Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84969 |
| ensemblid | ENSG00000124191.18 |
| hgncid | 16095 |
| symbol | TOX2 |
| name | TOX high mobility group box family member 2 |
| refseq_nuc | NM_001098797.2 |
| refseq_prot | NP_001092267.1 |
| ensembl_nuc | ENST00000341197.9 |
| ensembl_prot | ENSP00000344724.3 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 43914852 |
| end | 44069616 |
| strand | + |
| ver | v1.2 |
| region | chr20:43914852-44069616 |
| region5000 | chr20:43909852-44074616 |
| regionname0 | TOX2_chr20_43914852_44069616 |
| regionname5000 | TOX2_chr20_43909852_44074616 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 506 | 273 | 79 | 55 | 103 | 7 | 27 | 74 | TOX2_chr20_43909852_44074616 | TOX2 | MDVRL others(501): Show |
chr20 | 43909852 | 44074616 |
| a0002 | 0/0 | 506 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | MDVRL others(501): Show |
chr20 | 43909852 | 44074616 |
| a0003 | 0/0 | 507 | 4 | 1 | 2 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | MDVRL others(502): Show |
chr20 | 43909852 | 44074616 |
| a0004 | 0/0 | 506 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | MDVRL others(501): Show |
chr20 | 43909852 | 44074616 |
| a0005 | 0/0 | 506 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | MDVRL others(501): Show |
chr20 | 43909852 | 44074616 |
| a0006 | 0/0 | 506 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | MDVRL others(501): Show |
chr20 | 43909852 | 44074616 |
| a0007 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | MDVRL others(501): Show |
chr20 | 43909852 | 44074616 |
| a0008 | 0/0 | 506 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | MDVRL others(501): Show |
chr20 | 43909852 | 44074616 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1518 | 269 | 78 | 54 | 101 | 7 | 27 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0001c0007 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0001c0009 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0001c0011 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0001c0012 | 0/0 | 1518 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0002c0002 | 0/0 | 1518 | 4 | 3 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0003c0003 | 0/0 | 1521 | 4 | 1 | 2 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1516): Show |
chr20 | 43909852 | 44074616 | ||
| a0004c0005 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0005c0004 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0006c0008 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0007c0006 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 | ||
| a0008c0010 | 0/0 | 1518 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | ATGGA others(1513): Show |
chr20 | 43909852 | 44074616 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2491 | 218 | 48 | 50 | 88 | 7 | 24 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0002 | 0/1 | 2491 | 33 | 24 | 4 | 2 | 0 | 2 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0003 | 0/0 | 2491 | 6 | 4 | 0 | 1 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0004 | 0/0 | 2488 | 3 | 0 | 0 | 3 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2483): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0005 | 0/0 | 2491 | 2 | 0 | 0 | 2 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0006 | 0/0 | 2491 | 2 | 0 | 0 | 2 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0007 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0008 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0009 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0010 | 0/0 | 2488 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2483): Show |
chr20 | 43909852 | 44074616 |
| a0001c0001t0011 | 0/0 | 2488 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2483): Show |
chr20 | 43909852 | 44074616 |
| a0001c0007t0001 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0009t0002 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0011t0001 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0001c0012t0003 | 0/0 | 2491 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0002c0002t0001 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0002c0002t0002 | 0/0 | 2491 | 3 | 2 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0003c0003t0001 | 0/0 | 2494 | 4 | 1 | 2 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2489): Show |
chr20 | 43909852 | 44074616 |
| a0004c0005t0001 | 0/0 | 2491 | 2 | 2 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0005c0004t0002 | 0/0 | 2491 | 2 | 2 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0006c0008t0001 | 0/0 | 2491 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0007c0006t0001 | 0/0 | 2491 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| a0008c0010t0001 | 0/0 | 2491 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | ACTGC others(2486): Show |
chr20 | 43909852 | 44074616 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0008g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0001t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0007t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0009t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0011t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0001c0012t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0003c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0003c0003t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0003c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0004c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0004c0005t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0005c0004t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0005c0004t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0006c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0007c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| a0008c0010t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | FIN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0140 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0064 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01496 | hp1 | a0001 | c0012 | t0003 | g0013 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02129 | hp2 | a0006 | c0008 | t0001 | g0076 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0131 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0170 | EAS | CDX | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0175 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02572 | hp2 | a0004 | c0005 | t0001 | g0106 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02615 | hp1 | a0004 | c0005 | t0001 | g0107 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02717 | hp1 | a0005 | c0004 | t0002 | g0019 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02922 | hp2 | a0001 | c0009 | t0002 | g0152 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0145 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03486 | hp2 | a0007 | c0006 | t0001 | g0089 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | ESN | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | STU | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG04204 | hp2 | a0008 | c0010 | t0001 | g0164 | SAS | STU | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18942 | hp1 | a0001 | c0007 | t0001 | g0209 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19030 | hp1 | a0005 | c0004 | t0002 | g0020 | AFR | LWK | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | LWK | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | LWK | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | LWK | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19068 | hp1 | a0001 | c0001 | t0011 | g0168 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19083 | hp1 | a0001 | c0001 | t0010 | g0171 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19083 | hp2 | a0001 | c0001 | t0008 | g0108 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19088 | hp1 | a0001 | c0011 | t0001 | g0240 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19089 | hp2 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | YRI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | YRI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ASW | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ASW | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | TSI | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | USA | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | USA | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0263 | REF | REF | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0230 | REF | REF | TOX2_chr20_43909852_44074616 | TOX2 | chr20 | 43909852 | 44074616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43914955 | G | A | 1 | a0005 | 2 | HG02717.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.64G>A | p.Gly22Ser | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/9 | 104/2491 | 64/1521 | 22/506 | chr20 | 43914955 | |||
| chr20:43914985 | G | A | 1 | a0007 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.94G>A | p.Gly32Ser | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/9 | 134/2491 | 94/1521 | 32/506 | chr20 | 43914985 | |||
| chr20:44006569 | A | G | 1 | a0004 | 2 | HG02572.hp2 HG02615.hp1 |
missense_variant | MODERATE | c.188A>G | p.Asn63Ser | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/9 | 228/2491 | 188/1521 | 63/506 | chr20 | 44006569 | |||
| chr20:44051535 | T | C | 1 | a0002 | 4 | HG00741.hp2 HG02109.hp1 HG02145.hp2 others(1): Show |
missense_variant | MODERATE | c.641T>C | p.Val214Ala | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/9 | 681/2491 | 641/1521 | 214/506 | chr20 | 44051535 | |||
| chr20:44065844 | C | T | 1 | a0008 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1093C>T | p.Arg365Cys | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 7/9 | 1133/2491 | 1093/1521 | 365/506 | chr20 | 44065844 | |||
| chr20:44065918 | C | CCCG | 1 | a0003 | 4 | HG01106.hp1 HG01261.hp1 HG01515.hp2 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.1176_1178dupGCC | p.Pro393dup | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 7/9 | 1219/2491 | 1179/1521 | 393/506 | INFO_REALIGN_3_PRIME | chr20 | 44065918 | ||
| chr20:44066764 | C | T | 1 | a0006 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.1391C>T | p.Ser464Leu | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/9 | 1431/2491 | 1391/1521 | 464/506 | chr20 | 44066764 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:44051536 | G | T | 1 | a0001c0012 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.642G>T | p.Val214Val | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/9 | 682/2491 | 642/1521 | 214/506 | chr20 | 44051536 | |||
| chr20:44064848 | C | T | 1 | a0001c0011 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.951C>T | p.Leu317Leu | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 6/9 | 991/2491 | 951/1521 | 317/506 | chr20 | 44064848 | |||
| chr20:44065822 | G | A | 1 | a0001c0007 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.1071G>A | p.Thr357Thr | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 7/9 | 1111/2491 | 1071/1521 | 357/506 | chr20 | 44065822 | |||
| chr20:44065945 | C | G | 1 | a0001c0009 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1194C>G | p.Leu398Leu | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 7/9 | 1234/2491 | 1194/1521 | 398/506 | chr20 | 44065945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43914864 | AGCC | A | 3 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0011 |
5 | HG02165.hp2 NA18983.hp1 NA19068.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-10_-8delCGC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/9 | 8 | INFO_REALIGN_3_PRIME | chr20 | 43914864 | |||||
| chr20:44068705 | C | G | 1 | a0001c0001t0009 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*19C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 9/9 | 19 | chr20 | 44068705 | ||||||
| chr20:44068971 | C | T | 2 | a0001c0001t0003 a0001c0012t0003 |
7 | HG01496.hp1 HG02145.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*285C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 9/9 | 285 | chr20 | 44068971 | ||||||
| chr20:44069011 | G | C | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(4): Show |
46 | HG00741.hp2 HG01175.hp2 HG01346.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*325G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 9/9 | 325 | chr20 | 44069011 | ||||||
| chr20:44069074 | G | A | 1 | a0001c0001t0005 | 2 | NA18962.hp1 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*388G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 9/9 | 388 | chr20 | 44069074 | ||||||
| chr20:44069081 | C | G | 2 | a0001c0001t0006 a0001c0001t0011 |
3 | NA19011.hp1 NA19068.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*395C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 9/9 | 395 | chr20 | 44069081 | ||||||
| chr20:44069162 | G | A | 1 | a0001c0001t0007 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*476G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 9/9 | 476 | chr20 | 44069162 | ||||||
| chr20:44069350 | C | T | 1 | a0001c0001t0008 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 9/9 | 664 | chr20 | 44069350 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43915039 | T | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(14): Show |
17 | HG00735.hp2 HG01069.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+49T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915039 | |||||||
| chr20:43915370 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.99+380C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915370 | |||||||
| chr20:43915413 | C | G | 9 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+423C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915413 | |||||||
| chr20:43915467 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+477C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915467 | |||||||
| chr20:43915507 | T | G | 22 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
22 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(19): Show |
intron_variant | MODIFIER | c.99+517T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915507 | |||||||
| chr20:43915561 | CT | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | NA18944.hp2 NA18949.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+572delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915561 | |||||||
| chr20:43915706 | A | C | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+716A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915706 | |||||||
| chr20:43915865 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.99+875C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915865 | |||||||
| chr20:43915865 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.99+875C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915865 | |||||||
| chr20:43915895 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.99+905C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43915895 | |||||||
| chr20:43916318 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+1328C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43916318 | |||||||
| chr20:43916333 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0047 others(90): Show |
94 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.99+1343G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43916333 | |||||||
| chr20:43916353 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.99+1363C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43916353 | |||||||
| chr20:43916470 | G | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.99+1480G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43916470 | |||||||
| chr20:43916543 | G | A | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.99+1553G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43916543 | |||||||
| chr20:43916544 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.99+1554G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43916544 | |||||||
| chr20:43916761 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.99+1771G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43916761 | |||||||
| chr20:43917023 | T | C | 9 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+2033T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43917023 | |||||||
| chr20:43917116 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.99+2126A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43917116 | |||||||
| chr20:43917137 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
138 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.99+2147T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43917137 | |||||||
| chr20:43917196 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
138 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.99+2206T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43917196 | |||||||
| chr20:43917263 | TG | T | 12 | a0001c0001t0001g0046 a0001c0001t0001g0115 a0001c0001t0001g0116 others(9): Show |
12 | HG01175.hp2 HG01255.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+2279delG | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43917263 | ||||||
| chr20:43917307 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
138 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(135): Show |
intron_variant | MODIFIER | c.99+2317C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43917307 | |||||||
| chr20:43917682 | C | G | 5 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0002g0133 others(2): Show |
5 | HG02615.hp2 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2692C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43917682 | |||||||
| chr20:43917786 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0049 others(86): Show |
90 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.99+2796A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43917786 | |||||||
| chr20:43917796 | A | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): Show |
139 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.99+2806A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43917796 | |||||||
| chr20:43918052 | TC | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
134 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.99+3065delC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43918052 | ||||||
| chr20:43918210 | C | T | 1 | a0001c0001t0002g0273 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.99+3220C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43918210 | |||||||
| chr20:43918322 | A | G | 6 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0002g0133 others(3): Show |
6 | HG02615.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+3332A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43918322 | |||||||
| chr20:43918371 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99+3381A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43918371 | |||||||
| chr20:43918385 | T | A | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.99+3395T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43918385 | |||||||
| chr20:43918651 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+3661G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43918651 | |||||||
| chr20:43918663 | C | T | 19 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(16): Show |
19 | HG01167.hp1 HG02109.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+3673C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43918663 | |||||||
| chr20:43918871 | C | G | 1 | a0001c0001t0005g0272 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.99+3881C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43918871 | |||||||
| chr20:43918899 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(124): Show |
128 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.99+3909C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43918899 | |||||||
| chr20:43919012 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.99+4022C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919012 | |||||||
| chr20:43919018 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0049 others(87): Show |
91 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.99+4028A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919018 | |||||||
| chr20:43919190 | A | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(135): Show |
139 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.99+4200A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919190 | |||||||
| chr20:43919231 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(136): Show |
140 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.99+4241A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919231 | |||||||
| chr20:43919479 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18985.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.99+4489A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919479 | |||||||
| chr20:43919606 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(133): Show |
137 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.99+4616G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919606 | |||||||
| chr20:43919680 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(136): Show |
140 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.99+4690C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919680 | |||||||
| chr20:43919681 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.99+4691G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919681 | |||||||
| chr20:43919830 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0049 others(85): Show |
89 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.99+4840A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919830 | |||||||
| chr20:43919930 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(137): Show |
141 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.99+4940A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919930 | |||||||
| chr20:43919969 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(137): Show |
141 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.99+4979G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43919969 | |||||||
| chr20:43920011 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(137): Show |
141 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.99+5021A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43920011 | |||||||
| chr20:43920176 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0049 others(85): Show |
89 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.99+5186G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43920176 | |||||||
| chr20:43920229 | C | A | 1 | a0001c0001t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99+5239C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43920229 | |||||||
| chr20:43920311 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99+5321T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43920311 | |||||||
| chr20:43920392 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.99+5402T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43920392 | |||||||
| chr20:43920505 | G | A | 31 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(28): Show |
31 | HG00741.hp2 HG01884.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.99+5515G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43920505 | |||||||
| chr20:43920704 | A | C | 1 | a0001c0001t0002g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+5714A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43920704 | |||||||
| chr20:43920806 | G | T | 1 | a0001c0001t0002g0267 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.99+5816G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43920806 | |||||||
| chr20:43921007 | G | C | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(7): Show |
10 | HG01167.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+6017G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921007 | |||||||
| chr20:43921160 | C | T | 7 | a0001c0001t0001g0144 a0001c0001t0001g0148 a0001c0001t0002g0147 others(4): Show |
7 | HG02572.hp1 HG02970.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+6170C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921160 | |||||||
| chr20:43921245 | C | T | 25 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(22): Show |
25 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.99+6255C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921245 | |||||||
| chr20:43921321 | G | C | 5 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0002g0133 others(2): Show |
5 | HG02615.hp2 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+6331G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921321 | |||||||
| chr20:43921394 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.99+6404T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921394 | |||||||
| chr20:43921413 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+6423G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921413 | |||||||
| chr20:43921788 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.99+6798C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921788 | |||||||
| chr20:43921789 | G | T | 5 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0002g0133 others(2): Show |
5 | HG02615.hp2 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+6799G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921789 | |||||||
| chr20:43921790 | C | A | 5 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0002g0133 others(2): Show |
5 | HG02615.hp2 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+6800C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43921790 | |||||||
| chr20:43922046 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
177 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.99+7056G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43922046 | |||||||
| chr20:43922333 | C | T | 1 | a0002c0002t0002g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+7343C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43922333 | |||||||
| chr20:43922460 | C | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0023 others(64): Show |
67 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.99+7470C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43922460 | |||||||
| chr20:43922848 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
174 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.99+7858C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43922848 | |||||||
| chr20:43922993 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0048 |
2 | HG01361.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.99+8003C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43922993 | |||||||
| chr20:43922999 | C | T | 38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(35): Show |
38 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.99+8009C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43922999 | |||||||
| chr20:43923027 | C | CAG | 175 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
176 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.99+8038_99+8039dup others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43923027 | ||||||
| chr20:43923075 | T | TG | 47 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(44): Show |
47 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.99+8091dupG | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43923075 | ||||||
| chr20:43923173 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0002g0142 a0002c0002t0002g0131 |
3 | HG02145.hp2 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.99+8183A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923173 | |||||||
| chr20:43923197 | C | A | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.99+8207C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923197 | |||||||
| chr20:43923212 | T | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0132 others(11): Show |
14 | HG01071.hp1 HG02055.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+8222T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923212 | |||||||
| chr20:43923280 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
170 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.99+8290A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923280 | |||||||
| chr20:43923318 | GTCT | G | 23 | a0001c0001t0001g0049 a0001c0001t0001g0109 a0001c0001t0001g0110 others(20): Show |
23 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+8332_99+8334del others(3): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43923318 | ||||||
| chr20:43923350 | C | T | 45 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0048 others(42): Show |
45 | HG01071.hp1 HG01106.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.99+8360C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923350 | |||||||
| chr20:43923360 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99+8370C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923360 | |||||||
| chr20:43923643 | C | T | 45 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0038 others(42): Show |
45 | HG00639.hp2 HG00642.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.99+8653C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923643 | |||||||
| chr20:43923756 | G | A | 18 | a0001c0001t0001g0048 a0001c0001t0001g0151 a0001c0001t0001g0153 others(15): Show |
18 | HG01071.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+8766G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923756 | |||||||
| chr20:43923767 | C | T | 20 | a0001c0001t0001g0048 a0001c0001t0001g0151 a0001c0001t0001g0153 others(17): Show |
20 | HG00642.hp2 HG00733.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+8777C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923767 | |||||||
| chr20:43923809 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.99+8819C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923809 | |||||||
| chr20:43923846 | G | A | 46 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0050 others(43): Show |
46 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.99+8856G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923846 | |||||||
| chr20:43923856 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG00735.hp1 HG02683.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.99+8866C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43923856 | |||||||
| chr20:43924044 | C | T | 1 | a0004c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+9054C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924044 | |||||||
| chr20:43924056 | G | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
77 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.99+9066G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924056 | |||||||
| chr20:43924110 | G | A | 3 | a0001c0001t0001g0255 a0001c0001t0003g0143 a0001c0001t0003g0281 |
3 | HG02145.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.99+9120G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924110 | |||||||
| chr20:43924225 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0134 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+9235G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924225 | |||||||
| chr20:43924229 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(269): Show |
273 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.99+9239T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924229 | |||||||
| chr20:43924237 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(115): Show |
118 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.99+9247C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924237 | |||||||
| chr20:43924381 | T | TA | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(165): Show |
169 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(166): Show |
intron_variant | MODIFIER | c.99+9392dupA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43924381 | ||||||
| chr20:43924436 | CTG | C | 14 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(11): Show |
14 | HG00741.hp2 HG01071.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+9452_99+9453del others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43924436 | ||||||
| chr20:43924527 | C | T | 1 | a0001c0001t0008g0108 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.99+9537C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924527 | |||||||
| chr20:43924568 | G | T | 2 | a0001c0001t0001g0237 a0002c0002t0002g0033 |
2 | HG01261.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.99+9578G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924568 | |||||||
| chr20:43924601 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0024 others(78): Show |
81 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.99+9611T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924601 | |||||||
| chr20:43924797 | T | C | 52 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0051 others(49): Show |
52 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.99+9807T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924797 | |||||||
| chr20:43924917 | A | T | 61 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(58): Show |
61 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.99+9927A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924917 | |||||||
| chr20:43924955 | T | A | 3 | a0001c0001t0001g0237 a0001c0001t0002g0284 a0002c0002t0002g0033 |
3 | HG01261.hp2 HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.99+9965T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43924955 | |||||||
| chr20:43925017 | T | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0023 others(29): Show |
32 | HG01361.hp2 HG02055.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+10027T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925017 | |||||||
| chr20:43925162 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0023 others(91): Show |
94 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.99+10172A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925162 | |||||||
| chr20:43925261 | C | G | 58 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0051 others(55): Show |
58 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.99+10271C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925261 | |||||||
| chr20:43925262 | A | G | 58 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0051 others(55): Show |
58 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.99+10272A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925262 | |||||||
| chr20:43925353 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(148): Show |
152 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.99+10363T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925353 | |||||||
| chr20:43925404 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10414C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925404 | |||||||
| chr20:43925433 | G | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0127 others(5): Show |
8 | HG01361.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+10443G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925433 | |||||||
| chr20:43925476 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.99+10486C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925476 | |||||||
| chr20:43925533 | G | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0065 others(9): Show |
12 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+10543G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925533 | |||||||
| chr20:43925665 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0002g0235 a0001c0001t0002g0267 others(5): Show |
8 | HG00741.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+10675G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925665 | |||||||
| chr20:43925734 | G | A | 35 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0048 others(32): Show |
35 | HG00741.hp2 HG01261.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.99+10744G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925734 | |||||||
| chr20:43925940 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+10950A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925940 | |||||||
| chr20:43925994 | T | A | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+11004T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43925994 | |||||||
| chr20:43926041 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(54): Show |
57 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+11051T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926041 | |||||||
| chr20:43926136 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.99+11146T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926136 | |||||||
| chr20:43926153 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(52): Show |
55 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.99+11163A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926153 | |||||||
| chr20:43926208 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0002g0235 a0001c0001t0002g0267 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+11218C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926208 | |||||||
| chr20:43926251 | T | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0134 a0001c0001t0001g0237 others(3): Show |
6 | HG01261.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+11261T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926251 | |||||||
| chr20:43926270 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.99+11280C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926270 | |||||||
| chr20:43926386 | G | A | 88 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0040 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.99+11396G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926386 | |||||||
| chr20:43926407 | G | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0123 a0001c0001t0001g0155 |
3 | HG02004.hp2 HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.99+11417G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926407 | |||||||
| chr20:43926433 | C | T | 39 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0053 others(36): Show |
39 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.99+11443C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926433 | |||||||
| chr20:43926587 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(53): Show |
56 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.99+11597C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926587 | |||||||
| chr20:43926676 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(47): Show |
50 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.99+11686G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926676 | |||||||
| chr20:43926718 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.99+11728A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926718 | |||||||
| chr20:43926748 | G | C | 1 | a0003c0003t0001g0064 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.99+11758G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926748 | |||||||
| chr20:43926846 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(47): Show |
50 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.99+11856G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926846 | |||||||
| chr20:43926901 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+11911C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926901 | |||||||
| chr20:43926919 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(110): Show |
113 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.99+11929A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43926919 | |||||||
| chr20:43927030 | T | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(104): Show |
107 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.99+12040T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927030 | |||||||
| chr20:43927097 | T | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(144): Show |
147 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(144): Show |
intron_variant | MODIFIER | c.99+12107T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927097 | |||||||
| chr20:43927116 | C | A | 49 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(46): Show |
49 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.99+12126C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927116 | |||||||
| chr20:43927290 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0002g0035 a0001c0001t0002g0141 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+12300G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927290 | |||||||
| chr20:43927401 | C | T | 50 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(47): Show |
50 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.99+12411C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927401 | |||||||
| chr20:43927417 | A | T | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+12427A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927417 | |||||||
| chr20:43927456 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(105): Show |
108 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.99+12466A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927456 | |||||||
| chr20:43927458 | A | AAC | 12 | a0001c0001t0001g0071 a0001c0001t0001g0081 a0001c0001t0001g0116 others(9): Show |
12 | HG00597.hp1 HG00621.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+12520_99+12521d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | A | AACAC | 8 | a0001c0001t0001g0025 a0001c0001t0001g0092 a0001c0001t0001g0197 others(5): Show |
8 | HG00735.hp1 HG01106.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+12518_99+12521d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | A | AACACAC | 3 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0229 |
3 | HG00735.hp2 HG02683.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.99+12516_99+12521d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | A | AACACACA others(3): Show |
1 | a0001c0001t0001g0012 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.99+12512_99+12521d others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AAC | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
65 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.99+12520_99+12521d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AACAC | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(16): Show |
19 | HG01433.hp2 HG02523.hp1 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+12518_99+12521d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AACACAC | A | 18 | a0001c0001t0001g0060 a0001c0001t0001g0077 a0001c0001t0001g0087 others(15): Show |
18 | HG02056.hp1 HG02129.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+12516_99+12521d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0002g0236 |
3 | HG02559.hp1 HG03669.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.99+12514_99+12521d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AACACACA others(5): Show |
A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0042 others(12): Show |
15 | HG00408.hp2 HG01361.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+12510_99+12521d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AACACACA others(7): Show |
A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0024 others(33): Show |
36 | HG00621.hp2 HG00642.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+12508_99+12521d others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AACACACA others(9): Show |
A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0084 others(5): Show |
8 | HG01978.hp1 HG02148.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+12506_99+12521d others(18): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AACACACA others(11): Show |
A | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0080 others(6): Show |
9 | HG01167.hp1 HG02027.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+12504_99+12521d others(20): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927458 | AACACACA others(13): Show |
A | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+12502_99+12521d others(22): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927458 | ||||||
| chr20:43927511 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(105): Show |
108 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.99+12521A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927511 | |||||||
| chr20:43927529 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+12539G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927529 | |||||||
| chr20:43927552 | ATCTTGGC | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(143): Show |
146 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(143): Show |
intron_variant | MODIFIER | c.99+12571_99+12577d others(9): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927552 | ||||||
| chr20:43927614 | TTCCTTCC others(4): Show |
T | 2 | a0001c0001t0001g0276 a0004c0005t0001g0107 |
2 | HG02615.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.99+12637_99+12647d others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927614 | ||||||
| chr20:43927615 | T | C | 1 | a0004c0005t0001g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.99+12625T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927615 | |||||||
| chr20:43927618 | TTCCTTCC | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0126 a0001c0001t0001g0138 |
3 | HG01884.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.99+12637_99+12643d others(9): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927618 | ||||||
| chr20:43927622 | T | C | 1 | a0004c0005t0001g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.99+12632T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927622 | |||||||
| chr20:43927622 | TTCC | T | 39 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0016 others(36): Show |
39 | HG00733.hp1 HG01167.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.99+12637_99+12639d others(5): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927622 | ||||||
| chr20:43927624 | C | T | 1 | a0004c0005t0001g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.99+12634C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927624 | |||||||
| chr20:43927625 | C | CT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(77): Show |
80 | HG00323.hp1 HG00408.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.99+12636dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927625 | C | CTCCCCTT others(59): Show |
19 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0155 others(16): Show |
19 | HG00438.hp2 HG00738.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+12638_99+12639i others(68): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927625 | C | CTTCCT | 65 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(62): Show |
66 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.99+12636_99+12637i others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927625 | C | CTTCCTCC others(58): Show |
1 | a0001c0001t0001g0151 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.99+12636_99+12637i others(67): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927625 | C | CTTCCTTC others(14): Show |
1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+12636_99+12637i others(23): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927625 | C | CTTCCTTC others(2): Show |
34 | a0001c0001t0001g0050 a0001c0001t0001g0057 a0001c0001t0001g0058 others(31): Show |
34 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.99+12636_99+12637i others(11): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927625 | C | CTTCCTTC others(62): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0181 a0001c0001t0005g0185 |
3 | HG02738.hp2 HG03453.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.99+12636_99+12637i others(71): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927625 | C | CTTCCTTC others(6): Show |
7 | a0001c0001t0001g0077 a0001c0001t0001g0093 a0001c0001t0001g0096 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+12636_99+12637i others(15): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927625 | C | CTTCCTTC others(10): Show |
1 | a0001c0001t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.99+12636_99+12637i others(19): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927625 | ||||||
| chr20:43927626 | T | C | 1 | a0004c0005t0001g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.99+12636T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927626 | |||||||
| chr20:43927626 | T | TCCCCTTC others(11): Show |
24 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0053 others(21): Show |
24 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.99+12638_99+12639i others(20): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927626 | ||||||
| chr20:43927626 | T | TCCCCTTC others(51): Show |
3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0244 |
3 | HG01069.hp1 HG01071.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.99+12638_99+12639i others(60): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927626 | ||||||
| chr20:43927626 | T | TTCCTCCC others(15): Show |
1 | a0001c0001t0001g0056 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.99+12636_99+12637i others(24): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927626 | |||||||
| chr20:43927627 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+12637C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927627 | |||||||
| chr20:43927629 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+12639T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927629 | |||||||
| chr20:43927631 | C | T | 23 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0151 others(20): Show |
23 | HG00438.hp2 HG00738.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+12641C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927631 | |||||||
| chr20:43927634 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+12644T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927634 | |||||||
| chr20:43927639 | C | T | 15 | a0001c0001t0001g0031 a0001c0001t0001g0094 a0001c0001t0001g0144 others(12): Show |
15 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+12649C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927639 | |||||||
| chr20:43927640 | C | CTTTCT | 14 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(11): Show |
14 | HG00673.hp2 HG00733.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+12651_99+12652i others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927640 | ||||||
| chr20:43927640 | C | T | 3 | a0001c0001t0002g0035 a0001c0001t0002g0141 a0001c0001t0002g0147 |
3 | HG02258.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.99+12650C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927640 | |||||||
| chr20:43927641 | TC | T | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00408.hp2 HG00621.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+12655delC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927641 | ||||||
| chr20:43927642 | C | T | 42 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0045 others(39): Show |
42 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.99+12652C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927642 | |||||||
| chr20:43927642 | CCCCTT | C | 21 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0061 others(18): Show |
21 | HG02027.hp1 HG02071.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+12666_99+12670d others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927642 | ||||||
| chr20:43927643 | C | CCCTTCCC others(69): Show |
1 | a0001c0001t0001g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+12705_99+12706i others(78): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927643 | ||||||
| chr20:43927643 | C | CCTT | 19 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0078 others(16): Show |
19 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+12654_99+12655i others(5): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927643 | ||||||
| chr20:43927643 | C | CTT | 14 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(11): Show |
14 | HG00673.hp2 HG00733.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+12653_99+12654i others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927643 | |||||||
| chr20:43927643 | C | T | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00408.hp2 HG00621.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+12653C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927643 | |||||||
| chr20:43927647 | T | C | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
21 | HG00408.hp2 HG00621.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+12657T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927647 | |||||||
| chr20:43927648 | C | CCTTCCTT others(4): Show |
1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+12659_99+12660i others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927648 | ||||||
| chr20:43927652 | T | TC | 7 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0067 others(4): Show |
7 | HG00642.hp1 HG01361.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+12665dupC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927652 | ||||||
| chr20:43927653 | C | CCCCTT | 8 | a0001c0001t0001g0139 a0001c0001t0001g0151 a0001c0001t0001g0173 others(5): Show |
8 | HG01071.hp1 HG01978.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+12665_99+12666i others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927653 | ||||||
| chr20:43927653 | C | CCCCTTCC others(2): Show |
15 | a0001c0001t0001g0045 a0001c0001t0001g0153 a0001c0001t0001g0155 others(12): Show |
15 | HG00438.hp2 HG00738.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+12665_99+12666i others(11): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927653 | ||||||
| chr20:43927659 | C | CCCTTCCT others(17): Show |
2 | a0001c0001t0002g0035 a0001c0001t0002g0141 |
2 | HG02258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.99+12685_99+12686i others(26): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927659 | ||||||
| chr20:43927659 | C | CCCTTCCT others(21): Show |
1 | a0001c0001t0002g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99+12685_99+12686i others(30): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927659 | ||||||
| chr20:43927659 | C | CCCTTCCT others(25): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0242 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.99+12685_99+12686i others(34): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927659 | ||||||
| chr20:43927659 | C | CTT | 24 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0151 others(21): Show |
24 | HG00438.hp2 HG00738.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.99+12669_99+12670i others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927659 | |||||||
| chr20:43927659 | C | CTTCCTTC others(83): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0067 others(4): Show |
7 | HG00642.hp1 HG01361.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+12669_99+12670i others(92): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927659 | |||||||
| chr20:43927672 | C | T | 14 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(11): Show |
14 | HG00673.hp2 HG00733.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+12682C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927672 | |||||||
| chr20:43927676 | T | C | 62 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0031 others(59): Show |
62 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.99+12686T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927676 | |||||||
| chr20:43927683 | T | TC | 21 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0052 others(18): Show |
21 | HG00642.hp1 HG00673.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+12695dupC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927683 | ||||||
| chr20:43927688 | C | CCTT | 15 | a0001c0001t0001g0031 a0001c0001t0001g0094 a0001c0001t0001g0144 others(12): Show |
15 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+12699_99+12700i others(5): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927688 | ||||||
| chr20:43927694 | C | CCCTT | 44 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0023 others(41): Show |
44 | HG00642.hp1 HG00741.hp2 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.99+12713_99+12716d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCCTTCCT others(46): Show |
1 | a0001c0001t0001g0070 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.99+12716_99+12717i others(55): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCCTTCCT others(58): Show |
9 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(6): Show |
9 | HG01255.hp2 HG02004.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+12716_99+12717i others(67): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCCTTCCT others(62): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0111 |
2 | HG00673.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.99+12716_99+12717i others(71): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCCTTCCT others(66): Show |
1 | a0001c0001t0001g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.99+12716_99+12717i others(75): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCCTTCCT others(70): Show |
1 | a0001c0001t0001g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+12716_99+12717i others(79): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCC others(2): Show |
4 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0181 others(1): Show |
4 | HG01071.hp1 HG02738.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+12705_99+12706i others(11): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCC others(82): Show |
2 | a0001c0001t0001g0002 a0001c0001t0002g0015 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.99+12705_99+12706i others(91): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCC others(86): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0279 a0001c0001t0002g0236 |
3 | HG02109.hp2 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.99+12705_99+12706i others(95): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCC others(90): Show |
13 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(10): Show |
13 | HG02027.hp1 HG02071.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+12705_99+12706i others(99): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCC others(94): Show |
22 | a0001c0001t0001g0061 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG00408.hp2 HG02055.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.99+12705_99+12706i others(103): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCC others(99): Show |
1 | a0001c0001t0001g0276 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.99+12705_99+12706i others(108): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCC others(98): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0258 |
2 | HG00621.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.99+12705_99+12706i others(107): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCC others(106): Show |
5 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+12705_99+12706i others(115): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CCTTCCCT others(7): Show |
19 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0155 others(16): Show |
19 | HG00438.hp2 HG00738.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+12705_99+12706i others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43927694 | ||||||
| chr20:43927694 | C | CTTCCCTT others(21): Show |
3 | a0001c0001t0001g0094 a0001c0001t0001g0144 a0001c0001t0009g0145 |
3 | HG00639.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.99+12704_99+12705i others(30): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927694 | |||||||
| chr20:43927694 | C | CTTCCTTC others(20): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0223 a0001c0001t0001g0224 others(5): Show |
8 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+12704_99+12705i others(29): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927694 | |||||||
| chr20:43927694 | C | CTTCCTTC others(24): Show |
4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0244 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+12704_99+12705i others(33): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927694 | |||||||
| chr20:43927707 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+12717T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927707 | |||||||
| chr20:43927711 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+12721C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927711 | |||||||
| chr20:43927724 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+12734T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927724 | |||||||
| chr20:43927728 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+12738C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927728 | |||||||
| chr20:43927733 | A | T | 1 | a0001c0001t0003g0017 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+12743A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927733 | |||||||
| chr20:43927737 | T | A | 1 | a0001c0001t0003g0017 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+12747T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927737 | |||||||
| chr20:43927828 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+12838T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927828 | |||||||
| chr20:43927863 | T | C | 30 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(27): Show |
30 | HG00741.hp2 HG01261.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.99+12873T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927863 | |||||||
| chr20:43927881 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0127 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+12891A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927881 | |||||||
| chr20:43927941 | A | C | 12 | a0001c0001t0001g0040 a0001c0001t0001g0068 a0001c0001t0001g0069 others(9): Show |
12 | HG02056.hp2 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+12951A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927941 | |||||||
| chr20:43927957 | G | T | 2 | a0001c0001t0001g0002 a0001c0001t0002g0015 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.99+12967G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43927957 | |||||||
| chr20:43928084 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0002g0015 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.99+13094G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928084 | |||||||
| chr20:43928085 | T | C | 1 | a0001c0001t0002g0226 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99+13095T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928085 | |||||||
| chr20:43928256 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | NA18941.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.99+13266T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928256 | |||||||
| chr20:43928632 | C | T | 5 | a0001c0001t0002g0235 a0001c0001t0002g0267 a0001c0001t0002g0284 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+13642C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928632 | |||||||
| chr20:43928857 | G | A | 44 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0024 others(41): Show |
44 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.99+13867G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928857 | |||||||
| chr20:43928861 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(132): Show |
135 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.99+13871G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928861 | |||||||
| chr20:43928864 | G | A | 51 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(48): Show |
51 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.99+13874G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928864 | |||||||
| chr20:43928918 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0002g0273 |
2 | NA18950.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.99+13928C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928918 | |||||||
| chr20:43928981 | G | GA | 33 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0031 others(30): Show |
33 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.99+14009dupA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928981 | G | GAA | 44 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0053 others(41): Show |
44 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.99+14008_99+14009d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928981 | G | GAAA | 8 | a0001c0001t0001g0104 a0001c0001t0001g0155 a0001c0001t0001g0165 others(5): Show |
8 | HG02083.hp1 HG02148.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+14007_99+14009d others(5): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928981 | G | GAAAAA | 7 | a0001c0001t0001g0134 a0001c0001t0001g0237 a0001c0001t0001g0243 others(4): Show |
7 | HG00741.hp2 HG01261.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+14005_99+14009d others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928981 | G | GAAAAAAA others(1): Show |
6 | a0001c0001t0001g0040 a0001c0001t0001g0279 a0001c0001t0002g0035 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+14002_99+14009d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928981 | G | GAAAAAAA others(3): Show |
17 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0069 others(14): Show |
17 | HG00642.hp1 HG01071.hp1 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+14000_99+14009d others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928981 | G | GAAAAAAA others(4): Show |
21 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0043 others(18): Show |
21 | HG00408.hp2 HG01361.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+13999_99+14009d others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928981 | G | GAAAAAAA others(5): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0047 others(8): Show |
11 | HG00621.hp2 HG02027.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+13998_99+14009d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928981 | G | GAAAAAAA others(6): Show |
2 | a0001c0001t0002g0079 a0001c0001t0004g0162 |
2 | NA19089.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.99+13997_99+14009d others(15): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928981 | ||||||
| chr20:43928992 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.99+14002A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928992 | |||||||
| chr20:43928997 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+14009_99+14010i others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928997 | ||||||
| chr20:43928997 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0001g0023 a0007c0006t0001g0089 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.99+14009_99+14010i others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43928997 | ||||||
| chr20:43928997 | A | C | 1 | a0004c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+14007A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43928997 | |||||||
| chr20:43929000 | C | A | 13 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(10): Show |
13 | HG02056.hp1 HG02071.hp1 HG03654.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+14010C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929000 | |||||||
| chr20:43929006 | C | A | 13 | a0001c0001t0001g0031 a0001c0001t0001g0094 a0001c0001t0001g0144 others(10): Show |
13 | HG00639.hp2 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+14016C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929006 | |||||||
| chr20:43929100 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.99+14110A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929100 | |||||||
| chr20:43929359 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(133): Show |
136 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.99+14369T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929359 | |||||||
| chr20:43929493 | T | TC | 51 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(48): Show |
51 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.99+14509dupC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43929493 | ||||||
| chr20:43929515 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+14525G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929515 | |||||||
| chr20:43929645 | C | G | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+14655C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929645 | |||||||
| chr20:43929653 | T | C | 50 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0024 others(47): Show |
50 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.99+14663T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929653 | |||||||
| chr20:43929740 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+14750C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929740 | |||||||
| chr20:43929749 | G | T | 1 | a0004c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+14759G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929749 | |||||||
| chr20:43929850 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.99+14860C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929850 | |||||||
| chr20:43929968 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(131): Show |
134 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.99+14978G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929968 | |||||||
| chr20:43929973 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99+14983G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43929973 | |||||||
| chr20:43930000 | G | A | 13 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0094 others(10): Show |
13 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+15010G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930000 | |||||||
| chr20:43930028 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0127 a0001c0001t0001g0279 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+15038G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930028 | |||||||
| chr20:43930236 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+15246A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930236 | |||||||
| chr20:43930257 | T | A | 5 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0001t0002g0259 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+15267T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930257 | |||||||
| chr20:43930509 | G | A | 52 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(49): Show |
52 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.99+15519G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930509 | |||||||
| chr20:43930586 | A | C | 1 | a0001c0001t0001g0251 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.99+15596A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930586 | |||||||
| chr20:43930679 | G | T | 45 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0051 others(42): Show |
45 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.99+15689G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930679 | |||||||
| chr20:43930772 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0003g0017 |
2 | HG02056.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.99+15782A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930772 | |||||||
| chr20:43930891 | C | T | 52 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(49): Show |
52 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.99+15901C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43930891 | |||||||
| chr20:43931340 | G | T | 15 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(12): Show |
15 | HG02056.hp1 HG02071.hp1 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+16350G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43931340 | |||||||
| chr20:43931467 | C | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0126 |
2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.99+16477C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43931467 | |||||||
| chr20:43931525 | T | C | 8 | a0001c0001t0001g0138 a0001c0001t0001g0233 a0001c0001t0001g0285 others(5): Show |
8 | HG01884.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+16535T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43931525 | |||||||
| chr20:43931528 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+16538G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43931528 | |||||||
| chr20:43931585 | A | G | 2 | a0001c0001t0002g0235 a0001c0001t0002g0267 |
2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+16595A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43931585 | |||||||
| chr20:43931930 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0285 |
2 | HG01884.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.99+16940G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43931930 | |||||||
| chr20:43932207 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99+17217C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932207 | |||||||
| chr20:43932216 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+17226T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932216 | |||||||
| chr20:43932265 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0049 others(21): Show |
25 | HG00408.hp1 HG01175.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.99+17275C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932265 | |||||||
| chr20:43932266 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG02027.hp1 HG02071.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.99+17276G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932266 | |||||||
| chr20:43932476 | G | C | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0234 others(4): Show |
7 | HG02055.hp1 HG02056.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+17486G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932476 | |||||||
| chr20:43932520 | G | A | 8 | a0001c0001t0001g0062 a0001c0001t0001g0101 a0001c0001t0001g0102 others(5): Show |
8 | HG02132.hp2 NA18944.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+17530G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932520 | |||||||
| chr20:43932690 | C | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0242 a0001c0001t0002g0035 others(3): Show |
6 | HG02258.hp2 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+17700C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932690 | |||||||
| chr20:43932729 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.99+17739C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932729 | |||||||
| chr20:43932782 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(98): Show |
102 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.99+17792C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932782 | |||||||
| chr20:43932783 | C | CCCCCCG | 13 | a0001c0001t0001g0056 a0001c0001t0001g0080 a0001c0001t0001g0109 others(10): Show |
13 | HG00733.hp2 HG02083.hp2 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+17793_99+17794i others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932783 | |||||||
| chr20:43932783 | C | CCCCCG | 16 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0053 others(13): Show |
16 | HG00438.hp2 HG00673.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+17793_99+17794i others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932783 | |||||||
| chr20:43932783 | C | CCCCG | 17 | a0001c0001t0001g0042 a0001c0001t0001g0060 a0001c0001t0001g0110 others(14): Show |
17 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+17793_99+17794i others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932783 | |||||||
| chr20:43932783 | C | CCCG | 56 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0024 others(53): Show |
56 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.99+17793_99+17794i others(5): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932783 | |||||||
| chr20:43932783 | C | CGCCCG | 12 | a0001c0001t0001g0031 a0001c0001t0001g0094 a0001c0001t0001g0144 others(9): Show |
12 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+17796_99+17797i others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43932783 | ||||||
| chr20:43932783 | C | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0104 a0001c0001t0001g0166 |
3 | HG04204.hp1 NA18986.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.99+17793C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932783 | |||||||
| chr20:43932871 | G | A | 1 | a0001c0001t0004g0161 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.99+17881G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43932871 | |||||||
| chr20:43933035 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.99+18045C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933035 | |||||||
| chr20:43933064 | A | G | 3 | a0001c0001t0003g0286 a0001c0001t0007g0149 a0002c0002t0002g0140 |
3 | HG00741.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.99+18074A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933064 | |||||||
| chr20:43933235 | G | C | 36 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(33): Show |
36 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+18245G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933235 | |||||||
| chr20:43933388 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0242 others(8): Show |
11 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+18398T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933388 | |||||||
| chr20:43933425 | C | T | 45 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(42): Show |
45 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.99+18435C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933425 | |||||||
| chr20:43933528 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0027 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.99+18538G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933528 | |||||||
| chr20:43933529 | C | T | 38 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0053 others(35): Show |
38 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.99+18539C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933529 | |||||||
| chr20:43933720 | G | T | 41 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.99+18730G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933720 | |||||||
| chr20:43933725 | G | T | 5 | a0001c0001t0001g0127 a0001c0001t0002g0235 a0001c0001t0002g0267 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+18735G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933725 | |||||||
| chr20:43933734 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0163 |
2 | HG00597.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.99+18744G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933734 | |||||||
| chr20:43933917 | G | A | 71 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0031 others(68): Show |
71 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.99+18927G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933917 | |||||||
| chr20:43933937 | C | T | 10 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0134 others(7): Show |
10 | HG00741.hp2 HG02056.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+18947C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43933937 | |||||||
| chr20:43934136 | G | GGA | 24 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(21): Show |
24 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.99+19177_99+19178d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | G | GGAGA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(82): Show |
86 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.99+19175_99+19178d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | G | GGAGAGA | 26 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0073 others(23): Show |
26 | HG00642.hp2 HG00733.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.99+19173_99+19178d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | G | GGAGAGAG others(1): Show |
35 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0051 others(32): Show |
35 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.99+19171_99+19178d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | G | GGAGAGAG others(3): Show |
11 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0128 others(8): Show |
11 | HG00438.hp1 HG00735.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+19169_99+19178d others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | G | GGAGAGAG others(5): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0282 others(3): Show |
6 | HG02027.hp2 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+19167_99+19178d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | G | GGAGAGAG others(7): Show |
8 | a0001c0001t0001g0074 a0001c0001t0001g0113 a0001c0001t0001g0114 others(5): Show |
8 | HG00597.hp2 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+19165_99+19178d others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | G | GGAGAGAG others(11): Show |
1 | a0001c0001t0002g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+19161_99+19178d others(20): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | G | GGAGAGAG others(19): Show |
1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+19153_99+19178d others(28): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934136 | GGAGA | G | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG00621.hp2 HG00673.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+19175_99+19178d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934136 | ||||||
| chr20:43934167 | G | GAGAGAGA others(20): Show |
1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99+19178_99+19179i others(29): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934167 | ||||||
| chr20:43934167 | G | GAGAGAGA others(22): Show |
1 | a0002c0002t0002g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+19178_99+19179i others(31): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934167 | ||||||
| chr20:43934169 | C | A | 41 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(38): Show |
41 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.99+19179C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43934169 | |||||||
| chr20:43934317 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99+19327A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43934317 | |||||||
| chr20:43934436 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0234 others(3): Show |
6 | HG02056.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+19446C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43934436 | |||||||
| chr20:43934597 | C | T | 1 | a0004c0005t0001g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.99+19607C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43934597 | |||||||
| chr20:43934604 | A | T | 1 | a0001c0001t0001g0166 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.99+19614A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43934604 | |||||||
| chr20:43934798 | T | TTG | 23 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0057 others(20): Show |
23 | HG02055.hp1 HG02056.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+19834_99+19835d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934798 | ||||||
| chr20:43934798 | T | TTGTG | 25 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0027 others(22): Show |
26 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.99+19832_99+19835d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934798 | ||||||
| chr20:43934798 | T | TTGTGTG | 47 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0031 others(44): Show |
47 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.99+19830_99+19835d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934798 | ||||||
| chr20:43934798 | T | TTGTGTGT others(1): Show |
130 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
130 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.99+19828_99+19835d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934798 | ||||||
| chr20:43934798 | T | TTGTGTGT others(3): Show |
20 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0138 others(17): Show |
20 | HG00323.hp2 HG00642.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+19826_99+19835d others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934798 | ||||||
| chr20:43934798 | T | TTGTGTGT others(5): Show |
4 | a0001c0001t0001g0137 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | HG00733.hp1 HG01099.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+19824_99+19835d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43934798 | ||||||
| chr20:43934826 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.99+19836A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43934826 | |||||||
| chr20:43934931 | G | A | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+19941G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43934931 | |||||||
| chr20:43935007 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(264): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.99+20017A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935007 | |||||||
| chr20:43935096 | G | T | 1 | a0004c0005t0001g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.99+20106G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935096 | |||||||
| chr20:43935298 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.99+20308C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935298 | |||||||
| chr20:43935331 | T | C | 1 | a0001c0001t0002g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99+20341T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935331 | |||||||
| chr20:43935427 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+20437C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935427 | |||||||
| chr20:43935536 | A | C | 54 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(51): Show |
54 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.99+20546A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935536 | |||||||
| chr20:43935587 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+20597C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935587 | |||||||
| chr20:43935696 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(132): Show |
135 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.99+20706T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935696 | |||||||
| chr20:43935742 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+20752A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935742 | |||||||
| chr20:43935828 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.99+20838G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935828 | |||||||
| chr20:43935842 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0004g0161 |
2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.99+20852G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43935842 | |||||||
| chr20:43935927 | CA | C | 35 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0039 others(32): Show |
35 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.99+20962delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43935927 | ||||||
| chr20:43935927 | CAA | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
127 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.99+20961_99+20962d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43935927 | ||||||
| chr20:43935927 | CAAA | C | 90 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(87): Show |
90 | HG00408.hp2 HG00438.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.99+20960_99+20962d others(5): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43935927 | ||||||
| chr20:43935927 | CAAAA | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0242 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+20959_99+20962d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43935927 | ||||||
| chr20:43936061 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.99+21071C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43936061 | |||||||
| chr20:43936072 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+21082G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43936072 | |||||||
| chr20:43936119 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+21129C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43936119 | |||||||
| chr20:43936217 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.99+21227C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43936217 | |||||||
| chr20:43936287 | T | C | 5 | a0001c0001t0001g0127 a0001c0001t0002g0235 a0001c0001t0002g0267 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+21297T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43936287 | |||||||
| chr20:43936361 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99+21371T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43936361 | |||||||
| chr20:43936966 | G | A | 33 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(30): Show |
33 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.99+21976G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43936966 | |||||||
| chr20:43937120 | G | C | 1 | a0001c0001t0009g0145 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+22130G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937120 | |||||||
| chr20:43937122 | G | C | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.99+22132G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937122 | |||||||
| chr20:43937162 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.99+22172C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937162 | |||||||
| chr20:43937163 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.99+22173G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937163 | |||||||
| chr20:43937263 | G | C | 4 | a0001c0001t0002g0235 a0001c0001t0002g0267 a0001c0001t0002g0284 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+22273G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937263 | |||||||
| chr20:43937328 | C | T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(35): Show |
38 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.99+22338C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937328 | |||||||
| chr20:43937339 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0282 others(2): Show |
5 | HG02056.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+22349C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937339 | |||||||
| chr20:43937369 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(77): Show |
80 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.99+22379G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937369 | |||||||
| chr20:43937480 | A | C | 70 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0048 others(67): Show |
70 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+22490A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937480 | |||||||
| chr20:43937641 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.99+22651T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937641 | |||||||
| chr20:43937730 | C | T | 17 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(14): Show |
17 | HG02056.hp1 HG02071.hp1 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+22740C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937730 | |||||||
| chr20:43937735 | G | A | 2 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.99+22745G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937735 | |||||||
| chr20:43937755 | G | A | 33 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(30): Show |
33 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.99+22765G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937755 | |||||||
| chr20:43937758 | T | G | 134 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(131): Show |
134 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.99+22768T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937758 | |||||||
| chr20:43937937 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(84): Show |
87 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.99+22947A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937937 | |||||||
| chr20:43937995 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0234 |
2 | NA18747.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.99+23005G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43937995 | |||||||
| chr20:43938033 | C | A | 3 | a0001c0001t0002g0035 a0001c0001t0002g0141 a0001c0001t0002g0147 |
3 | HG02258.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.99+23043C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938033 | |||||||
| chr20:43938120 | C | T | 33 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(30): Show |
33 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.99+23130C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938120 | |||||||
| chr20:43938336 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.99+23346C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938336 | |||||||
| chr20:43938585 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0242 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+23595G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938585 | |||||||
| chr20:43938608 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0242 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+23618C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938608 | |||||||
| chr20:43938611 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+23621G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938611 | |||||||
| chr20:43938658 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.99+23668C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938658 | |||||||
| chr20:43938738 | T | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+23748T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938738 | |||||||
| chr20:43938808 | G | A | 1 | a0002c0002t0002g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+23818G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938808 | |||||||
| chr20:43938892 | G | T | 2 | a0001c0001t0002g0235 a0001c0001t0002g0267 |
2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+23902G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938892 | |||||||
| chr20:43938893 | T | G | 17 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0068 others(14): Show |
17 | HG02056.hp2 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+23903T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43938893 | |||||||
| chr20:43939021 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.99+24031C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939021 | |||||||
| chr20:43939055 | A | G | 2 | a0001c0001t0002g0235 a0001c0001t0002g0267 |
2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.99+24065A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939055 | |||||||
| chr20:43939175 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.99+24185C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939175 | |||||||
| chr20:43939177 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.99+24187T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939177 | |||||||
| chr20:43939190 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.99+24200C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939190 | |||||||
| chr20:43939301 | C | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(80): Show |
83 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.99+24311C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939301 | |||||||
| chr20:43939426 | C | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+24436C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939426 | |||||||
| chr20:43939512 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(85): Show |
88 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(85): Show |
intron_variant | MODIFIER | c.99+24522A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939512 | |||||||
| chr20:43939524 | C | T | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+24534C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939524 | |||||||
| chr20:43939525 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.99+24535G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939525 | |||||||
| chr20:43939902 | C | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0148 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+24912C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43939902 | |||||||
| chr20:43940189 | C | T | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+25199C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43940189 | |||||||
| chr20:43940476 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.99+25486G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43940476 | |||||||
| chr20:43940513 | C | T | 35 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(32): Show |
35 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.99+25523C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43940513 | |||||||
| chr20:43940525 | C | CT | 90 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(87): Show |
90 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.99+25546dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43940525 | ||||||
| chr20:43940536 | T | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0127 a0001c0001t0002g0029 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+25546T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43940536 | |||||||
| chr20:43940537 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(88): Show |
91 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(88): Show |
intron_variant | MODIFIER | c.99+25547C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43940537 | |||||||
| chr20:43940582 | G | C | 15 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(12): Show |
15 | HG02056.hp1 HG02071.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+25592G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43940582 | |||||||
| chr20:43941050 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0264 |
2 | HG00733.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.99+26060G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941050 | |||||||
| chr20:43941221 | T | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0068 others(14): Show |
17 | HG02056.hp2 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+26231T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941221 | |||||||
| chr20:43941271 | G | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(124): Show |
127 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.99+26281G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941271 | |||||||
| chr20:43941323 | C | CT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0180 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+26348dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43941323 | ||||||
| chr20:43941323 | C | CTT | 65 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0048 others(62): Show |
65 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.99+26347_99+26348d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43941323 | ||||||
| chr20:43941363 | G | A | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+26373G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941363 | |||||||
| chr20:43941431 | C | T | 4 | a0001c0001t0001g0278 a0001c0001t0003g0286 a0001c0001t0007g0149 others(1): Show |
4 | HG00741.hp2 HG02055.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+26441C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941431 | |||||||
| chr20:43941442 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99+26452C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941442 | |||||||
| chr20:43941579 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0172 |
2 | HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.99+26589C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941579 | |||||||
| chr20:43941584 | C | T | 5 | a0001c0001t0001g0087 a0001c0001t0001g0172 a0001c0001t0001g0228 others(2): Show |
5 | HG00323.hp2 HG02165.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+26594C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941584 | |||||||
| chr20:43941666 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.99+26676C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941666 | |||||||
| chr20:43941704 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.99+26714G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941704 | |||||||
| chr20:43941807 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0048 others(30): Show |
33 | HG02055.hp1 HG02056.hp1 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.99+26817A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941807 | |||||||
| chr20:43941891 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+26901G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43941891 | |||||||
| chr20:43942004 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+27014C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43942004 | |||||||
| chr20:43942162 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+27172T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43942162 | |||||||
| chr20:43942223 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.99+27233A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43942223 | |||||||
| chr20:43942367 | A | T | 3 | a0001c0001t0002g0035 a0001c0001t0002g0141 a0001c0001t0002g0147 |
3 | HG02258.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.99+27377A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43942367 | |||||||
| chr20:43942380 | C | G | 98 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0024 others(95): Show |
98 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.99+27390C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43942380 | |||||||
| chr20:43942677 | C | A | 1 | a0001c0001t0002g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+27687C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43942677 | |||||||
| chr20:43942760 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99+27770A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43942760 | |||||||
| chr20:43943030 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+28040C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43943030 | |||||||
| chr20:43943242 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0126 others(1): Show |
4 | HG01167.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+28252C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43943242 | |||||||
| chr20:43943302 | CT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(108): Show |
112 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.99+28313delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43943302 | |||||||
| chr20:43943513 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0282 others(2): Show |
5 | HG02056.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+28523G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43943513 | |||||||
| chr20:43943663 | T | C | 54 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(51): Show |
54 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.99+28673T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43943663 | |||||||
| chr20:43943803 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.99+28813C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43943803 | |||||||
| chr20:43943862 | G | GATTT | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(263): Show |
267 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.99+28875_99+28878d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43943862 | ||||||
| chr20:43944181 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-29186G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944181 | |||||||
| chr20:43944252 | A | G | 55 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(52): Show |
55 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.100-29115A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944252 | |||||||
| chr20:43944403 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0068 others(14): Show |
17 | HG02055.hp1 HG02056.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-28964C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944403 | |||||||
| chr20:43944514 | CT | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(76): Show |
79 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.100-28847delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43944514 | ||||||
| chr20:43944550 | CCAG | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(76): Show |
79 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.100-28815_100-2881 others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43944550 | ||||||
| chr20:43944563 | C | T | 38 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(35): Show |
38 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.100-28804C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944563 | |||||||
| chr20:43944683 | C | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0049 others(21): Show |
25 | HG00408.hp1 HG01175.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-28684C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944683 | |||||||
| chr20:43944739 | C | G | 15 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(12): Show |
15 | HG02056.hp1 HG02071.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-28628C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944739 | |||||||
| chr20:43944952 | C | T | 35 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0041 others(32): Show |
35 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-28415C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944952 | |||||||
| chr20:43944960 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0242 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.100-28407C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944960 | |||||||
| chr20:43944968 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0197 |
2 | NA18952.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.100-28399A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43944968 | |||||||
| chr20:43945182 | C | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(76): Show |
79 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.100-28185C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43945182 | |||||||
| chr20:43945191 | T | C | 20 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0048 others(17): Show |
20 | HG02056.hp1 HG02071.hp1 HG02523.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-28176T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43945191 | |||||||
| chr20:43945519 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100-27848G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43945519 | |||||||
| chr20:43945529 | T | G | 1 | a0001c0001t0003g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100-27838T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43945529 | |||||||
| chr20:43945722 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
109 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.100-27645C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43945722 | |||||||
| chr20:43945802 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(240): Show |
244 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.100-27565T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43945802 | |||||||
| chr20:43945808 | G | C | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-27559G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43945808 | |||||||
| chr20:43945809 | G | C | 3 | a0001c0001t0003g0286 a0001c0001t0007g0149 a0002c0002t0002g0140 |
3 | HG00741.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.100-27558G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43945809 | |||||||
| chr20:43946154 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG02027.hp1 HG02071.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.100-27213C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946154 | |||||||
| chr20:43946169 | A | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0234 others(3): Show |
6 | HG02056.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-27198A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946169 | |||||||
| chr20:43946295 | A | ATCAT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0179 others(12): Show |
15 | HG02027.hp1 HG02071.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-27048_100-2704 others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43946295 | ||||||
| chr20:43946295 | ATCATTCA others(5): Show |
A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0234 others(3): Show |
6 | HG02056.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-27056_100-2704 others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43946295 | ||||||
| chr20:43946400 | A | G | 2 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.100-26967A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946400 | |||||||
| chr20:43946591 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.100-26776C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946591 | |||||||
| chr20:43946599 | G | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0048 others(28): Show |
31 | HG02056.hp1 HG02056.hp2 HG02071.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-26768G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946599 | |||||||
| chr20:43946759 | C | T | 1 | a0003c0003t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.100-26608C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946759 | |||||||
| chr20:43946768 | G | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0126 |
3 | HG01167.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.100-26599G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946768 | |||||||
| chr20:43946968 | G | A | 1 | a0001c0012t0003g0013 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.100-26399G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946968 | |||||||
| chr20:43946974 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0148 others(2): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-26393C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946974 | |||||||
| chr20:43946975 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0126 others(1): Show |
4 | HG01167.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-26392G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946975 | |||||||
| chr20:43946990 | C | G | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-26377C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43946990 | |||||||
| chr20:43947093 | C | T | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-26274C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43947093 | |||||||
| chr20:43947129 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.100-26238C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43947129 | |||||||
| chr20:43947133 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0242 a0002c0002t0002g0131 |
3 | HG02145.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.100-26234G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43947133 | |||||||
| chr20:43947159 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0027 others(96): Show |
99 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.100-26208A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43947159 | |||||||
| chr20:43947170 | T | C | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-26197T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43947170 | |||||||
| chr20:43947201 | G | A | 53 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(50): Show |
53 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-26166G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43947201 | |||||||
| chr20:43947373 | T | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0048 others(33): Show |
36 | HG02055.hp1 HG02055.hp2 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-25994T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43947373 | |||||||
| chr20:43947529 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.100-25838C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43947529 | |||||||
| chr20:43948181 | C | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0048 others(32): Show |
35 | HG02055.hp1 HG02055.hp2 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-25186C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948181 | |||||||
| chr20:43948358 | G | T | 55 | a0001c0001t0001g0031 a0001c0001t0001g0045 a0001c0001t0001g0052 others(52): Show |
55 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.100-25009G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948358 | |||||||
| chr20:43948380 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0234 others(3): Show |
6 | HG02056.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-24987C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948380 | |||||||
| chr20:43948406 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0266 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-24961G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948406 | |||||||
| chr20:43948437 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100-24930C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948437 | |||||||
| chr20:43948620 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-24747C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948620 | |||||||
| chr20:43948695 | AGCCAGGG others(15): Show |
A | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100-24671_100-2465 others(26): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948695 | |||||||
| chr20:43948722 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(112): Show |
116 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.100-24645C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948722 | |||||||
| chr20:43948880 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.100-24487A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948880 | |||||||
| chr20:43948977 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100-24390G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43948977 | |||||||
| chr20:43949382 | G | T | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100-23985G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43949382 | |||||||
| chr20:43949425 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0242 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.100-23942C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43949425 | |||||||
| chr20:43949708 | C | T | 15 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0058 others(12): Show |
15 | HG02056.hp1 HG02071.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-23659C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43949708 | |||||||
| chr20:43949759 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.100-23608C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43949759 | |||||||
| chr20:43949796 | G | A | 2 | a0001c0001t0002g0103 a0004c0005t0001g0107 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.100-23571G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43949796 | |||||||
| chr20:43949962 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100-23405A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43949962 | |||||||
| chr20:43950007 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0266 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-23360A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950007 | |||||||
| chr20:43950035 | CT | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(245): Show |
249 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.100-23329delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43950035 | ||||||
| chr20:43950161 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02647.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-23206A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950161 | |||||||
| chr20:43950353 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.100-23014G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950353 | |||||||
| chr20:43950411 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(194): Show |
198 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.100-22956T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950411 | |||||||
| chr20:43950456 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.100-22911T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950456 | |||||||
| chr20:43950508 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(194): Show |
198 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.100-22859T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950508 | |||||||
| chr20:43950548 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(104): Show |
108 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.100-22819C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950548 | |||||||
| chr20:43950807 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-22560C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950807 | |||||||
| chr20:43950833 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0040 others(60): Show |
63 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.100-22534G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950833 | |||||||
| chr20:43950911 | G | C | 2 | a0001c0001t0001g0023 a0007c0006t0001g0089 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.100-22456G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950911 | |||||||
| chr20:43950917 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.100-22450C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43950917 | |||||||
| chr20:43951071 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.100-22296G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951071 | |||||||
| chr20:43951099 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.100-22268G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951099 | |||||||
| chr20:43951236 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0237 a0001c0001t0002g0133 |
3 | HG01261.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-22131T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951236 | |||||||
| chr20:43951282 | ATAGAG | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0237 a0001c0001t0002g0133 |
3 | HG01261.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-22080_100-2207 others(9): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951282 | ||||||
| chr20:43951310 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100-22057C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951310 | |||||||
| chr20:43951365 | C | A | 52 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0023 others(49): Show |
52 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.100-22002C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951365 | |||||||
| chr20:43951365 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.100-22002C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951365 | |||||||
| chr20:43951427 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.100-21940A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951427 | |||||||
| chr20:43951445 | C | T | 109 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): Show |
109 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.100-21922C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951445 | |||||||
| chr20:43951587 | CA | C | 6 | a0001c0001t0001g0115 a0001c0001t0001g0244 a0001c0001t0001g0245 others(3): Show |
6 | HG01934.hp2 HG01975.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-21776delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951587 | ||||||
| chr20:43951705 | A | ATT | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0088 others(2): Show |
5 | HG02056.hp2 HG02071.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-21661_100-2166 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951705 | ||||||
| chr20:43951707 | G | GGTTTTT | 3 | a0001c0001t0002g0035 a0001c0001t0002g0141 a0001c0001t0002g0147 |
3 | HG02258.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.100-21660_100-2165 others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951707 | G | GGTTTTTT others(7): Show |
1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-21660_100-2165 others(18): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951707 | G | GGTTTTTT others(8): Show |
1 | a0007c0006t0001g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.100-21660_100-2165 others(19): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951707 | G | GGTTTTTT others(13): Show |
6 | a0001c0001t0001g0101 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-21660_100-2165 others(24): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951707 | G | GGTTTTTT others(14): Show |
3 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0202 |
3 | HG00408.hp1 NA18970.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.100-21660_100-2165 others(25): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951707 | G | GGTTTTTT others(15): Show |
4 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0001g0180 others(1): Show |
4 | HG02132.hp2 NA18953.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-21660_100-2165 others(26): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951707 | G | GGTTTTTT others(16): Show |
1 | a0001c0001t0001g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.100-21660_100-2165 others(27): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951707 | G | GGTTTTTT others(17): Show |
2 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.100-21660_100-2165 others(28): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951707 | G | GTTGTTTT others(14): Show |
1 | a0001c0001t0001g0188 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100-21658_100-2165 others(25): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0045 others(58): Show |
62 | HG00438.hp2 HG00639.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.100-21643_100-2163 others(9): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTT | 11 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0155 others(8): Show |
11 | HG00738.hp2 HG01884.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-21644_100-2163 others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT | 6 | a0001c0001t0001g0048 a0001c0001t0001g0154 a0001c0001t0001g0252 others(3): Show |
6 | HG02165.hp2 HG02615.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-21645_100-2163 others(11): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(2): Show |
9 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0075 others(6): Show |
9 | HG01071.hp1 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-21647_100-2163 others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0003g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100-21648_100-2163 others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0104 a0001c0001t0007g0149 a0002c0002t0002g0140 |
3 | HG00741.hp2 HG04204.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.100-21649_100-2163 others(15): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(15): Show |
3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0011t0001g0240 |
3 | NA18941.hp2 NA18960.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.100-21649_100-2164 others(26): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0184 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.100-21650_100-2163 others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0078 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.100-21652_100-2163 others(18): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(10): Show |
3 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0126 |
3 | HG01167.hp1 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.100-21655_100-2163 others(21): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-21656_100-2163 others(22): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(12): Show |
1 | a0001c0001t0001g0279 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.100-21657_100-2163 others(23): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(13): Show |
1 | a0001c0001t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-21658_100-2163 others(24): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(14): Show |
8 | a0001c0001t0001g0058 a0001c0001t0001g0097 a0001c0001t0001g0137 others(5): Show |
8 | HG01255.hp1 HG02523.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-21659_100-2163 others(25): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(15): Show |
14 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(11): Show |
14 | HG00323.hp1 HG02280.hp1 HG03490.hp1 others(11): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(26): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(16): Show |
8 | a0001c0001t0001g0095 a0001c0001t0001g0159 a0001c0001t0001g0160 others(5): Show |
8 | HG01433.hp1 HG02970.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(27): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(17): Show |
8 | a0001c0001t0001g0060 a0001c0001t0001g0255 a0001c0001t0002g0262 others(5): Show |
8 | HG01106.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(28): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(18): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0198 others(2): Show |
5 | HG01361.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(29): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(19): Show |
5 | a0001c0001t0001g0009 a0001c0001t0001g0256 a0001c0001t0001g0258 others(2): Show |
5 | HG01069.hp2 HG01978.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(30): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(20): Show |
12 | a0001c0001t0001g0066 a0001c0001t0001g0081 a0001c0001t0001g0084 others(9): Show |
12 | HG00438.hp1 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(31): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(21): Show |
11 | a0001c0001t0001g0051 a0001c0001t0001g0090 a0001c0001t0001g0174 others(8): Show |
11 | HG00639.hp1 HG00642.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(32): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(22): Show |
8 | a0001c0001t0001g0074 a0001c0001t0001g0093 a0001c0001t0001g0113 others(5): Show |
8 | HG00597.hp2 HG00673.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(33): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(23): Show |
10 | a0001c0001t0001g0061 a0001c0001t0001g0067 a0001c0001t0001g0091 others(7): Show |
10 | HG00735.hp1 HG01433.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(34): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(24): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0071 others(1): Show |
4 | HG00621.hp1 NA18944.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-21639_100-2163 others(35): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(25): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0072 |
3 | HG02027.hp2 NA18949.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.100-21639_100-2163 others(36): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(26): Show |
1 | a0001c0001t0001g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.100-21639_100-2163 others(37): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(27): Show |
1 | a0001c0001t0001g0163 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.100-21639_100-2163 others(38): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(28): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0065 |
2 | HG02300.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.100-21639_100-2163 others(39): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(30): Show |
2 | a0001c0001t0001g0012 a0001c0001t0001g0183 |
2 | HG01257.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.100-21639_100-2163 others(41): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(31): Show |
1 | a0001c0001t0001g0182 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.100-21639_100-2163 others(42): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(33): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0181 |
2 | HG02258.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.100-21639_100-2163 others(44): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | GTTTTTTT others(34): Show |
1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-21639_100-2163 others(45): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951707 | ||||||
| chr20:43951707 | G | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0088 others(2): Show |
5 | HG02056.hp2 HG02071.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-21660G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951707 | |||||||
| chr20:43951710 | T | G | 5 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0002g0026 others(2): Show |
5 | HG02630.hp2 HG02717.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-21657T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951710 | |||||||
| chr20:43951713 | T | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0278 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.100-21654T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951713 | |||||||
| chr20:43951728 | T | TTTTTTTT others(21): Show |
1 | a0001c0001t0001g0077 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.100-21639_100-2163 others(32): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951728 | |||||||
| chr20:43951742 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-21625T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951742 | |||||||
| chr20:43951818 | C | T | 120 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
120 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.100-21549C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951818 | |||||||
| chr20:43951853 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0045 others(90): Show |
94 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.100-21514A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951853 | |||||||
| chr20:43951887 | TTTTG | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(237): Show |
241 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.100-21460_100-2145 others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43951887 | ||||||
| chr20:43951936 | G | A | 2 | a0001c0001t0002g0284 a0002c0002t0002g0033 |
2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.100-21431G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951936 | |||||||
| chr20:43951942 | G | C | 1 | a0003c0003t0001g0004 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.100-21425G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43951942 | |||||||
| chr20:43952074 | A | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(221): Show |
225 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.100-21293A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952074 | |||||||
| chr20:43952075 | A | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(221): Show |
225 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.100-21292A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952075 | |||||||
| chr20:43952091 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0024 others(92): Show |
96 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.100-21276T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952091 | |||||||
| chr20:43952099 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0127 a0001c0001t0001g0237 others(1): Show |
4 | HG01261.hp2 HG02615.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-21268C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952099 | |||||||
| chr20:43952103 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0282 others(3): Show |
6 | HG01106.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-21264A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952103 | |||||||
| chr20:43952108 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0257 others(1): Show |
4 | HG01167.hp1 HG02486.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-21259A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952108 | |||||||
| chr20:43952122 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
135 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.100-21245C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952122 | |||||||
| chr20:43952150 | C | G | 13 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0098 others(10): Show |
13 | HG00408.hp1 HG00438.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-21217C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952150 | |||||||
| chr20:43952152 | T | C | 1 | a0001c0001t0008g0108 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.100-21215T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952152 | |||||||
| chr20:43952180 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0242 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.100-21187C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952180 | |||||||
| chr20:43952190 | T | C | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-21177T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952190 | |||||||
| chr20:43952209 | AT | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | NA18944.hp2 NA18949.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-21149delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43952209 | ||||||
| chr20:43952372 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-20995G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952372 | |||||||
| chr20:43952379 | C | A | 5 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0001g0237 others(2): Show |
5 | HG01261.hp2 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-20988C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952379 | |||||||
| chr20:43952409 | A | C | 1 | a0001c0001t0003g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100-20958A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952409 | |||||||
| chr20:43952584 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.100-20783C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952584 | |||||||
| chr20:43952585 | C | A | 3 | a0001c0001t0001g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG01978.hp1 HG02148.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.100-20782C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952585 | |||||||
| chr20:43952717 | A | C | 1 | a0001c0007t0001g0209 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.100-20650A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952717 | |||||||
| chr20:43952747 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100-20620A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952747 | |||||||
| chr20:43952762 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-20605C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952762 | |||||||
| chr20:43952794 | T | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0126 a0001c0001t0001g0266 |
3 | HG02451.hp2 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.100-20573T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952794 | |||||||
| chr20:43952800 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
220 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.100-20567G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952800 | |||||||
| chr20:43952805 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-20562T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952805 | |||||||
| chr20:43952907 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(91): Show |
95 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.100-20460G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952907 | |||||||
| chr20:43952983 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0249 a0001c0001t0001g0255 others(4): Show |
7 | HG02109.hp2 HG02135.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-20384C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43952983 | |||||||
| chr20:43953139 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.100-20228C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43953139 | |||||||
| chr20:43953233 | A | ATAATT | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
220 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.100-20132_100-2013 others(9): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43953233 | ||||||
| chr20:43953274 | A | G | 14 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0094 others(11): Show |
14 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.100-20093A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43953274 | |||||||
| chr20:43953341 | G | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0037 others(42): Show |
45 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.100-20026G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43953341 | |||||||
| chr20:43953502 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.100-19865A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43953502 | |||||||
| chr20:43953692 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0002g0142 |
3 | HG02818.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.100-19675G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43953692 | |||||||
| chr20:43953809 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.100-19558C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43953809 | |||||||
| chr20:43954007 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0002g0028 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100-19360C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954007 | |||||||
| chr20:43954034 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0095 |
3 | HG00323.hp1 HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.100-19333T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954034 | |||||||
| chr20:43954047 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.100-19320A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954047 | |||||||
| chr20:43954063 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0229 others(2): Show |
5 | HG02970.hp2 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-19304A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954063 | |||||||
| chr20:43954383 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0048 others(26): Show |
29 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-18984C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954383 | |||||||
| chr20:43954460 | CTG | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0048 others(27): Show |
30 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.100-18903_100-1890 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43954460 | ||||||
| chr20:43954472 | T | G | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-18895T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954472 | |||||||
| chr20:43954524 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.100-18843C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954524 | |||||||
| chr20:43954556 | G | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(78): Show |
82 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.100-18811G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954556 | |||||||
| chr20:43954562 | T | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0180 a0005c0004t0002g0019 others(1): Show |
4 | HG02717.hp1 NA18522.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-18805T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954562 | |||||||
| chr20:43954574 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(78): Show |
82 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.100-18793G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954574 | |||||||
| chr20:43954739 | C | G | 1 | a0001c0001t0002g0022 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-18628C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954739 | |||||||
| chr20:43954807 | G | A | 3 | a0001c0001t0002g0035 a0001c0001t0002g0141 a0001c0001t0002g0147 |
3 | HG02258.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.100-18560G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954807 | |||||||
| chr20:43954840 | T | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0048 others(27): Show |
30 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.100-18527T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954840 | |||||||
| chr20:43954922 | A | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | NA18990.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.100-18445A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954922 | |||||||
| chr20:43954957 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-18410C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954957 | |||||||
| chr20:43954977 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
142 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.100-18390A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954977 | |||||||
| chr20:43954996 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-18371G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954996 | |||||||
| chr20:43954998 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.100-18369C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43954998 | |||||||
| chr20:43955031 | A | G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0037 others(42): Show |
45 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.100-18336A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955031 | |||||||
| chr20:43955093 | C | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0037 others(42): Show |
45 | HG00621.hp2 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.100-18274C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955093 | |||||||
| chr20:43955202 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.100-18165A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955202 | |||||||
| chr20:43955272 | T | A | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-18095T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955272 | |||||||
| chr20:43955299 | G | A | 2 | a0001c0001t0001g0023 a0007c0006t0001g0089 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.100-18068G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955299 | |||||||
| chr20:43955520 | T | A | 7 | a0001c0001t0001g0243 a0001c0001t0002g0035 a0001c0001t0002g0141 others(4): Show |
7 | HG00741.hp2 HG02258.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-17847T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955520 | |||||||
| chr20:43955580 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.100-17787G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955580 | |||||||
| chr20:43955594 | A | G | 11 | a0001c0001t0001g0130 a0001c0001t0001g0180 a0001c0001t0001g0243 others(8): Show |
11 | HG00741.hp2 HG02258.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-17773A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955594 | |||||||
| chr20:43955747 | A | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0039 others(3): Show |
6 | HG01167.hp1 HG01361.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-17620A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955747 | |||||||
| chr20:43955758 | G | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(108): Show |
112 | HG00621.hp2 HG00642.hp2 HG00673.hp2 others(109): Show |
intron_variant | MODIFIER | c.100-17609G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955758 | |||||||
| chr20:43955778 | T | C | 11 | a0001c0001t0001g0130 a0001c0001t0001g0180 a0001c0001t0001g0243 others(8): Show |
11 | HG00741.hp2 HG02258.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-17589T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955778 | |||||||
| chr20:43955794 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0006g0167 |
2 | NA19068.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.100-17573G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955794 | |||||||
| chr20:43955819 | C | T | 15 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0094 others(12): Show |
15 | HG00639.hp2 HG01261.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-17548C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955819 | |||||||
| chr20:43955887 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.100-17480C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955887 | |||||||
| chr20:43955922 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0126 others(9): Show |
12 | HG00323.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-17445G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43955922 | |||||||
| chr20:43956006 | G | T | 1 | a0001c0001t0001g0043 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.100-17361G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956006 | |||||||
| chr20:43956024 | T | TAG | 97 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(94): Show |
98 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.100-17343_100-1734 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956024 | |||||||
| chr20:43956056 | A | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0066 others(26): Show |
29 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-17311A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956056 | |||||||
| chr20:43956371 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.100-16996G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956371 | |||||||
| chr20:43956559 | T | TA | 14 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0094 others(11): Show |
14 | HG00639.hp2 HG01261.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.100-16786dupA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43956559 | ||||||
| chr20:43956559 | T | TAAAAAAA others(308): Show |
1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-16792_100-1679 others(319): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43956559 | ||||||
| chr20:43956559 | TA | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(117): Show |
121 | HG00621.hp2 HG00642.hp2 HG00673.hp2 others(118): Show |
intron_variant | MODIFIER | c.100-16786delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43956559 | ||||||
| chr20:43956559 | TAA | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0001g0172 others(9): Show |
12 | HG00323.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-16787_100-1678 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43956559 | ||||||
| chr20:43956565 | A | G | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-16802A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956565 | |||||||
| chr20:43956580 | A | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0200 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-16787A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956580 | |||||||
| chr20:43956582 | G | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0200 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-16785G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956582 | |||||||
| chr20:43956583 | A | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0200 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-16784A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956583 | |||||||
| chr20:43956584 | C | CTG | 91 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(88): Show |
92 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.100-16781_100-1678 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43956584 | ||||||
| chr20:43956584 | C | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0200 others(3): Show |
6 | HG02896.hp2 HG02897.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-16783C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956584 | |||||||
| chr20:43956670 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-16697G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956670 | |||||||
| chr20:43956754 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-16613G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956754 | |||||||
| chr20:43956843 | C | T | 3 | a0001c0001t0001g0130 a0005c0004t0002g0019 a0005c0004t0002g0020 |
3 | HG02717.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.100-16524C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43956843 | |||||||
| chr20:43957131 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(93): Show |
97 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.100-16236C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957131 | |||||||
| chr20:43957167 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(94): Show |
98 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.100-16200T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957167 | |||||||
| chr20:43957409 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100-15958C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957409 | |||||||
| chr20:43957453 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-15914G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957453 | |||||||
| chr20:43957567 | C | CT | 29 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0058 others(26): Show |
29 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.100-15780dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43957567 | ||||||
| chr20:43957567 | C | CTT | 7 | a0001c0001t0001g0130 a0001c0001t0001g0243 a0001c0001t0001g0249 others(4): Show |
7 | HG02135.hp1 HG02717.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-15781_100-1578 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43957567 | ||||||
| chr20:43957567 | CT | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0127 a0001c0001t0001g0134 others(6): Show |
9 | HG01515.hp1 HG01515.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-15780delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43957567 | ||||||
| chr20:43957569 | T | TTG | 79 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(76): Show |
80 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.100-15797_100-1579 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43957569 | ||||||
| chr20:43957571 | T | G | 16 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0048 others(13): Show |
16 | HG00639.hp2 HG01261.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-15796T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957571 | |||||||
| chr20:43957678 | G | C | 1 | a0001c0001t0001g0018 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.100-15689G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957678 | |||||||
| chr20:43957712 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100-15655A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957712 | |||||||
| chr20:43957830 | T | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(95): Show |
99 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.100-15537T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957830 | |||||||
| chr20:43957831 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(95): Show |
99 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.100-15536G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957831 | |||||||
| chr20:43957907 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-15460C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43957907 | |||||||
| chr20:43958083 | C | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0066 others(13): Show |
16 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-15284C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958083 | |||||||
| chr20:43958136 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(78): Show |
82 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.100-15231G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958136 | |||||||
| chr20:43958240 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-15127C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958240 | |||||||
| chr20:43958247 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0002g0028 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100-15120T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958247 | |||||||
| chr20:43958313 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.100-15054G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958313 | |||||||
| chr20:43958385 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(78): Show |
82 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.100-14982A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958385 | |||||||
| chr20:43958442 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.100-14925C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958442 | |||||||
| chr20:43958533 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-14834C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958533 | |||||||
| chr20:43958803 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.100-14564C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958803 | |||||||
| chr20:43958983 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(79): Show |
83 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.100-14384G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43958983 | |||||||
| chr20:43959058 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0002g0142 |
3 | HG02818.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.100-14309G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959058 | |||||||
| chr20:43959083 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.100-14284G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959083 | |||||||
| chr20:43959084 | G | C | 2 | a0001c0001t0001g0278 a0001c0001t0002g0103 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.100-14283G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959084 | |||||||
| chr20:43959116 | T | C | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-14251T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959116 | |||||||
| chr20:43959316 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0066 others(18): Show |
21 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-14051C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959316 | |||||||
| chr20:43959340 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0009g0145 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.100-14027C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959340 | |||||||
| chr20:43959439 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(78): Show |
82 | HG00673.hp2 HG00733.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.100-13928G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959439 | |||||||
| chr20:43959587 | C | T | 3 | a0001c0001t0001g0130 a0005c0004t0002g0019 a0005c0004t0002g0020 |
3 | HG02717.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.100-13780C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959587 | |||||||
| chr20:43959604 | T | A | 2 | a0001c0001t0001g0002 a0001c0001t0002g0015 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100-13763T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959604 | |||||||
| chr20:43959714 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(12): Show |
15 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-13653C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959714 | |||||||
| chr20:43959822 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-13545G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959822 | |||||||
| chr20:43959849 | T | C | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-13518T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959849 | |||||||
| chr20:43959948 | G | C | 12 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(9): Show |
12 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-13419G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43959948 | |||||||
| chr20:43960035 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.100-13332C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43960035 | |||||||
| chr20:43960041 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.100-13326C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43960041 | |||||||
| chr20:43960151 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0231 others(8): Show |
11 | HG00323.hp2 HG02109.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-13216T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43960151 | |||||||
| chr20:43960358 | T | C | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100-13009T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43960358 | |||||||
| chr20:43960513 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.100-12854C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43960513 | |||||||
| chr20:43960765 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.100-12602C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43960765 | |||||||
| chr20:43960788 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.100-12579G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43960788 | |||||||
| chr20:43960837 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.100-12530A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43960837 | |||||||
| chr20:43961191 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0231 others(6): Show |
9 | HG00323.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-12176C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43961191 | |||||||
| chr20:43961212 | C | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0039 others(13): Show |
16 | HG00639.hp2 HG01167.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-12155C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43961212 | |||||||
| chr20:43961336 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-12031G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43961336 | |||||||
| chr20:43961366 | TG | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0077 others(4): Show |
7 | HG00735.hp1 HG01069.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-11998delG | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43961366 | ||||||
| chr20:43961600 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.100-11767C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43961600 | |||||||
| chr20:43961648 | G | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0048 others(23): Show |
26 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-11719G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43961648 | |||||||
| chr20:43961798 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0009g0145 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.100-11569G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43961798 | |||||||
| chr20:43961961 | G | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0231 others(8): Show |
11 | HG00323.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-11406G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43961961 | |||||||
| chr20:43962047 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-11320C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43962047 | |||||||
| chr20:43962301 | C | T | 14 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(11): Show |
14 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.100-11066C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43962301 | |||||||
| chr20:43962474 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-10893C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43962474 | |||||||
| chr20:43962531 | T | A | 1 | a0001c0001t0002g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.100-10836T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43962531 | |||||||
| chr20:43962581 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-10786G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43962581 | |||||||
| chr20:43962602 | T | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(108): Show |
112 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.100-10765T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43962602 | |||||||
| chr20:43963038 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.100-10329G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963038 | |||||||
| chr20:43963100 | T | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(43): Show |
46 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.100-10267T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963100 | |||||||
| chr20:43963101 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.100-10266G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963101 | |||||||
| chr20:43963165 | T | A | 1 | a0001c0001t0001g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100-10202T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963165 | |||||||
| chr20:43963270 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(54): Show |
57 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.100-10097C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963270 | |||||||
| chr20:43963380 | CA | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(48): Show |
51 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.100-9986delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963380 | |||||||
| chr20:43963584 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0002g0133 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-9783C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963584 | |||||||
| chr20:43963639 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(29): Show |
32 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.100-9728G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963639 | |||||||
| chr20:43963662 | G | A | 1 | a0003c0003t0001g0004 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.100-9705G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963662 | |||||||
| chr20:43963696 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.100-9671A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963696 | |||||||
| chr20:43963700 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
135 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(132): Show |
intron_variant | MODIFIER | c.100-9667T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963700 | |||||||
| chr20:43963819 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.100-9548A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43963819 | |||||||
| chr20:43964166 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.100-9201C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43964166 | |||||||
| chr20:43964328 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0229 others(2): Show |
5 | HG02970.hp2 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-9039G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43964328 | |||||||
| chr20:43964368 | T | C | 1 | a0001c0001t0002g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-8999T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43964368 | |||||||
| chr20:43964580 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(35): Show |
38 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.100-8787G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43964580 | |||||||
| chr20:43964807 | T | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(38): Show |
41 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.100-8560T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43964807 | |||||||
| chr20:43964915 | G | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG02895.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.100-8452G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43964915 | |||||||
| chr20:43965083 | C | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(12): Show |
15 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-8284C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965083 | |||||||
| chr20:43965124 | G | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | NA18944.hp2 NA18949.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-8243G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965124 | |||||||
| chr20:43965165 | A | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0027 others(77): Show |
81 | HG00323.hp2 HG00673.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.100-8202A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965165 | |||||||
| chr20:43965357 | T | C | 18 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(15): Show |
18 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-8010T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965357 | |||||||
| chr20:43965480 | C | T | 10 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0255 others(7): Show |
10 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-7887C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965480 | |||||||
| chr20:43965510 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100-7857G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965510 | |||||||
| chr20:43965564 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG02027.hp1 HG02071.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7803G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965564 | |||||||
| chr20:43965744 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0039 others(4): Show |
7 | HG00639.hp2 HG01167.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-7623C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965744 | |||||||
| chr20:43965767 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-7600G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43965767 | |||||||
| chr20:43966103 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.100-7264G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43966103 | |||||||
| chr20:43966523 | C | T | 1 | a0001c0001t0004g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.100-6844C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43966523 | |||||||
| chr20:43966715 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(63): Show |
66 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.100-6652T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43966715 | |||||||
| chr20:43966730 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-6637G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43966730 | |||||||
| chr20:43966753 | C | CA | 47 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(44): Show |
47 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.100-6597dupA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43966753 | ||||||
| chr20:43966772 | T | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100-6595T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43966772 | |||||||
| chr20:43966781 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-6586T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43966781 | |||||||
| chr20:43966873 | T | C | 3 | a0001c0001t0001g0130 a0005c0004t0002g0019 a0005c0004t0002g0020 |
3 | HG02717.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.100-6494T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43966873 | |||||||
| chr20:43966915 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0094 others(2): Show |
5 | HG00639.hp2 HG01361.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-6452C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43966915 | |||||||
| chr20:43966959 | CCACCAA | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
235 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(232): Show |
intron_variant | MODIFIER | c.100-6399_100-6394d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr20 | 43966959 | ||||||
| chr20:43967004 | G | A | 3 | a0001c0001t0001g0257 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG02895.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.100-6363G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43967004 | |||||||
| chr20:43967169 | A | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(12): Show |
15 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-6198A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43967169 | |||||||
| chr20:43967320 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0037 a0001c0001t0001g0144 others(6): Show |
9 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-6047T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43967320 | |||||||
| chr20:43967430 | C | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0130 others(12): Show |
15 | HG02027.hp1 HG02071.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-5937C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43967430 | |||||||
| chr20:43967486 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.100-5881G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43967486 | |||||||
| chr20:43967494 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100-5873A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43967494 | |||||||
| chr20:43967816 | A | G | 3 | a0001c0001t0001g0126 a0001c0001t0001g0266 a0001c0001t0001g0278 |
3 | HG02055.hp1 HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100-5551A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43967816 | |||||||
| chr20:43968089 | C | T | 1 | a0004c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.100-5278C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43968089 | |||||||
| chr20:43968090 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-5277G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43968090 | |||||||
| chr20:43968182 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.100-5185A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43968182 | |||||||
| chr20:43968272 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | NA18941.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.100-5095C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43968272 | |||||||
| chr20:43968484 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.100-4883G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43968484 | |||||||
| chr20:43968542 | A | C | 8 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0002g0035 others(5): Show |
8 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-4825A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43968542 | |||||||
| chr20:43968548 | T | G | 1 | a0001c0001t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.100-4819T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43968548 | |||||||
| chr20:43968618 | A | C | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-4749A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43968618 | |||||||
| chr20:43969021 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.100-4346T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43969021 | |||||||
| chr20:43969321 | T | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100-4046T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43969321 | |||||||
| chr20:43969487 | G | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0215 a0001c0001t0001g0219 others(2): Show |
5 | NA18971.hp1 NA19000.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-3880G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43969487 | |||||||
| chr20:43969520 | C | G | 15 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0109 others(12): Show |
15 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-3847C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43969520 | |||||||
| chr20:43969661 | A | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100-3706A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43969661 | |||||||
| chr20:43969756 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.100-3611G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43969756 | |||||||
| chr20:43969931 | C | G | 13 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(10): Show |
13 | HG00408.hp2 HG02132.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-3436C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43969931 | |||||||
| chr20:43970006 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.100-3361G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970006 | |||||||
| chr20:43970020 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100-3347C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970020 | |||||||
| chr20:43970088 | T | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0034 others(16): Show |
19 | HG01261.hp2 HG01361.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.100-3279T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970088 | |||||||
| chr20:43970291 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.100-3076G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970291 | |||||||
| chr20:43970526 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100-2841G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970526 | |||||||
| chr20:43970528 | T | TGGTATGC others(16): Show |
2 | a0001c0001t0002g0141 a0001c0001t0002g0147 |
2 | HG02258.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-2839_100-2838i others(25): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970528 | |||||||
| chr20:43970615 | A | G | 3 | a0001c0001t0001g0257 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG02895.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.100-2752A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970615 | |||||||
| chr20:43970635 | A | T | 1 | a0001c0001t0003g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100-2732A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970635 | |||||||
| chr20:43970875 | C | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0176 a0001c0001t0001g0222 |
3 | HG03654.hp1 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.100-2492C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43970875 | |||||||
| chr20:43971607 | C | G | 10 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0255 others(7): Show |
10 | HG00741.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-1760C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43971607 | |||||||
| chr20:43971733 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.100-1634T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43971733 | |||||||
| chr20:43972635 | C | T | 1 | a0003c0003t0001g0004 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.100-732C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43972635 | |||||||
| chr20:43972909 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.100-458C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43972909 | |||||||
| chr20:43972984 | C | G | 1 | a0001c0001t0006g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.100-383C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43972984 | |||||||
| chr20:43973104 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-263G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43973104 | |||||||
| chr20:43973167 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-200G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43973167 | |||||||
| chr20:43973170 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.100-197G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43973170 | |||||||
| chr20:43973252 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0009g0145 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.100-115C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43973252 | |||||||
| chr20:43973325 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0039 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-42G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 1/8 | chr20 | 43973325 | |||||||
| chr20:43973502 | T | G | 18 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(15): Show |
18 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+70T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43973502 | |||||||
| chr20:43973725 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0002g0236 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.165+293G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43973725 | |||||||
| chr20:43973795 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0002g0103 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.165+363G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43973795 | |||||||
| chr20:43973808 | T | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+376T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43973808 | |||||||
| chr20:43973817 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.165+385G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43973817 | |||||||
| chr20:43973892 | G | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0127 others(15): Show |
18 | HG02027.hp1 HG02071.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+460G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43973892 | |||||||
| chr20:43973963 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.165+531C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43973963 | |||||||
| chr20:43973964 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.165+532G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43973964 | |||||||
| chr20:43974472 | C | T | 1 | a0001c0001t0006g0167 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.165+1040C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43974472 | |||||||
| chr20:43974793 | G | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+1361G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43974793 | |||||||
| chr20:43975060 | C | A | 2 | a0001c0001t0001g0278 a0001c0001t0002g0103 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.165+1628C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43975060 | |||||||
| chr20:43975679 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(12): Show |
15 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+2247G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43975679 | |||||||
| chr20:43975680 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 others(1): Show |
4 | HG02922.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+2248C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43975680 | |||||||
| chr20:43975823 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165+2391C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43975823 | |||||||
| chr20:43975826 | A | G | 2 | a0001c0001t0002g0141 a0001c0001t0002g0147 |
2 | HG02258.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.165+2394A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43975826 | |||||||
| chr20:43976501 | C | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0039 others(5): Show |
8 | HG00639.hp2 HG01167.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+3069C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43976501 | |||||||
| chr20:43976507 | C | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0039 others(5): Show |
8 | HG00639.hp2 HG01167.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+3075C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43976507 | |||||||
| chr20:43976773 | A | AGCGC | 5 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0077 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+3348_165+3351d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976773 | ||||||
| chr20:43976777 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0252 a0001c0001t0004g0161 others(2): Show |
5 | HG02165.hp2 NA18981.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+3345C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43976777 | |||||||
| chr20:43976780 | G | A | 5 | a0001c0001t0001g0139 a0001c0001t0001g0215 a0001c0001t0001g0219 others(2): Show |
5 | NA18971.hp1 NA19000.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+3348G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43976780 | |||||||
| chr20:43976782 | G | GCA | 24 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0127 others(21): Show |
24 | HG01975.hp2 HG02027.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.165+3371_165+3372d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | G | GCACA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0046 others(70): Show |
74 | HG00323.hp2 HG00673.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.165+3369_165+3372d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | G | GCACACA | 11 | a0001c0001t0001g0024 a0001c0001t0001g0116 a0001c0001t0001g0166 others(8): Show |
11 | HG02055.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+3367_165+3372d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0056 a0001c0001t0001g0241 a0001c0001t0007g0149 others(1): Show |
4 | HG00741.hp2 HG02257.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+3365_165+3372d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | G | GCACACAC others(3): Show |
1 | a0001c0001t0003g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165+3363_165+3372d others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0038 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.165+3360_165+3361i others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | G | GCGCA | 11 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0070 others(8): Show |
11 | HG00621.hp2 HG00642.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+3351_165+3352i others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | G | GCGCACAC others(3): Show |
1 | a0001c0001t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.165+3351_165+3352i others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | G | GCGCGCAC others(3): Show |
1 | a0001c0001t0009g0145 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165+3351_165+3352i others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976782 | GCA | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0098 a0001c0001t0001g0114 |
3 | HG00597.hp2 NA18953.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.165+3371_165+3372d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976782 | ||||||
| chr20:43976783 | C | CACACACA others(3): Show |
14 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(11): Show |
14 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+3360_165+3361i others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43976783 | ||||||
| chr20:43976784 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0077 others(5): Show |
8 | HG00735.hp1 HG01069.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+3352A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43976784 | |||||||
| chr20:43977172 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0002g0236 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.165+3740G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977172 | |||||||
| chr20:43977214 | A | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(12): Show |
15 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+3782A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977214 | |||||||
| chr20:43977222 | C | T | 3 | a0001c0001t0003g0286 a0001c0001t0007g0149 a0002c0002t0002g0140 |
3 | HG00741.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.165+3790C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977222 | |||||||
| chr20:43977273 | G | T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(10): Show |
13 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+3841G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977273 | |||||||
| chr20:43977363 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.165+3931G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977363 | |||||||
| chr20:43977523 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.165+4091A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977523 | |||||||
| chr20:43977568 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.165+4136C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977568 | |||||||
| chr20:43977578 | G | GT | 3 | a0001c0001t0001g0027 a0001c0001t0002g0267 a0001c0009t0002g0152 |
3 | HG02896.hp1 HG02896.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.165+4147dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43977578 | ||||||
| chr20:43977580 | G | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(134): Show |
138 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(135): Show |
intron_variant | MODIFIER | c.165+4148G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977580 | |||||||
| chr20:43977785 | G | T | 2 | a0001c0001t0001g0255 a0001c0001t0002g0236 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.165+4353G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43977785 | |||||||
| chr20:43978035 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0066 |
2 | HG01069.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.165+4603T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978035 | |||||||
| chr20:43978120 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(36): Show |
39 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.165+4688T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978120 | |||||||
| chr20:43978165 | A | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(12): Show |
15 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+4733A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978165 | |||||||
| chr20:43978185 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.165+4753A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978185 | |||||||
| chr20:43978399 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.165+4967G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978399 | |||||||
| chr20:43978481 | C | CTTATTA | 63 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0023 others(60): Show |
63 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.165+5052_165+5057d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978481 | ||||||
| chr20:43978638 | G | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0229 others(4): Show |
7 | HG02109.hp2 HG02280.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+5206G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978638 | |||||||
| chr20:43978639 | G | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0130 others(11): Show |
14 | HG02027.hp1 HG02071.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+5207G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978639 | |||||||
| chr20:43978654 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0048 others(12): Show |
15 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+5222C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978654 | |||||||
| chr20:43978694 | C | T | 3 | a0001c0001t0001g0266 a0001c0001t0001g0278 a0001c0001t0002g0103 |
3 | HG02055.hp1 HG02622.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.165+5262C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978694 | |||||||
| chr20:43978736 | A | AT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(27): Show |
30 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.165+5310dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978736 | ||||||
| chr20:43978763 | T | TTG | 37 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0018 others(34): Show |
37 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.165+5365_165+5366d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | T | TTGTG | 5 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0039 others(2): Show |
5 | HG01167.hp1 HG02896.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+5363_165+5366d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | T | TTGTGTG | 13 | a0001c0001t0001g0024 a0001c0001t0001g0139 a0001c0001t0001g0153 others(10): Show |
13 | HG01106.hp1 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+5361_165+5366d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | T | TTGTGTGT others(1): Show |
43 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0053 others(40): Show |
44 | HG00323.hp2 HG00673.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.165+5359_165+5366d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | T | TTGTGTGT others(3): Show |
15 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0056 others(12): Show |
15 | HG01069.hp1 HG01169.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.165+5357_165+5366d others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | T | TTGTGTGT others(5): Show |
5 | a0001c0001t0001g0121 a0001c0001t0001g0200 a0001c0001t0001g0203 others(2): Show |
5 | NA18944.hp1 NA18978.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+5355_165+5366d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0221 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.165+5353_165+5366d others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | T | TTGTGTGT others(9): Show |
1 | a0001c0001t0002g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.165+5351_165+5366d others(18): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | TTG | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0025 others(23): Show |
26 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.165+5365_165+5366d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978763 | TTGTG | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0048 others(20): Show |
23 | HG00741.hp2 HG02027.hp1 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.165+5363_165+5366d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43978763 | ||||||
| chr20:43978893 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0009g0145 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+5461G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43978893 | |||||||
| chr20:43979210 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+5778T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43979210 | |||||||
| chr20:43979504 | A | G | 17 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(14): Show |
17 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+6072A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43979504 | |||||||
| chr20:43979541 | C | G | 1 | a0001c0001t0001g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.165+6109C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43979541 | |||||||
| chr20:43979633 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(145): Show |
149 | HG00323.hp2 HG00621.hp2 HG00642.hp2 others(146): Show |
intron_variant | MODIFIER | c.165+6201T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43979633 | |||||||
| chr20:43979731 | A | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0037 others(12): Show |
15 | HG01261.hp2 HG01884.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+6299A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43979731 | |||||||
| chr20:43979836 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+6404C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43979836 | |||||||
| chr20:43979855 | A | AT | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0067 others(2): Show |
5 | HG02132.hp1 NA18970.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+6424dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43979855 | ||||||
| chr20:43979891 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(27): Show |
30 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.165+6459G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43979891 | |||||||
| chr20:43980354 | G | T | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+6922G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43980354 | |||||||
| chr20:43980502 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.165+7070G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43980502 | |||||||
| chr20:43980545 | A | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(62): Show |
65 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.165+7113A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43980545 | |||||||
| chr20:43980904 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+7472A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43980904 | |||||||
| chr20:43980917 | A | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0048 others(13): Show |
16 | HG00621.hp2 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+7485A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43980917 | |||||||
| chr20:43981061 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.165+7629T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981061 | |||||||
| chr20:43981389 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.165+7957T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981389 | |||||||
| chr20:43981398 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.165+7966A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981398 | |||||||
| chr20:43981492 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0049 others(7): Show |
11 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+8060C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981492 | |||||||
| chr20:43981506 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0009g0145 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+8074A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981506 | |||||||
| chr20:43981544 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0147 |
2 | HG02258.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.165+8112G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981544 | |||||||
| chr20:43981575 | T | C | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.165+8143T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981575 | |||||||
| chr20:43981581 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+8149G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981581 | |||||||
| chr20:43981773 | T | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0039 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+8341T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981773 | |||||||
| chr20:43981806 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+8374G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981806 | |||||||
| chr20:43981928 | G | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0148 a0001c0001t0001g0285 others(1): Show |
4 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+8496G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43981928 | |||||||
| chr20:43981935 | C | CT | 62 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0046 others(59): Show |
63 | HG00323.hp2 HG00673.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.165+8519dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43981935 | ||||||
| chr20:43981935 | CT | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(50): Show |
53 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.165+8519delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43981935 | ||||||
| chr20:43982140 | G | A | 1 | a0001c0001t0010g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.165+8708G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43982140 | |||||||
| chr20:43982249 | G | C | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165+8817G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43982249 | |||||||
| chr20:43982258 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0002g0142 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+8826G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43982258 | |||||||
| chr20:43982266 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0002g0103 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.165+8834G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43982266 | |||||||
| chr20:43982541 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.165+9109G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43982541 | |||||||
| chr20:43982561 | G | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG01167.hp2 HG01169.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.165+9129G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43982561 | |||||||
| chr20:43982665 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.165+9233A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43982665 | |||||||
| chr20:43982838 | GA | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0027 others(76): Show |
80 | HG00323.hp2 HG00673.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.165+9408delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43982838 | ||||||
| chr20:43983075 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.165+9643G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983075 | |||||||
| chr20:43983177 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.165+9745G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983177 | |||||||
| chr20:43983402 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+9970A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983402 | |||||||
| chr20:43983471 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+10039A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983471 | |||||||
| chr20:43983501 | A | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(23): Show |
26 | HG00323.hp1 HG00642.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.165+10069A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983501 | |||||||
| chr20:43983604 | C | T | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+10172C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983604 | |||||||
| chr20:43983642 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+10210C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983642 | |||||||
| chr20:43983684 | G | GT | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(54): Show |
57 | HG00323.hp1 HG00642.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.165+10258dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43983684 | ||||||
| chr20:43983694 | G | C | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+10262G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983694 | |||||||
| chr20:43983699 | A | G | 2 | a0004c0005t0001g0106 a0004c0005t0001g0107 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.165+10267A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983699 | |||||||
| chr20:43983930 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0159 |
2 | HG01258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.165+10498C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43983930 | |||||||
| chr20:43984044 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.165+10612C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984044 | |||||||
| chr20:43984093 | C | T | 1 | a0007c0006t0001g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+10661C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984093 | |||||||
| chr20:43984103 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.165+10671C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984103 | |||||||
| chr20:43984130 | C | CT | 4 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 others(1): Show |
4 | HG02055.hp2 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+10699dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43984130 | ||||||
| chr20:43984482 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(62): Show |
65 | HG00323.hp1 HG00642.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.165+11050C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984482 | |||||||
| chr20:43984537 | T | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
76 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.165+11105T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984537 | |||||||
| chr20:43984633 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+11201G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984633 | |||||||
| chr20:43984656 | G | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0130 others(6): Show |
9 | HG02258.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+11224G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984656 | |||||||
| chr20:43984690 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+11258A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984690 | |||||||
| chr20:43984876 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.165+11444G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984876 | |||||||
| chr20:43984895 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+11463C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984895 | |||||||
| chr20:43984948 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.165+11516G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43984948 | |||||||
| chr20:43985114 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0153 a0001c0009t0002g0152 others(1): Show |
4 | HG02109.hp1 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+11682C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43985114 | |||||||
| chr20:43985180 | T | A | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+11748T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43985180 | |||||||
| chr20:43985352 | C | T | 4 | a0001c0001t0001g0257 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+11920C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43985352 | |||||||
| chr20:43985501 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.165+12069C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43985501 | |||||||
| chr20:43985511 | T | A | 1 | a0001c0001t0002g0262 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.165+12079T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43985511 | |||||||
| chr20:43985702 | C | G | 2 | a0001c0001t0001g0047 a0001c0001t0009g0145 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+12270C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43985702 | |||||||
| chr20:43985910 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0261 a0001c0001t0009g0145 |
3 | HG01099.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+12478G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43985910 | |||||||
| chr20:43986256 | A | AATGT | 10 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0204 others(7): Show |
10 | HG00639.hp1 HG01106.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+12853_165+1285 others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43986256 | ||||||
| chr20:43986256 | A | AATGTATG others(1): Show |
3 | a0001c0001t0001g0255 a0001c0001t0001g0278 a0001c0001t0002g0236 |
3 | HG02055.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.165+12849_165+1285 others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43986256 | ||||||
| chr20:43986256 | A | AATGTATG others(5): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(47): Show |
50 | HG00408.hp2 HG00639.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.165+12845_165+1285 others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43986256 | ||||||
| chr20:43986256 | A | AATGTATG others(9): Show |
38 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0038 others(35): Show |
38 | HG00408.hp1 HG00438.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.165+12841_165+1285 others(20): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43986256 | ||||||
| chr20:43986256 | A | AATGTATG others(13): Show |
2 | a0001c0001t0002g0026 a0001c0001t0002g0133 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+12837_165+1285 others(24): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43986256 | ||||||
| chr20:43986285 | A | ATGTATGT others(17): Show |
3 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0265 |
3 | HG00642.hp2 HG02071.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.165+12856_165+1285 others(28): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43986285 | ||||||
| chr20:43986285 | A | ATGTATGT others(13): Show |
12 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0018 others(9): Show |
12 | HG01069.hp2 HG01099.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+12856_165+1285 others(24): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43986285 | ||||||
| chr20:43986285 | A | ATGTATGT others(9): Show |
8 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0087 others(5): Show |
8 | HG00323.hp1 HG00735.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+12856_165+1285 others(20): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43986285 | ||||||
| chr20:43986299 | T | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | NA18960.hp1 NA18974.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+12867T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43986299 | |||||||
| chr20:43986406 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.165+12974C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43986406 | |||||||
| chr20:43986625 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.165+13193A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43986625 | |||||||
| chr20:43986925 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.165+13493G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43986925 | |||||||
| chr20:43987024 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.165+13592A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987024 | |||||||
| chr20:43987070 | A | C | 1 | a0001c0001t0001g0038 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.165+13638A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987070 | |||||||
| chr20:43987143 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.165+13711T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987143 | |||||||
| chr20:43987172 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.165+13740G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987172 | |||||||
| chr20:43987277 | C | G | 1 | a0001c0001t0001g0007 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.165+13845C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987277 | |||||||
| chr20:43987364 | G | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0018 others(15): Show |
18 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.165+13932G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987364 | |||||||
| chr20:43987365 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0009g0145 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.165+13933G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987365 | |||||||
| chr20:43987409 | C | G | 1 | a0001c0001t0001g0007 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.165+13977C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987409 | |||||||
| chr20:43987439 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.165+14007C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987439 | |||||||
| chr20:43987447 | A | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0130 others(12): Show |
15 | HG00741.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+14015A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987447 | |||||||
| chr20:43987480 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0133 |
3 | HG02922.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+14048C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987480 | |||||||
| chr20:43987515 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+14083T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987515 | |||||||
| chr20:43987531 | G | A | 57 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(54): Show |
57 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.165+14099G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987531 | |||||||
| chr20:43987823 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.165+14391C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987823 | |||||||
| chr20:43987872 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(248): Show |
252 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.165+14440T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987872 | |||||||
| chr20:43987912 | C | CT | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(76): Show |
79 | HG00438.hp1 HG00621.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.165+14505dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43987912 | ||||||
| chr20:43987912 | CT | C | 14 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0067 others(11): Show |
14 | HG00738.hp1 HG01167.hp2 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+14505delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43987912 | ||||||
| chr20:43987946 | T | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
131 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.165+14514T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43987946 | |||||||
| chr20:43988236 | G | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0206 |
2 | HG00408.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.165+14804G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43988236 | |||||||
| chr20:43988288 | G | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0049 others(27): Show |
31 | HG00673.hp2 HG01175.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.165+14856G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43988288 | |||||||
| chr20:43988330 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.165+14898A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43988330 | |||||||
| chr20:43988554 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | NA18960.hp1 NA18974.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+15122C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43988554 | |||||||
| chr20:43988612 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0130 others(6): Show |
9 | HG02258.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+15180G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43988612 | |||||||
| chr20:43989225 | C | G | 4 | a0001c0001t0001g0257 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+15793C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43989225 | |||||||
| chr20:43989231 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.165+15799C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43989231 | |||||||
| chr20:43989486 | A | G | 1 | a0001c0001t0003g0286 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165+16054A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43989486 | |||||||
| chr20:43989497 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0134 a0001c0001t0002g0129 others(1): Show |
4 | HG02818.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+16065G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43989497 | |||||||
| chr20:43989509 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0002g0236 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.165+16077G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43989509 | |||||||
| chr20:43989736 | C | T | 55 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(52): Show |
55 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.165+16304C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43989736 | |||||||
| chr20:43989781 | G | GA | 20 | a0001c0001t0001g0047 a0001c0001t0001g0060 a0001c0001t0001g0127 others(17): Show |
20 | HG01106.hp1 HG01433.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.165+16365dupA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43989781 | ||||||
| chr20:43989781 | GA | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0257 a0001c0001t0001g0282 others(3): Show |
6 | HG02258.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+16365delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43989781 | ||||||
| chr20:43990059 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
129 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.166-16488A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43990059 | |||||||
| chr20:43990162 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.166-16385A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43990162 | |||||||
| chr20:43990346 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(126): Show |
129 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.166-16201T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43990346 | |||||||
| chr20:43990608 | T | G | 1 | a0001c0001t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.166-15939T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43990608 | |||||||
| chr20:43990698 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.166-15849C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43990698 | |||||||
| chr20:43991275 | G | GGGA | 57 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(54): Show |
57 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.166-15270_166-1526 others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991275 | ||||||
| chr20:43991305 | G | A | 2 | a0001c0001t0002g0136 a0001c0001t0002g0259 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.166-15242G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991305 | |||||||
| chr20:43991349 | C | A | 1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.166-15198C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991349 | |||||||
| chr20:43991445 | T | C | 57 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(54): Show |
57 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.166-15102T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991445 | |||||||
| chr20:43991464 | C | G | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.166-15083C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991464 | |||||||
| chr20:43991614 | C | CATT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0199 others(3): Show |
6 | HG00741.hp2 HG02896.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-14890_166-1488 others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | C | CATTATT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0241 others(4): Show |
7 | HG02257.hp1 HG02258.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-14893_166-1488 others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | C | CATTATTA others(2): Show |
3 | a0001c0001t0001g0130 a0005c0004t0002g0019 a0005c0004t0002g0020 |
3 | HG02717.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.166-14896_166-1488 others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | CATT | C | 43 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0023 others(40): Show |
43 | HG00621.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.166-14890_166-1488 others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | CATTATT | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
133 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.166-14893_166-1488 others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | CATTATTA others(2): Show |
C | 3 | a0001c0001t0001g0189 a0001c0001t0009g0145 a0003c0003t0001g0004 |
3 | HG01261.hp1 HG02129.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.166-14896_166-1488 others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | CATTATTA others(5): Show |
C | 1 | a0001c0001t0002g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.166-14899_166-1488 others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | CATTATTA others(8): Show |
C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0001t0001g0282 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-14902_166-1488 others(19): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | CATTATTA others(11): Show |
C | 1 | a0001c0001t0002g0135 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.166-14905_166-1488 others(22): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | CATTATTA others(14): Show |
C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.166-14908_166-1488 others(25): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991614 | CATTATTA others(17): Show |
C | 57 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(54): Show |
57 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.166-14911_166-1488 others(28): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43991614 | ||||||
| chr20:43991620 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.166-14927T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991620 | |||||||
| chr20:43991623 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.166-14924T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991623 | |||||||
| chr20:43991914 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0002g0129 |
2 | HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.166-14633C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991914 | |||||||
| chr20:43991915 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.166-14632G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991915 | |||||||
| chr20:43991952 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(147): Show |
151 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.166-14595G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43991952 | |||||||
| chr20:43992094 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0243 a0001c0001t0009g0145 |
3 | HG02886.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.166-14453C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43992094 | |||||||
| chr20:43992255 | C | T | 58 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.166-14292C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43992255 | |||||||
| chr20:43992364 | G | A | 4 | a0001c0001t0001g0257 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-14183G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43992364 | |||||||
| chr20:43992586 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.166-13961C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43992586 | |||||||
| chr20:43992759 | T | C | 58 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.166-13788T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43992759 | |||||||
| chr20:43992849 | C | CA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0034 others(38): Show |
41 | HG00733.hp1 HG00741.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.166-13681dupA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43992849 | ||||||
| chr20:43992849 | C | CAA | 10 | a0001c0001t0001g0038 a0001c0001t0001g0255 a0001c0001t0001g0257 others(7): Show |
10 | HG02258.hp2 HG02559.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-13682_166-1368 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43992849 | ||||||
| chr20:43992863 | A | AAG | 24 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(21): Show |
24 | HG00323.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-13683_166-1368 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43992863 | ||||||
| chr20:43992863 | A | AG | 3 | a0001c0001t0001g0047 a0001c0001t0001g0093 a0001c0001t0009g0145 |
3 | HG03225.hp2 HG03453.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.166-13684_166-1368 others(5): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43992863 | |||||||
| chr20:43992888 | A | C | 58 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.166-13659A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43992888 | |||||||
| chr20:43993053 | G | C | 58 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.166-13494G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993053 | |||||||
| chr20:43993189 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0002g0236 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.166-13358A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993189 | |||||||
| chr20:43993210 | T | TAA | 58 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.166-13336_166-1333 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43993210 | ||||||
| chr20:43993222 | G | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.166-13325G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993222 | |||||||
| chr20:43993255 | G | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(55): Show |
58 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.166-13292G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993255 | |||||||
| chr20:43993828 | T | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(66): Show |
69 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.166-12719T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993828 | |||||||
| chr20:43993843 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0278 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.166-12704G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993843 | |||||||
| chr20:43993846 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0009g0145 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.166-12701A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993846 | |||||||
| chr20:43993890 | C | T | 45 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(42): Show |
45 | HG00408.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.166-12657C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993890 | |||||||
| chr20:43993910 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.166-12637C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993910 | |||||||
| chr20:43993944 | G | A | 60 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0016 others(57): Show |
60 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.166-12603G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993944 | |||||||
| chr20:43993980 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.166-12567C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43993980 | |||||||
| chr20:43994066 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.166-12481G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994066 | |||||||
| chr20:43994071 | A | G | 2 | a0001c0001t0001g0232 a0001c0012t0003g0013 |
2 | HG01496.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.166-12476A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994071 | |||||||
| chr20:43994109 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00408.hp2 NA18944.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-12438C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994109 | |||||||
| chr20:43994134 | G | C | 2 | a0001c0001t0001g0126 a0001c0001t0002g0129 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.166-12413G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994134 | |||||||
| chr20:43994172 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.166-12375A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994172 | |||||||
| chr20:43994200 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.166-12347C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994200 | |||||||
| chr20:43994254 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0255 |
2 | HG03710.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.166-12293C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994254 | |||||||
| chr20:43994255 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.166-12292A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994255 | |||||||
| chr20:43994290 | A | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
109 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.166-12257A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994290 | |||||||
| chr20:43994299 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
105 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.166-12248T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994299 | |||||||
| chr20:43994301 | CA | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.166-12238delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43994301 | ||||||
| chr20:43994318 | G | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
116 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.166-12229G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994318 | |||||||
| chr20:43994388 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0090 others(12): Show |
15 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-12159G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994388 | |||||||
| chr20:43994421 | T | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
115 | HG00323.hp1 HG00323.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.166-12126T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994421 | |||||||
| chr20:43994459 | C | CACAAAA | 75 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0018 others(72): Show |
75 | HG00323.hp1 HG00597.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.166-12087_166-1208 others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43994459 | ||||||
| chr20:43994459 | C | CACAAAAA | 25 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0024 others(22): Show |
25 | HG00323.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.166-12087_166-1208 others(11): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43994459 | ||||||
| chr20:43994460 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.166-12087A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994460 | |||||||
| chr20:43994461 | A | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0123 others(2): Show |
5 | HG01071.hp1 HG01934.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-12086A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994461 | |||||||
| chr20:43994643 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.166-11904C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994643 | |||||||
| chr20:43994691 | T | TG | 3 | a0001c0001t0002g0147 a0001c0001t0002g0226 a0002c0002t0002g0033 |
3 | HG02109.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-11855dupG | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43994691 | ||||||
| chr20:43994752 | C | T | 4 | a0001c0001t0001g0102 a0001c0001t0001g0109 a0001c0001t0001g0264 others(1): Show |
4 | HG00733.hp1 HG00733.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-11795C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994752 | |||||||
| chr20:43994878 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.166-11669G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994878 | |||||||
| chr20:43994941 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.166-11606G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994941 | |||||||
| chr20:43994974 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0184 |
2 | HG00621.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.166-11573G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43994974 | |||||||
| chr20:43995223 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.166-11324T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995223 | |||||||
| chr20:43995327 | G | A | 33 | a0001c0001t0001g0061 a0001c0001t0001g0080 a0001c0001t0001g0109 others(30): Show |
33 | HG00408.hp2 HG00733.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.166-11220G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995327 | |||||||
| chr20:43995333 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.166-11214C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995333 | |||||||
| chr20:43995379 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.166-11168C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995379 | |||||||
| chr20:43995380 | G | A | 30 | a0001c0001t0001g0061 a0001c0001t0001g0080 a0001c0001t0001g0122 others(27): Show |
30 | HG00741.hp2 HG02109.hp1 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.166-11167G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995380 | |||||||
| chr20:43995420 | T | A | 33 | a0001c0001t0001g0061 a0001c0001t0001g0080 a0001c0001t0001g0109 others(30): Show |
33 | HG00733.hp2 HG00741.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.166-11127T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995420 | |||||||
| chr20:43995466 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.166-11081A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995466 | |||||||
| chr20:43995593 | A | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(214): Show |
217 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(214): Show |
intron_variant | MODIFIER | c.166-10954A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995593 | |||||||
| chr20:43995660 | C | A | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.166-10887C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995660 | |||||||
| chr20:43995697 | T | G | 39 | a0001c0001t0001g0023 a0001c0001t0001g0061 a0001c0001t0001g0080 others(36): Show |
39 | HG00733.hp2 HG00741.hp2 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.166-10850T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995697 | |||||||
| chr20:43995818 | C | T | 13 | a0001c0001t0001g0024 a0001c0001t0001g0093 a0001c0001t0001g0094 others(10): Show |
13 | HG00639.hp2 HG01515.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-10729C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995818 | |||||||
| chr20:43995984 | CAT | C | 3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0188 |
3 | NA18983.hp2 NA19010.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.166-10562_166-1056 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995984 | |||||||
| chr20:43995985 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(231): Show |
235 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(232): Show |
intron_variant | MODIFIER | c.166-10562A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43995985 | |||||||
| chr20:43996031 | G | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0093 a0001c0001t0001g0094 others(10): Show |
13 | HG00639.hp2 HG01515.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-10516G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43996031 | |||||||
| chr20:43996076 | T | A | 32 | a0001c0001t0001g0061 a0001c0001t0001g0080 a0001c0001t0001g0121 others(29): Show |
32 | HG00741.hp2 HG02109.hp1 HG02280.hp2 others(29): Show |
intron_variant | MODIFIER | c.166-10471T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43996076 | |||||||
| chr20:43996393 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.166-10154T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43996393 | |||||||
| chr20:43996418 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0180 |
2 | NA18953.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.166-10129C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43996418 | |||||||
| chr20:43996796 | G | GC | 42 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(39): Show |
42 | HG00639.hp2 HG00733.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.166-9748dupC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43996796 | ||||||
| chr20:43996978 | G | A | 39 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(36): Show |
39 | HG00639.hp2 HG00733.hp1 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.166-9569G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43996978 | |||||||
| chr20:43997635 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0002g0147 |
2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.166-8912T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43997635 | |||||||
| chr20:43997913 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-8634C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43997913 | |||||||
| chr20:43998024 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.166-8523C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998024 | |||||||
| chr20:43998196 | G | A | 27 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0047 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-8351G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998196 | |||||||
| chr20:43998264 | A | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.166-8283A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998264 | |||||||
| chr20:43998464 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(193): Show |
196 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.166-8083C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998464 | |||||||
| chr20:43998497 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(189): Show |
192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.166-8050T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998497 | |||||||
| chr20:43998499 | A | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0285 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-8048A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998499 | |||||||
| chr20:43998557 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.166-7990C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998557 | |||||||
| chr20:43998580 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(163): Show |
166 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.166-7967A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998580 | |||||||
| chr20:43998648 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0205 |
2 | HG00642.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.166-7899T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998648 | |||||||
| chr20:43998719 | A | ACATC | 36 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0023 others(33): Show |
36 | HG00639.hp2 HG01175.hp2 HG01978.hp1 others(33): Show |
intron_variant | MODIFIER | c.166-7827_166-7824d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43998719 | ||||||
| chr20:43998720 | C | CATCT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0049 others(17): Show |
20 | HG00735.hp1 HG01106.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.166-7780_166-7777d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43998720 | ||||||
| chr20:43998720 | CATCT | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
124 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.166-7780_166-7777d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43998720 | ||||||
| chr20:43998720 | CATCTATC others(1): Show |
C | 12 | a0001c0001t0001g0040 a0001c0001t0001g0097 a0001c0001t0001g0112 others(9): Show |
12 | HG02132.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-7784_166-7777d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43998720 | ||||||
| chr20:43998720 | CATCTATC others(5): Show |
C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0139 a0001c0001t0001g0269 |
3 | HG01496.hp2 HG03017.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.166-7788_166-7777d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43998720 | ||||||
| chr20:43998720 | CATCTATC others(13): Show |
C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0196 |
2 | HG01255.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.166-7796_166-7777d others(22): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43998720 | ||||||
| chr20:43998721 | A | ATCCATCT others(1): Show |
7 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0104 others(4): Show |
7 | HG00673.hp2 HG00741.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-7824_166-7823i others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 43998721 | ||||||
| chr20:43998724 | T | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(41): Show |
44 | HG00408.hp2 HG00673.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.166-7823T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998724 | |||||||
| chr20:43998725 | A | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0023 others(32): Show |
35 | HG00639.hp2 HG01175.hp2 HG01978.hp1 others(32): Show |
intron_variant | MODIFIER | c.166-7822A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998725 | |||||||
| chr20:43998728 | T | C | 95 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0024 others(92): Show |
95 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.166-7819T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998728 | |||||||
| chr20:43998729 | A | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(41): Show |
44 | HG00408.hp2 HG00673.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.166-7818A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998729 | |||||||
| chr20:43998732 | T | C | 7 | a0001c0001t0001g0040 a0001c0001t0001g0126 a0001c0001t0001g0229 others(4): Show |
7 | HG02451.hp2 HG02647.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-7815T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998732 | |||||||
| chr20:43998733 | A | G | 95 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0024 others(92): Show |
95 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.166-7814A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998733 | |||||||
| chr20:43998736 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0139 |
2 | HG03017.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.166-7811T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998736 | |||||||
| chr20:43998737 | A | G | 7 | a0001c0001t0001g0040 a0001c0001t0001g0126 a0001c0001t0001g0229 others(4): Show |
7 | HG02451.hp2 HG02647.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-7810A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998737 | |||||||
| chr20:43998741 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0139 |
2 | HG03017.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.166-7806A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998741 | |||||||
| chr20:43998791 | A | G | 24 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0047 others(21): Show |
24 | HG00639.hp2 HG00673.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.166-7756A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998791 | |||||||
| chr20:43998879 | C | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0047 others(19): Show |
22 | HG00639.hp2 HG00673.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.166-7668C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43998879 | |||||||
| chr20:43999055 | C | T | 1 | a0001c0012t0003g0013 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.166-7492C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43999055 | |||||||
| chr20:43999185 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(202): Show |
206 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.166-7362A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43999185 | |||||||
| chr20:43999426 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.166-7121C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43999426 | |||||||
| chr20:43999537 | A | T | 21 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0047 others(18): Show |
21 | HG00639.hp2 HG00673.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-7010A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43999537 | |||||||
| chr20:43999540 | C | T | 1 | a0002c0002t0002g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-7007C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43999540 | |||||||
| chr20:43999794 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0270 |
2 | HG01261.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.166-6753G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43999794 | |||||||
| chr20:43999957 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(187): Show |
190 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.166-6590G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 43999957 | |||||||
| chr20:44000047 | G | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(147): Show |
150 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.166-6500G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44000047 | |||||||
| chr20:44000091 | T | A | 1 | a0001c0001t0001g0251 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.166-6456T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44000091 | |||||||
| chr20:44000157 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.166-6390G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44000157 | |||||||
| chr20:44000207 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.166-6340G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44000207 | |||||||
| chr20:44000292 | A | T | 3 | a0001c0001t0002g0022 a0002c0002t0001g0146 a0002c0002t0002g0131 |
3 | HG02145.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.166-6255A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44000292 | |||||||
| chr20:44000769 | G | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.166-5778G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44000769 | |||||||
| chr20:44000772 | A | C | 17 | a0001c0001t0001g0126 a0001c0001t0001g0148 a0001c0001t0001g0153 others(14): Show |
17 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-5775A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44000772 | |||||||
| chr20:44001097 | C | T | 183 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(180): Show |
183 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.166-5450C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001097 | |||||||
| chr20:44001263 | T | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-5284T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001263 | |||||||
| chr20:44001286 | C | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(168): Show |
171 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.166-5261C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001286 | |||||||
| chr20:44001417 | A | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(188): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.166-5130A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001417 | |||||||
| chr20:44001637 | G | T | 3 | a0001c0001t0001g0225 a0001c0001t0002g0103 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.166-4910G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001637 | |||||||
| chr20:44001671 | G | A | 15 | a0001c0001t0001g0126 a0001c0001t0001g0148 a0001c0001t0001g0153 others(12): Show |
15 | HG02145.hp2 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.166-4876G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001671 | |||||||
| chr20:44001677 | TCTCTGTG others(10): Show |
T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(189): Show |
192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.166-4853_166-4837d others(19): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 44001677 | ||||||
| chr20:44001704 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.166-4843A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001704 | |||||||
| chr20:44001718 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(189): Show |
192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.166-4829C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001718 | |||||||
| chr20:44001719 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(190): Show |
193 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.166-4828A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001719 | |||||||
| chr20:44001731 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0254 others(5): Show |
8 | HG00738.hp1 HG01361.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-4816C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001731 | |||||||
| chr20:44001826 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(202): Show |
206 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.166-4721T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001826 | |||||||
| chr20:44001847 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0195 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.166-4700G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44001847 | |||||||
| chr20:44002209 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0205 |
2 | HG00642.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.166-4338T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44002209 | |||||||
| chr20:44002242 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA18990.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.166-4305C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44002242 | |||||||
| chr20:44002281 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.166-4266T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44002281 | |||||||
| chr20:44002752 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.166-3795C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44002752 | |||||||
| chr20:44002753 | G | A | 28 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0126 others(25): Show |
28 | HG00642.hp1 HG02145.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.166-3794G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44002753 | |||||||
| chr20:44002789 | C | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0104 a0001c0001t0001g0228 others(1): Show |
4 | HG00673.hp2 HG03492.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-3758C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44002789 | |||||||
| chr20:44003061 | A | T | 28 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0126 others(25): Show |
28 | HG00642.hp1 HG02145.hp2 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.166-3486A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003061 | |||||||
| chr20:44003117 | C | T | 3 | a0001c0001t0002g0022 a0002c0002t0001g0146 a0002c0002t0002g0131 |
3 | HG02145.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.166-3430C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003117 | |||||||
| chr20:44003183 | CT | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0063 others(16): Show |
19 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.166-3343delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 44003183 | ||||||
| chr20:44003310 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.166-3237G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003310 | |||||||
| chr20:44003516 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.166-3031G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003516 | |||||||
| chr20:44003601 | C | T | 3 | a0001c0001t0002g0022 a0002c0002t0001g0146 a0002c0002t0002g0131 |
3 | HG02145.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.166-2946C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003601 | |||||||
| chr20:44003747 | TGTGTGGC others(7): Show |
T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0009g0145 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-2796_166-2783d others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 44003747 | ||||||
| chr20:44003766 | A | G | 4 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0009g0145 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-2781A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003766 | |||||||
| chr20:44003856 | A | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0007c0006t0001g0089 |
3 | HG02572.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.166-2691A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003856 | |||||||
| chr20:44003900 | G | A | 7 | a0001c0001t0001g0067 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG02132.hp1 NA18942.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-2647G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003900 | |||||||
| chr20:44003988 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.166-2559G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44003988 | |||||||
| chr20:44004044 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.166-2503G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44004044 | |||||||
| chr20:44004342 | G | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(195): Show |
198 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.166-2205G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44004342 | |||||||
| chr20:44004687 | A | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-1860A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44004687 | |||||||
| chr20:44005043 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.166-1504A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44005043 | |||||||
| chr20:44005319 | A | G | 3 | a0001c0001t0001g0243 a0001c0001t0002g0035 a0001c0001t0002g0036 |
3 | HG02886.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.166-1228A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44005319 | |||||||
| chr20:44005387 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0002g0103 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.166-1160A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44005387 | |||||||
| chr20:44005656 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(193): Show |
196 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.166-891C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44005656 | |||||||
| chr20:44005722 | C | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(199): Show |
202 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.166-825C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44005722 | |||||||
| chr20:44005739 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0094 a0001c0001t0002g0026 |
3 | HG00639.hp2 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.166-808A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44005739 | |||||||
| chr20:44005765 | G | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.166-782G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44005765 | |||||||
| chr20:44005835 | GGT | G | 16 | a0001c0001t0001g0067 a0001c0001t0001g0114 a0001c0001t0001g0122 others(13): Show |
16 | HG02132.hp1 NA18941.hp1 NA18942.hp1 others(13): Show |
intron_variant | MODIFIER | c.166-710_166-709del others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr20 | 44005835 | ||||||
| chr20:44005963 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.166-584T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44005963 | |||||||
| chr20:44006056 | C | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0255 a0001c0001t0001g0280 |
3 | HG02280.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.166-491C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44006056 | |||||||
| chr20:44006292 | C | A | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.166-255C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44006292 | |||||||
| chr20:44006292 | C | T | 1 | a0003c0003t0001g0064 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.166-255C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 2/8 | chr20 | 44006292 | |||||||
| chr20:44006836 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0166 a0001c0001t0001g0214 |
3 | HG00673.hp1 NA18962.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.411+44G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44006836 | |||||||
| chr20:44007263 | G | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0279 |
2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.411+471G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44007263 | |||||||
| chr20:44007320 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.411+528G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44007320 | |||||||
| chr20:44007394 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.411+602G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44007394 | |||||||
| chr20:44007408 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.411+616T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44007408 | |||||||
| chr20:44007830 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.411+1038T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44007830 | |||||||
| chr20:44007878 | G | A | 6 | a0001c0001t0001g0225 a0001c0001t0002g0022 a0001c0001t0002g0103 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+1086G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44007878 | |||||||
| chr20:44007980 | T | G | 1 | a0001c0001t0001g0203 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.411+1188T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44007980 | |||||||
| chr20:44008109 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18983.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.411+1317G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008109 | |||||||
| chr20:44008172 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.411+1380C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008172 | |||||||
| chr20:44008229 | T | C | 31 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0050 others(28): Show |
31 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.411+1437T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008229 | |||||||
| chr20:44008269 | G | C | 1 | a0001c0009t0002g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.411+1477G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008269 | |||||||
| chr20:44008541 | C | T | 17 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0055 others(14): Show |
17 | HG00673.hp2 HG00741.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.411+1749C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008541 | |||||||
| chr20:44008559 | CA | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(194): Show |
197 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.411+1780delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44008559 | ||||||
| chr20:44008570 | A | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(163): Show |
166 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.411+1778A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008570 | |||||||
| chr20:44008743 | T | TAGTCATG others(4): Show |
1 | a0001c0001t0001g0061 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.411+1952_411+1962d others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44008743 | ||||||
| chr20:44008759 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(200): Show |
203 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.411+1967G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008759 | |||||||
| chr20:44008830 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.411+2038C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008830 | |||||||
| chr20:44008840 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0225 others(11): Show |
14 | HG02145.hp2 HG02622.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.411+2048G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44008840 | |||||||
| chr20:44009018 | T | TCA | 5 | a0001c0001t0001g0023 a0001c0001t0001g0094 a0001c0001t0001g0258 others(2): Show |
5 | HG00639.hp2 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+2231_411+2232d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44009018 | ||||||
| chr20:44009025 | T | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(201): Show |
204 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.411+2233T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009025 | |||||||
| chr20:44009073 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.411+2281A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009073 | |||||||
| chr20:44009078 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.411+2286C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009078 | |||||||
| chr20:44009109 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0241 a0001c0001t0001g0242 others(2): Show |
5 | HG02257.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+2317C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009109 | |||||||
| chr20:44009140 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.411+2348G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009140 | |||||||
| chr20:44009258 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(145): Show |
148 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.411+2466G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009258 | |||||||
| chr20:44009314 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0094 a0001c0001t0001g0258 others(2): Show |
5 | HG00639.hp2 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+2522C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009314 | |||||||
| chr20:44009402 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.411+2610C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009402 | |||||||
| chr20:44009427 | C | G | 9 | a0001c0001t0001g0049 a0001c0001t0001g0056 a0001c0001t0001g0084 others(6): Show |
9 | HG01346.hp1 HG01496.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.411+2635C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009427 | |||||||
| chr20:44009510 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+2718G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009510 | |||||||
| chr20:44009525 | T | C | 18 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0055 others(15): Show |
18 | HG00673.hp2 HG00741.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.411+2733T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009525 | |||||||
| chr20:44009661 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0125 a0001c0001t0001g0172 others(1): Show |
4 | HG00408.hp1 HG02523.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+2869C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009661 | |||||||
| chr20:44009857 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.411+3065G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009857 | |||||||
| chr20:44009867 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.411+3075A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44009867 | |||||||
| chr20:44010006 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(200): Show |
203 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.411+3214G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010006 | |||||||
| chr20:44010026 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(166): Show |
169 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.411+3234G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010026 | |||||||
| chr20:44010145 | C | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0037 others(8): Show |
11 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.411+3353C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010145 | |||||||
| chr20:44010263 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(200): Show |
203 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.411+3471G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010263 | |||||||
| chr20:44010351 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+3559T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010351 | |||||||
| chr20:44010547 | G | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+3755G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010547 | |||||||
| chr20:44010643 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.411+3851C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010643 | |||||||
| chr20:44010710 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+3918C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010710 | |||||||
| chr20:44010726 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+3934C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010726 | |||||||
| chr20:44010882 | C | A | 3 | a0001c0001t0001g0243 a0001c0001t0002g0035 a0001c0001t0002g0036 |
3 | HG02886.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.411+4090C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010882 | |||||||
| chr20:44010920 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+4128G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44010920 | |||||||
| chr20:44011056 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+4264G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44011056 | |||||||
| chr20:44011429 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+4637T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44011429 | |||||||
| chr20:44011455 | GC | G | 17 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0055 others(14): Show |
17 | HG00673.hp2 HG00741.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.411+4667delC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44011455 | ||||||
| chr20:44011641 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+4849T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44011641 | |||||||
| chr20:44011703 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.411+4911T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44011703 | |||||||
| chr20:44011707 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.411+4915C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44011707 | |||||||
| chr20:44011831 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.411+5039G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44011831 | |||||||
| chr20:44011864 | C | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0047 others(17): Show |
20 | HG00639.hp2 HG00673.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.411+5072C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44011864 | |||||||
| chr20:44011973 | T | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(205): Show |
208 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.411+5181T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44011973 | |||||||
| chr20:44012002 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.411+5210C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44012002 | |||||||
| chr20:44012014 | A | C | 3 | a0001c0001t0001g0243 a0001c0001t0002g0035 a0001c0001t0002g0036 |
3 | HG02886.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.411+5222A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44012014 | |||||||
| chr20:44012019 | A | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+5227A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44012019 | |||||||
| chr20:44012501 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+5709T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44012501 | |||||||
| chr20:44012516 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+5724T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44012516 | |||||||
| chr20:44012742 | T | C | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+5950T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44012742 | |||||||
| chr20:44012834 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.411+6042C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44012834 | |||||||
| chr20:44013081 | G | A | 1 | a0002c0002t0002g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.411+6289G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013081 | |||||||
| chr20:44013251 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+6459G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013251 | |||||||
| chr20:44013309 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+6517C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013309 | |||||||
| chr20:44013417 | A | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+6625A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013417 | |||||||
| chr20:44013444 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.411+6652G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013444 | |||||||
| chr20:44013796 | A | G | 1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.411+7004A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013796 | |||||||
| chr20:44013827 | G | A | 10 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(7): Show |
10 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.411+7035G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013827 | |||||||
| chr20:44013923 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.411+7131A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013923 | |||||||
| chr20:44013992 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.411+7200T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013992 | |||||||
| chr20:44013993 | A | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+7201A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44013993 | |||||||
| chr20:44014056 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+7264G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014056 | |||||||
| chr20:44014094 | G | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0102 a0001c0001t0001g0200 |
3 | NA18949.hp2 NA18981.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.411+7302G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014094 | |||||||
| chr20:44014104 | G | A | 21 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0047 others(18): Show |
21 | HG00639.hp2 HG00673.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.411+7312G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014104 | |||||||
| chr20:44014128 | C | CA | 152 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(149): Show |
153 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(150): Show |
intron_variant | MODIFIER | c.411+7363dupA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44014128 | ||||||
| chr20:44014128 | C | CAA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0041 others(38): Show |
41 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.411+7362_411+7363d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44014128 | ||||||
| chr20:44014128 | CA | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0097 a0001c0001t0001g0125 others(9): Show |
12 | HG00408.hp1 HG01255.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.411+7363delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44014128 | ||||||
| chr20:44014128 | CAAAAAA | C | 9 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(6): Show |
9 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.411+7358_411+7363d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44014128 | ||||||
| chr20:44014128 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0004g0162 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.411+7352_411+7363d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44014128 | ||||||
| chr20:44014259 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.411+7467T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014259 | |||||||
| chr20:44014274 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.411+7482G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014274 | |||||||
| chr20:44014289 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
221 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.411+7497T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014289 | |||||||
| chr20:44014402 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0002g0142 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.411+7610G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014402 | |||||||
| chr20:44014564 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+7772T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014564 | |||||||
| chr20:44014703 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0270 |
2 | HG01261.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.411+7911C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014703 | |||||||
| chr20:44014713 | A | G | 3 | a0001c0001t0009g0145 a0005c0004t0002g0019 a0005c0004t0002g0020 |
3 | HG02717.hp1 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.411+7921A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014713 | |||||||
| chr20:44014715 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+7923T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014715 | |||||||
| chr20:44014761 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+7969C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014761 | |||||||
| chr20:44014801 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+8009G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44014801 | |||||||
| chr20:44015213 | G | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0274 |
2 | NA18971.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.411+8421G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015213 | |||||||
| chr20:44015321 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.411+8529C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015321 | |||||||
| chr20:44015354 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.411+8562G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015354 | |||||||
| chr20:44015364 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(214): Show |
218 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.411+8572G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015364 | |||||||
| chr20:44015727 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+8935G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015727 | |||||||
| chr20:44015945 | C | T | 10 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.411+9153C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015945 | |||||||
| chr20:44015970 | A | C | 2 | a0001c0001t0001g0258 a0001c0001t0002g0142 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.411+9178A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015970 | |||||||
| chr20:44015974 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.411+9182C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015974 | |||||||
| chr20:44015984 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+9192C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44015984 | |||||||
| chr20:44016027 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.411+9235G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44016027 | |||||||
| chr20:44016095 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+9303C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44016095 | |||||||
| chr20:44016413 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+9621T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44016413 | |||||||
| chr20:44016437 | T | C | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+9645T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44016437 | |||||||
| chr20:44016691 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0110 a0001c0001t0002g0085 others(5): Show |
8 | HG01175.hp2 HG01346.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+9899C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44016691 | |||||||
| chr20:44016738 | A | C | 18 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0055 others(15): Show |
18 | HG00673.hp2 HG00741.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.411+9946A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44016738 | |||||||
| chr20:44017292 | C | T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0282 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+10500C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44017292 | |||||||
| chr20:44017318 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+10526C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44017318 | |||||||
| chr20:44017420 | T | G | 3 | a0001c0001t0009g0145 a0005c0004t0002g0019 a0005c0004t0002g0020 |
3 | HG02717.hp1 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.411+10628T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44017420 | |||||||
| chr20:44017460 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+10668G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44017460 | |||||||
| chr20:44017587 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+10795T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44017587 | |||||||
| chr20:44017795 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(170): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.411+11003A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44017795 | |||||||
| chr20:44017956 | A | T | 3 | a0001c0001t0001g0243 a0001c0001t0002g0035 a0001c0001t0002g0036 |
3 | HG02886.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.411+11164A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44017956 | |||||||
| chr20:44018067 | T | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+11275T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018067 | |||||||
| chr20:44018094 | G | T | 3 | a0001c0001t0001g0243 a0001c0001t0002g0035 a0001c0001t0002g0036 |
3 | HG02886.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.411+11302G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018094 | |||||||
| chr20:44018192 | C | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(154): Show |
157 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.411+11400C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018192 | |||||||
| chr20:44018194 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(154): Show |
157 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.411+11402G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018194 | |||||||
| chr20:44018244 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+11452T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018244 | |||||||
| chr20:44018373 | C | G | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.411+11581C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018373 | |||||||
| chr20:44018398 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0144 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.411+11606T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018398 | |||||||
| chr20:44018399 | A | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+11607A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018399 | |||||||
| chr20:44018410 | G | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0144 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.411+11618G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018410 | |||||||
| chr20:44018552 | A | C | 1 | a0001c0001t0001g0050 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.411+11760A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018552 | |||||||
| chr20:44018599 | C | T | 4 | a0001c0001t0003g0021 a0001c0001t0003g0143 a0001c0001t0003g0281 others(1): Show |
4 | HG02145.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+11807C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018599 | |||||||
| chr20:44018650 | A | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+11858A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018650 | |||||||
| chr20:44018673 | A | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+11881A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018673 | |||||||
| chr20:44018751 | G | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(200): Show |
203 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.411+11959G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018751 | |||||||
| chr20:44018921 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0094 a0001c0001t0002g0026 |
3 | HG00639.hp2 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.411+12129A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018921 | |||||||
| chr20:44018950 | C | G | 2 | a0001c0001t0001g0201 a0001c0001t0004g0161 |
2 | NA18946.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.411+12158C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018950 | |||||||
| chr20:44018996 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.411+12204G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44018996 | |||||||
| chr20:44019003 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(200): Show |
203 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.411+12211G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019003 | |||||||
| chr20:44019080 | TTGAC | T | 4 | a0001c0001t0001g0232 a0001c0001t0009g0145 a0005c0004t0002g0019 others(1): Show |
4 | HG01975.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+12316_411+1231 others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44019080 | ||||||
| chr20:44019097 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12305T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019097 | |||||||
| chr20:44019103 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.411+12311A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019103 | |||||||
| chr20:44019105 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12313T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019105 | |||||||
| chr20:44019110 | GAAA | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12321_411+1232 others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44019110 | ||||||
| chr20:44019115 | A | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12323A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019115 | |||||||
| chr20:44019119 | AT | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12328delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019119 | |||||||
| chr20:44019176 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.411+12384T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019176 | |||||||
| chr20:44019208 | A | G | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12416A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019208 | |||||||
| chr20:44019284 | C | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12492C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019284 | |||||||
| chr20:44019386 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.411+12594C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019386 | |||||||
| chr20:44019480 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+12688C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019480 | |||||||
| chr20:44019556 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12764T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019556 | |||||||
| chr20:44019558 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+12766T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019558 | |||||||
| chr20:44019873 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0002g0103 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.411+13081C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019873 | |||||||
| chr20:44019964 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0225 others(11): Show |
14 | HG02145.hp2 HG02622.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.411+13172G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019964 | |||||||
| chr20:44019977 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(194): Show |
197 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.411+13185G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44019977 | |||||||
| chr20:44020050 | G | A | 1 | a0001c0001t0001g0005 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.411+13258G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020050 | |||||||
| chr20:44020609 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0279 |
2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.411+13817G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020609 | |||||||
| chr20:44020774 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.411+13982T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020774 | |||||||
| chr20:44020852 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.411+14060G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020852 | |||||||
| chr20:44020867 | G | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.411+14075G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020867 | |||||||
| chr20:44020885 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.411+14093T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020885 | |||||||
| chr20:44020893 | C | A | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.411+14101C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020893 | |||||||
| chr20:44020904 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0002g0142 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.411+14112G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020904 | |||||||
| chr20:44020947 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.411+14155C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44020947 | |||||||
| chr20:44021042 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.411+14250C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021042 | |||||||
| chr20:44021049 | C | T | 1 | a0001c0001t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.411+14257C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021049 | |||||||
| chr20:44021202 | T | A | 1 | a0001c0001t0010g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.411+14410T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021202 | |||||||
| chr20:44021349 | G | T | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.411+14557G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021349 | |||||||
| chr20:44021450 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.411+14658T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021450 | |||||||
| chr20:44021494 | C | A | 1 | a0001c0001t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.411+14702C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021494 | |||||||
| chr20:44021522 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.411+14730T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021522 | |||||||
| chr20:44021606 | T | C | 3 | a0001c0001t0001g0225 a0001c0001t0002g0103 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.411+14814T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021606 | |||||||
| chr20:44021651 | A | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(171): Show |
175 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.411+14859A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021651 | |||||||
| chr20:44021711 | C | A | 1 | a0001c0001t0001g0062 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.411+14919C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021711 | |||||||
| chr20:44021775 | C | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+14983C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021775 | |||||||
| chr20:44021802 | A | AT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(164): Show |
168 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.411+15025dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44021802 | ||||||
| chr20:44021802 | AT | A | 21 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0055 others(18): Show |
21 | HG00673.hp2 HG00741.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.411+15025delT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44021802 | ||||||
| chr20:44021899 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.411+15107G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44021899 | |||||||
| chr20:44022030 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+15238C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022030 | |||||||
| chr20:44022053 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+15261G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022053 | |||||||
| chr20:44022062 | A | G | 4 | a0001c0001t0001g0258 a0001c0001t0002g0141 a0001c0001t0002g0142 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+15270A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022062 | |||||||
| chr20:44022089 | T | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+15297T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022089 | |||||||
| chr20:44022240 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+15448C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022240 | |||||||
| chr20:44022269 | G | A | 4 | a0001c0001t0001g0258 a0001c0001t0002g0141 a0001c0001t0002g0142 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+15477G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022269 | |||||||
| chr20:44022290 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0266 |
2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.411+15498C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022290 | |||||||
| chr20:44022298 | ACTTTAGT others(4): Show |
A | 1 | a0001c0001t0010g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.411+15507_411+1551 others(15): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022298 | |||||||
| chr20:44022314 | T | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0258 a0001c0001t0002g0141 others(2): Show |
5 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+15522T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022314 | |||||||
| chr20:44022316 | G | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0225 a0001c0001t0002g0032 others(2): Show |
5 | HG01167.hp1 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+15524G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022316 | |||||||
| chr20:44022317 | T | A | 4 | a0001c0001t0001g0258 a0001c0001t0002g0141 a0001c0001t0002g0142 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+15525T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022317 | |||||||
| chr20:44022463 | T | G | 4 | a0001c0001t0001g0258 a0001c0001t0002g0141 a0001c0001t0002g0142 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+15671T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022463 | |||||||
| chr20:44022640 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(154): Show |
158 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.411+15848G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022640 | |||||||
| chr20:44022766 | C | T | 4 | a0001c0001t0001g0258 a0001c0001t0002g0141 a0001c0001t0002g0142 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+15974C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022766 | |||||||
| chr20:44022811 | T | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+16019T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022811 | |||||||
| chr20:44022824 | A | C | 4 | a0001c0001t0001g0258 a0001c0001t0002g0141 a0001c0001t0002g0142 others(1): Show |
4 | HG02258.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+16032A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022824 | |||||||
| chr20:44022870 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.411+16078G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022870 | |||||||
| chr20:44022917 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.411+16125T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022917 | |||||||
| chr20:44022941 | C | A | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411+16149C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022941 | |||||||
| chr20:44022960 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.411+16168C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022960 | |||||||
| chr20:44022961 | G | A | 1 | a0001c0001t0004g0162 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.411+16169G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44022961 | |||||||
| chr20:44023005 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0258 a0001c0001t0001g0270 others(1): Show |
4 | HG01261.hp2 HG01884.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+16213G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023005 | |||||||
| chr20:44023022 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.411+16230C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023022 | |||||||
| chr20:44023136 | A | C | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411+16344A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023136 | |||||||
| chr20:44023236 | CTGGCCAA others(5): Show |
C | 1 | a0001c0001t0002g0079 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.411+16447_411+1645 others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44023236 | ||||||
| chr20:44023303 | AC | A | 14 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0038 others(11): Show |
14 | HG02622.hp1 HG02622.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.411+16513delC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44023303 | ||||||
| chr20:44023311 | TC | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0186 a0001c0001t0010g0171 |
3 | NA18987.hp1 NA18987.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.411+16522delC | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44023311 | ||||||
| chr20:44023378 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.411+16586C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023378 | |||||||
| chr20:44023407 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.411+16615G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023407 | |||||||
| chr20:44023431 | G | GAAAAA | 24 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0055 others(21): Show |
24 | HG00639.hp2 HG00673.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.411+16654_411+1665 others(9): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44023431 | ||||||
| chr20:44023431 | G | GAAAAAAA others(1): Show |
9 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0225 others(6): Show |
9 | HG02622.hp1 HG02622.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.411+16651_411+1665 others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44023431 | ||||||
| chr20:44023431 | G | GGAAA | 3 | a0001c0001t0001g0127 a0001c0001t0001g0186 a0001c0001t0001g0201 |
3 | HG03209.hp2 NA18946.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.411+16639_411+1664 others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023431 | |||||||
| chr20:44023431 | G | GGAAAA | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
157 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.411+16639_411+1664 others(9): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023431 | |||||||
| chr20:44023431 | G | GGAAAAA | 7 | a0001c0001t0001g0052 a0001c0001t0001g0088 a0001c0001t0001g0144 others(4): Show |
7 | HG02071.hp1 HG02572.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+16639_411+1664 others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023431 | |||||||
| chr20:44023431 | G | GGGAAAAA others(3): Show |
1 | a0005c0004t0002g0020 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.411+16639_411+1664 others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023431 | |||||||
| chr20:44023451 | G | A | 1 | a0004c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.411+16659G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023451 | |||||||
| chr20:44023457 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.411+16665A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023457 | |||||||
| chr20:44023667 | G | A | 1 | a0001c0001t0008g0108 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.411+16875G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023667 | |||||||
| chr20:44023689 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.411+16897A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023689 | |||||||
| chr20:44023696 | C | G | 3 | a0001c0001t0002g0022 a0002c0002t0001g0146 a0002c0002t0002g0131 |
3 | HG02145.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.411+16904C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023696 | |||||||
| chr20:44023983 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.411+17191C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44023983 | |||||||
| chr20:44024284 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0038 others(9): Show |
12 | HG02622.hp1 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.411+17492C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44024284 | |||||||
| chr20:44024293 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(194): Show |
198 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.411+17501A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44024293 | |||||||
| chr20:44024308 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0279 |
2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.411+17516T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44024308 | |||||||
| chr20:44024408 | C | CTTTATG | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(182): Show |
186 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.411+17617_411+1762 others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44024408 | ||||||
| chr20:44024433 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.411+17641G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44024433 | |||||||
| chr20:44024778 | GATAATAT others(5): Show |
G | 12 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0038 others(9): Show |
12 | HG02622.hp1 HG02622.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.411+18002_411+1801 others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44024778 | ||||||
| chr20:44024795 | TATATACA others(10): Show |
T | 3 | a0001c0001t0002g0022 a0002c0002t0001g0146 a0002c0002t0002g0131 |
3 | HG02145.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.411+18024_411+1804 others(21): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44024795 | ||||||
| chr20:44025047 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411+18255A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025047 | |||||||
| chr20:44025094 | C | A | 15 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0038 others(12): Show |
15 | HG02145.hp2 HG02622.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.411+18302C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025094 | |||||||
| chr20:44025153 | A | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0183 a0001c0001t0001g0220 |
3 | NA18952.hp2 NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.411+18361A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025153 | |||||||
| chr20:44025327 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+18535G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025327 | |||||||
| chr20:44025337 | C | T | 1 | a0003c0003t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.411+18545C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025337 | |||||||
| chr20:44025339 | C | G | 1 | a0001c0012t0003g0013 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.411+18547C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025339 | |||||||
| chr20:44025353 | C | T | 3 | a0001c0001t0001g0258 a0001c0001t0002g0136 a0001c0001t0002g0142 |
3 | HG02615.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.411+18561C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025353 | |||||||
| chr20:44025453 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(157): Show |
161 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.411+18661A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025453 | |||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0002g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0001g0264 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
72 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0014 others(69): Show |
72 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0001g0071 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
8 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0094 others(5): Show |
8 | HG00323.hp1 HG00639.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0001g0006 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1771): Show |
1 | a0001c0001t0001g0043 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1782): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0001g0228 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
3 | a0001c0001t0001g0258 a0001c0001t0002g0136 a0001c0001t0002g0142 |
3 | HG02615.hp2 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0001g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
18 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0038 others(15): Show |
18 | HG02451.hp2 HG02559.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(162): Show |
166 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0001g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0001g0090 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
1 | a0001c0001t0001g0109 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
4 | a0001c0001t0001g0130 a0001c0001t0001g0144 a0001c0001t0001g0237 others(1): Show |
4 | HG01261.hp2 HG01884.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025526 | T | TGCTATAT others(1770): Show |
2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+18736_411+1873 others(1781): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44025526 | ||||||
| chr20:44025577 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0066 |
2 | HG01099.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.411+18785C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025577 | |||||||
| chr20:44025707 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(180): Show |
184 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.411+18915T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025707 | |||||||
| chr20:44025920 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
157 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.411+19128G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025920 | |||||||
| chr20:44025924 | A | G | 20 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0055 others(17): Show |
20 | HG00639.hp2 HG00673.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.411+19132A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025924 | |||||||
| chr20:44025982 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.411+19190G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44025982 | |||||||
| chr20:44026079 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0154 a0001c0001t0001g0178 |
3 | NA18954.hp2 NA19002.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.411+19287G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026079 | |||||||
| chr20:44026209 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.411+19417G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026209 | |||||||
| chr20:44026214 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0002g0103 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.411+19422G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026214 | |||||||
| chr20:44026227 | T | TTATATAT others(9): Show |
1 | a0001c0001t0001g0265 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.411+19435_411+1943 others(20): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026227 | |||||||
| chr20:44026228 | G | GAGATATA others(17): Show |
1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.411+19437_411+1943 others(28): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GAT | 7 | a0001c0001t0001g0203 a0001c0001t0001g0243 a0001c0001t0002g0035 others(4): Show |
7 | HG02258.hp2 HG02886.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+19456_411+1945 others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATAT | 7 | a0001c0001t0001g0055 a0001c0001t0001g0201 a0001c0001t0001g0223 others(4): Show |
7 | HG00673.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.411+19452_411+1945 others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(1): Show |
13 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0176 others(10): Show |
13 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.411+19450_411+1945 others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(3): Show |
5 | a0001c0001t0001g0038 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+19448_411+1945 others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(5): Show |
2 | a0001c0001t0001g0023 a0001c0001t0002g0015 |
2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.411+19446_411+1945 others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(7): Show |
13 | a0001c0001t0001g0018 a0001c0001t0001g0037 a0001c0001t0001g0052 others(10): Show |
13 | HG00323.hp2 HG01175.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.411+19444_411+1945 others(18): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(9): Show |
17 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0041 others(14): Show |
17 | HG00735.hp2 HG01261.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.411+19442_411+1945 others(20): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(11): Show |
25 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(22): Show |
25 | HG00639.hp1 HG01167.hp1 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.411+19440_411+1945 others(22): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(13): Show |
23 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0031 others(20): Show |
23 | HG00438.hp1 HG00597.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.411+19438_411+1945 others(24): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(15): Show |
22 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0048 others(19): Show |
22 | HG00673.hp1 HG01106.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.411+19457_411+1945 others(26): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(17): Show |
15 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0114 others(12): Show |
15 | HG01099.hp2 HG02109.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.411+19457_411+1945 others(28): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(19): Show |
13 | a0001c0001t0001g0034 a0001c0001t0001g0105 a0001c0001t0001g0109 others(10): Show |
13 | HG00733.hp2 HG02055.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.411+19457_411+1945 others(30): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(21): Show |
3 | a0001c0001t0001g0090 a0001c0001t0001g0174 a0001c0001t0001g0287 |
3 | HG00642.hp1 HG02717.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.411+19457_411+1945 others(32): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(23): Show |
14 | a0001c0001t0001g0016 a0001c0001t0001g0073 a0001c0001t0001g0156 others(11): Show |
14 | HG00408.hp2 HG01361.hp2 HG02683.hp1 others(11): Show |
intron_variant | MODIFIER | c.411+19457_411+1945 others(34): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(25): Show |
5 | a0001c0001t0001g0068 a0001c0001t0001g0134 a0001c0001t0001g0225 others(2): Show |
5 | HG02056.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+19457_411+1945 others(36): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | GATATATA others(29): Show |
2 | a0001c0001t0001g0111 a0002c0002t0002g0131 |
2 | HG01169.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.411+19457_411+1945 others(40): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026228 | ||||||
| chr20:44026228 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.411+19436G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026228 | |||||||
| chr20:44026229 | A | ATATATAT others(16): Show |
1 | a0001c0001t0010g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.411+19457_411+1945 others(27): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026229 | ||||||
| chr20:44026242 | T | TATATATT others(13): Show |
1 | a0001c0001t0001g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.411+19456_411+1945 others(24): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026242 | ||||||
| chr20:44026248 | T | TATATATA others(25): Show |
1 | a0001c0001t0002g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.411+19457_411+1945 others(36): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026248 | ||||||
| chr20:44026248 | T | TATATATA others(29): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0229 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.411+19457_411+1945 others(40): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026248 | ||||||
| chr20:44026248 | T | TATATATA others(33): Show |
2 | a0001c0001t0002g0236 a0001c0001t0002g0268 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.411+19457_411+1945 others(44): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026248 | ||||||
| chr20:44026248 | T | TATATATA others(35): Show |
1 | a0001c0001t0001g0257 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411+19457_411+1945 others(46): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026248 | ||||||
| chr20:44026248 | T | TATATATA others(49): Show |
1 | a0001c0001t0002g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.411+19457_411+1945 others(60): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44026248 | ||||||
| chr20:44026250 | G | C | 10 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(7): Show |
10 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.411+19458G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026250 | |||||||
| chr20:44026250 | G | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(179): Show |
182 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.411+19458G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026250 | |||||||
| chr20:44026252 | C | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(169): Show |
172 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.411+19460C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026252 | |||||||
| chr20:44026254 | C | T | 153 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(150): Show |
153 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.411+19462C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026254 | |||||||
| chr20:44026340 | TA | T | 3 | a0001c0001t0001g0243 a0001c0001t0002g0035 a0001c0001t0002g0036 |
3 | HG02886.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.411+19549delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026340 | |||||||
| chr20:44026484 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.411+19692G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026484 | |||||||
| chr20:44026639 | G | C | 1 | a0001c0001t0002g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.411+19847G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026639 | |||||||
| chr20:44026942 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.411+20150C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026942 | |||||||
| chr20:44026978 | T | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | NA18944.hp2 NA18949.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+20186T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44026978 | |||||||
| chr20:44027035 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+20243G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027035 | |||||||
| chr20:44027308 | G | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0038 others(13): Show |
16 | HG00733.hp1 HG02145.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.411+20516G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027308 | |||||||
| chr20:44027399 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.411+20607G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027399 | |||||||
| chr20:44027410 | C | G | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+20618C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027410 | |||||||
| chr20:44027603 | T | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0038 others(6): Show |
9 | HG02818.hp2 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.411+20811T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027603 | |||||||
| chr20:44027609 | A | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0276 |
2 | NA18969.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.411+20817A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027609 | |||||||
| chr20:44027616 | A | G | 1 | a0003c0003t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.411+20824A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027616 | |||||||
| chr20:44027670 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(187): Show |
191 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.411+20878C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027670 | |||||||
| chr20:44027765 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.411+20973G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027765 | |||||||
| chr20:44027845 | A | T | 1 | a0001c0001t0005g0272 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.411+21053A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44027845 | |||||||
| chr20:44028137 | G | C | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.411+21345G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44028137 | |||||||
| chr20:44028309 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.411+21517G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44028309 | |||||||
| chr20:44028369 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.411+21577G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44028369 | |||||||
| chr20:44028511 | C | T | 44 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0034 others(41): Show |
44 | HG01069.hp2 HG01175.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.411+21719C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44028511 | |||||||
| chr20:44028633 | TACAG | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(179): Show |
183 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.411+21849_411+2185 others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44028633 | ||||||
| chr20:44028685 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(179): Show |
183 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.411+21893A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44028685 | |||||||
| chr20:44028908 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.411+22116T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44028908 | |||||||
| chr20:44028951 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411+22159G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44028951 | |||||||
| chr20:44029060 | G | A | 12 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0176 others(9): Show |
12 | HG00673.hp2 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.412-22246G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029060 | |||||||
| chr20:44029201 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.412-22105T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029201 | |||||||
| chr20:44029222 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.412-22084T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029222 | |||||||
| chr20:44029312 | C | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.412-21994C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029312 | |||||||
| chr20:44029344 | T | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.412-21962T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029344 | |||||||
| chr20:44029387 | C | G | 3 | a0001c0001t0001g0225 a0001c0001t0002g0103 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.412-21919C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029387 | |||||||
| chr20:44029443 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.412-21863A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029443 | |||||||
| chr20:44029541 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
157 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.412-21765G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029541 | |||||||
| chr20:44029634 | A | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
171 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.412-21672A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029634 | |||||||
| chr20:44029687 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.412-21619C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029687 | |||||||
| chr20:44029891 | G | A | 1 | a0003c0003t0001g0004 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-21415G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029891 | |||||||
| chr20:44029946 | T | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(159): Show |
163 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.412-21360T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029946 | |||||||
| chr20:44029973 | C | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(163): Show |
167 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.412-21333C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44029973 | |||||||
| chr20:44030119 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(166): Show |
170 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.412-21187A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44030119 | |||||||
| chr20:44030742 | G | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0094 a0001c0001t0001g0225 others(6): Show |
9 | HG00639.hp2 HG00733.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-20564G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44030742 | |||||||
| chr20:44030979 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.412-20327G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44030979 | |||||||
| chr20:44031200 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.412-20106C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031200 | |||||||
| chr20:44031248 | T | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(160): Show |
164 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.412-20058T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031248 | |||||||
| chr20:44031261 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0094 a0001c0001t0002g0026 |
3 | HG00639.hp2 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.412-20045G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031261 | |||||||
| chr20:44031434 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0221 others(5): Show |
8 | HG00738.hp2 HG01361.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.412-19872T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031434 | |||||||
| chr20:44031543 | T | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-19763T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031543 | |||||||
| chr20:44031603 | C | G | 7 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-19703C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031603 | |||||||
| chr20:44031646 | C | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(168): Show |
172 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.412-19660C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031646 | |||||||
| chr20:44031796 | A | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(195): Show |
199 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.412-19510A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031796 | |||||||
| chr20:44031909 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(232): Show |
236 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.412-19397C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44031909 | |||||||
| chr20:44032083 | A | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0282 others(3): Show |
6 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-19223A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44032083 | |||||||
| chr20:44032176 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
13 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.412-19130G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44032176 | |||||||
| chr20:44032189 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0282 others(3): Show |
6 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-19117G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44032189 | |||||||
| chr20:44032375 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.412-18931C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44032375 | |||||||
| chr20:44032731 | T | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0282 others(3): Show |
6 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-18575T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44032731 | |||||||
| chr20:44032864 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(195): Show |
199 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(196): Show |
intron_variant | MODIFIER | c.412-18442T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44032864 | |||||||
| chr20:44032890 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-18416G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44032890 | |||||||
| chr20:44033231 | T | C | 1 | a0001c0001t0001g0005 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.412-18075T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44033231 | |||||||
| chr20:44033448 | T | A | 1 | a0001c0001t0002g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.412-17858T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44033448 | |||||||
| chr20:44033643 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0260 a0001c0012t0003g0013 |
3 | HG01069.hp2 HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.412-17663G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44033643 | |||||||
| chr20:44033681 | CA | C | 21 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0034 others(18): Show |
21 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.412-17609delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44033681 | ||||||
| chr20:44033715 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0166 a0001c0001t0001g0201 |
3 | NA18946.hp2 NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.412-17591C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44033715 | |||||||
| chr20:44033736 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(156): Show |
160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.412-17570C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44033736 | |||||||
| chr20:44033923 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0066 |
2 | HG01099.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.412-17383G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44033923 | |||||||
| chr20:44033927 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-17379C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44033927 | |||||||
| chr20:44033936 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-17370C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44033936 | |||||||
| chr20:44034093 | C | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0144 a0001c0001t0001g0237 others(3): Show |
6 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-17213C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034093 | |||||||
| chr20:44034150 | A | G | 27 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0034 others(24): Show |
27 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.412-17156A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034150 | |||||||
| chr20:44034237 | C | G | 1 | a0001c0001t0011g0168 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.412-17069C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034237 | |||||||
| chr20:44034239 | G | GT | 9 | a0001c0001t0001g0227 a0001c0001t0001g0258 a0001c0001t0002g0015 others(6): Show |
9 | HG01175.hp2 HG02615.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.412-17056dupT | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44034239 | ||||||
| chr20:44034357 | G | T | 26 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0034 others(23): Show |
26 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.412-16949G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034357 | |||||||
| chr20:44034386 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.412-16920C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034386 | |||||||
| chr20:44034531 | T | C | 7 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-16775T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034531 | |||||||
| chr20:44034556 | A | G | 1 | a0003c0003t0001g0004 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-16750A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034556 | |||||||
| chr20:44034562 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-16744G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034562 | |||||||
| chr20:44034854 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.412-16452T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034854 | |||||||
| chr20:44034886 | A | G | 13 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(10): Show |
13 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.412-16420A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034886 | |||||||
| chr20:44034923 | C | T | 1 | a0003c0003t0001g0003 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.412-16383C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034923 | |||||||
| chr20:44034957 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0144 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.412-16349T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44034957 | |||||||
| chr20:44035026 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(158): Show |
162 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.412-16280C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035026 | |||||||
| chr20:44035075 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-16231G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035075 | |||||||
| chr20:44035187 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-16119G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035187 | |||||||
| chr20:44035202 | C | T | 7 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-16104C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035202 | |||||||
| chr20:44035253 | C | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0038 others(12): Show |
15 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.412-16053C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035253 | |||||||
| chr20:44035314 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.412-15992A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035314 | |||||||
| chr20:44035357 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.412-15949G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035357 | |||||||
| chr20:44035456 | C | T | 1 | a0002c0002t0002g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.412-15850C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035456 | |||||||
| chr20:44035513 | T | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0283 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.412-15793T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035513 | |||||||
| chr20:44035625 | T | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0282 others(3): Show |
6 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-15681T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035625 | |||||||
| chr20:44035730 | T | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(2): Show |
5 | HG02451.hp2 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-15576T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035730 | |||||||
| chr20:44035863 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.412-15443A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035863 | |||||||
| chr20:44035960 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.412-15346C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035960 | |||||||
| chr20:44035991 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.412-15315G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035991 | |||||||
| chr20:44035997 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.412-15309G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44035997 | |||||||
| chr20:44036224 | C | T | 2 | a0001c0001t0002g0129 a0004c0005t0001g0106 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.412-15082C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036224 | |||||||
| chr20:44036398 | C | A | 2 | a0001c0001t0002g0129 a0004c0005t0001g0106 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.412-14908C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036398 | |||||||
| chr20:44036403 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(185): Show |
189 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.412-14903G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036403 | |||||||
| chr20:44036507 | T | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(188): Show |
192 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.412-14799T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036507 | |||||||
| chr20:44036561 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-14745C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036561 | |||||||
| chr20:44036564 | T | A | 3 | a0001c0001t0002g0129 a0001c0001t0002g0284 a0004c0005t0001g0106 |
3 | HG02055.hp2 HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.412-14742T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036564 | |||||||
| chr20:44036573 | C | T | 24 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0034 others(21): Show |
24 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.412-14733C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036573 | |||||||
| chr20:44036644 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0030 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.412-14662C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036644 | |||||||
| chr20:44036646 | T | G | 2 | a0001c0012t0003g0013 a0003c0003t0001g0003 |
2 | HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.412-14660T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036646 | |||||||
| chr20:44036900 | G | A | 8 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(5): Show |
8 | HG02451.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.412-14406G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44036900 | |||||||
| chr20:44037057 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-14249C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037057 | |||||||
| chr20:44037093 | A | G | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-14213A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037093 | |||||||
| chr20:44037203 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.412-14103C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037203 | |||||||
| chr20:44037212 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.412-14094C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037212 | |||||||
| chr20:44037440 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.412-13866T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037440 | |||||||
| chr20:44037593 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.412-13713A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037593 | |||||||
| chr20:44037666 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.412-13640C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037666 | |||||||
| chr20:44037704 | A | G | 6 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0074 others(3): Show |
6 | HG00597.hp2 NA18942.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-13602A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037704 | |||||||
| chr20:44037723 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(200): Show |
204 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.412-13583A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037723 | |||||||
| chr20:44037726 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0093 a0001c0001t0001g0264 others(2): Show |
5 | HG00733.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-13580C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037726 | |||||||
| chr20:44037835 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(183): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.412-13471C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037835 | |||||||
| chr20:44037837 | A | G | 13 | a0001c0001t0001g0126 a0001c0001t0001g0224 a0001c0001t0001g0229 others(10): Show |
13 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.412-13469A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037837 | |||||||
| chr20:44037888 | G | C | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-13418G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44037888 | |||||||
| chr20:44038055 | A | C | 9 | a0001c0001t0001g0224 a0001c0001t0001g0258 a0001c0001t0002g0015 others(6): Show |
9 | HG02486.hp1 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-13251A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038055 | |||||||
| chr20:44038090 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.412-13216T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038090 | |||||||
| chr20:44038125 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-13181G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038125 | |||||||
| chr20:44038253 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-13053C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038253 | |||||||
| chr20:44038254 | G | A | 7 | a0001c0001t0001g0224 a0001c0001t0001g0258 a0001c0001t0002g0015 others(4): Show |
7 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-13052G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038254 | |||||||
| chr20:44038442 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.412-12864G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038442 | |||||||
| chr20:44038529 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0130 a0001c0001t0001g0144 |
3 | HG03540.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.412-12777T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038529 | |||||||
| chr20:44038535 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.412-12771C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038535 | |||||||
| chr20:44038554 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.412-12752A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038554 | |||||||
| chr20:44038756 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0002g0103 a0001c0001t0002g0135 |
3 | HG02622.hp1 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.412-12550G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44038756 | |||||||
| chr20:44039089 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-12217G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039089 | |||||||
| chr20:44039302 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0003g0021 a0001c0001t0003g0143 others(3): Show |
6 | HG01361.hp2 HG02145.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-12004C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039302 | |||||||
| chr20:44039412 | T | A | 6 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-11894T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039412 | |||||||
| chr20:44039415 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.412-11891A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039415 | |||||||
| chr20:44039482 | A | G | 2 | a0001c0012t0003g0013 a0003c0003t0001g0003 |
2 | HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.412-11824A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039482 | |||||||
| chr20:44039536 | A | C | 3 | a0001c0001t0001g0233 a0001c0001t0002g0029 a0001c0001t0002g0030 |
3 | HG02970.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.412-11770A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039536 | |||||||
| chr20:44039586 | G | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(163): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.412-11720G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039586 | |||||||
| chr20:44039717 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.412-11589C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039717 | |||||||
| chr20:44039748 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(199): Show |
203 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.412-11558G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039748 | |||||||
| chr20:44039766 | A | AG | 6 | a0001c0001t0001g0083 a0001c0001t0001g0159 a0001c0001t0001g0174 others(3): Show |
6 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-11536dupG | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44039766 | ||||||
| chr20:44039893 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(151): Show |
155 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.412-11413C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039893 | |||||||
| chr20:44039926 | T | C | 4 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0001c0001t0006g0212 others(1): Show |
4 | NA18941.hp1 NA18985.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-11380T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44039926 | |||||||
| chr20:44040031 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.412-11275G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040031 | |||||||
| chr20:44040103 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.412-11203G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040103 | |||||||
| chr20:44040188 | G | A | 3 | a0001c0001t0002g0129 a0001c0001t0002g0284 a0004c0005t0001g0106 |
3 | HG02055.hp2 HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.412-11118G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040188 | |||||||
| chr20:44040362 | T | A | 1 | a0006c0008t0001g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.412-10944T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040362 | |||||||
| chr20:44040616 | T | A | 18 | a0001c0001t0001g0024 a0001c0001t0001g0126 a0001c0001t0001g0132 others(15): Show |
18 | HG01496.hp1 HG01515.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.412-10690T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040616 | |||||||
| chr20:44040629 | A | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(198): Show |
202 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.412-10677A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040629 | |||||||
| chr20:44040636 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.412-10670A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040636 | |||||||
| chr20:44040664 | A | C | 6 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-10642A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040664 | |||||||
| chr20:44040869 | A | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0267 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.412-10437A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44040869 | |||||||
| chr20:44041123 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(154): Show |
158 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.412-10183C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44041123 | |||||||
| chr20:44041346 | G | C | 9 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0233 others(6): Show |
9 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-9960G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44041346 | |||||||
| chr20:44041351 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0278 others(4): Show |
7 | HG01496.hp1 HG01515.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-9955G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44041351 | |||||||
| chr20:44041353 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(174): Show |
178 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.412-9953G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44041353 | |||||||
| chr20:44041488 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.412-9818T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44041488 | |||||||
| chr20:44041601 | G | A | 2 | a0001c0001t0002g0129 a0004c0005t0001g0106 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.412-9705G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44041601 | |||||||
| chr20:44041860 | A | T | 4 | a0001c0001t0001g0225 a0001c0001t0002g0022 a0001c0001t0002g0103 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-9446A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44041860 | |||||||
| chr20:44042013 | T | C | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-9293T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042013 | |||||||
| chr20:44042207 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.412-9099A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042207 | |||||||
| chr20:44042228 | G | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-9078G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042228 | |||||||
| chr20:44042346 | G | A | 4 | a0001c0001t0001g0258 a0001c0001t0002g0015 a0001c0001t0002g0136 others(1): Show |
4 | HG02615.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-8960G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042346 | |||||||
| chr20:44042431 | G | A | 1 | a0004c0005t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.412-8875G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042431 | |||||||
| chr20:44042516 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0278 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-8790G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042516 | |||||||
| chr20:44042530 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(161): Show |
165 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.412-8776T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042530 | |||||||
| chr20:44042538 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.412-8768A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042538 | |||||||
| chr20:44042543 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(201): Show |
205 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.412-8763A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042543 | |||||||
| chr20:44042793 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(159): Show |
163 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.412-8513A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042793 | |||||||
| chr20:44042936 | A | G | 30 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0034 others(27): Show |
30 | HG00323.hp2 HG00733.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.412-8370A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042936 | |||||||
| chr20:44042939 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.412-8367G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44042939 | |||||||
| chr20:44043070 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-8236G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043070 | |||||||
| chr20:44043087 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0138 others(4): Show |
7 | HG00733.hp2 HG01884.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-8219C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043087 | |||||||
| chr20:44043119 | C | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(202): Show |
206 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.412-8187C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043119 | |||||||
| chr20:44043227 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-8079G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043227 | |||||||
| chr20:44043307 | T | C | 6 | a0001c0001t0001g0258 a0001c0001t0002g0015 a0001c0001t0002g0136 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-7999T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043307 | |||||||
| chr20:44043356 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0261 others(1): Show |
4 | HG00639.hp1 HG01099.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-7950A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043356 | |||||||
| chr20:44043528 | A | C | 6 | a0001c0001t0001g0258 a0001c0001t0002g0015 a0001c0001t0002g0136 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-7778A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043528 | |||||||
| chr20:44043536 | T | G | 3 | a0001c0001t0002g0129 a0001c0001t0002g0284 a0004c0005t0001g0106 |
3 | HG02055.hp2 HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.412-7770T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043536 | |||||||
| chr20:44043598 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.412-7708G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043598 | |||||||
| chr20:44043598 | G | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(203): Show |
207 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.412-7708G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043598 | |||||||
| chr20:44043617 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-7689G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043617 | |||||||
| chr20:44043629 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.412-7677C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043629 | |||||||
| chr20:44043637 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.412-7669C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043637 | |||||||
| chr20:44043771 | G | A | 25 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0034 others(22): Show |
25 | HG00323.hp2 HG00733.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.412-7535G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043771 | |||||||
| chr20:44043773 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.412-7533A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44043773 | |||||||
| chr20:44044090 | T | C | 1 | a0001c0011t0001g0240 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.412-7216T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044090 | |||||||
| chr20:44044095 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.412-7211C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044095 | |||||||
| chr20:44044116 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(167): Show |
171 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.412-7190C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044116 | |||||||
| chr20:44044128 | G | GGAT | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(159): Show |
163 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.412-7176_412-7175i others(5): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44044128 | ||||||
| chr20:44044131 | C | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(159): Show |
163 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.412-7175C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044131 | |||||||
| chr20:44044132 | A | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(159): Show |
163 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.412-7174A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044132 | |||||||
| chr20:44044160 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-7146G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044160 | |||||||
| chr20:44044161 | G | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-7145G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044161 | |||||||
| chr20:44044170 | C | T | 1 | a0002c0002t0002g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.412-7136C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044170 | |||||||
| chr20:44044279 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.412-7027G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044279 | |||||||
| chr20:44044291 | G | A | 2 | a0001c0001t0002g0129 a0004c0005t0001g0106 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.412-7015G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044291 | |||||||
| chr20:44044366 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0002g0035 a0001c0001t0002g0036 |
3 | HG02886.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.412-6940G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044366 | |||||||
| chr20:44044422 | TA | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(157): Show |
161 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.412-6870delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44044422 | ||||||
| chr20:44044551 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.412-6755A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044551 | |||||||
| chr20:44044917 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.412-6389G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044917 | |||||||
| chr20:44044923 | T | G | 1 | a0001c0001t0002g0236 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.412-6383T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044923 | |||||||
| chr20:44044967 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-6339G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044967 | |||||||
| chr20:44044991 | G | A | 3 | a0001c0001t0001g0233 a0001c0001t0002g0029 a0001c0001t0002g0030 |
3 | HG02970.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.412-6315G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44044991 | |||||||
| chr20:44045208 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(166): Show |
170 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.412-6098C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44045208 | |||||||
| chr20:44045301 | TA | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0122 a0001c0001t0001g0201 |
3 | NA18946.hp1 NA18946.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.412-5998delA | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44045301 | ||||||
| chr20:44045316 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-5990C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44045316 | |||||||
| chr20:44045351 | AAAAT | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(166): Show |
170 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.412-5949_412-5946d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44045351 | ||||||
| chr20:44045426 | G | A | 1 | a0001c0011t0001g0240 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.412-5880G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44045426 | |||||||
| chr20:44045484 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.412-5822T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44045484 | |||||||
| chr20:44045773 | C | T | 6 | a0001c0001t0001g0258 a0001c0001t0002g0015 a0001c0001t0002g0136 others(3): Show |
6 | HG02258.hp2 HG02615.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-5533C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44045773 | |||||||
| chr20:44045774 | G | A | 9 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0233 others(6): Show |
9 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-5532G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44045774 | |||||||
| chr20:44045796 | A | C | 1 | a0001c0001t0001g0221 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.412-5510A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44045796 | |||||||
| chr20:44046048 | T | A | 2 | a0001c0012t0003g0013 a0003c0003t0001g0003 |
2 | HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.412-5258T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44046048 | |||||||
| chr20:44046303 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.412-5003C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44046303 | |||||||
| chr20:44046319 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.412-4987A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44046319 | |||||||
| chr20:44046479 | A | T | 1 | a0001c0001t0002g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.412-4827A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44046479 | |||||||
| chr20:44046530 | T | C | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-4776T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44046530 | |||||||
| chr20:44046899 | T | A | 4 | a0001c0001t0001g0258 a0001c0001t0002g0015 a0001c0001t0002g0136 others(1): Show |
4 | HG02615.hp2 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-4407T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44046899 | |||||||
| chr20:44046971 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(178): Show |
182 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.412-4335T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44046971 | |||||||
| chr20:44047063 | C | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-4243C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44047063 | |||||||
| chr20:44047385 | T | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA18990.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.412-3921T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44047385 | |||||||
| chr20:44047390 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(177): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.412-3916A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44047390 | |||||||
| chr20:44047485 | TTAACATC others(392): Show |
T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(280): Show |
284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.412-3817_412-3419d others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44047485 | ||||||
| chr20:44047940 | C | T | 2 | a0001c0012t0003g0013 a0003c0003t0001g0003 |
2 | HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.412-3366C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44047940 | |||||||
| chr20:44048075 | CG | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG00323.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.412-3228delG | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048075 | ||||||
| chr20:44048099 | A | T | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412-3207A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048099 | |||||||
| chr20:44048138 | G | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0251 |
2 | NA18985.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.412-3168G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048138 | |||||||
| chr20:44048175 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(151): Show |
155 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.412-3131A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048175 | |||||||
| chr20:44048220 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0094 a0001c0001t0002g0026 others(5): Show |
8 | HG00639.hp2 HG00741.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.412-3086G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048220 | |||||||
| chr20:44048232 | TAAATA | T | 9 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(6): Show |
9 | HG02451.hp2 HG02615.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.412-3066_412-3062d others(7): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048232 | ||||||
| chr20:44048310 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0195 others(2): Show |
5 | HG02258.hp1 HG02965.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-2996A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048310 | |||||||
| chr20:44048377 | A | G | 16 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0038 others(13): Show |
16 | HG00323.hp2 HG00733.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.412-2929A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048377 | |||||||
| chr20:44048388 | T | TATATATA others(16): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0214 |
2 | HG00673.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.412-2918_412-2917i others(25): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048388 | |||||||
| chr20:44048388 | T | TATATATA others(28): Show |
1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.412-2918_412-2917i others(37): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048388 | |||||||
| chr20:44048388 | T | TTA | 16 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0046 others(13): Show |
16 | HG01261.hp2 HG01361.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.412-2894_412-2893d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATA | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(56): Show |
60 | HG00408.hp2 HG00438.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.412-2896_412-2893d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATA | 15 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0070 others(12): Show |
15 | HG00323.hp2 HG00621.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.412-2898_412-2893d others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(1): Show |
11 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0055 others(8): Show |
11 | HG00673.hp2 HG00735.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.412-2900_412-2893d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(3): Show |
8 | a0001c0001t0001g0050 a0001c0001t0001g0097 a0001c0001t0001g0101 others(5): Show |
8 | HG02083.hp1 HG02615.hp2 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-2902_412-2893d others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(5): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0053 a0001c0001t0001g0160 others(8): Show |
11 | HG01433.hp1 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.412-2904_412-2893d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0210 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.412-2906_412-2893d others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(9): Show |
5 | a0001c0001t0001g0126 a0001c0001t0001g0148 a0001c0001t0001g0153 others(2): Show |
5 | HG02451.hp2 HG02572.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-2908_412-2893d others(18): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(11): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0074 a0001c0001t0001g0102 others(1): Show |
4 | HG00597.hp2 HG01258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-2910_412-2893d others(20): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(13): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0134 |
3 | HG01099.hp1 HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.412-2912_412-2893d others(22): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(15): Show |
6 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0200 others(3): Show |
6 | HG02630.hp2 HG02647.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-2914_412-2893d others(24): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(17): Show |
4 | a0001c0001t0001g0051 a0001c0001t0002g0015 a0001c0001t0002g0085 others(1): Show |
4 | HG00639.hp1 HG02148.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-2916_412-2893d others(26): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(44): Show |
1 | a0001c0001t0001g0234 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.412-2894_412-2893i others(53): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(19): Show |
9 | a0001c0001t0001g0023 a0001c0001t0001g0062 a0001c0001t0001g0067 others(6): Show |
9 | HG00642.hp2 HG00738.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.412-2893_412-2892i others(28): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(21): Show |
11 | a0001c0001t0001g0027 a0001c0001t0001g0094 a0001c0001t0001g0109 others(8): Show |
11 | HG00639.hp2 HG00733.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.412-2893_412-2892i others(30): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(23): Show |
6 | a0001c0001t0001g0063 a0001c0001t0001g0099 a0001c0001t0001g0100 others(3): Show |
6 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-2893_412-2892i others(32): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(25): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0011t0001g0240 others(2): Show |
5 | HG00741.hp2 HG01167.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-2893_412-2892i others(34): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(27): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0073 a0001c0001t0001g0211 others(4): Show |
7 | HG01361.hp2 HG03516.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.412-2893_412-2892i others(36): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | T | TTATATAT others(33): Show |
1 | a0001c0001t0005g0272 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.412-2893_412-2892i others(42): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048388 | TTA | T | 3 | a0001c0001t0001g0042 a0001c0001t0002g0141 a0001c0001t0002g0226 |
3 | HG02258.hp2 NA19005.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-2894_412-2893d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048388 | ||||||
| chr20:44048390 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.412-2916A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048390 | |||||||
| chr20:44048394 | A | T | 1 | a0001c0001t0002g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412-2912A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048394 | |||||||
| chr20:44048400 | ATATATAT others(7): Show |
A | 1 | a0001c0007t0001g0209 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.412-2901_412-2888d others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048400 | ||||||
| chr20:44048412 | ATG | A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0261 a0001c0001t0007g0149 others(1): Show |
4 | HG01099.hp2 HG02559.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-2892_412-2891d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44048412 | ||||||
| chr20:44048414 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(192): Show |
196 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.412-2892G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048414 | |||||||
| chr20:44048417 | T | A | 3 | a0001c0001t0001g0224 a0005c0004t0002g0019 a0005c0004t0002g0020 |
3 | HG02559.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.412-2889T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048417 | |||||||
| chr20:44048418 | A | ATATATAT others(4): Show |
1 | a0001c0001t0004g0162 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.412-2888_412-2887i others(13): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048418 | |||||||
| chr20:44048418 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.412-2888_412-2887i others(31): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048418 | |||||||
| chr20:44048718 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.412-2588A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048718 | |||||||
| chr20:44048950 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.412-2356A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048950 | |||||||
| chr20:44048958 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.412-2348G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44048958 | |||||||
| chr20:44049087 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0229 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.412-2219G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049087 | |||||||
| chr20:44049164 | A | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(192): Show |
196 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.412-2142A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049164 | |||||||
| chr20:44049282 | T | G | 2 | a0001c0001t0002g0141 a0001c0001t0002g0226 |
2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.412-2024T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049282 | |||||||
| chr20:44049439 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.412-1867C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049439 | |||||||
| chr20:44049503 | A | G | 4 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-1803A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049503 | |||||||
| chr20:44049521 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.412-1785A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049521 | |||||||
| chr20:44049602 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(185): Show |
189 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.412-1704G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049602 | |||||||
| chr20:44049664 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-1642G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049664 | |||||||
| chr20:44049698 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(187): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.412-1608C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049698 | |||||||
| chr20:44049719 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(182): Show |
186 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.412-1587A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049719 | |||||||
| chr20:44049740 | G | GTGTT | 4 | a0001c0001t0001g0225 a0001c0001t0002g0022 a0001c0001t0002g0103 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-1563_412-1560d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44049740 | ||||||
| chr20:44049978 | G | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0195 others(1): Show |
4 | HG02258.hp1 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-1328G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44049978 | |||||||
| chr20:44050165 | C | T | 2 | a0001c0001t0001g0234 a0001c0001t0001g0251 |
2 | NA18985.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.412-1141C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050165 | |||||||
| chr20:44050166 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0002g0032 |
2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.412-1140G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050166 | |||||||
| chr20:44050367 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.412-939C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050367 | |||||||
| chr20:44050471 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0229 a0001c0001t0001g0257 others(1): Show |
4 | HG02451.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-835G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050471 | |||||||
| chr20:44050474 | A | G | 6 | a0001c0001t0001g0258 a0001c0001t0002g0015 a0001c0001t0002g0136 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-832A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050474 | |||||||
| chr20:44050494 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.412-812G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050494 | |||||||
| chr20:44050551 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(172): Show |
176 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.412-755A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050551 | |||||||
| chr20:44050774 | AG | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(179): Show |
183 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.412-530delG | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr20 | 44050774 | ||||||
| chr20:44050858 | A | G | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.412-448A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050858 | |||||||
| chr20:44050928 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.412-378C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050928 | |||||||
| chr20:44050969 | T | C | 4 | a0001c0001t0001g0225 a0001c0001t0002g0022 a0001c0001t0002g0103 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-337T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 3/8 | chr20 | 44050969 | |||||||
| chr20:44051762 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.651+217C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44051762 | |||||||
| chr20:44052007 | C | T | 2 | a0001c0001t0003g0017 a0002c0002t0002g0140 |
2 | HG00741.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.651+462C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052007 | |||||||
| chr20:44052114 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0047 others(24): Show |
27 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.651+569C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052114 | |||||||
| chr20:44052171 | G | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(221): Show |
225 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.651+626G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052171 | |||||||
| chr20:44052240 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.651+695G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052240 | |||||||
| chr20:44052268 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.651+723G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052268 | |||||||
| chr20:44052331 | A | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0001g0229 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.651+786A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052331 | |||||||
| chr20:44052430 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(97): Show |
101 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.651+885G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052430 | |||||||
| chr20:44052448 | G | A | 28 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0060 others(25): Show |
28 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.651+903G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052448 | |||||||
| chr20:44052834 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.651+1289C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44052834 | |||||||
| chr20:44053092 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.652-1207C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053092 | |||||||
| chr20:44053256 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0006g0167 a0001c0001t0006g0212 others(1): Show |
4 | NA19005.hp1 NA19011.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.652-1043C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053256 | |||||||
| chr20:44053367 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.652-932C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053367 | |||||||
| chr20:44053429 | G | A | 1 | a0001c0012t0003g0013 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.652-870G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053429 | |||||||
| chr20:44053433 | G | GAT | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0004c0005t0001g0106 |
3 | HG02572.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.652-860_652-859dup others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053433 | ||||||
| chr20:44053433 | G | GATATATA others(1): Show |
8 | a0001c0001t0001g0243 a0001c0001t0002g0022 a0001c0001t0002g0035 others(5): Show |
8 | HG02258.hp2 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.652-859_652-858ins others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053433 | ||||||
| chr20:44053437 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.652-861_652-860ins others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053437 | ||||||
| chr20:44053439 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0001g0274 a0006c0008t0001g0076 |
3 | HG02129.hp2 HG02965.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.652-860T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053439 | |||||||
| chr20:44053439 | T | TAC | 22 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(19): Show |
23 | HG01071.hp1 HG01257.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.652-828_652-827dup others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | T | TACAC | 3 | a0001c0001t0002g0136 a0001c0001t0002g0142 a0001c0001t0002g0235 |
3 | HG02615.hp2 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.652-830_652-827dup others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | T | TATACAC | 19 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0061 others(16): Show |
19 | HG00639.hp2 HG00738.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.652-859_652-858ins others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | T | TATACACA others(1): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0031 others(4): Show |
7 | HG01099.hp1 HG01258.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.652-859_652-858ins others(8): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | T | TATACACA others(3): Show |
1 | a0001c0001t0001g0160 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.652-859_652-858ins others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | T | TATACACA others(5): Show |
1 | a0001c0001t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.652-859_652-858ins others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | T | TATATATA others(3): Show |
1 | a0001c0001t0002g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.652-859_652-858ins others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | TAC | T | 142 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(139): Show |
142 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.652-828_652-827del others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | TACAC | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0189 a0001c0001t0001g0276 |
3 | HG02129.hp1 NA18953.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.652-830_652-827del others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.652-836_652-827del others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | TACACACA others(9): Show |
T | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.652-842_652-827del others(16): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053439 | TACACACA others(11): Show |
T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0047 others(4): Show |
7 | HG01069.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-844_652-827del others(18): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053439 | ||||||
| chr20:44053441 | C | T | 10 | a0001c0001t0001g0114 a0001c0001t0001g0194 a0001c0001t0002g0028 others(7): Show |
10 | HG02109.hp1 HG02572.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.652-858C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053441 | |||||||
| chr20:44053443 | C | T | 111 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(108): Show |
111 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.652-856C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053443 | |||||||
| chr20:44053445 | C | T | 103 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(100): Show |
103 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.652-854C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053445 | |||||||
| chr20:44053447 | C | T | 7 | a0001c0001t0001g0123 a0001c0001t0001g0189 a0001c0001t0001g0256 others(4): Show |
7 | HG02004.hp2 HG02129.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.652-852C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053447 | |||||||
| chr20:44053449 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.652-850C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053449 | |||||||
| chr20:44053473 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0016 others(24): Show |
27 | HG00639.hp2 HG00738.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.652-826T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053473 | |||||||
| chr20:44053501 | CATATATA others(33): Show |
C | 1 | a0001c0001t0001g0169 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.652-787_652-748del others(40): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053501 | ||||||
| chr20:44053522 | C | CAT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0047 others(4): Show |
7 | HG01069.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-769_652-768dup others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053522 | ||||||
| chr20:44053522 | CAT | C | 12 | a0001c0001t0001g0243 a0001c0001t0002g0022 a0001c0001t0002g0035 others(9): Show |
12 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.652-769_652-768del others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053522 | ||||||
| chr20:44053522 | CATATATA others(12): Show |
C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(105): Show |
108 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.652-750_652-732del others(19): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053522 | ||||||
| chr20:44053522 | CATATATA others(14): Show |
C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.652-769_652-749del others(21): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053522 | ||||||
| chr20:44053551 | C | CATATATA others(48): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0047 others(4): Show |
7 | HG01069.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-726_652-725ins others(55): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053551 | ||||||
| chr20:44053574 | C | CAT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0151 others(3): Show |
6 | HG01071.hp1 HG01257.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.652-717_652-716dup others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053574 | ||||||
| chr20:44053591 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.652-708T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053591 | |||||||
| chr20:44053599 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.652-700C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053599 | |||||||
| chr20:44053602 | A | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0047 others(4): Show |
7 | HG01069.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-697A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053602 | |||||||
| chr20:44053607 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0109 |
2 | HG00733.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.652-692T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053607 | |||||||
| chr20:44053609 | C | CAT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(229): Show |
233 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(230): Show |
intron_variant | MODIFIER | c.652-686_652-685dup others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053609 | ||||||
| chr20:44053609 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0109 |
2 | HG00733.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.652-690C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053609 | |||||||
| chr20:44053629 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
234 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(231): Show |
intron_variant | MODIFIER | c.652-670C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053629 | |||||||
| chr20:44053652 | GCA | G | 10 | a0001c0001t0001g0243 a0001c0001t0002g0022 a0001c0001t0002g0035 others(7): Show |
10 | HG02258.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.652-639_652-638del others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44053652 | ||||||
| chr20:44053794 | C | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0047 others(4): Show |
7 | HG01069.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-505C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053794 | |||||||
| chr20:44053845 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0039 others(21): Show |
25 | HG01071.hp1 HG01167.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.652-454G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053845 | |||||||
| chr20:44053939 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.652-360G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44053939 | |||||||
| chr20:44054145 | GTGTC | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0047 others(4): Show |
7 | HG01069.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-145_652-142del others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr20 | 44054145 | ||||||
| chr20:44054195 | T | C | 1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.652-104T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 4/8 | chr20 | 44054195 | |||||||
| chr20:44054614 | A | G | 1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.879+88A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44054614 | |||||||
| chr20:44054753 | C | T | 42 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0024 others(39): Show |
42 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.879+227C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44054753 | |||||||
| chr20:44054807 | A | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0047 others(4): Show |
7 | HG01069.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+281A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44054807 | |||||||
| chr20:44054866 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.879+340A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44054866 | |||||||
| chr20:44054919 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.879+393A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44054919 | |||||||
| chr20:44054963 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(26): Show |
30 | HG01071.hp1 HG01257.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.879+437A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44054963 | |||||||
| chr20:44054963 | A | T | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.879+437A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44054963 | |||||||
| chr20:44055071 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.879+545C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44055071 | |||||||
| chr20:44055228 | C | T | 20 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0027 others(17): Show |
20 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.879+702C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44055228 | |||||||
| chr20:44055602 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(47): Show |
50 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.879+1076G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44055602 | |||||||
| chr20:44055632 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
244 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(241): Show |
intron_variant | MODIFIER | c.879+1106T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44055632 | |||||||
| chr20:44055650 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.879+1124G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44055650 | |||||||
| chr20:44055870 | A | G | 1 | a0001c0001t0009g0145 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.879+1344A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44055870 | |||||||
| chr20:44055954 | G | C | 29 | a0001c0001t0001g0266 a0001c0001t0002g0015 a0001c0001t0002g0026 others(26): Show |
29 | HG01175.hp2 HG01346.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.879+1428G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44055954 | |||||||
| chr20:44056445 | G | A | 48 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0024 others(45): Show |
48 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.879+1919G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44056445 | |||||||
| chr20:44056532 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0049 others(20): Show |
24 | HG01071.hp1 HG01257.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.879+2006G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44056532 | |||||||
| chr20:44056581 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.879+2055G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44056581 | |||||||
| chr20:44056684 | C | T | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.879+2158C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44056684 | |||||||
| chr20:44056850 | T | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(24): Show |
27 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+2324T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44056850 | |||||||
| chr20:44057053 | C | T | 28 | a0001c0001t0002g0015 a0001c0001t0002g0026 a0001c0001t0002g0028 others(25): Show |
28 | HG01175.hp2 HG01346.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.879+2527C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057053 | |||||||
| chr20:44057243 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.879+2717C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057243 | |||||||
| chr20:44057263 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(24): Show |
27 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+2737C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057263 | |||||||
| chr20:44057402 | G | C | 1 | a0001c0001t0001g0282 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.879+2876G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057402 | |||||||
| chr20:44057677 | T | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(24): Show |
27 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+3151T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057677 | |||||||
| chr20:44057736 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.879+3210A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057736 | |||||||
| chr20:44057911 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.879+3385T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057911 | |||||||
| chr20:44057936 | C | T | 7 | a0001c0001t0003g0017 a0001c0001t0003g0021 a0001c0001t0003g0059 others(4): Show |
7 | HG01496.hp1 HG02145.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+3410C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057936 | |||||||
| chr20:44057952 | G | GCAAGTCA others(32): Show |
4 | a0001c0001t0002g0136 a0001c0001t0002g0142 a0001c0001t0002g0235 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+3427_879+3465d others(41): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44057952 | ||||||
| chr20:44057959 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.879+3433A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057959 | |||||||
| chr20:44057993 | G | T | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.879+3467G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057993 | |||||||
| chr20:44057996 | G | GAGTTCCA others(3): Show |
2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.879+3470_879+3471i others(12): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057996 | |||||||
| chr20:44057998 | A | C | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.879+3472A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44057998 | |||||||
| chr20:44058072 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(16): Show |
19 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.879+3546C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058072 | |||||||
| chr20:44058124 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(19): Show |
23 | HG01071.hp1 HG01257.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.879+3598T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058124 | |||||||
| chr20:44058132 | T | C | 138 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(135): Show |
138 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.879+3606T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058132 | |||||||
| chr20:44058183 | C | T | 28 | a0001c0001t0001g0266 a0001c0001t0002g0026 a0001c0001t0002g0028 others(25): Show |
28 | HG01175.hp2 HG01346.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.879+3657C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058183 | |||||||
| chr20:44058207 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0190 |
2 | HG02523.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.879+3681G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058207 | |||||||
| chr20:44058213 | T | TG | 28 | a0001c0001t0001g0266 a0001c0001t0002g0026 a0001c0001t0002g0028 others(25): Show |
28 | HG01175.hp2 HG01346.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.879+3691dupG | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44058213 | ||||||
| chr20:44058376 | A | G | 160 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.879+3850A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058376 | |||||||
| chr20:44058399 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.879+3873C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058399 | |||||||
| chr20:44058494 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(24): Show |
27 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+3968C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058494 | |||||||
| chr20:44058557 | T | A | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.879+4031T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058557 | |||||||
| chr20:44058758 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(24): Show |
27 | HG00639.hp2 HG00738.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+4232C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058758 | |||||||
| chr20:44058800 | A | G | 13 | a0001c0001t0002g0022 a0001c0001t0002g0035 a0001c0001t0002g0036 others(10): Show |
13 | HG00741.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.879+4274A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44058800 | |||||||
| chr20:44058968 | GTTAT | G | 44 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0024 others(41): Show |
44 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.879+4446_879+4449d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44058968 | ||||||
| chr20:44059519 | C | T | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.879+4993C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44059519 | |||||||
| chr20:44059693 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.880-5084C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44059693 | |||||||
| chr20:44060139 | C | T | 4 | a0001c0001t0002g0026 a0001c0001t0002g0029 a0001c0001t0002g0030 others(1): Show |
4 | HG02630.hp2 HG02970.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-4638C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060139 | |||||||
| chr20:44060306 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0138 |
2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.880-4471C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060306 | |||||||
| chr20:44060318 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0224 |
2 | HG01433.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.880-4459A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060318 | |||||||
| chr20:44060440 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.880-4337G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060440 | |||||||
| chr20:44060557 | C | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0138 a0001c0001t0001g0223 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-4220C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060557 | |||||||
| chr20:44060627 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.880-4150G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060627 | |||||||
| chr20:44060794 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0224 |
2 | HG01433.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.880-3983T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060794 | |||||||
| chr20:44060842 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0047 |
2 | HG01069.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.880-3935C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060842 | |||||||
| chr20:44060844 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.880-3933C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060844 | |||||||
| chr20:44060854 | A | G | 47 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0024 others(44): Show |
47 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.880-3923A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060854 | |||||||
| chr20:44060870 | C | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(115): Show |
118 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.880-3907C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060870 | |||||||
| chr20:44060989 | T | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(20): Show |
23 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-3788T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44060989 | |||||||
| chr20:44061037 | A | G | 127 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(124): Show |
127 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.880-3740A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44061037 | |||||||
| chr20:44061050 | A | G | 1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.880-3727A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44061050 | |||||||
| chr20:44061076 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.880-3701C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44061076 | |||||||
| chr20:44061115 | T | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(16): Show |
19 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.880-3662T>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44061115 | |||||||
| chr20:44061352 | A | G | 128 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(125): Show |
128 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.880-3425A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44061352 | |||||||
| chr20:44061489 | A | G | 21 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0047 others(18): Show |
21 | HG00741.hp2 HG01069.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-3288A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44061489 | |||||||
| chr20:44061523 | G | GAAAAATT others(266): Show |
1 | a0001c0001t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.880-3240_880-3239i others(275): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44061523 | ||||||
| chr20:44061781 | C | T | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.880-2996C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44061781 | |||||||
| chr20:44061937 | T | TAAAACCC others(318): Show |
1 | a0001c0001t0001g0258 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.880-2825_880-2824i others(327): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44061937 | ||||||
| chr20:44061937 | T | TAAAACCC others(325): Show |
1 | a0001c0001t0001g0134 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.880-2825_880-2824i others(334): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44061937 | ||||||
| chr20:44061937 | T | TAAAACCC others(326): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0265 a0001c0001t0001g0270 |
3 | HG00642.hp2 HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.880-2825_880-2824i others(335): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44061937 | ||||||
| chr20:44061937 | T | TAAAACCC others(327): Show |
14 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0048 others(11): Show |
14 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.880-2825_880-2824i others(336): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44061937 | ||||||
| chr20:44061937 | T | TAAAACCC others(328): Show |
1 | a0001c0001t0001g0205 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.880-2825_880-2824i others(337): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44061937 | ||||||
| chr20:44061937 | T | TAAAACCC others(329): Show |
1 | a0001c0001t0001g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.880-2825_880-2824i others(338): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44061937 | ||||||
| chr20:44061956 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.880-2821G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44061956 | |||||||
| chr20:44062011 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.880-2766C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062011 | |||||||
| chr20:44062059 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.880-2718C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062059 | |||||||
| chr20:44062215 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.880-2562C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062215 | |||||||
| chr20:44062312 | C | A | 34 | a0001c0001t0002g0015 a0001c0001t0002g0026 a0001c0001t0002g0028 others(31): Show |
34 | HG01175.hp2 HG01346.hp2 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.880-2465C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062312 | |||||||
| chr20:44062314 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | NA18941.hp2 NA18960.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.880-2463C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062314 | |||||||
| chr20:44062366 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.880-2411C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062366 | |||||||
| chr20:44062367 | A | AAAAT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
143 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.880-2373_880-2370d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062367 | ||||||
| chr20:44062367 | A | AAAATAAA others(1): Show |
19 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0044 others(16): Show |
19 | HG00597.hp2 HG00738.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.880-2377_880-2370d others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062367 | ||||||
| chr20:44062367 | AAAAT | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0207 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-2373_880-2370d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062367 | ||||||
| chr20:44062367 | AAAATAAA others(5): Show |
A | 3 | a0001c0001t0001g0201 a0001c0001t0005g0185 a0001c0001t0005g0272 |
3 | NA18946.hp2 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.880-2381_880-2370d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062367 | ||||||
| chr20:44062396 | AAATAAAT others(5): Show |
A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0066 |
3 | HG01099.hp1 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.880-2370_880-2359d others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062396 | ||||||
| chr20:44062404 | A | AAATAAAT others(5): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0047 |
2 | HG01069.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.880-2370_880-2369i others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062404 | ||||||
| chr20:44062404 | A | AAATAAAT others(1): Show |
8 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0126 others(5): Show |
8 | HG01361.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-2370_880-2369i others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062404 | ||||||
| chr20:44062404 | A | AAATAAAT others(5): Show |
2 | a0001c0001t0002g0129 a0004c0005t0001g0106 |
2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.880-2370_880-2369i others(14): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062404 | ||||||
| chr20:44062404 | A | AAATGAAT others(1): Show |
10 | a0001c0001t0002g0022 a0001c0001t0002g0035 a0001c0001t0002g0036 others(7): Show |
10 | HG00741.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.880-2366_880-2365i others(10): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062404 | ||||||
| chr20:44062404 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0224 a0001c0001t0001g0283 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.880-2373A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062404 | |||||||
| chr20:44062404 | AAATG | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0048 others(13): Show |
16 | HG00639.hp2 HG00738.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.880-2369_880-2366d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062404 | ||||||
| chr20:44062408 | G | A | 2 | a0001c0001t0009g0145 a0002c0002t0001g0146 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.880-2369G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062408 | |||||||
| chr20:44062425 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.880-2352A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062425 | |||||||
| chr20:44062608 | A | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0047 others(19): Show |
22 | HG00741.hp2 HG01069.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.880-2169A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062608 | |||||||
| chr20:44062747 | A | G | 31 | a0001c0001t0001g0266 a0001c0001t0002g0026 a0001c0001t0002g0028 others(28): Show |
31 | HG01175.hp2 HG01346.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.880-2030A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44062747 | |||||||
| chr20:44062782 | T | TAAAA | 19 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(16): Show |
19 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.880-1993_880-1990d others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44062782 | ||||||
| chr20:44063000 | G | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(15): Show |
18 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.880-1777G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063000 | |||||||
| chr20:44063001 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(15): Show |
18 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.880-1776G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063001 | |||||||
| chr20:44063055 | A | G | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.880-1722A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063055 | |||||||
| chr20:44063116 | T | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(39): Show |
43 | HG00639.hp2 HG00738.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.880-1661T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063116 | |||||||
| chr20:44063299 | C | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(15): Show |
18 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.880-1478C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063299 | |||||||
| chr20:44063309 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0229 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.880-1468T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063309 | |||||||
| chr20:44063312 | G | A | 1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.880-1465G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063312 | |||||||
| chr20:44063321 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.880-1456G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063321 | |||||||
| chr20:44063536 | A | C | 1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.880-1241A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063536 | |||||||
| chr20:44063628 | T | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0047 others(19): Show |
22 | HG00741.hp2 HG01069.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.880-1149T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063628 | |||||||
| chr20:44063637 | A | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(15): Show |
18 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.880-1140A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063637 | |||||||
| chr20:44063649 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0276 |
2 | NA18969.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.880-1128C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063649 | |||||||
| chr20:44063733 | T | C | 215 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(212): Show |
215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.880-1044T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063733 | |||||||
| chr20:44063759 | T | TAC | 7 | a0001c0001t0002g0022 a0001c0001t0002g0035 a0001c0001t0002g0036 others(4): Show |
7 | HG02622.hp2 HG02647.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-1006_880-1005d others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44063759 | ||||||
| chr20:44063759 | TACACACA others(25): Show |
T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0024 others(51): Show |
54 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.880-1004_880-973de others(33): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44063759 | ||||||
| chr20:44063761 | CACACACA others(19): Show |
C | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.880-1004_880-979de others(27): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44063761 | ||||||
| chr20:44063763 | CACACACA others(17): Show |
C | 1 | a0001c0001t0004g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.880-1004_880-981de others(25): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44063763 | ||||||
| chr20:44063787 | T | TAC | 6 | a0001c0001t0002g0015 a0001c0001t0002g0136 a0001c0001t0002g0142 others(3): Show |
6 | HG02055.hp2 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-974_880-973dup others(2): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44063787 | ||||||
| chr20:44063787 | T | TACAC | 105 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(102): Show |
105 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.880-976_880-973dup others(4): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44063787 | ||||||
| chr20:44063787 | T | TACACAC | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0109 others(2): Show |
5 | HG00733.hp2 HG01106.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-978_880-973dup others(6): Show |
TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr20 | 44063787 | ||||||
| chr20:44063797 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0047 |
2 | HG01069.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.880-980C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063797 | |||||||
| chr20:44063812 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.880-965T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44063812 | |||||||
| chr20:44064135 | G | C | 47 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0024 others(44): Show |
47 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.880-642G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44064135 | |||||||
| chr20:44064443 | A | G | 47 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0024 others(44): Show |
47 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.880-334A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44064443 | |||||||
| chr20:44064468 | A | C | 70 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0014 others(67): Show |
70 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.880-309A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44064468 | |||||||
| chr20:44064576 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.880-201A>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44064576 | |||||||
| chr20:44064722 | C | T | 8 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0073 others(5): Show |
8 | HG00621.hp1 HG02132.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-55C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 5/8 | chr20 | 44064722 | |||||||
| chr20:44064932 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0031 others(16): Show |
19 | HG00639.hp2 HG00738.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.960+75C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 6/8 | chr20 | 44064932 | |||||||
| chr20:44065010 | A | G | 215 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(212): Show |
215 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.960+153A>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 6/8 | chr20 | 44065010 | |||||||
| chr20:44065074 | C | G | 1 | a0001c0001t0002g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+217C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 6/8 | chr20 | 44065074 | |||||||
| chr20:44065084 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0224 |
2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.960+227T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 6/8 | chr20 | 44065084 | |||||||
| chr20:44065237 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0283 a0008c0010t0001g0164 |
3 | HG02895.hp1 HG02897.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.960+380G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 6/8 | chr20 | 44065237 | |||||||
| chr20:44065390 | A | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
237 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.961-322A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 6/8 | chr20 | 44065390 | |||||||
| chr20:44065437 | G | T | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.961-275G>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 6/8 | chr20 | 44065437 | |||||||
| chr20:44066140 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1356+33G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 7/8 | chr20 | 44066140 | |||||||
| chr20:44066348 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1356+241C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 7/8 | chr20 | 44066348 | |||||||
| chr20:44066358 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1356+251T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 7/8 | chr20 | 44066358 | |||||||
| chr20:44066560 | G | A | 2 | a0005c0004t0002g0019 a0005c0004t0002g0020 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1357-170G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 7/8 | chr20 | 44066560 | |||||||
| chr20:44066891 | C | A | 1 | a0001c0001t0001g0207 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1484+34C>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44066891 | |||||||
| chr20:44067028 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0151 |
2 | HG01071.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1484+171C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067028 | |||||||
| chr20:44067141 | C | G | 1 | a0002c0002t0002g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1484+284C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067141 | |||||||
| chr20:44067155 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1484+298G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067155 | |||||||
| chr20:44067246 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0176 |
2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1484+389G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067246 | |||||||
| chr20:44067581 | T | G | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1484+724T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067581 | |||||||
| chr20:44067611 | T | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0034 others(11): Show |
14 | HG01261.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1484+754T>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067611 | |||||||
| chr20:44067754 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1485-896G>A | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067754 | |||||||
| chr20:44067871 | G | C | 1 | a0002c0002t0002g0131 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1485-779G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067871 | |||||||
| chr20:44067878 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0255 a0001c0001t0001g0270 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485-772C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067878 | |||||||
| chr20:44067940 | A | C | 129 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(126): Show |
129 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1485-710A>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067940 | |||||||
| chr20:44067975 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1485-675C>G | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44067975 | |||||||
| chr20:44068009 | T | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0010 others(123): Show |
126 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1485-641T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44068009 | |||||||
| chr20:44068032 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1485-618C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44068032 | |||||||
| chr20:44068250 | C | T | 5 | a0001c0001t0002g0028 a0001c0001t0002g0147 a0001c0001t0002g0267 others(2): Show |
5 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485-400C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44068250 | |||||||
| chr20:44068494 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1485-156G>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44068494 | |||||||
| chr20:44068547 | T | C | 38 | a0001c0001t0001g0127 a0001c0001t0001g0224 a0001c0001t0001g0266 others(35): Show |
38 | HG01175.hp2 HG01346.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.1485-103T>C | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44068547 | |||||||
| chr20:44068615 | C | T | 47 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0024 others(44): Show |
47 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1485-35C>T | TOX2 | ENSG00000124191.18 | transcript | ENST00000341197.9 | protein_coding | 8/8 | chr20 | 44068615 |