG02027.hp1 HG02083.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.-49-2444_-49-2441d others(6): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | C | CAGAGAG | 13 | a0001c0001t0002g0111 a0001c0001t0002g0122 a0001c0001t0002g0283 others(10): Show |
14 | HG01192.hp1 HG01891.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.-49-2446_-49-2441d others(8): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | C | CAGAGAGA others(1): Show |
4 | a0001c0001t0002g0103 a0001c0002t0001g0021 a0001c0004t0001g0161 others(1): Show |
5 | HG02040.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-2448_-49-2441d others(10): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | C | CAGAGAGA others(3): Show |
3 | a0001c0001t0002g0319 a0001c0002t0001g0164 a0001c0004t0001g0331 |
3 | HG03654.hp2 NA18951.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-49-2450_-49-2441d others(12): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | C | CAGAGAGA others(5): Show |
3 | a0001c0004t0001g0160 a0001c0004t0001g0340 a0002c0003t0001g0351 |
3 | HG02145.hp1 NA18944.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.-49-2452_-49-2441d others(14): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | C | CAGAGAGA others(7): Show |
1 | a0001c0004t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-49-2454_-49-2441d others(16): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | C | CAGAGAGA others(9): Show |
1 | a0001c0002t0001g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-49-2456_-49-2441d others(18): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | C | CAGAGAGA others(13): Show |
1 | a0001c0004t0001g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-49-2460_-49-2441d others(22): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAG | C | 45 | a0001c0001t0002g0010 a0001c0001t0002g0026 a0001c0001t0002g0050 others(42): Show |
56 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.-49-2442_-49-2441d others(4): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAG | C | 60 | a0001c0001t0001g0249 a0001c0001t0002g0008 a0001c0001t0002g0011 others(57): Show |
64 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.-49-2444_-49-2441d others(6): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAGAG | C | 46 | a0001c0001t0001g0045 a0001c0001t0001g0110 a0001c0001t0001g0252 others(43): Show |
50 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-49-2446_-49-2441d others(8): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAGAGA others(1): Show |
C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(35): Show |
48 | HG00558.hp1 HG00609.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.-49-2448_-49-2441d others(10): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAGAGA others(3): Show |
C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0250 a0001c0001t0001g0294 others(8): Show |
12 | HG00438.hp2 HG00741.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.-49-2450_-49-2441d others(12): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAGAGA others(5): Show |
C | 8 | a0001c0001t0001g0157 a0001c0001t0001g0247 a0001c0001t0002g0061 others(5): Show |
9 | HG00733.hp2 HG01069.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-49-2452_-49-2441d others(14): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAGAGA others(7): Show |
C | 10 | a0001c0001t0001g0113 a0001c0001t0001g0158 a0001c0001t0001g0238 others(7): Show |
10 | HG00140.hp2 HG00323.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-2454_-49-2441d others(16): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAGAGA others(9): Show |
C | 3 | a0001c0001t0002g0234 a0001c0002t0001g0034 a0001c0002t0001g0278 |
3 | HG00735.hp1 HG02004.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-49-2456_-49-2441d others(18): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAGAGA others(11): Show |
C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0140 a0001c0002t0001g0227 others(1): Show |
4 | HG01109.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-2458_-49-2441d others(20): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737347 | CAGAGAGA others(17): Show |
C | 6 | a0001c0002t0001g0229 a0001c0002t0001g0236 a0001c0002t0001g0237 others(3): Show |
6 | HG02109.hp2 HG02559.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-2464_-49-2441d others(26): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737347 | |||||||
| chr3:187737366 | A | G | 3 | a0001c0001t0003g0085 a0001c0001t0003g0129 a0001c0001t0003g0318 |
3 | HG00642.hp1 HG01346.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-49-2459T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737366 | |||||||
| chr3:187737379 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49-2472C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737379 | |||||||
| chr3:187737381 | G | A | 24 | a0001c0001t0001g0147 a0001c0001t0001g0205 a0001c0001t0002g0135 others(21): Show |
33 | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-49-2474C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737381 | |||||||
| chr3:187737381 | G | GAA | 17 | a0001c0001t0002g0120 a0001c0002t0001g0185 a0002c0003t0001g0007 others(14): Show |
19 | HG00099.hp1 HG01081.hp2 HG03041.hp1 others(16): Show |
intron_variant | MODIFIER | c.-49-2475_-49-2474i others(4): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737381 | |||||||
| chr3:187737381 | G | GAGAA | 7 | a0001c0002t0008g0187 a0002c0003t0001g0062 a0002c0003t0001g0143 others(4): Show |
7 | HG02056.hp1 HG03041.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-2475_-49-2474i others(6): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737381 | |||||||
| chr3:187737381 | G | GAGAGAA | 2 | a0001c0002t0001g0028 a0002c0003t0001g0233 |
3 | HG01358.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-49-2475_-49-2474i others(8): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737381 | |||||||
| chr3:187737381 | G | GAGAGAGA others(3): Show |
1 | a0001c0002t0001g0186 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-49-2475_-49-2474i others(12): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737381 | |||||||
| chr3:187737382 | A | T | 1 | a0001c0001t0002g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49-2475T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737382 | |||||||
| chr3:187737393 | GAGA | G | 7 | a0001c0001t0002g0003 a0001c0001t0002g0184 a0001c0001t0002g0262 others(4): Show |
7 | HG00544.hp1 HG00597.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-49-2489_-49-2487d others(5): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737393 | |||||||
| chr3:187737395 | GA | G | 3 | a0001c0001t0001g0254 a0001c0001t0002g0101 a0001c0001t0002g0217 |
3 | HG02132.hp2 HG02738.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-49-2489delT | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737395 | |||||||
| chr3:187737396 | A | AG | 4 | a0001c0001t0002g0037 a0001c0001t0002g0130 a0001c0001t0002g0248 others(1): Show |
4 | HG01123.hp2 HG03927.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-2490_-49-2489i others(3): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737396 | |||||||
| chr3:187737397 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0095 |
2 | HG02027.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-49-2490T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737397 | |||||||
| chr3:187737461 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-49-2554G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737461 | |||||||
| chr3:187737462 | CT | C | 6 | a0002c0003t0001g0094 a0002c0003t0001g0235 a0002c0003t0001g0351 others(3): Show |
7 | HG02145.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-2556delA | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737462 | |||||||
| chr3:187737583 | C | G | 1 | a0001c0001t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-49-2676G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737583 | |||||||
| chr3:187737664 | C | T | 6 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(3): Show |
6 | NA18957.hp1 NA18968.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-49-2757G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737664 | |||||||
| chr3:187737719 | G | C | 360 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(357): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.-49-2812C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737719 | |||||||
| chr3:187737720 | G | T | 1 | a0002c0003t0001g0305 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-49-2813C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737720 | |||||||
| chr3:187737752 | C | CT | 63 | a0001c0001t0001g0013 a0001c0001t0001g0238 a0001c0001t0001g0254 others(60): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-49-2846dupA | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737752 | |||||||
| chr3:187737752 | C | CTT | 54 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0029 others(51): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-49-2847_-49-2846d others(4): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737752 | |||||||
| chr3:187737752 | C | CTTT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0045 others(116): Show |
135 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-49-2848_-49-2846d others(5): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737752 | |||||||
| chr3:187737752 | C | CTTTT | 59 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0002g0010 others(56): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-49-2849_-49-2846d others(6): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737752 | |||||||
| chr3:187737752 | C | CTTTTT | 8 | a0001c0001t0002g0052 a0001c0001t0002g0078 a0001c0001t0002g0079 others(5): Show |
8 | HG00438.hp1 HG01952.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-49-2850_-49-2846d others(7): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737752 | |||||||
| chr3:187737955 | C | A | 46 | a0001c0001t0002g0120 a0001c0002t0001g0179 a0001c0002t0001g0180 others(43): Show |
58 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.-49-3048G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737955 | |||||||
| chr3:187737983 | A | G | 353 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(350): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.-49-3076T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187737983 | |||||||
| chr3:187738170 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(191): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-49-3263T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738170 | |||||||
| chr3:187738331 | C | G | 1 | a0001c0001t0002g0312 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-49-3424G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738331 | |||||||
| chr3:187738345 | C | A | 2 | a0001c0001t0002g0072 a0001c0001t0002g0241 |
2 | NA18968.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-49-3438G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738345 | |||||||
| chr3:187738345 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-49-3438G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738345 | |||||||
| chr3:187738422 | T | C | 1 | a0001c0002t0001g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-49-3515A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738422 | |||||||
| chr3:187738499 | A | G | 6 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 others(3): Show |
6 | HG01256.hp1 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-49-3592T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738499 | |||||||
| chr3:187738541 | C | T | 2 | a0002c0003t0001g0150 a0002c0003t0001g0151 |
2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-49-3634G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738541 | |||||||
| chr3:187738624 | A | T | 8 | a0002c0003t0001g0143 a0002c0003t0001g0206 a0002c0003t0001g0207 others(5): Show |
8 | HG01074.hp1 HG02630.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-3717T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738624 | |||||||
| chr3:187738649 | G | A | 8 | a0002c0003t0001g0143 a0002c0003t0001g0206 a0002c0003t0001g0207 others(5): Show |
8 | HG01074.hp1 HG02630.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-3742C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738649 | |||||||
| chr3:187738758 | C | A | 1 | a0001c0002t0001g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-49-3851G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738758 | |||||||
| chr3:187738806 | A | C | 165 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0008 others(162): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.-49-3899T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738806 | |||||||
| chr3:187738921 | T | G | 47 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0051 others(44): Show |
51 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.-49-4014A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738921 | |||||||
| chr3:187738945 | C | T | 1 | a0001c0004t0001g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-49-4038G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738945 | |||||||
| chr3:187738967 | C | T | 31 | a0001c0001t0002g0120 a0002c0003t0001g0001 a0002c0003t0001g0005 others(28): Show |
41 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.-49-4060G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187738967 | |||||||
| chr3:187739116 | C | G | 79 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0051 others(76): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-49-4209G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739116 | |||||||
| chr3:187739238 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(38): Show |
49 | HG00323.hp1 HG00741.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.-49-4331T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739238 | |||||||
| chr3:187739362 | C | T | 3 | a0002c0003t0001g0094 a0002c0003t0001g0235 a0002c0003t0001g0351 |
3 | HG02145.hp1 HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-49-4455G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739362 | |||||||
| chr3:187739379 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-49-4472C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739379 | |||||||
| chr3:187739388 | G | A | 8 | a0002c0003t0001g0143 a0002c0003t0001g0206 a0002c0003t0001g0207 others(5): Show |
8 | HG01074.hp1 HG02630.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.-49-4481C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739388 | |||||||
| chr3:187739621 | G | C | 1 | a0001c0001t0002g0328 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-49-4714C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739621 | |||||||
| chr3:187739668 | A | G | 1 | a0001c0002t0001g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-49-4761T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739668 | |||||||
| chr3:187739782 | C | T | 5 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 others(2): Show |
5 | HG01256.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-4875G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739782 | |||||||
| chr3:187739804 | G | T | 2 | a0001c0001t0002g0210 a0001c0001t0002g0211 |
2 | HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-49-4897C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739804 | |||||||
| chr3:187739953 | A | G | 1 | a0001c0001t0002g0311 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-49-5046T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739953 | |||||||
| chr3:187739988 | G | A | 1 | a0001c0002t0001g0199 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-49-5081C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187739988 | |||||||
| chr3:187740033 | G | A | 346 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(343): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-49-5126C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740033 | |||||||
| chr3:187740044 | G | T | 1 | a0001c0013t0002g0125 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-49-5137C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740044 | |||||||
| chr3:187740225 | C | A | 1 | a0001c0001t0002g0222 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-50+5185G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740225 | |||||||
| chr3:187740333 | C | G | 153 | a0001c0001t0001g0133 a0001c0001t0002g0003 a0001c0001t0002g0008 others(150): Show |
166 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.-50+5077G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740333 | |||||||
| chr3:187740349 | C | A | 3 | a0001c0004t0001g0149 a0002c0003t0001g0150 a0002c0003t0001g0151 |
3 | HG02055.hp2 HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-50+5061G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740349 | |||||||
| chr3:187740364 | C | T | 2 | a0002c0003t0001g0203 a0002c0003t0004g0359 |
2 | HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-50+5046G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740364 | |||||||
| chr3:187740366 | C | G | 6 | a0001c0002t0001g0146 a0001c0002t0001g0154 a0001c0002t0001g0155 others(3): Show |
6 | HG02572.hp2 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50+5044G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740366 | |||||||
| chr3:187740385 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-50+5025T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740385 | |||||||
| chr3:187740508 | C | A | 1 | a0001c0001t0002g0136 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-50+4902G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740508 | |||||||
| chr3:187740510 | T | G | 3 | a0001c0004t0001g0149 a0002c0003t0001g0150 a0002c0003t0001g0151 |
3 | HG02055.hp2 HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-50+4900A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740510 | |||||||
| chr3:187740581 | C | G | 1 | a0002c0003t0001g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-50+4829G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740581 | |||||||
| chr3:187740628 | T | C | 1 | a0002c0012t0001g0337 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-50+4782A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740628 | |||||||
| chr3:187740859 | G | A | 1 | a0002c0003t0001g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-50+4551C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740859 | |||||||
| chr3:187740929 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-50+4481C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740929 | |||||||
| chr3:187740968 | A | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0110 a0001c0001t0001g0113 others(6): Show |
10 | HG01106.hp1 HG01255.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50+4442T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740968 | |||||||
| chr3:187740982 | G | A | 29 | a0001c0001t0002g0120 a0001c0002t0002g0202 a0002c0003t0001g0001 others(26): Show |
38 | HG00099.hp1 HG00544.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-50+4428C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187740982 | |||||||
| chr3:187741057 | C | G | 1 | a0001c0001t0002g0262 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-50+4353G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187741057 | |||||||
| chr3:187741300 | T | G | 118 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0051 others(115): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.-50+4110A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187741300 | |||||||
| chr3:187741605 | A | G | 1 | a0001c0013t0002g0125 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-50+3805T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187741605 | |||||||
| chr3:187741709 | T | C | 163 | a0001c0001t0001g0045 a0001c0001t0001g0126 a0001c0001t0001g0133 others(160): Show |
174 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-50+3701A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187741709 | |||||||
| chr3:187741913 | G | T | 10 | a0001c0002t0001g0179 a0001c0002t0001g0180 a0001c0002t0001g0181 others(7): Show |
10 | HG01109.hp2 HG01256.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50+3497C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187741913 | |||||||
| chr3:187741979 | C | CA | 12 | a0001c0001t0002g0044 a0002c0003t0001g0143 a0002c0003t0001g0206 others(9): Show |
13 | HG01074.hp1 HG01978.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50+3430dupT | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187741979 | |||||||
| chr3:187741991 | C | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(304): Show |
337 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.-50+3419G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187741991 | |||||||
| chr3:187742112 | A | G | 1 | a0001c0002t0001g0344 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-50+3298T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742112 | |||||||
| chr3:187742119 | G | A | 149 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0002g0003 others(146): Show |
160 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.-50+3291C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742119 | |||||||
| chr3:187742224 | A | C | 1 | a0002c0003t0001g0351 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-50+3186T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742224 | |||||||
| chr3:187742279 | A | C | 3 | a0001c0002t0001g0227 a0001c0002t0001g0236 a0001c0002t0001g0237 |
3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-50+3131T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742279 | |||||||
| chr3:187742311 | G | A | 194 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0147 others(191): Show |
208 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.-50+3099C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742311 | |||||||
| chr3:187742314 | G | T | 1 | a0001c0004t0001g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-50+3096C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742314 | |||||||
| chr3:187742321 | T | C | 1 | a0001c0002t0001g0246 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-50+3089A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742321 | |||||||
| chr3:187742642 | G | T | 17 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0002t0001g0027 others(14): Show |
18 | HG01074.hp2 HG01123.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-50+2768C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742642 | |||||||
| chr3:187742861 | A | G | 1 | a0001c0001t0007g0336 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-50+2549T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742861 | |||||||
| chr3:187742890 | G | C | 2 | a0001c0001t0002g0036 a0001c0001t0002g0269 |
2 | HG02027.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-50+2520C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742890 | |||||||
| chr3:187742920 | T | G | 1 | a0006c0008t0001g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-50+2490A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742920 | |||||||
| chr3:187742985 | A | G | 6 | a0001c0002t0001g0028 a0001c0002t0001g0138 a0001c0002t0001g0185 others(3): Show |
7 | HG01081.hp2 HG01358.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+2425T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187742985 | |||||||
| chr3:187743022 | C | CT | 61 | a0001c0001t0001g0110 a0001c0001t0002g0050 a0001c0001t0002g0064 others(58): Show |
65 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-50+2387dupA | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743022 | |||||||
| chr3:187743022 | C | CTT | 92 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0041 others(89): Show |
101 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-50+2386_-50+2387d others(4): Show |
BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743022 | |||||||
| chr3:187743269 | C | G | 1 | a0002c0003t0001g0107 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-50+2141G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743269 | |||||||
| chr3:187743350 | AG | A | 7 | a0001c0001t0002g0332 a0001c0002t0001g0146 a0001c0002t0001g0226 others(4): Show |
7 | HG01109.hp2 HG01261.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+2059delC | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743350 | |||||||
| chr3:187743354 | G | A | 1 | a0001c0009t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-50+2056C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743354 | |||||||
| chr3:187743355 | G | T | 1 | a0002c0003t0001g0152 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-50+2055C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743355 | |||||||
| chr3:187743447 | A | G | 3 | a0001c0004t0001g0149 a0002c0003t0001g0150 a0002c0003t0001g0151 |
3 | HG02055.hp2 HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-50+1963T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743447 | |||||||
| chr3:187743536 | TA | T | 12 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0047 others(9): Show |
14 | HG00408.hp1 HG02080.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50+1873delT | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743536 | |||||||
| chr3:187743537 | A | T | 69 | a0001c0001t0001g0156 a0001c0001t0002g0008 a0001c0001t0002g0026 others(66): Show |
81 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.-50+1873T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743537 | |||||||
| chr3:187743584 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-50+1826T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743584 | |||||||
| chr3:187743723 | G | GC | 29 | a0001c0001t0001g0045 a0001c0001t0001g0334 a0001c0001t0002g0035 others(26): Show |
29 | HG00323.hp2 HG00735.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.-50+1686dupG | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743723 | |||||||
| chr3:187743743 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-50+1667G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743743 | |||||||
| chr3:187743832 | T | C | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+1578A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743832 | |||||||
| chr3:187743867 | A | G | 1 | a0001c0001t0002g0352 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-50+1543T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743867 | |||||||
| chr3:187743947 | T | C | 1 | a0002c0003t0001g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-50+1463A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743947 | |||||||
| chr3:187743968 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-50+1442T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743968 | |||||||
| chr3:187743990 | T | G | 1 | a0001c0001t0002g0035 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-50+1420A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187743990 | |||||||
| chr3:187744023 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-50+1387A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744023 | |||||||
| chr3:187744025 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-50+1385G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744025 | |||||||
| chr3:187744063 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-50+1347A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744063 | |||||||
| chr3:187744079 | C | G | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+1331G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744079 | |||||||
| chr3:187744103 | T | C | 1 | a0002c0003t0001g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-50+1307A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744103 | |||||||
| chr3:187744112 | G | A | 1 | a0002c0003t0001g0351 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-50+1298C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744112 | |||||||
| chr3:187744130 | A | G | 1 | a0001c0002t0001g0146 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+1280T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744130 | |||||||
| chr3:187744166 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-50+1244A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744166 | |||||||
| chr3:187744201 | T | G | 1 | a0001c0001t0002g0038 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-50+1209A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744201 | |||||||
| chr3:187744302 | G | A | 1 | a0001c0001t0002g0052 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-50+1108C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744302 | |||||||
| chr3:187744303 | G | C | 1 | a0001c0001t0002g0052 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-50+1107C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744303 | |||||||
| chr3:187744306 | C | A | 1 | a0001c0001t0002g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-50+1104G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744306 | |||||||
| chr3:187744322 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-50+1088G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744322 | |||||||
| chr3:187744356 | G | C | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+1054C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744356 | |||||||
| chr3:187744365 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-50+1045G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744365 | |||||||
| chr3:187744371 | A | G | 3 | a0001c0001t0001g0238 a0001c0004t0001g0239 a0003c0006t0001g0145 |
3 | HG01123.hp1 HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-50+1039T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744371 | |||||||
| chr3:187744375 | G | C | 1 | a0001c0004t0001g0341 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-50+1035C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744375 | |||||||
| chr3:187744376 | C | G | 1 | a0001c0001t0002g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+1034G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744376 | |||||||
| chr3:187744416 | A | T | 1 | a0001c0001t0002g0353 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-50+994T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744416 | |||||||
| chr3:187744417 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-50+993G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744417 | |||||||
| chr3:187744418 | C | G | 1 | a0001c0001t0002g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-50+992G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744418 | |||||||
| chr3:187744430 | A | C | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+980T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744430 | |||||||
| chr3:187744437 | A | G | 1 | a0001c0001t0002g0353 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-50+973T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744437 | |||||||
| chr3:187744460 | A | C | 1 | a0001c0001t0002g0353 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-50+950T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744460 | |||||||
| chr3:187744461 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-50+949T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744461 | |||||||
| chr3:187744479 | G | A | 1 | a0001c0004t0001g0032 | 2 | HG01081.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.-50+931C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744479 | |||||||
| chr3:187744486 | A | C | 1 | a0001c0001t0002g0038 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-50+924T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744486 | |||||||
| chr3:187744508 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(231): Show |
263 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-50+902T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744508 | |||||||
| chr3:187744511 | A | G | 1 | a0001c0001t0002g0357 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-50+899T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744511 | |||||||
| chr3:187744537 | T | G | 1 | a0001c0001t0001g0362 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-50+873A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744537 | |||||||
| chr3:187744541 | A | G | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+869T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744541 | |||||||
| chr3:187744542 | G | A | 1 | a0002c0003t0001g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-50+868C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744542 | |||||||
| chr3:187744548 | A | G | 1 | a0002c0003t0001g0143 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-50+862T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744548 | |||||||
| chr3:187744549 | T | G | 1 | a0002c0003t0001g0342 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-50+861A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744549 | |||||||
| chr3:187744565 | G | C | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+845C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744565 | |||||||
| chr3:187744573 | A | G | 1 | a0001c0001t0002g0142 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-50+837T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744573 | |||||||
| chr3:187744577 | A | C | 1 | a0001c0001t0002g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-50+833T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744577 | |||||||
| chr3:187744600 | A | G | 1 | a0002c0003t0001g0141 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-50+810T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744600 | |||||||
| chr3:187744602 | A | G | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+808T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744602 | |||||||
| chr3:187744604 | T | G | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+806A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744604 | |||||||
| chr3:187744626 | A | T | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+784T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744626 | |||||||
| chr3:187744647 | G | C | 1 | a0001c0002t0001g0348 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-50+763C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744647 | |||||||
| chr3:187744667 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0002g0361 |
2 | HG01515.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-50+743T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744667 | |||||||
| chr3:187744688 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-50+722G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744688 | |||||||
| chr3:187744709 | C | G | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+701G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744709 | |||||||
| chr3:187744709 | C | T | 1 | a0001c0001t0002g0343 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-50+701G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744709 | |||||||
| chr3:187744717 | T | G | 1 | a0001c0001t0002g0343 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-50+693A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744717 | |||||||
| chr3:187744739 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-50+671T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744739 | |||||||
| chr3:187744809 | G | T | 1 | a0001c0001t0002g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-50+601C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744809 | |||||||
| chr3:187744810 | GA | G | 61 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0018 others(58): Show |
73 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.-50+599delT | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744810 | |||||||
| chr3:187744812 | G | C | 1 | a0001c0002t0001g0344 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-50+598C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744812 | |||||||
| chr3:187744816 | G | A | 1 | a0001c0001t0001g0345 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-50+594C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744816 | |||||||
| chr3:187744824 | G | C | 1 | a0001c0001t0002g0099 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-50+586C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744824 | |||||||
| chr3:187744828 | G | C | 1 | a0002c0005t0001g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+582C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744828 | |||||||
| chr3:187744828 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-50+582C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744828 | |||||||
| chr3:187744832 | G | A | 2 | a0001c0001t0002g0095 a0001c0004t0001g0346 |
2 | HG02027.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-50+578C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744832 | |||||||
| chr3:187744842 | A | G | 1 | a0001c0001t0002g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-50+568T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744842 | |||||||
| chr3:187744844 | G | A | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+566C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744844 | |||||||
| chr3:187744846 | A | G | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+564T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744846 | |||||||
| chr3:187744851 | A | C | 2 | a0001c0001t0002g0100 a0001c0002t0001g0034 |
2 | HG02080.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-50+559T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744851 | |||||||
| chr3:187744865 | A | T | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+545T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744865 | |||||||
| chr3:187744867 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-50+543G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744867 | |||||||
| chr3:187744875 | A | C | 1 | a0001c0001t0002g0099 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-50+535T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744875 | |||||||
| chr3:187744879 | C | G | 1 | a0001c0001t0002g0098 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-50+531G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744879 | |||||||
| chr3:187744883 | C | G | 1 | a0001c0001t0001g0362 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-50+527G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744883 | |||||||
| chr3:187744897 | C | T | 1 | a0002c0003t0001g0351 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-50+513G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744897 | |||||||
| chr3:187744898 | A | T | 1 | a0001c0002t0001g0097 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-50+512T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744898 | |||||||
| chr3:187744899 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-50+511C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744899 | |||||||
| chr3:187744899 | G | T | 1 | a0001c0002t0001g0097 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-50+511C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744899 | |||||||
| chr3:187744903 | A | C | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+507T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744903 | |||||||
| chr3:187744904 | A | G | 1 | a0001c0001t0002g0096 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-50+506T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744904 | |||||||
| chr3:187744908 | G | C | 3 | a0001c0001t0002g0363 a0001c0002t0001g0348 a0002c0003t0001g0347 |
3 | HG02970.hp1 HG03540.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-50+502C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744908 | |||||||
| chr3:187744910 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-50+500C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744910 | |||||||
| chr3:187744924 | G | A | 1 | a0002c0003t0001g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-50+486C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744924 | |||||||
| chr3:187744934 | C | G | 48 | a0001c0001t0001g0002 a0001c0001t0002g0009 a0001c0001t0002g0010 others(45): Show |
52 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.-50+476G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744934 | |||||||
| chr3:187744937 | G | T | 1 | a0001c0002t0001g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-50+473C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744937 | |||||||
| chr3:187744939 | T | C | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+471A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744939 | |||||||
| chr3:187744946 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-50+464G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744946 | |||||||
| chr3:187744962 | C | G | 1 | a0001c0001t0002g0051 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-50+448G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744962 | |||||||
| chr3:187744962 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-50+448G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744962 | |||||||
| chr3:187744965 | G | T | 1 | a0001c0001t0002g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+445C>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744965 | |||||||
| chr3:187744981 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-50+429T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744981 | |||||||
| chr3:187744988 | G | A | 1 | a0001c0001t0002g0352 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-50+422C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744988 | |||||||
| chr3:187744996 | C | G | 1 | a0001c0001t0002g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-50+414G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187744996 | |||||||
| chr3:187745047 | T | C | 1 | a0001c0002t0001g0349 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-50+363A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745047 | |||||||
| chr3:187745061 | A | G | 1 | a0001c0001t0002g0047 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-50+349T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745061 | |||||||
| chr3:187745069 | A | G | 1 | a0002c0003t0001g0360 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-50+341T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745069 | |||||||
| chr3:187745082 | A | C | 1 | a0002c0003t0001g0046 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-50+328T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745082 | |||||||
| chr3:187745102 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-50+308G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745102 | |||||||
| chr3:187745106 | T | C | 1 | a0002c0003t0001g0043 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-50+304A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745106 | |||||||
| chr3:187745107 | C | A | 1 | a0001c0002t0001g0350 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-50+303G>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745107 | |||||||
| chr3:187745122 | A | T | 1 | a0001c0001t0002g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-50+288T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745122 | |||||||
| chr3:187745125 | A | G | 1 | a0002c0005t0001g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+285T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745125 | |||||||
| chr3:187745126 | T | A | 1 | a0002c0003t0001g0043 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-50+284A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745126 | |||||||
| chr3:187745127 | A | G | 1 | a0001c0001t0002g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-50+283T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745127 | |||||||
| chr3:187745129 | T | C | 1 | a0001c0001t0002g0352 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-50+281A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745129 | |||||||
| chr3:187745136 | T | G | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+274A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745136 | |||||||
| chr3:187745140 | T | G | 1 | a0002c0003t0001g0356 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-50+270A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745140 | |||||||
| chr3:187745142 | A | C | 1 | a0001c0001t0002g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-50+268T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745142 | |||||||
| chr3:187745142 | A | G | 1 | a0002c0003t0001g0356 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-50+268T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745142 | |||||||
| chr3:187745153 | C | G | 1 | a0002c0003t0001g0043 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-50+257G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745153 | |||||||
| chr3:187745154 | C | T | 1 | a0002c0003t0001g0043 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-50+256G>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745154 | |||||||
| chr3:187745158 | G | A | 1 | a0002c0003t0001g0351 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-50+252C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745158 | |||||||
| chr3:187745160 | T | A | 1 | a0001c0001t0002g0352 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-50+250A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745160 | |||||||
| chr3:187745164 | A | G | 1 | a0002c0003t0001g0356 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-50+246T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745164 | |||||||
| chr3:187745178 | A | G | 1 | a0001c0004t0001g0042 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-50+232T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745178 | |||||||
| chr3:187745179 | A | C | 1 | a0001c0001t0002g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-50+231T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745179 | |||||||
| chr3:187745186 | G | C | 1 | a0001c0001t0002g0353 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-50+224C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745186 | |||||||
| chr3:187745194 | T | C | 1 | a0001c0004t0001g0354 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-50+216A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745194 | |||||||
| chr3:187745196 | T | C | 1 | a0001c0004t0001g0354 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-50+214A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745196 | |||||||
| chr3:187745204 | G | A | 1 | a0001c0001t0002g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-50+206C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745204 | |||||||
| chr3:187745208 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+202C>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745208 | |||||||
| chr3:187745208 | G | C | 1 | a0002c0005t0001g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+202C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745208 | |||||||
| chr3:187745212 | G | C | 1 | a0001c0002t0001g0355 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-50+198C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745212 | |||||||
| chr3:187745219 | T | G | 1 | a0001c0001t0002g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-50+191A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745219 | |||||||
| chr3:187745220 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-50+190T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745220 | |||||||
| chr3:187745223 | T | G | 1 | a0002c0003t0001g0356 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-50+187A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745223 | |||||||
| chr3:187745224 | A | C | 1 | a0001c0001t0002g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+186T>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745224 | |||||||
| chr3:187745224 | A | T | 1 | a0002c0005t0001g0040 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-50+186T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745224 | |||||||
| chr3:187745226 | A | G | 1 | a0001c0002t0001g0039 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-50+184T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745226 | |||||||
| chr3:187745229 | C | G | 1 | a0001c0001t0001g0362 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-50+181G>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745229 | |||||||
| chr3:187745231 | T | C | 1 | a0001c0001t0002g0357 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-50+179A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745231 | |||||||
| chr3:187745232 | T | C | 1 | a0001c0001t0001g0362 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-50+178A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745232 | |||||||
| chr3:187745233 | T | C | 1 | a0001c0001t0002g0358 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50+177A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745233 | |||||||
| chr3:187745235 | T | A | 2 | a0001c0001t0002g0357 a0001c0001t0002g0363 |
2 | HG01952.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-50+175A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745235 | |||||||
| chr3:187745241 | T | G | 1 | a0001c0001t0002g0358 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-50+169A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745241 | |||||||
| chr3:187745242 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-50+168T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745242 | |||||||
| chr3:187745243 | G | C | 2 | a0002c0003t0001g0360 a0002c0003t0004g0359 |
2 | HG03017.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-50+167C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745243 | |||||||
| chr3:187745245 | T | C | 1 | a0001c0001t0002g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-50+165A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745245 | |||||||
| chr3:187745250 | A | G | 1 | a0001c0001t0002g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+160T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745250 | |||||||
| chr3:187745255 | A | T | 1 | a0001c0001t0002g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+155T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745255 | |||||||
| chr3:187745256 | A | G | 1 | a0002c0003t0001g0360 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-50+154T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745256 | |||||||
| chr3:187745269 | A | G | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+141T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745269 | |||||||
| chr3:187745273 | T | A | 1 | a0002c0003t0001g0360 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-50+137A>T | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745273 | |||||||
| chr3:187745273 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+137A>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745273 | |||||||
| chr3:187745277 | G | C | 1 | a0001c0001t0002g0361 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+133C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745277 | |||||||
| chr3:187745286 | G | C | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+124C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745286 | |||||||
| chr3:187745288 | A | G | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+122T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745288 | |||||||
| chr3:187745293 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-50+117T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745293 | |||||||
| chr3:187745295 | A | G | 1 | a0001c0001t0002g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-50+115T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745295 | |||||||
| chr3:187745308 | A | G | 1 | a0001c0001t0002g0035 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-50+102T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745308 | |||||||
| chr3:187745310 | A | T | 1 | a0001c0002t0001g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-50+100T>A | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745310 | |||||||
| chr3:187745311 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-50+99T>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745311 | |||||||
| chr3:187745318 | T | G | 1 | a0001c0001t0001g0362 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-50+92A>C | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745318 | |||||||
| chr3:187745324 | G | C | 1 | a0001c0001t0002g0363 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-50+86C>G | BCL6 | ENSG00000113916.18 | transcript | ENST00000406870.7 | protein_coding | 1/9 | chr3 | 187745324 |