Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 440097 |
| ensemblid | ENSG00000185610.6 |
| hgncid | 33186 |
| symbol | DBX2 |
| name | developing brain homeobox 2 |
| refseq_nuc | NM_001004329.3 |
| refseq_prot | NP_001004329.2 |
| ensembl_nuc | ENST00000332700.6 |
| ensembl_prot | ENSP00000331470.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 45014672 |
| end | 45051099 |
| strand | - |
| ver | v1.2 |
| region | chr12:45014672-45051099 |
| region5000 | chr12:45009672-45056099 |
| regionname0 | DBX2_chr12_45014672_45051099 |
| regionname5000 | DBX2_chr12_45009672_45056099 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 339 | 299 | 61 | 54 | 154 | 5 | 25 | 124 | DBX2_chr12_45009672_45056099 | DBX2 | MLPSA others(334): Show |
chr12 | 45009672 | 45056099 |
| a0002 | 1/1 | 339 | 111 | 33 | 22 | 44 | 5 | 5 | 32 | DBX2_chr12_45009672_45056099 | DBX2 | MLPSA others(334): Show |
chr12 | 45009672 | 45056099 |
| a0003 | 0/0 | 339 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | MLPSA others(334): Show |
chr12 | 45009672 | 45056099 |
| a0004 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | MLPSA others(334): Show |
chr12 | 45009672 | 45056099 |
| a0005 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | MLPSA others(334): Show |
chr12 | 45009672 | 45056099 |
| a0006 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | MLPSA others(334): Show |
chr12 | 45009672 | 45056099 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1017 | 236 | 58 | 49 | 103 | 5 | 21 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0001c0003 | 0/0 | 1017 | 49 | 0 | 5 | 41 | 0 | 3 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0001c0005 | 0/0 | 1017 | 7 | 1 | 0 | 5 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0001c0006 | 0/0 | 1017 | 5 | 0 | 0 | 5 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0001c0008 | 0/0 | 1017 | 2 | 2 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0002c0002 | 1/1 | 1017 | 101 | 24 | 22 | 43 | 5 | 5 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0002c0004 | 0/0 | 1017 | 9 | 9 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0002c0011 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0003c0007 | 0/0 | 1017 | 3 | 3 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0004c0010 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0005c0009 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 | ||
| a0006c0012 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATGCT others(1012): Show |
chr12 | 45009672 | 45056099 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2806 | 202 | 37 | 45 | 94 | 5 | 21 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0005 | 0/0 | 2806 | 15 | 14 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0006 | 0/0 | 2806 | 6 | 0 | 0 | 6 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0009 | 0/0 | 2806 | 3 | 3 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0010 | 0/0 | 2806 | 2 | 0 | 2 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0011 | 0/0 | 2806 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0013 | 0/0 | 2806 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0014 | 0/0 | 2806 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0015 | 0/0 | 2806 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0016 | 0/0 | 2806 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0018 | 0/0 | 2806 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0019 | 0/0 | 2806 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0001t0020 | 0/0 | 2806 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0003t0003 | 0/0 | 2806 | 31 | 0 | 5 | 23 | 0 | 3 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0003t0004 | 0/0 | 2806 | 18 | 0 | 0 | 18 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0005t0002 | 0/0 | 2806 | 7 | 1 | 0 | 5 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0006t0001 | 0/0 | 2806 | 5 | 0 | 0 | 5 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0001c0008t0001 | 0/0 | 2806 | 2 | 2 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0002c0002t0002 | 1/1 | 2806 | 96 | 24 | 18 | 42 | 5 | 5 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0002c0002t0007 | 0/0 | 2806 | 4 | 0 | 4 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0002c0002t0012 | 0/0 | 2806 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0002c0004t0001 | 0/0 | 2806 | 4 | 4 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0002c0004t0002 | 0/0 | 2806 | 5 | 5 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0002c0011t0002 | 0/0 | 2806 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0003c0007t0008 | 0/0 | 2806 | 3 | 3 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0004c0010t0002 | 0/0 | 2806 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0005c0009t0017 | 0/0 | 2806 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| a0006c0012t0003 | 0/0 | 2806 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | ATCGT others(2801): Show |
chr12 | 45009672 | 45056099 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0006g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0010g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0014g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0015g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0016g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0018g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0019g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0001t0020g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0003t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0005t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0005t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0005t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0005t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0005t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0005t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0006t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0008t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0001c0008t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0001 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0002 | 0/0 | 8 | 0 | 1 | 4 | 2 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0010 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0007g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0007g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0002t0012g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0004t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0004t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0004t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0002c0011t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0003c0007t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0003c0007t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0003c0007t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0004c0010t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0005c0009t0017g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| a0006c0012t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0112 | EUR | FIN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00408 | hp1 | a0001 | c0003 | t0003 | g0007 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00423 | hp2 | a0001 | c0006 | t0001 | g0023 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00544 | hp1 | a0001 | c0003 | t0003 | g0303 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00558 | hp1 | a0001 | c0003 | t0003 | g0298 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0234 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01069 | hp2 | a0002 | c0002 | t0007 | g0032 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0115 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0163 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0183 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0166 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0031 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0111 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0097 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01257 | hp1 | a0002 | c0002 | t0007 | g0032 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01261 | hp1 | a0002 | c0002 | t0007 | g0138 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01261 | hp2 | a0001 | c0001 | t0010 | g0246 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01346 | hp1 | a0002 | c0002 | t0007 | g0137 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | IBS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0028 | EUR | IBS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0308 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0309 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01952 | hp2 | a0001 | c0003 | t0003 | g0306 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01981 | hp2 | a0001 | c0003 | t0003 | g0305 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01993 | hp2 | a0001 | c0003 | t0003 | g0307 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02004 | hp1 | a0001 | c0001 | t0020 | g0057 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02015 | hp2 | a0002 | c0011 | t0002 | g0292 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02040 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02055 | hp1 | a0002 | c0004 | t0001 | g0186 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0294 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02080 | hp2 | a0001 | c0006 | t0001 | g0061 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02083 | hp1 | a0002 | c0002 | t0012 | g0134 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02083 | hp2 | a0001 | c0006 | t0001 | g0064 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0195 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0304 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02145 | hp1 | a0002 | c0004 | t0002 | g0154 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02155 | hp2 | a0001 | c0005 | t0002 | g0072 | EAS | CDX | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02165 | hp2 | a0001 | c0006 | t0001 | g0023 | EAS | CDX | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02258 | hp1 | a0002 | c0004 | t0002 | g0094 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0174 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0114 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0168 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02523 | hp1 | a0001 | c0003 | t0003 | g0007 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | KHV | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02572 | hp2 | a0003 | c0007 | t0008 | g0279 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0182 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0126 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0178 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02630 | hp1 | a0003 | c0007 | t0008 | g0278 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0119 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0171 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02896 | hp1 | a0001 | c0008 | t0001 | g0314 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02922 | hp2 | a0001 | c0005 | t0002 | g0165 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0099 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02970 | hp2 | a0001 | c0008 | t0001 | g0315 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0167 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0164 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0262 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03225 | hp2 | a0002 | c0004 | t0001 | g0185 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0049 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0251 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0296 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03516 | hp2 | a0004 | c0010 | t0002 | g0282 | AFR | ESN | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0180 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03669 | hp2 | a0001 | c0005 | t0002 | g0148 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0155 | SAS | BEB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG04184 | hp1 | a0001 | c0003 | t0003 | g0310 | SAS | BEB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0031 | SAS | BEB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0033 | SAS | STU | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0090 | AFR | YRI | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18747 | hp2 | a0001 | c0003 | t0003 | g0046 | EAS | CHB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0160 | AFR | YRI | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | YRI | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18941 | hp1 | a0001 | c0003 | t0003 | g0291 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18941 | hp2 | a0001 | c0003 | t0003 | g0311 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18943 | hp1 | a0001 | c0006 | t0001 | g0086 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18946 | hp2 | a0001 | c0003 | t0003 | g0047 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0293 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18950 | hp1 | a0001 | c0003 | t0003 | g0297 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18954 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18959 | hp2 | a0005 | c0009 | t0017 | g0190 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18961 | hp1 | a0001 | c0003 | t0004 | g0289 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18963 | hp2 | a0001 | c0003 | t0004 | g0003 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18965 | hp1 | a0001 | c0003 | t0004 | g0021 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18966 | hp1 | a0001 | c0003 | t0004 | g0283 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18967 | hp2 | a0001 | c0003 | t0003 | g0046 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18968 | hp2 | a0001 | c0003 | t0004 | g0003 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18973 | hp2 | a0001 | c0003 | t0004 | g0285 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18975 | hp1 | a0001 | c0003 | t0004 | g0021 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0220 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18982 | hp2 | a0001 | c0003 | t0004 | g0287 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18989 | hp1 | a0001 | c0003 | t0004 | g0021 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18989 | hp2 | a0001 | c0001 | t0014 | g0228 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0048 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18993 | hp2 | a0006 | c0012 | t0003 | g0313 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18999 | hp1 | a0001 | c0003 | t0004 | g0003 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19003 | hp2 | a0001 | c0003 | t0003 | g0300 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0295 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19006 | hp2 | a0001 | c0001 | t0013 | g0069 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | LWK | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | LWK | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19055 | hp1 | a0001 | c0003 | t0003 | g0047 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19056 | hp2 | a0001 | c0003 | t0004 | g0288 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19057 | hp1 | a0001 | c0005 | t0002 | g0144 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19057 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19058 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19062 | hp2 | a0001 | c0003 | t0004 | g0003 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19063 | hp2 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19065 | hp1 | a0001 | c0005 | t0002 | g0145 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19065 | hp2 | a0001 | c0001 | t0018 | g0077 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19067 | hp1 | a0001 | c0003 | t0004 | g0290 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19068 | hp1 | a0001 | c0003 | t0004 | g0003 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19072 | hp1 | a0001 | c0003 | t0003 | g0301 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19075 | hp2 | a0001 | c0003 | t0004 | g0286 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19078 | hp2 | a0001 | c0003 | t0004 | g0284 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19081 | hp1 | a0001 | c0005 | t0002 | g0150 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19082 | hp1 | a0001 | c0003 | t0004 | g0003 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19087 | hp1 | a0001 | c0005 | t0002 | g0147 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19088 | hp1 | a0001 | c0003 | t0004 | g0302 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19088 | hp2 | a0001 | c0003 | t0003 | g0048 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19089 | hp2 | a0001 | c0003 | t0003 | g0299 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19240 | hp1 | a0002 | c0004 | t0002 | g0016 | AFR | YRI | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA19240 | hp2 | a0003 | c0007 | t0008 | g0259 | AFR | YRI | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | ASW | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA20129 | hp2 | a0002 | c0004 | t0002 | g0016 | AFR | ASW | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0116 | EUR | TSI | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA20905 | hp1 | a0001 | c0003 | t0003 | g0312 | SAS | GIH | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | GIH | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0159 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0131 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0140 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0161 | AFR | MSL | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0117 | AFR | USA | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | USA | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | USA | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA20300 | hp2 | a0002 | c0004 | t0002 | g0016 | AFR | USA | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0125 | AFR | LWK | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0118 | AFR | LWK | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0136 | REF | REF | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0120 | REF | REF | DBX2_chr12_45009672_45056099 | DBX2 | chr12 | 45009672 | 45056099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45016506 | C | T | 1 | a0006 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.800G>A | p.Arg267Gln | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 972/2806 | 800/1020 | 267/339 | chr12 | 45016506 | |||
| chr12:45023858 | G | C | 1 | a0003 | 3 | HG02572.hp2 HG02630.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.536C>G | p.Ser179Cys | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/4 | 708/2806 | 536/1020 | 179/339 | chr12 | 45023858 | |||
| chr12:45023883 | T | C | 4 | a0001 a0003 a0005 others(1): Show |
304 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(301): Show |
missense_variant | MODERATE | c.511A>G | p.Met171Val | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/4 | 683/2806 | 511/1020 | 171/339 | chr12 | 45023883 | |||
| chr12:45036061 | C | T | 1 | a0005 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.457G>A | p.Gly153Ser | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/4 | 629/2806 | 457/1020 | 153/339 | chr12 | 45036061 | |||
| chr12:45050636 | G | A | 1 | a0004 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.292C>T | p.Pro98Ser | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/4 | 464/2806 | 292/1020 | 98/339 | chr12 | 45050636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45016292 | A | G | 8 | a0001c0001 a0001c0003 a0001c0006 others(5): Show |
306 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(303): Show |
synonymous_variant | LOW | c.1014T>C | p.Ala338Ala | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 1186/2806 | 1014/1020 | 338/339 | chr12 | 45016292 | |||
| chr12:45016505 | C | T | 1 | a0001c0006 | 5 | HG00423.hp2 HG02080.hp2 HG02083.hp2 others(2): Show |
synonymous_variant | LOW | c.801G>A | p.Arg267Arg | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 973/2806 | 801/1020 | 267/339 | chr12 | 45016505 | |||
| chr12:45036038 | T | G | 1 | a0001c0008 | 2 | HG02896.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.480A>C | p.Ala160Ala | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/4 | 652/2806 | 480/1020 | 160/339 | chr12 | 45036038 | |||
| chr12:45050733 | G | A | 4 | a0001c0003 a0001c0008 a0002c0011 others(1): Show |
53 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(50): Show |
synonymous_variant | LOW | c.195C>T | p.Ala65Ala | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/4 | 367/2806 | 195/1020 | 65/339 | chr12 | 45050733 | |||
| chr12:45050856 | G | A | 1 | a0001c0008 | 2 | HG02896.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.72C>T | p.Asn24Asn | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/4 | 244/2806 | 72/1020 | 24/339 | chr12 | 45050856 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45014699 | A | G | 1 | a0001c0001t0016 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1587T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 1587 | chr12 | 45014699 | ||||||
| chr12:45014728 | C | G | 3 | a0001c0001t0005 a0001c0001t0011 a0003c0007t0008 |
19 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1558G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 1558 | chr12 | 45014728 | ||||||
| chr12:45014823 | T | C | 21 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(18): Show |
301 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*1463A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 1463 | chr12 | 45014823 | ||||||
| chr12:45014925 | T | C | 21 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(18): Show |
301 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*1361A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 1361 | chr12 | 45014925 | ||||||
| chr12:45015030 | G | T | 1 | a0001c0001t0015 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1256C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 1256 | chr12 | 45015030 | ||||||
| chr12:45015066 | T | G | 1 | a0001c0001t0010 | 2 | HG00639.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1220A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 1220 | chr12 | 45015066 | ||||||
| chr12:45015331 | G | T | 1 | a0003c0007t0008 | 3 | HG02572.hp2 HG02630.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*955C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 955 | chr12 | 45015331 | ||||||
| chr12:45015384 | G | C | 1 | a0001c0001t0019 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*902C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 902 | chr12 | 45015384 | ||||||
| chr12:45015434 | T | G | 1 | a0005c0009t0017 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 852 | chr12 | 45015434 | ||||||
| chr12:45015437 | T | G | 1 | a0001c0001t0018 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*849A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 849 | chr12 | 45015437 | ||||||
| chr12:45015534 | G | A | 1 | a0001c0003t0004 | 18 | NA18961.hp1 NA18963.hp2 NA18965.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*752C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 752 | chr12 | 45015534 | ||||||
| chr12:45015601 | C | T | 1 | a0001c0001t0014 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*685G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 685 | chr12 | 45015601 | ||||||
| chr12:45015676 | T | C | 2 | a0001c0001t0009 a0001c0001t0019 |
4 | HG02818.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*610A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 610 | chr12 | 45015676 | ||||||
| chr12:45015702 | T | C | 1 | a0001c0001t0020 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 584 | chr12 | 45015702 | ||||||
| chr12:45015823 | A | G | 1 | a0001c0001t0013 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*463T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 463 | chr12 | 45015823 | ||||||
| chr12:45016012 | T | C | 3 | a0001c0003t0003 a0001c0003t0004 a0006c0012t0003 |
50 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*274A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 274 | chr12 | 45016012 | ||||||
| chr12:45016146 | G | T | 1 | a0001c0001t0006 | 6 | HG02129.hp2 NA18944.hp2 NA18977.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*140C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 140 | chr12 | 45016146 | ||||||
| chr12:45016251 | C | T | 1 | a0002c0002t0012 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 35 | chr12 | 45016251 | ||||||
| chr12:45016280 | T | C | 1 | a0002c0002t0007 | 4 | HG01069.hp2 HG01257.hp1 HG01261.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 4/4 | 6 | chr12 | 45016280 | ||||||
| chr12:45050987 | C | T | 1 | a0001c0001t0011 | 1 | HG03453.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/4 | 60 | chr12 | 45050987 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45016708 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.688-90G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45016708 | |||||||
| chr12:45016767 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.688-149C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45016767 | |||||||
| chr12:45016787 | T | C | 214 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
273 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.688-169A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45016787 | |||||||
| chr12:45016801 | A | ATT | 3 | a0003c0007t0008g0259 a0003c0007t0008g0278 a0003c0007t0008g0279 |
3 | HG02572.hp2 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.688-185_688-184dup others(2): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45016801 | |||||||
| chr12:45016831 | T | C | 2 | a0001c0001t0006g0017 a0001c0001t0006g0219 |
4 | NA18944.hp2 NA18977.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-213A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45016831 | |||||||
| chr12:45016860 | T | C | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(112): Show |
144 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.688-242A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45016860 | |||||||
| chr12:45016945 | G | A | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
272 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.688-327C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45016945 | |||||||
| chr12:45016991 | G | T | 1 | a0001c0003t0003g0294 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.688-373C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45016991 | |||||||
| chr12:45017025 | A | G | 214 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
273 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.688-407T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017025 | |||||||
| chr12:45017030 | C | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.688-412G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017030 | |||||||
| chr12:45017056 | G | A | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(89): Show |
121 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.688-438C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017056 | |||||||
| chr12:45017195 | T | G | 243 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
307 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.688-577A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017195 | |||||||
| chr12:45017215 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.688-597T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017215 | |||||||
| chr12:45017362 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0179 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.688-744T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017362 | |||||||
| chr12:45017374 | C | T | 18 | a0001c0001t0005g0030 a0001c0001t0005g0097 a0001c0001t0005g0098 others(15): Show |
19 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.688-756G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017374 | |||||||
| chr12:45017398 | T | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
301 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.688-780A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017398 | |||||||
| chr12:45017442 | T | C | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(47): Show |
65 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.688-824A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017442 | |||||||
| chr12:45017505 | G | T | 2 | a0002c0002t0002g0009 a0002c0002t0002g0090 |
5 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.688-887C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017505 | |||||||
| chr12:45017614 | T | C | 3 | a0001c0001t0001g0091 a0001c0008t0001g0314 a0001c0008t0001g0315 |
3 | HG02896.hp1 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.688-996A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017614 | |||||||
| chr12:45017679 | T | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.688-1061A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017679 | |||||||
| chr12:45017850 | G | C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-1232C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017850 | |||||||
| chr12:45017906 | T | C | 15 | a0001c0001t0005g0030 a0001c0001t0005g0097 a0001c0001t0005g0098 others(12): Show |
16 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.688-1288A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017906 | |||||||
| chr12:45017910 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.688-1292T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45017910 | |||||||
| chr12:45018265 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.688-1647G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45018265 | |||||||
| chr12:45018479 | G | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.688-1861C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45018479 | |||||||
| chr12:45018700 | G | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.688-2082C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45018700 | |||||||
| chr12:45019236 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.688-2618A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45019236 | |||||||
| chr12:45019424 | C | T | 2 | a0001c0001t0006g0017 a0001c0001t0006g0219 |
4 | NA18944.hp2 NA18977.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-2806G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45019424 | |||||||
| chr12:45019511 | T | C | 2 | a0002c0002t0002g0121 a0002c0002t0002g0125 |
2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.688-2893A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45019511 | |||||||
| chr12:45019563 | T | G | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.688-2945A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45019563 | |||||||
| chr12:45019671 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0006g0195 |
3 | HG02129.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.688-3053G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45019671 | |||||||
| chr12:45019715 | A | T | 5 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.688-3097T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45019715 | |||||||
| chr12:45020047 | C | T | 2 | a0002c0002t0002g0027 a0002c0002t0002g0092 |
3 | HG02886.hp2 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.688-3429G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020047 | |||||||
| chr12:45020123 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.688-3505G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020123 | |||||||
| chr12:45020169 | C | T | 3 | a0001c0001t0001g0257 a0002c0002t0002g0182 a0002c0002t0002g0183 |
3 | HG01167.hp2 HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.687+3538G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020169 | |||||||
| chr12:45020191 | A | G | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
301 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.687+3516T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020191 | |||||||
| chr12:45020191 | A | T | 1 | a0001c0003t0004g0290 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.687+3516T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020191 | |||||||
| chr12:45020237 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.687+3470G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020237 | |||||||
| chr12:45020420 | C | T | 170 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
214 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.687+3287G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020420 | |||||||
| chr12:45020442 | A | G | 5 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+3265T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020442 | |||||||
| chr12:45020550 | G | GA | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+3156dupT | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020550 | |||||||
| chr12:45020675 | G | GTA | 56 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(53): Show |
73 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.687+3030_687+3031d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020675 | |||||||
| chr12:45020675 | G | GTATA | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
199 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.687+3028_687+3031d others(6): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020675 | |||||||
| chr12:45020675 | G | GTATATA | 11 | a0001c0001t0001g0037 a0001c0001t0001g0083 a0001c0001t0001g0091 others(8): Show |
12 | HG00673.hp1 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.687+3026_687+3031d others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020675 | |||||||
| chr12:45020675 | G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0227 a0003c0007t0008g0259 a0003c0007t0008g0278 others(1): Show |
4 | HG02572.hp2 HG02630.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+3024_687+3031d others(10): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020675 | |||||||
| chr12:45020690 | T | TATAC | 10 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0194 others(7): Show |
12 | HG00621.hp2 HG02074.hp2 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.687+3016_687+3017i others(6): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020690 | |||||||
| chr12:45020690 | T | TATATATA others(1): Show |
3 | a0001c0001t0009g0117 a0001c0001t0009g0118 a0001c0001t0009g0119 |
3 | HG02818.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.687+3016_687+3017i others(10): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020690 | |||||||
| chr12:45020692 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0153 others(4): Show |
9 | HG01167.hp1 HG01169.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.687+3015G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020692 | |||||||
| chr12:45020774 | G | C | 1 | a0002c0002t0002g0033 | 2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.687+2933C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020774 | |||||||
| chr12:45020812 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0139 |
2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.687+2895A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020812 | |||||||
| chr12:45020813 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.687+2894C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020813 | |||||||
| chr12:45020848 | C | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+2859G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020848 | |||||||
| chr12:45020906 | G | A | 36 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(33): Show |
50 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.687+2801C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45020906 | |||||||
| chr12:45021406 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.687+2301A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021406 | |||||||
| chr12:45021440 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2267C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021440 | |||||||
| chr12:45021468 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2239A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021468 | |||||||
| chr12:45021490 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2217C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021490 | |||||||
| chr12:45021499 | A | C | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2208T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021499 | |||||||
| chr12:45021503 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2204A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021503 | |||||||
| chr12:45021504 | A | T | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2203T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021504 | |||||||
| chr12:45021505 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2202C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021505 | |||||||
| chr12:45021506 | C | A | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2201G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021506 | |||||||
| chr12:45021509 | C | A | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2198G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021509 | |||||||
| chr12:45021510 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2197C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021510 | |||||||
| chr12:45021518 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2189C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021518 | |||||||
| chr12:45021524 | C | A | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2183G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021524 | |||||||
| chr12:45021531 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2176A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021531 | |||||||
| chr12:45021532 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2175C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021532 | |||||||
| chr12:45021538 | T | A | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2169A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021538 | |||||||
| chr12:45021539 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2168T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021539 | |||||||
| chr12:45021546 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2161C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021546 | |||||||
| chr12:45021547 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.687+2160A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021547 | |||||||
| chr12:45021578 | T | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+2129A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021578 | |||||||
| chr12:45021631 | T | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+2076A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021631 | |||||||
| chr12:45021632 | G | A | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.687+2075C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021632 | |||||||
| chr12:45021747 | G | A | 3 | a0001c0001t0001g0091 a0001c0008t0001g0314 a0001c0008t0001g0315 |
3 | HG02896.hp1 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.687+1960C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021747 | |||||||
| chr12:45021749 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0153 others(1): Show |
6 | HG01167.hp1 HG01169.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1958G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021749 | |||||||
| chr12:45021789 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
375 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(372): Show |
intron_variant | MODIFIER | c.687+1918T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021789 | |||||||
| chr12:45021849 | ATGATACT others(29): Show |
A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
275 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.687+1822_687+1857d others(38): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021849 | |||||||
| chr12:45021861 | A | G | 1 | a0002c0002t0012g0134 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.687+1846T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021861 | |||||||
| chr12:45021887 | T | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
275 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.687+1820A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021887 | |||||||
| chr12:45021888 | T | G | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
275 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.687+1819A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021888 | |||||||
| chr12:45021902 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.687+1805G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021902 | |||||||
| chr12:45021908 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.687+1799C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021908 | |||||||
| chr12:45021980 | C | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
219 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.687+1727G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45021980 | |||||||
| chr12:45022005 | C | G | 3 | a0001c0001t0005g0174 a0001c0001t0005g0175 a0001c0001t0011g0049 |
3 | HG02055.hp2 HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.687+1702G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022005 | |||||||
| chr12:45022211 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1496G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022211 | |||||||
| chr12:45022298 | G | GT | 57 | a0001c0001t0001g0055 a0001c0001t0001g0141 a0001c0001t0001g0194 others(54): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.687+1408dupA | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022298 | |||||||
| chr12:45022298 | G | GTT | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
173 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.687+1407_687+1408d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022298 | |||||||
| chr12:45022298 | G | GTTT | 39 | a0001c0001t0001g0026 a0001c0001t0001g0038 a0001c0001t0001g0040 others(36): Show |
44 | HG00544.hp2 HG00621.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.687+1406_687+1408d others(5): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022298 | |||||||
| chr12:45022298 | G | GTTTTT | 7 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0107 others(4): Show |
7 | HG01361.hp1 HG01978.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.687+1404_687+1408d others(7): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022298 | |||||||
| chr12:45022298 | G | GTTTTTT | 11 | a0001c0001t0005g0030 a0001c0001t0005g0098 a0001c0001t0005g0099 others(8): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.687+1403_687+1408d others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022298 | |||||||
| chr12:45022322 | G | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0037 a0001c0001t0001g0153 others(1): Show |
6 | HG01167.hp1 HG01169.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1385C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022322 | |||||||
| chr12:45022328 | G | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(89): Show |
121 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.687+1379C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022328 | |||||||
| chr12:45022357 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.687+1350C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022357 | |||||||
| chr12:45022396 | T | G | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+1311A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022396 | |||||||
| chr12:45022428 | C | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+1279G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022428 | |||||||
| chr12:45022448 | C | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+1259G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022448 | |||||||
| chr12:45022452 | A | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+1255T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022452 | |||||||
| chr12:45022512 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.687+1195C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022512 | |||||||
| chr12:45022594 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.687+1113C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022594 | |||||||
| chr12:45022600 | G | A | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
284 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.687+1107C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022600 | |||||||
| chr12:45022711 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.687+996G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022711 | |||||||
| chr12:45022821 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+886G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022821 | |||||||
| chr12:45022826 | T | C | 19 | a0001c0001t0005g0030 a0001c0001t0005g0097 a0001c0001t0005g0098 others(16): Show |
20 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+881A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022826 | |||||||
| chr12:45022844 | G | A | 1 | a0002c0002t0002g0090 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.687+863C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022844 | |||||||
| chr12:45022904 | T | A | 6 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+803A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45022904 | |||||||
| chr12:45023027 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+680C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023027 | |||||||
| chr12:45023069 | G | A | 1 | a0001c0003t0004g0286 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.687+638C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023069 | |||||||
| chr12:45023224 | A | G | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+483T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023224 | |||||||
| chr12:45023271 | G | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+436C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023271 | |||||||
| chr12:45023304 | T | C | 26 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(23): Show |
27 | HG01192.hp2 HG01361.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.687+403A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023304 | |||||||
| chr12:45023312 | G | A | 7 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(4): Show |
7 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.687+395C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023312 | |||||||
| chr12:45023321 | A | G | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+386T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023321 | |||||||
| chr12:45023412 | A | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+295T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023412 | |||||||
| chr12:45023444 | G | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.687+263C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023444 | |||||||
| chr12:45023497 | C | T | 1 | a0001c0001t0010g0234 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.687+210G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023497 | |||||||
| chr12:45023629 | C | T | 7 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
7 | HG01361.hp1 HG01975.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.687+78G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 3/3 | chr12 | 45023629 | |||||||
| chr12:45023923 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0179 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.500-29G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45023923 | |||||||
| chr12:45023939 | A | T | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-45T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45023939 | |||||||
| chr12:45024129 | G | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0211 |
2 | HG00323.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.500-235C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024129 | |||||||
| chr12:45024171 | G | T | 6 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-277C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024171 | |||||||
| chr12:45024179 | A | ATGGTT | 2 | a0002c0002t0002g0009 a0002c0002t0002g0090 |
5 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-290_500-286dup others(5): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024179 | |||||||
| chr12:45024244 | A | C | 2 | a0002c0002t0002g0127 a0002c0002t0002g0131 |
2 | HG01255.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.500-350T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024244 | |||||||
| chr12:45024249 | A | G | 238 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
299 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.500-355T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024249 | |||||||
| chr12:45024251 | G | T | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-357C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024251 | |||||||
| chr12:45024259 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.500-365A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024259 | |||||||
| chr12:45024281 | G | A | 3 | a0001c0001t0001g0091 a0001c0008t0001g0314 a0001c0008t0001g0315 |
3 | HG02896.hp1 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.500-387C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024281 | |||||||
| chr12:45024308 | C | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-414G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024308 | |||||||
| chr12:45024350 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0179 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.500-456T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024350 | |||||||
| chr12:45024362 | C | T | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-468G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024362 | |||||||
| chr12:45024363 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0060 a0001c0001t0001g0080 |
3 | NA18944.hp1 NA19010.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.500-469C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024363 | |||||||
| chr12:45024469 | C | T | 12 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(9): Show |
18 | HG00408.hp1 HG00558.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.500-575G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024469 | |||||||
| chr12:45024489 | A | T | 36 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(33): Show |
50 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.500-595T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024489 | |||||||
| chr12:45024501 | G | A | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-607C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024501 | |||||||
| chr12:45024528 | C | T | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
267 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.500-634G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024528 | |||||||
| chr12:45024533 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.500-639G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024533 | |||||||
| chr12:45024600 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.500-706A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024600 | |||||||
| chr12:45024675 | G | A | 243 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
307 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.500-781C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024675 | |||||||
| chr12:45024697 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.500-803G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024697 | |||||||
| chr12:45024875 | G | C | 1 | a0001c0001t0001g0006 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.500-981C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024875 | |||||||
| chr12:45024906 | C | T | 5 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(2): Show |
5 | HG01884.hp1 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-1012G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024906 | |||||||
| chr12:45024907 | C | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.500-1013G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45024907 | |||||||
| chr12:45025134 | A | T | 1 | a0002c0002t0002g0156 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.500-1240T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025134 | |||||||
| chr12:45025167 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.500-1273G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025167 | |||||||
| chr12:45025186 | G | A | 1 | a0002c0002t0002g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.500-1292C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025186 | |||||||
| chr12:45025243 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(52): Show |
70 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.500-1349C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025243 | |||||||
| chr12:45025538 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.500-1644G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025538 | |||||||
| chr12:45025619 | T | C | 282 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(279): Show |
368 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(365): Show |
intron_variant | MODIFIER | c.500-1725A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025619 | |||||||
| chr12:45025761 | T | TAGAAAGA others(309): Show |
1 | a0001c0003t0004g0284 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.500-1868_500-1867i others(318): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(304): Show |
6 | a0001c0001t0005g0097 a0001c0001t0005g0152 a0001c0001t0011g0049 others(3): Show |
6 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(313): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(305): Show |
12 | a0001c0001t0001g0104 a0001c0001t0005g0030 a0001c0001t0005g0098 others(9): Show |
13 | HG01975.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(314): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(306): Show |
8 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(5): Show |
8 | HG01361.hp1 HG01978.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(315): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(295): Show |
1 | a0001c0001t0001g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(304): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(305): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(314): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(310): Show |
1 | a0001c0003t0003g0301 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(319): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(311): Show |
30 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(27): Show |
43 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(320): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(312): Show |
4 | a0001c0003t0003g0048 a0001c0003t0003g0293 a0001c0003t0004g0286 others(1): Show |
5 | NA18948.hp1 NA18990.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(321): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(325): Show |
2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01884.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(334): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(326): Show |
3 | a0001c0001t0001g0252 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG02257.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(335): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(308): Show |
2 | a0001c0001t0001g0091 a0001c0008t0001g0314 |
2 | HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(317): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(309): Show |
1 | a0001c0008t0001g0315 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.500-1868_500-1867i others(318): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(302): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0200 |
2 | HG01255.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(311): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(303): Show |
61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(58): Show |
81 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(312): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(304): Show |
2 | a0001c0001t0001g0227 a0005c0009t0017g0190 |
2 | NA18959.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(313): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(305): Show |
2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(314): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(309): Show |
1 | a0001c0001t0001g0066 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.500-1868_500-1867i others(318): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(313): Show |
1 | a0001c0006t0001g0086 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(322): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(316): Show |
3 | a0001c0001t0001g0059 a0001c0001t0001g0065 a0001c0001t0001g0067 |
3 | HG00099.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(325): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(321): Show |
1 | a0001c0001t0001g0052 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(330): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(322): Show |
6 | a0001c0001t0001g0053 a0001c0001t0001g0068 a0001c0001t0001g0088 others(3): Show |
6 | HG01496.hp1 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(331): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(323): Show |
11 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0063 others(8): Show |
14 | HG00423.hp2 HG01943.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(332): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(324): Show |
13 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0054 others(10): Show |
20 | HG00558.hp2 HG00733.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(333): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(325): Show |
8 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0076 others(5): Show |
8 | HG00673.hp2 HG02080.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(334): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(326): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0058 a0001c0001t0001g0060 others(1): Show |
6 | NA18939.hp1 NA19003.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(335): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(327): Show |
7 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0079 others(4): Show |
9 | HG02622.hp2 HG03225.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(336): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(328): Show |
5 | a0001c0001t0001g0051 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG02129.hp1 HG02809.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(337): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(329): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0270 |
2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(338): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(330): Show |
3 | a0001c0001t0001g0025 a0001c0001t0001g0083 a0001c0001t0001g0170 |
4 | HG02015.hp1 HG02976.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(339): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(332): Show |
1 | a0001c0001t0001g0139 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.500-1868_500-1867i others(341): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(333): Show |
1 | a0002c0004t0001g0186 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(342): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(334): Show |
1 | a0001c0001t0001g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(343): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(335): Show |
1 | a0001c0001t0001g0258 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(344): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(340): Show |
1 | a0001c0001t0001g0093 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.500-1868_500-1867i others(349): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(346): Show |
1 | a0001c0001t0001g0096 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(355): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(347): Show |
1 | a0001c0001t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(356): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(303): Show |
3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0206 |
3 | HG01099.hp2 HG02132.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(312): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(327): Show |
1 | a0001c0001t0001g0272 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.500-1868_500-1867i others(336): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(328): Show |
1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.500-1868_500-1867i others(337): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(302): Show |
2 | a0001c0001t0001g0230 a0001c0001t0001g0236 |
2 | NA18946.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.500-1868_500-1867i others(311): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025761 | T | TAGAAAGA others(303): Show |
21 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
30 | HG00544.hp2 HG00621.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.500-1868_500-1867i others(312): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025761 | |||||||
| chr12:45025804 | G | C | 2 | a0001c0001t0009g0117 a0001c0001t0009g0118 |
2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.500-1910C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45025804 | |||||||
| chr12:45026067 | A | G | 1 | a0001c0003t0003g0305 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.500-2173T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026067 | |||||||
| chr12:45026128 | A | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-2234T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026128 | |||||||
| chr12:45026255 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.500-2361C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026255 | |||||||
| chr12:45026322 | C | A | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-2428G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026322 | |||||||
| chr12:45026344 | A | G | 208 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
266 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.500-2450T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026344 | |||||||
| chr12:45026589 | A | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.500-2695T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026589 | |||||||
| chr12:45026595 | T | G | 1 | a0001c0001t0019g0251 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.500-2701A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026595 | |||||||
| chr12:45026673 | T | C | 1 | a0002c0002t0002g0133 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.500-2779A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026673 | |||||||
| chr12:45026895 | C | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(47): Show |
65 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.500-3001G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026895 | |||||||
| chr12:45026973 | CT | C | 8 | a0001c0005t0002g0165 a0002c0002t0002g0160 a0002c0002t0002g0161 others(5): Show |
8 | HG01109.hp1 HG01175.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-3080delA | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026973 | |||||||
| chr12:45026976 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0274 |
2 | HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.500-3082A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026976 | |||||||
| chr12:45026996 | C | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-3102G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026996 | |||||||
| chr12:45026997 | A | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-3103T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45026997 | |||||||
| chr12:45027011 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-3117A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027011 | |||||||
| chr12:45027345 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.500-3451G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027345 | |||||||
| chr12:45027348 | A | C | 1 | a0001c0006t0001g0061 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.500-3454T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027348 | |||||||
| chr12:45027378 | C | A | 2 | a0002c0002t0002g0166 a0002c0002t0002g0167 |
2 | HG01175.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.500-3484G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027378 | |||||||
| chr12:45027401 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0179 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.500-3507A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027401 | |||||||
| chr12:45027420 | C | T | 5 | a0001c0001t0005g0097 a0001c0001t0005g0152 a0003c0007t0008g0259 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-3526G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027420 | |||||||
| chr12:45027550 | C | A | 2 | a0002c0002t0002g0128 a0002c0002t0002g0129 |
2 | HG01099.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.500-3656G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027550 | |||||||
| chr12:45027646 | A | G | 1 | a0001c0006t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.500-3752T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027646 | |||||||
| chr12:45027661 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.500-3767A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027661 | |||||||
| chr12:45027698 | G | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.500-3804C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027698 | |||||||
| chr12:45027738 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.500-3844G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027738 | |||||||
| chr12:45027741 | C | T | 36 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(33): Show |
50 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.500-3847G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45027741 | |||||||
| chr12:45028027 | G | C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-4133C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028027 | |||||||
| chr12:45028114 | C | G | 8 | a0001c0001t0001g0091 a0001c0001t0001g0252 a0001c0001t0001g0253 others(5): Show |
8 | HG01884.hp1 HG02257.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.500-4220G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028114 | |||||||
| chr12:45028124 | A | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0153 a0001c0001t0001g0177 |
4 | HG01167.hp1 HG01169.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-4230T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028124 | |||||||
| chr12:45028192 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.500-4298A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028192 | |||||||
| chr12:45028387 | C | T | 72 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0147 others(69): Show |
112 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.500-4493G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028387 | |||||||
| chr12:45028404 | CT | C | 18 | a0001c0001t0005g0030 a0001c0001t0005g0097 a0001c0001t0005g0098 others(15): Show |
19 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.500-4511delA | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028404 | |||||||
| chr12:45028453 | A | G | 55 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0147 others(52): Show |
74 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.500-4559T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028453 | |||||||
| chr12:45028476 | T | C | 1 | a0001c0003t0004g0287 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.500-4582A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028476 | |||||||
| chr12:45028499 | G | A | 4 | a0001c0001t0001g0103 a0001c0003t0003g0308 a0002c0002t0002g0027 others(1): Show |
5 | HG01934.hp1 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-4605C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028499 | |||||||
| chr12:45028552 | G | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
7 | HG02040.hp1 NA18612.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.500-4658C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028552 | |||||||
| chr12:45028561 | A | G | 18 | a0001c0001t0005g0030 a0001c0001t0005g0097 a0001c0001t0005g0098 others(15): Show |
19 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.500-4667T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028561 | |||||||
| chr12:45028659 | C | T | 18 | a0001c0001t0005g0030 a0001c0001t0005g0097 a0001c0001t0005g0098 others(15): Show |
19 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.500-4765G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028659 | |||||||
| chr12:45028660 | G | A | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(113): Show |
145 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.500-4766C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028660 | |||||||
| chr12:45028716 | G | T | 1 | a0002c0004t0002g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.500-4822C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028716 | |||||||
| chr12:45028752 | C | T | 1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.500-4858G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45028752 | |||||||
| chr12:45029269 | G | A | 1 | a0004c0010t0002g0282 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.500-5375C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029269 | |||||||
| chr12:45029306 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0179 |
2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.500-5412C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029306 | |||||||
| chr12:45029516 | G | A | 7 | a0001c0003t0003g0048 a0001c0003t0003g0303 a0001c0003t0003g0305 others(4): Show |
8 | HG00544.hp1 HG01934.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.500-5622C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029516 | |||||||
| chr12:45029734 | G | A | 9 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.500-5840C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029734 | |||||||
| chr12:45029863 | TA | T | 28 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0028 others(25): Show |
42 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.500-5970delT | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029863 | |||||||
| chr12:45029871 | A | AATAAT | 13 | a0001c0003t0003g0048 a0001c0003t0003g0300 a0001c0003t0003g0301 others(10): Show |
14 | HG00544.hp1 HG01934.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.500-5978_500-5977i others(7): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029871 | |||||||
| chr12:45029871 | A | T | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0005g0097 others(4): Show |
7 | HG01192.hp2 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.500-5977T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029871 | |||||||
| chr12:45029874 | T | A | 13 | a0001c0003t0003g0048 a0001c0003t0003g0300 a0001c0003t0003g0301 others(10): Show |
14 | HG00544.hp1 HG01934.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.500-5980A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029874 | |||||||
| chr12:45029877 | T | A | 3 | a0001c0001t0001g0103 a0002c0002t0002g0044 a0002c0002t0002g0262 |
4 | HG00738.hp1 HG02280.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.500-5983A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029877 | |||||||
| chr12:45029879 | A | AAAAT | 10 | a0001c0001t0001g0093 a0001c0001t0001g0173 a0001c0001t0001g0208 others(7): Show |
11 | HG01109.hp2 HG01884.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.500-5989_500-5986d others(6): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029879 | A | AAAATAAA others(9): Show |
1 | a0001c0001t0001g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.500-5986_500-5985i others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029879 | A | AAAATAAA others(1): Show |
109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(106): Show |
138 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.500-5993_500-5986d others(10): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029879 | A | AAAATAAA others(5): Show |
56 | a0001c0001t0001g0096 a0001c0001t0001g0103 a0001c0001t0001g0141 others(53): Show |
69 | HG00408.hp1 HG00738.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.500-5997_500-5986d others(14): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029879 | A | AAAATAAA others(9): Show |
2 | a0001c0001t0001g0214 a0001c0003t0003g0299 |
2 | HG03834.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.500-6001_500-5986d others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029879 | A | AAT | 4 | a0001c0003t0003g0048 a0001c0003t0003g0300 a0001c0003t0003g0303 others(1): Show |
5 | HG00544.hp1 HG01943.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-5986_500-5985i others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029879 | A | AATAAAT | 9 | a0001c0003t0003g0301 a0001c0003t0003g0304 a0001c0003t0003g0305 others(6): Show |
9 | HG01934.hp1 HG01952.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.500-5986_500-5985i others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029879 | A | AT | 2 | a0002c0002t0002g0044 a0002c0002t0002g0262 |
3 | HG00738.hp1 HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.500-5986_500-5985i others(3): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029879 | AAAATAAA others(5): Show |
A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(85): Show |
128 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.500-5997_500-5986d others(14): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029879 | |||||||
| chr12:45029911 | T | TAAATAAA others(9): Show |
1 | a0001c0001t0001g0037 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.500-6018_500-6017i others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029911 | |||||||
| chr12:45029916 | A | G | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.500-6022T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029916 | |||||||
| chr12:45029945 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.500-6051A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029945 | |||||||
| chr12:45029984 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(78): Show |
115 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.499+6035G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029984 | |||||||
| chr12:45029998 | C | T | 30 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0028 others(27): Show |
45 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.499+6021G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45029998 | |||||||
| chr12:45030013 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.499+6006G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030013 | |||||||
| chr12:45030095 | A | G | 1 | a0002c0002t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.499+5924T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030095 | |||||||
| chr12:45030109 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.499+5910C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030109 | |||||||
| chr12:45030242 | CCAAA | C | 29 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0028 others(26): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.499+5773_499+5776d others(6): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030242 | |||||||
| chr12:45030286 | C | T | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.499+5733G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030286 | |||||||
| chr12:45030393 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.499+5626T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030393 | |||||||
| chr12:45030422 | T | C | 2 | a0002c0002t0002g0009 a0002c0002t0002g0090 |
5 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+5597A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030422 | |||||||
| chr12:45030475 | C | T | 9 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0194 others(6): Show |
11 | HG00621.hp2 HG02074.hp2 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.499+5544G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030475 | |||||||
| chr12:45030487 | T | C | 1 | a0001c0003t0003g0294 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.499+5532A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030487 | |||||||
| chr12:45030553 | ATGGCAC | A | 25 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0153 others(22): Show |
27 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.499+5460_499+5465d others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030553 | |||||||
| chr12:45030633 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(85): Show |
128 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.499+5386C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030633 | |||||||
| chr12:45030760 | G | GT | 25 | a0001c0001t0001g0037 a0001c0001t0001g0093 a0001c0001t0001g0153 others(22): Show |
27 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.499+5258dupA | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030760 | |||||||
| chr12:45030764 | G | C | 1 | a0002c0004t0002g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.499+5255C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030764 | |||||||
| chr12:45030842 | A | G | 310 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(307): Show |
411 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(408): Show |
intron_variant | MODIFIER | c.499+5177T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030842 | |||||||
| chr12:45030870 | G | T | 1 | a0001c0001t0001g0063 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.499+5149C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45030870 | |||||||
| chr12:45031023 | G | A | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.499+4996C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031023 | |||||||
| chr12:45031121 | G | C | 9 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(6): Show |
9 | HG02055.hp2 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.499+4898C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031121 | |||||||
| chr12:45031147 | G | A | 1 | a0001c0001t0015g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.499+4872C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031147 | |||||||
| chr12:45031191 | A | AGT | 11 | a0001c0001t0001g0170 a0001c0001t0001g0252 a0001c0001t0001g0253 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.499+4826_499+4827d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031191 | |||||||
| chr12:45031191 | A | AGTGT | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(3): Show |
6 | HG02109.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+4824_499+4827d others(6): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031191 | |||||||
| chr12:45031191 | A | AGTGTGTG others(3): Show |
12 | a0001c0001t0001g0236 a0001c0003t0003g0048 a0001c0003t0003g0301 others(9): Show |
13 | HG01934.hp1 HG01943.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.499+4818_499+4827d others(12): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031191 | |||||||
| chr12:45031191 | A | AGTGTGTG others(5): Show |
5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG00544.hp1 HG01978.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+4816_499+4827d others(14): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031191 | |||||||
| chr12:45031191 | A | AGTGTGTG others(7): Show |
5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG01361.hp1 HG01975.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+4814_499+4827d others(16): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031191 | |||||||
| chr12:45031191 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.499+4828T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031191 | |||||||
| chr12:45031194 | G | A | 1 | a0002c0002t0002g0113 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.499+4825C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031194 | |||||||
| chr12:45031213 | TGTGTGTG others(11): Show |
T | 1 | a0001c0001t0001g0062 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.499+4788_499+4805d others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031213 | |||||||
| chr12:45031215 | TGTGTGTG others(11): Show |
T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(40): Show |
59 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.499+4786_499+4803d others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031215 | |||||||
| chr12:45031215 | TGTGTGTG others(15): Show |
T | 1 | a0001c0001t0001g0087 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.499+4782_499+4803d others(24): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031215 | |||||||
| chr12:45031217 | TGTGTGTG others(9): Show |
T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0083 |
2 | HG00099.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.499+4786_499+4801d others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031217 | |||||||
| chr12:45031217 | TGTGTGTG others(11): Show |
T | 35 | a0001c0001t0001g0091 a0001c0005t0002g0144 a0001c0005t0002g0145 others(32): Show |
52 | HG00423.hp1 HG00621.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.499+4784_499+4801d others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031217 | |||||||
| chr12:45031218 | GTGTGTGT others(10): Show |
G | 1 | a0002c0004t0002g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.499+4784_499+4800d others(19): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031218 | |||||||
| chr12:45031219 | TGTGTGTG others(9): Show |
T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0002c0004t0002g0016 others(1): Show |
5 | HG01256.hp1 HG01258.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+4784_499+4799d others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031219 | |||||||
| chr12:45031219 | TGTGTGTG others(11): Show |
T | 1 | a0002c0002t0002g0001 | 2 | NA19002.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.499+4782_499+4799d others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031219 | |||||||
| chr12:45031219 | TGTGTGTG others(13): Show |
T | 2 | a0002c0002t0002g0009 a0002c0002t0002g0090 |
5 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+4780_499+4799d others(22): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031219 | |||||||
| chr12:45031221 | T | TGA | 2 | a0002c0002t0007g0032 a0002c0002t0007g0138 |
3 | HG01069.hp2 HG01257.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.499+4797_499+4798i others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031221 | |||||||
| chr12:45031223 | T | A | 3 | a0002c0002t0007g0032 a0002c0002t0007g0137 a0002c0002t0007g0138 |
4 | HG01069.hp2 HG01257.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+4796A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031223 | |||||||
| chr12:45031223 | T | TGAGAGA | 3 | a0002c0002t0002g0128 a0002c0002t0002g0129 a0002c0002t0002g0159 |
3 | HG01099.hp1 HG01123.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.499+4795_499+4796i others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031223 | |||||||
| chr12:45031223 | TGTGAGAG others(3): Show |
T | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.499+4786_499+4795d others(12): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031223 | |||||||
| chr12:45031225 | T | A | 6 | a0002c0002t0002g0128 a0002c0002t0002g0129 a0002c0002t0002g0159 others(3): Show |
7 | HG01069.hp2 HG01099.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+4794A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGA | 2 | a0002c0002t0002g0044 a0002c0002t0002g0262 |
3 | HG00738.hp1 HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.499+4792_499+4793d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGAGAGA | 13 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0028 others(10): Show |
18 | HG00323.hp2 HG00642.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.499+4788_499+4793d others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGAGAGAG others(1): Show |
7 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0031 others(4): Show |
10 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+4786_499+4793d others(10): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGAGAGAG others(5): Show |
1 | a0002c0002t0002g0127 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.499+4782_499+4793d others(14): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGAGA | 3 | a0001c0001t0001g0212 a0002c0002t0002g0125 a0002c0002t0002g0130 |
3 | HG01361.hp2 NA19009.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGAGAG others(3): Show |
2 | a0001c0001t0005g0174 a0001c0001t0005g0175 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(12): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGAG others(1): Show |
6 | a0001c0001t0001g0194 a0001c0001t0005g0098 a0001c0001t0005g0099 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(10): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGAG others(3): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0192 |
2 | HG00408.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(12): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(1): Show |
5 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0226 others(2): Show |
6 | HG00639.hp2 HG01433.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(10): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(3): Show |
40 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(37): Show |
48 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(12): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(5): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0204 others(4): Show |
7 | HG01109.hp2 HG01261.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(14): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0213 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.499+4793_499+4794i others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(3): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0249 a0001c0001t0001g0272 |
3 | HG00323.hp1 HG02976.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(12): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(5): Show |
18 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0042 others(15): Show |
21 | HG00642.hp2 HG00738.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(14): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(7): Show |
6 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0196 others(3): Show |
6 | HG02486.hp2 HG04115.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(16): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(9): Show |
3 | a0001c0003t0003g0007 a0001c0003t0003g0291 a0001c0003t0004g0003 |
3 | NA18941.hp1 NA18954.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(11): Show |
2 | a0001c0003t0003g0047 a0001c0003t0004g0284 |
2 | NA19055.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(5): Show |
7 | a0001c0001t0001g0093 a0001c0001t0001g0210 a0001c0001t0001g0247 others(4): Show |
8 | HG02145.hp2 HG02451.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(14): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(7): Show |
22 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): Show |
27 | HG00544.hp2 HG00621.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(16): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.499+4793_499+4794i others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(11): Show |
9 | a0001c0001t0001g0039 a0001c0003t0003g0007 a0001c0003t0003g0046 others(6): Show |
12 | HG00558.hp1 HG02040.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(15): Show |
1 | a0001c0003t0004g0003 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.499+4793_499+4794i others(24): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0177 a0001c0001t0001g0243 |
2 | HG02056.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(16): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(9): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0229 a0001c0001t0001g0237 |
4 | NA18961.hp2 NA19001.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(13): Show |
11 | a0001c0003t0003g0007 a0001c0003t0003g0047 a0001c0003t0004g0003 others(8): Show |
16 | HG00408.hp1 HG02523.hp1 NA18946.hp2 others(13): Show |
intron_variant | MODIFIER | c.499+4793_499+4794i others(22): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(15): Show |
2 | a0001c0003t0003g0296 a0001c0003t0004g0021 |
2 | HG03491.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(24): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0037 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0245 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.499+4793_499+4794i others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(15): Show |
2 | a0001c0003t0003g0299 a0001c0003t0004g0283 |
2 | NA18966.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.499+4793_499+4794i others(24): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031225 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.499+4793_499+4794i others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031225 | |||||||
| chr12:45031227 | A | T | 24 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(21): Show |
24 | HG01361.hp1 HG01891.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.499+4792T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031227 | |||||||
| chr12:45031229 | A | T | 8 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0141 others(5): Show |
8 | HG01981.hp2 HG02145.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.499+4790T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031229 | |||||||
| chr12:45031231 | A | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0179 a0002c0004t0002g0154 |
3 | HG02145.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.499+4788T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031231 | |||||||
| chr12:45031233 | A | T | 1 | a0001c0001t0001g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.499+4786T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031233 | |||||||
| chr12:45031235 | A | T | 1 | a0001c0001t0001g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.499+4784T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031235 | |||||||
| chr12:45031570 | A | T | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.499+4449T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031570 | |||||||
| chr12:45031654 | G | A | 3 | a0001c0001t0001g0091 a0002c0002t0002g0027 a0002c0002t0002g0092 |
4 | HG02886.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+4365C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031654 | |||||||
| chr12:45031697 | G | A | 1 | a0002c0002t0002g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.499+4322C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031697 | |||||||
| chr12:45031792 | C | T | 11 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(8): Show |
11 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.499+4227G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031792 | |||||||
| chr12:45031876 | C | T | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.499+4143G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031876 | |||||||
| chr12:45031941 | T | C | 1 | a0001c0003t0003g0309 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.499+4078A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45031941 | |||||||
| chr12:45032070 | G | A | 2 | a0002c0002t0002g0182 a0002c0002t0002g0183 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.499+3949C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45032070 | |||||||
| chr12:45032267 | T | C | 1 | a0002c0002t0007g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.499+3752A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45032267 | |||||||
| chr12:45032733 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(83): Show |
126 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.499+3286T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45032733 | |||||||
| chr12:45032734 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.499+3285A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45032734 | |||||||
| chr12:45032876 | T | A | 1 | a0001c0001t0020g0057 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.499+3143A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45032876 | |||||||
| chr12:45033143 | G | A | 11 | a0001c0003t0004g0003 a0001c0003t0004g0021 a0001c0003t0004g0283 others(8): Show |
18 | NA18961.hp1 NA18963.hp2 NA18965.hp1 others(15): Show |
intron_variant | MODIFIER | c.499+2876C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45033143 | |||||||
| chr12:45033385 | C | T | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.499+2634G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45033385 | |||||||
| chr12:45033639 | T | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(86): Show |
129 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.499+2380A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45033639 | |||||||
| chr12:45033664 | A | G | 1 | a0001c0003t0003g0303 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.499+2355T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45033664 | |||||||
| chr12:45033987 | A | G | 2 | a0002c0002t0002g0182 a0002c0002t0002g0183 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.499+2032T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45033987 | |||||||
| chr12:45033997 | C | G | 4 | a0001c0001t0006g0017 a0001c0001t0006g0195 a0001c0001t0006g0219 others(1): Show |
6 | HG02129.hp2 NA18944.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.499+2022G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45033997 | |||||||
| chr12:45034012 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.499+2007G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034012 | |||||||
| chr12:45034121 | C | A | 1 | a0002c0002t0002g0115 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.499+1898G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034121 | |||||||
| chr12:45034128 | C | CCA | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(112): Show |
145 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.499+1889_499+1890d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034128 | |||||||
| chr12:45034202 | G | A | 151 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(148): Show |
208 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.499+1817C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034202 | |||||||
| chr12:45034256 | C | G | 2 | a0002c0002t0002g0182 a0002c0002t0002g0183 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.499+1763G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034256 | |||||||
| chr12:45034634 | C | G | 2 | a0001c0001t0016g0126 a0002c0002t0002g0121 |
2 | HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.499+1385G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034634 | |||||||
| chr12:45034675 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.499+1344A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034675 | |||||||
| chr12:45034811 | C | T | 1 | a0002c0002t0002g0146 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.499+1208G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034811 | |||||||
| chr12:45034898 | C | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0002c0004t0001g0178 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1121G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034898 | |||||||
| chr12:45034928 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.499+1091C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034928 | |||||||
| chr12:45034941 | G | C | 1 | a0002c0004t0002g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.499+1078C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034941 | |||||||
| chr12:45034998 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0002c0004t0001g0178 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.499+1021A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45034998 | |||||||
| chr12:45035168 | C | T | 2 | a0002c0002t0002g0009 a0002c0002t0002g0090 |
5 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.499+851G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45035168 | |||||||
| chr12:45035627 | C | G | 12 | a0001c0001t0001g0093 a0001c0001t0001g0173 a0001c0001t0005g0098 others(9): Show |
12 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+392G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45035627 | |||||||
| chr12:45035675 | C | T | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.499+344G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45035675 | |||||||
| chr12:45035753 | G | A | 11 | a0001c0003t0004g0003 a0001c0003t0004g0021 a0001c0003t0004g0283 others(8): Show |
18 | NA18961.hp1 NA18963.hp2 NA18965.hp1 others(15): Show |
intron_variant | MODIFIER | c.499+266C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45035753 | |||||||
| chr12:45035772 | G | A | 12 | a0001c0001t0001g0093 a0001c0001t0001g0173 a0001c0001t0005g0098 others(9): Show |
12 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.499+247C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 2/3 | chr12 | 45035772 | |||||||
| chr12:45036128 | A | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(81): Show |
119 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.404-14T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45036128 | |||||||
| chr12:45036162 | A | G | 1 | a0001c0001t0006g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.404-48T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45036162 | |||||||
| chr12:45036317 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.404-203C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45036317 | |||||||
| chr12:45036322 | G | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(69): Show |
106 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.404-208C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45036322 | |||||||
| chr12:45036364 | G | T | 1 | a0001c0001t0001g0263 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.404-250C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45036364 | |||||||
| chr12:45036402 | T | C | 1 | a0002c0002t0002g0129 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.404-288A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45036402 | |||||||
| chr12:45036601 | T | C | 1 | a0002c0002t0002g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.404-487A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45036601 | |||||||
| chr12:45037003 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.404-889C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45037003 | |||||||
| chr12:45037181 | G | A | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.404-1067C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45037181 | |||||||
| chr12:45037295 | G | C | 37 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(34): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-1181C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45037295 | |||||||
| chr12:45037445 | G | A | 2 | a0001c0001t0010g0234 a0001c0001t0010g0246 |
2 | HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.404-1331C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45037445 | |||||||
| chr12:45037608 | G | A | 1 | a0001c0006t0001g0086 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.404-1494C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45037608 | |||||||
| chr12:45037671 | T | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(11): Show |
17 | HG02723.hp1 HG02895.hp2 HG03579.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-1557A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45037671 | |||||||
| chr12:45037987 | T | G | 3 | a0001c0001t0001g0170 a0001c0001t0005g0097 a0001c0001t0015g0171 |
3 | HG01192.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.404-1873A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45037987 | |||||||
| chr12:45038313 | T | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(69): Show |
106 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.404-2199A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038313 | |||||||
| chr12:45038322 | A | G | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.404-2208T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038322 | |||||||
| chr12:45038326 | GA | G | 38 | a0001c0001t0001g0026 a0001c0001t0001g0103 a0001c0001t0001g0104 others(35): Show |
56 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.404-2213delT | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038326 | |||||||
| chr12:45038515 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.404-2401T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038515 | |||||||
| chr12:45038585 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.404-2471A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038585 | |||||||
| chr12:45038593 | ATCCCAAC others(75): Show |
A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(128): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.404-2561_404-2480d others(84): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038593 | |||||||
| chr12:45038647 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.404-2533C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038647 | |||||||
| chr12:45038694 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.404-2580T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038694 | |||||||
| chr12:45038723 | T | A | 17 | a0001c0001t0001g0093 a0001c0001t0001g0170 a0001c0001t0001g0173 others(14): Show |
17 | HG01167.hp2 HG01192.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-2609A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038723 | |||||||
| chr12:45038836 | CTATTA | C | 2 | a0002c0004t0002g0016 a0002c0004t0002g0094 |
4 | HG02258.hp1 NA19240.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-2727_404-2723d others(7): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038836 | |||||||
| chr12:45038954 | T | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0274 |
2 | HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.404-2840A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45038954 | |||||||
| chr12:45039155 | C | CT | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(122): Show |
177 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.404-3042dupA | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039155 | |||||||
| chr12:45039161 | T | C | 13 | a0001c0003t0003g0048 a0001c0003t0003g0300 a0001c0003t0003g0301 others(10): Show |
14 | HG00544.hp1 HG01934.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.404-3047A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039161 | |||||||
| chr12:45039219 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.404-3105C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039219 | |||||||
| chr12:45039268 | G | T | 1 | a0001c0006t0001g0061 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.404-3154C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039268 | |||||||
| chr12:45039276 | G | GGT | 7 | a0001c0003t0003g0007 a0001c0003t0003g0293 a0001c0003t0003g0294 others(4): Show |
11 | HG00408.hp1 HG02015.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.404-3164_404-3163d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039276 | |||||||
| chr12:45039277 | G | GTA | 5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0267 others(2): Show |
5 | HG02074.hp2 HG03540.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-3165_404-3164d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | G | GTATA | 3 | a0001c0001t0001g0020 a0001c0001t0006g0195 a0002c0002t0007g0138 |
5 | HG01069.hp1 HG01071.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-3167_404-3164d others(6): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | G | GTGTA | 4 | a0001c0003t0003g0047 a0001c0003t0003g0310 a0001c0003t0003g0311 others(1): Show |
5 | HG04184.hp1 NA18941.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-3164_404-3163i others(6): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | G | GTGTATA | 4 | a0001c0003t0003g0298 a0001c0003t0003g0312 a0001c0003t0004g0021 others(1): Show |
6 | HG00558.hp1 NA18965.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.404-3164_404-3163i others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTA | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0038 others(26): Show |
41 | HG00639.hp1 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.404-3165_404-3164d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATA | G | 34 | a0001c0001t0001g0037 a0001c0001t0001g0041 a0001c0001t0001g0142 others(31): Show |
37 | HG00323.hp2 HG00621.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.404-3167_404-3164d others(6): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATA | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0141 others(14): Show |
22 | HG00642.hp2 HG01167.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.404-3169_404-3164d others(8): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATAT others(1): Show |
G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0153 a0001c0001t0001g0205 others(16): Show |
25 | HG01123.hp2 HG01169.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.404-3171_404-3164d others(10): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATAT others(3): Show |
G | 27 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0040 others(24): Show |
35 | HG00323.hp1 HG00673.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.404-3173_404-3164d others(12): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATAT others(5): Show |
G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0257 a0001c0001t0005g0122 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.404-3175_404-3164d others(14): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATAT others(9): Show |
G | 2 | a0001c0001t0001g0209 a0002c0002t0002g0140 |
2 | HG02486.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.404-3179_404-3164d others(18): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATAT others(11): Show |
G | 1 | a0002c0002t0002g0044 | 2 | HG00738.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.404-3181_404-3164d others(20): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATAT others(15): Show |
G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(7): Show |
10 | HG01099.hp1 HG01361.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.404-3185_404-3164d others(24): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATAT others(21): Show |
G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(70): Show |
107 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.404-3191_404-3164d others(30): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039277 | GTATATAT others(23): Show |
G | 6 | a0001c0001t0001g0026 a0001c0001t0005g0097 a0001c0001t0015g0171 others(3): Show |
10 | HG01192.hp2 HG01255.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.404-3193_404-3164d others(32): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039277 | |||||||
| chr12:45039279 | A | G | 20 | a0001c0003t0003g0048 a0001c0003t0003g0295 a0001c0003t0003g0296 others(17): Show |
26 | HG00544.hp1 HG01934.hp1 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.404-3165T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039279 | |||||||
| chr12:45039283 | A | G | 1 | a0001c0003t0003g0291 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.404-3169T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039283 | |||||||
| chr12:45039287 | A | G | 1 | a0001c0003t0003g0046 | 2 | NA18747.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.404-3173T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039287 | |||||||
| chr12:45039301 | ATATATAT others(15): Show |
A | 6 | a0001c0003t0003g0305 a0001c0003t0003g0306 a0001c0003t0003g0307 others(3): Show |
6 | HG01934.hp1 HG01943.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-3209_404-3188d others(24): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039301 | |||||||
| chr12:45039317 | A | G | 1 | a0002c0002t0002g0002 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.404-3203T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039317 | |||||||
| chr12:45039319 | A | C | 1 | a0001c0003t0003g0047 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.404-3205T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039319 | |||||||
| chr12:45039319 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.404-3205T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039319 | |||||||
| chr12:45039321 | A | G | 6 | a0001c0001t0005g0098 a0001c0001t0005g0099 a0001c0001t0005g0100 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.404-3207T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039321 | |||||||
| chr12:45039321 | ATG | A | 9 | a0001c0003t0003g0048 a0001c0003t0003g0303 a0001c0003t0003g0304 others(6): Show |
11 | HG00544.hp1 HG02132.hp2 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.404-3209_404-3208d others(4): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039321 | |||||||
| chr12:45039322 | T | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-3208A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039322 | |||||||
| chr12:45039323 | G | A | 15 | a0001c0003t0003g0007 a0001c0003t0003g0296 a0001c0003t0003g0298 others(12): Show |
17 | HG00558.hp1 HG02015.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-3209C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039323 | |||||||
| chr12:45039323 | G | C | 9 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(6): Show |
14 | HG00408.hp1 HG02071.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.404-3209C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039323 | |||||||
| chr12:45039443 | T | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-3329A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039443 | |||||||
| chr12:45039448 | T | C | 17 | a0001c0001t0001g0093 a0001c0001t0001g0170 a0001c0001t0001g0173 others(14): Show |
17 | HG01167.hp2 HG01192.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-3334A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039448 | |||||||
| chr12:45039488 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.404-3374G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039488 | |||||||
| chr12:45039621 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.404-3507A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039621 | |||||||
| chr12:45039787 | G | A | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-3673C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039787 | |||||||
| chr12:45039869 | T | G | 1 | a0002c0002t0002g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.404-3755A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039869 | |||||||
| chr12:45039880 | G | GA | 110 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(107): Show |
158 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.404-3767dupT | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039880 | |||||||
| chr12:45039880 | GAAAAA | G | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-3771_404-3767d others(7): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45039880 | |||||||
| chr12:45040240 | T | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(69): Show |
106 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.404-4126A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040240 | |||||||
| chr12:45040285 | G | A | 37 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(34): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-4171C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040285 | |||||||
| chr12:45040353 | C | T | 310 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(307): Show |
411 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(408): Show |
intron_variant | MODIFIER | c.404-4239G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040353 | |||||||
| chr12:45040382 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(69): Show |
106 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.404-4268T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040382 | |||||||
| chr12:45040395 | C | T | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-4281G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040395 | |||||||
| chr12:45040415 | C | G | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-4301G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040415 | |||||||
| chr12:45040460 | T | C | 17 | a0001c0001t0001g0093 a0001c0001t0001g0170 a0001c0001t0001g0173 others(14): Show |
17 | HG01167.hp2 HG01192.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-4346A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040460 | |||||||
| chr12:45040603 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(91): Show |
123 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.404-4489G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040603 | |||||||
| chr12:45040698 | A | G | 9 | a0001c0005t0002g0165 a0002c0002t0002g0160 a0002c0002t0002g0161 others(6): Show |
9 | HG01109.hp1 HG01175.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.404-4584T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040698 | |||||||
| chr12:45040769 | T | A | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.404-4655A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040769 | |||||||
| chr12:45040804 | C | T | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-4690G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040804 | |||||||
| chr12:45040817 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.404-4703G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040817 | |||||||
| chr12:45040818 | T | G | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-4704A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040818 | |||||||
| chr12:45040945 | A | G | 1 | a0002c0002t0002g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.404-4831T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45040945 | |||||||
| chr12:45041041 | G | C | 17 | a0001c0001t0001g0093 a0001c0001t0001g0170 a0001c0001t0001g0173 others(14): Show |
17 | HG01167.hp2 HG01192.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-4927C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041041 | |||||||
| chr12:45041300 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.404-5186G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041300 | |||||||
| chr12:45041428 | T | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-5314A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041428 | |||||||
| chr12:45041477 | T | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-5363A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041477 | |||||||
| chr12:45041577 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.404-5463A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041577 | |||||||
| chr12:45041602 | C | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(61): Show |
94 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.404-5488G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041602 | |||||||
| chr12:45041664 | G | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-5550C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041664 | |||||||
| chr12:45041678 | A | C | 9 | a0001c0001t0001g0039 a0001c0001t0001g0201 a0001c0001t0001g0202 others(6): Show |
10 | HG01099.hp2 HG01109.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.404-5564T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041678 | |||||||
| chr12:45041692 | G | A | 15 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(12): Show |
16 | HG00738.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.404-5578C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041692 | |||||||
| chr12:45041709 | T | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
7 | HG02040.hp1 NA18612.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-5595A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041709 | |||||||
| chr12:45041763 | A | C | 2 | a0002c0002t0002g0035 a0002c0002t0002g0155 |
3 | HG00423.hp1 HG03927.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.404-5649T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041763 | |||||||
| chr12:45041768 | T | C | 10 | a0002c0002t0002g0001 a0002c0002t0002g0035 a0002c0002t0002g0036 others(7): Show |
25 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.404-5654A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041768 | |||||||
| chr12:45041935 | A | G | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-5821T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45041935 | |||||||
| chr12:45042136 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(11): Show |
17 | HG02723.hp1 HG02895.hp2 HG03579.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-6022A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042136 | |||||||
| chr12:45042140 | A | G | 310 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(307): Show |
411 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(408): Show |
intron_variant | MODIFIER | c.404-6026T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042140 | |||||||
| chr12:45042408 | A | G | 2 | a0001c0001t0005g0098 a0001c0001t0005g0281 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.404-6294T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042408 | |||||||
| chr12:45042522 | A | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(128): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.404-6408T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042522 | |||||||
| chr12:45042651 | C | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(128): Show |
183 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.404-6537G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042651 | |||||||
| chr12:45042722 | G | A | 1 | a0002c0002t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.404-6608C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042722 | |||||||
| chr12:45042815 | A | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0002c0004t0001g0178 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.404-6701T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042815 | |||||||
| chr12:45042865 | C | T | 3 | a0001c0001t0001g0091 a0002c0002t0002g0027 a0002c0002t0002g0092 |
4 | HG02886.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.404-6751G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042865 | |||||||
| chr12:45042876 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.404-6762C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042876 | |||||||
| chr12:45042920 | C | T | 1 | a0002c0002t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.404-6806G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042920 | |||||||
| chr12:45042946 | T | C | 37 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(34): Show |
51 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-6832A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45042946 | |||||||
| chr12:45043010 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0173 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.404-6896T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043010 | |||||||
| chr12:45043105 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.404-6991G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043105 | |||||||
| chr12:45043303 | T | C | 2 | a0002c0002t0002g0182 a0002c0002t0002g0183 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.404-7189A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043303 | |||||||
| chr12:45043409 | T | C | 3 | a0002c0002t0007g0032 a0002c0002t0007g0137 a0002c0002t0007g0138 |
4 | HG01069.hp2 HG01257.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+7116A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043409 | |||||||
| chr12:45043459 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.403+7066A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043459 | |||||||
| chr12:45043576 | G | C | 1 | a0002c0002t0002g0090 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.403+6949C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043576 | |||||||
| chr12:45043671 | T | C | 1 | a0002c0004t0002g0016 | 3 | NA19240.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.403+6854A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043671 | |||||||
| chr12:45043690 | T | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+6835A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043690 | |||||||
| chr12:45043712 | C | A | 12 | a0001c0001t0001g0093 a0001c0001t0001g0173 a0001c0001t0005g0098 others(9): Show |
12 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+6813G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043712 | |||||||
| chr12:45043768 | T | C | 2 | a0002c0004t0002g0016 a0002c0004t0002g0094 |
4 | HG02258.hp1 NA19240.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+6757A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043768 | |||||||
| chr12:45043772 | C | T | 1 | a0001c0001t0006g0195 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.403+6753G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043772 | |||||||
| chr12:45043803 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.403+6722A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043803 | |||||||
| chr12:45043857 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.403+6668C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043857 | |||||||
| chr12:45043951 | T | G | 3 | a0001c0001t0001g0091 a0002c0002t0002g0027 a0002c0002t0002g0092 |
4 | HG02886.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+6574A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45043951 | |||||||
| chr12:45044062 | C | T | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+6463G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044062 | |||||||
| chr12:45044074 | C | T | 1 | a0002c0002t0002g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.403+6451G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044074 | |||||||
| chr12:45044087 | C | A | 310 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(307): Show |
411 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(408): Show |
intron_variant | MODIFIER | c.403+6438G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044087 | |||||||
| chr12:45044093 | T | C | 1 | a0002c0002t0002g0158 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.403+6432A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044093 | |||||||
| chr12:45044106 | AG | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0052 others(30): Show |
51 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.403+6418delC | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044106 | |||||||
| chr12:45044158 | T | C | 1 | a0001c0005t0002g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.403+6367A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044158 | |||||||
| chr12:45044167 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.403+6358T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044167 | |||||||
| chr12:45044230 | CT | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(125): Show |
177 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.403+6294delA | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044230 | |||||||
| chr12:45044248 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0005g0097 a0001c0001t0015g0171 others(2): Show |
5 | HG01167.hp2 HG01192.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+6277G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044248 | |||||||
| chr12:45044275 | G | C | 59 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0170 others(56): Show |
77 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.403+6250C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044275 | |||||||
| chr12:45044297 | A | C | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+6228T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044297 | |||||||
| chr12:45044313 | A | T | 5 | a0001c0001t0001g0170 a0001c0001t0005g0097 a0001c0001t0015g0171 others(2): Show |
5 | HG01167.hp2 HG01192.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+6212T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044313 | |||||||
| chr12:45044425 | G | T | 1 | a0001c0001t0001g0194 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.403+6100C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044425 | |||||||
| chr12:45044517 | A | G | 1 | a0002c0002t0002g0029 | 2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.403+6008T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044517 | |||||||
| chr12:45044640 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.403+5885G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044640 | |||||||
| chr12:45044865 | A | G | 1 | a0002c0002t0002g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.403+5660T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044865 | |||||||
| chr12:45044871 | C | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
5 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+5654G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044871 | |||||||
| chr12:45044879 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.403+5646T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044879 | |||||||
| chr12:45044959 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(11): Show |
17 | HG02723.hp1 HG02895.hp2 HG03579.hp2 others(14): Show |
intron_variant | MODIFIER | c.403+5566A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45044959 | |||||||
| chr12:45045002 | G | A | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(112): Show |
145 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.403+5523C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045002 | |||||||
| chr12:45045172 | G | C | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.403+5353C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045172 | |||||||
| chr12:45045185 | G | T | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+5340C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045185 | |||||||
| chr12:45045260 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0002c0004t0001g0178 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+5265A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045260 | |||||||
| chr12:45045281 | G | A | 1 | a0002c0002t0002g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.403+5244C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045281 | |||||||
| chr12:45045288 | A | T | 2 | a0002c0004t0002g0016 a0002c0004t0002g0094 |
4 | HG02258.hp1 NA19240.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+5237T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045288 | |||||||
| chr12:45045320 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.403+5205C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045320 | |||||||
| chr12:45045337 | T | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+5188A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045337 | |||||||
| chr12:45045398 | T | C | 13 | a0001c0003t0003g0007 a0001c0003t0003g0046 a0001c0003t0003g0047 others(10): Show |
19 | HG00408.hp1 HG00558.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.403+5127A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045398 | |||||||
| chr12:45045426 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.403+5099T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045426 | |||||||
| chr12:45045452 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG00733.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.403+5073G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045452 | |||||||
| chr12:45045519 | G | A | 10 | a0002c0002t0002g0001 a0002c0002t0002g0035 a0002c0002t0002g0036 others(7): Show |
25 | HG00423.hp1 HG00621.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.403+5006C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045519 | |||||||
| chr12:45045704 | C | T | 1 | a0002c0002t0002g0151 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.403+4821G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045704 | |||||||
| chr12:45045751 | G | A | 1 | a0002c0002t0002g0033 | 2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.403+4774C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045751 | |||||||
| chr12:45045778 | G | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
96 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.403+4747C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045778 | |||||||
| chr12:45045779 | G | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
96 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.403+4746C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045779 | |||||||
| chr12:45045796 | C | T | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+4729G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045796 | |||||||
| chr12:45045818 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0005g0097 a0001c0001t0015g0171 |
3 | HG01192.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.403+4707G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045818 | |||||||
| chr12:45045819 | G | A | 7 | a0002c0002t0002g0028 a0002c0002t0002g0111 a0002c0002t0002g0112 others(4): Show |
8 | HG00323.hp2 HG01081.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+4706C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045819 | |||||||
| chr12:45045871 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403+4654A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045871 | |||||||
| chr12:45045877 | C | T | 1 | a0005c0009t0017g0190 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.403+4648G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045877 | |||||||
| chr12:45045960 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0005g0097 a0001c0001t0015g0171 others(2): Show |
5 | HG01167.hp2 HG01192.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+4565G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045960 | |||||||
| chr12:45045996 | C | T | 7 | a0002c0002t0002g0028 a0002c0002t0002g0111 a0002c0002t0002g0112 others(4): Show |
8 | HG00323.hp2 HG01081.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+4529G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45045996 | |||||||
| chr12:45046004 | A | C | 1 | a0002c0002t0002g0160 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.403+4521T>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046004 | |||||||
| chr12:45046009 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403+4516G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046009 | |||||||
| chr12:45046024 | T | C | 1 | a0001c0001t0015g0171 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.403+4501A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046024 | |||||||
| chr12:45046028 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.403+4497G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046028 | |||||||
| chr12:45046062 | AT | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(11): Show |
17 | HG02723.hp1 HG02895.hp2 HG03579.hp2 others(14): Show |
intron_variant | MODIFIER | c.403+4462delA | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046062 | |||||||
| chr12:45046143 | T | A | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.403+4382A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046143 | |||||||
| chr12:45046194 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.403+4331G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046194 | |||||||
| chr12:45046401 | C | A | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+4124G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046401 | |||||||
| chr12:45046541 | A | T | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+3984T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046541 | |||||||
| chr12:45046565 | C | G | 47 | a0001c0001t0001g0026 a0001c0001t0001g0170 a0001c0001t0005g0097 others(44): Show |
65 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.403+3960G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046565 | |||||||
| chr12:45046677 | C | T | 1 | a0002c0004t0002g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.403+3848G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046677 | |||||||
| chr12:45046837 | T | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(63): Show |
94 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.403+3688A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046837 | |||||||
| chr12:45046901 | C | T | 59 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0170 others(56): Show |
77 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.403+3624G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45046901 | |||||||
| chr12:45047121 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.403+3404T>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047121 | |||||||
| chr12:45047146 | T | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+3379A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047146 | |||||||
| chr12:45047208 | C | G | 1 | a0002c0002t0002g0111 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.403+3317G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047208 | |||||||
| chr12:45047244 | G | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+3281C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047244 | |||||||
| chr12:45047254 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.403+3271T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047254 | |||||||
| chr12:45047299 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.403+3226G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047299 | |||||||
| chr12:45047358 | G | A | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+3167C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047358 | |||||||
| chr12:45047380 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.403+3145A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047380 | |||||||
| chr12:45047443 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.403+3082A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047443 | |||||||
| chr12:45047642 | A | G | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+2883T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047642 | |||||||
| chr12:45047708 | T | A | 2 | a0002c0002t0002g0182 a0002c0002t0002g0183 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.403+2817A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047708 | |||||||
| chr12:45047892 | T | C | 42 | a0001c0001t0001g0026 a0001c0003t0003g0007 a0001c0003t0003g0046 others(39): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.403+2633A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45047892 | |||||||
| chr12:45048013 | G | C | 1 | a0002c0002t0002g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.403+2512C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048013 | |||||||
| chr12:45048094 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.403+2431C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048094 | |||||||
| chr12:45048134 | C | T | 17 | a0001c0001t0001g0093 a0001c0001t0001g0170 a0001c0001t0001g0173 others(14): Show |
17 | HG01167.hp2 HG01192.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.403+2391G>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048134 | |||||||
| chr12:45048187 | G | C | 1 | a0002c0002t0002g0169 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.403+2338C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048187 | |||||||
| chr12:45048290 | G | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+2235C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048290 | |||||||
| chr12:45048326 | T | G | 59 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0170 others(56): Show |
77 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.403+2199A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048326 | |||||||
| chr12:45048430 | T | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+2095A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048430 | |||||||
| chr12:45048439 | C | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(5): Show |
8 | HG01361.hp1 HG01975.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+2086G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048439 | |||||||
| chr12:45048572 | T | C | 9 | a0001c0005t0002g0165 a0002c0002t0002g0160 a0002c0002t0002g0161 others(6): Show |
9 | HG01109.hp1 HG01175.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.403+1953A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048572 | |||||||
| chr12:45048672 | G | T | 1 | a0002c0002t0002g0169 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.403+1853C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048672 | |||||||
| chr12:45048673 | T | C | 1 | a0002c0002t0002g0169 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.403+1852A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048673 | |||||||
| chr12:45048674 | C | A | 1 | a0002c0002t0002g0169 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.403+1851G>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048674 | |||||||
| chr12:45048710 | T | G | 17 | a0001c0001t0001g0093 a0001c0001t0001g0170 a0001c0001t0001g0173 others(14): Show |
17 | HG01167.hp2 HG01192.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.403+1815A>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45048710 | |||||||
| chr12:45049155 | T | C | 42 | a0001c0001t0001g0026 a0001c0003t0003g0007 a0001c0003t0003g0046 others(39): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.403+1370A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049155 | |||||||
| chr12:45049385 | T | A | 1 | a0001c0003t0003g0299 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.403+1140A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049385 | |||||||
| chr12:45049400 | G | T | 12 | a0001c0001t0001g0093 a0001c0001t0001g0173 a0001c0001t0005g0098 others(9): Show |
12 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+1125C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049400 | |||||||
| chr12:45049402 | T | C | 42 | a0001c0001t0001g0026 a0001c0003t0003g0007 a0001c0003t0003g0046 others(39): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.403+1123A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049402 | |||||||
| chr12:45049507 | G | A | 4 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0002c0004t0001g0178 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+1018C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049507 | |||||||
| chr12:45049516 | A | G | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+1009T>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049516 | |||||||
| chr12:45049593 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0173 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.403+932C>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049593 | |||||||
| chr12:45049662 | C | CA | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(111): Show |
144 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.403+862dupT | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049662 | |||||||
| chr12:45049662 | C | CAA | 7 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0002c0002t0002g0181 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+861_403+862dup others(2): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049662 | |||||||
| chr12:45049662 | CA | C | 35 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0050 others(32): Show |
54 | HG00408.hp1 HG00558.hp1 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.403+862delT | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049662 | |||||||
| chr12:45049662 | CAA | C | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+861_403+862del others(2): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049662 | |||||||
| chr12:45049936 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403+589C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049936 | |||||||
| chr12:45049991 | G | T | 2 | a0002c0004t0001g0185 a0002c0004t0001g0186 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.403+534C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049991 | |||||||
| chr12:45049993 | A | ACTTTGCG others(19): Show |
1 | a0001c0001t0001g0184 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.403+506_403+531dup others(26): Show |
DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049993 | |||||||
| chr12:45049998 | G | C | 1 | a0001c0001t0001g0280 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.403+527C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45049998 | |||||||
| chr12:45050063 | C | G | 42 | a0001c0001t0001g0026 a0001c0003t0003g0007 a0001c0003t0003g0046 others(39): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.403+462G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050063 | |||||||
| chr12:45050093 | G | T | 3 | a0001c0001t0001g0091 a0002c0002t0002g0027 a0002c0002t0002g0092 |
4 | HG02886.hp2 HG02922.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+432C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050093 | |||||||
| chr12:45050108 | T | C | 1 | a0002c0002t0002g0090 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.403+417A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050108 | |||||||
| chr12:45050109 | C | G | 3 | a0001c0001t0001g0026 a0002c0002t0002g0009 a0002c0002t0002g0090 |
7 | HG02258.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+416G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050109 | |||||||
| chr12:45050173 | T | C | 1 | a0002c0004t0002g0016 | 3 | NA19240.hp1 NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.403+352A>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050173 | |||||||
| chr12:45050181 | G | T | 1 | a0002c0002t0002g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.403+344C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050181 | |||||||
| chr12:45050211 | G | T | 2 | a0002c0002t0002g0182 a0002c0002t0002g0183 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.403+314C>A | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050211 | |||||||
| chr12:45050224 | C | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(44): Show |
62 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.403+301G>C | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050224 | |||||||
| chr12:45050299 | G | C | 2 | a0001c0008t0001g0314 a0001c0008t0001g0315 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+226C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050299 | |||||||
| chr12:45050327 | G | C | 2 | a0002c0002t0002g0182 a0002c0002t0002g0183 |
2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.403+198C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050327 | |||||||
| chr12:45050455 | T | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(110): Show |
143 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.403+70A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050455 | |||||||
| chr12:45050481 | G | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(110): Show |
143 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.403+44C>G | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050481 | |||||||
| chr12:45050517 | T | A | 1 | a0001c0001t0005g0281 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.403+8A>T | DBX2 | ENSG00000185610.6 | transcript | ENST00000332700.6 | protein_coding | 1/3 | chr12 | 45050517 |