Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29121 |
| ensemblid | ENSG00000069493.15 |
| hgncid | 14351 |
| symbol | CLEC2D |
| name | C-type lectin domain family 2 member D |
| refseq_nuc | NM_013269.6 |
| refseq_prot | NP_037401.1 |
| ensembl_nuc | ENST00000290855.11 |
| ensembl_prot | ENSP00000290855.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 9669713 |
| end | 9699553 |
| strand | + |
| ver | v1.2 |
| region | chr12:9669713-9699553 |
| region5000 | chr12:9664713-9704553 |
| regionname0 | CLEC2D_chr12_9669713_9699553 |
| regionname5000 | CLEC2D_chr12_9664713_9704553 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 191 | 193 | 34 | 38 | 89 | 4 | 26 | 70 | CLEC2D_chr12_9664713_9704553 | CLEC2D | MHDSN others(186): Show |
chr12 | 9664713 | 9704553 |
| a0002 | 0/0 | 191 | 131 | 8 | 22 | 79 | 5 | 17 | 56 | CLEC2D_chr12_9664713_9704553 | CLEC2D | MHDSN others(186): Show |
chr12 | 9664713 | 9704553 |
| a0003 | 0/0 | 191 | 55 | 40 | 12 | 0 | 2 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | MHDSN others(186): Show |
chr12 | 9664713 | 9704553 |
| a0004 | 0/0 | 191 | 7 | 6 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | MHDSN others(186): Show |
chr12 | 9664713 | 9704553 |
| a0005 | 0/0 | 191 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | MHDSN others(186): Show |
chr12 | 9664713 | 9704553 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 573 | 187 | 30 | 38 | 89 | 4 | 24 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ATGCA others(568): Show |
chr12 | 9664713 | 9704553 | ||
| a0001c0006 | 0/0 | 573 | 6 | 4 | 0 | 0 | 0 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ATGCA others(568): Show |
chr12 | 9664713 | 9704553 | ||
| a0002c0002 | 0/0 | 573 | 128 | 8 | 22 | 79 | 5 | 14 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ATGCA others(568): Show |
chr12 | 9664713 | 9704553 | ||
| a0002c0007 | 0/0 | 573 | 3 | 0 | 0 | 0 | 0 | 3 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ATGCA others(568): Show |
chr12 | 9664713 | 9704553 | ||
| a0003c0003 | 0/0 | 573 | 40 | 29 | 9 | 0 | 1 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ATGCA others(568): Show |
chr12 | 9664713 | 9704553 | ||
| a0003c0004 | 0/0 | 573 | 15 | 11 | 3 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ATGCA others(568): Show |
chr12 | 9664713 | 9704553 | ||
| a0004c0005 | 0/0 | 573 | 7 | 6 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ATGCA others(568): Show |
chr12 | 9664713 | 9704553 | ||
| a0005c0008 | 0/0 | 573 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ATGCA others(568): Show |
chr12 | 9664713 | 9704553 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5275 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0002 | 0/0 | 5273 | 102 | 4 | 14 | 69 | 3 | 12 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0004 | 0/0 | 5277 | 15 | 0 | 9 | 2 | 1 | 3 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5272): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0005 | 0/0 | 5275 | 6 | 3 | 2 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0006 | 0/0 | 5273 | 7 | 0 | 0 | 6 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0009 | 0/0 | 5266 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5261): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0010 | 0/0 | 5273 | 3 | 1 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0011 | 0/0 | 5273 | 6 | 1 | 5 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0013 | 1/0 | 5277 | 4 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5272): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0014 | 0/0 | 5271 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0015 | 0/0 | 5273 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0017 | 0/0 | 5268 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5263): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0019 | 0/0 | 5281 | 3 | 2 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5276): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0020 | 0/0 | 5278 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5273): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0021 | 0/0 | 5273 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0022 | 0/0 | 5271 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0025 | 0/0 | 5273 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0026 | 0/0 | 5275 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0032 | 0/0 | 5274 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5269): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0033 | 0/0 | 5281 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5276): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0038 | 0/0 | 5271 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0039 | 0/0 | 5274 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5269): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0040 | 0/0 | 5273 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0041 | 0/0 | 5273 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0042 | 0/0 | 5277 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5272): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0043 | 0/0 | 5274 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5269): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0044 | 0/0 | 5273 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0045 | 0/0 | 5273 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0046 | 0/0 | 5274 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5269): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0048 | 0/0 | 5273 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0049 | 0/0 | 5273 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0050 | 0/0 | 5273 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0051 | 0/0 | 5273 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0052 | 0/0 | 5273 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0054 | 0/0 | 5273 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0001t0055 | 0/1 | 5276 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5271): Show |
chr12 | 9664713 | 9704553 |
| a0001c0006t0003 | 0/0 | 5271 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0001c0006t0007 | 0/0 | 5273 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0001c0006t0016 | 0/0 | 5271 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0001 | 0/0 | 5275 | 111 | 3 | 18 | 74 | 3 | 13 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0008 | 0/0 | 5270 | 4 | 3 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5265): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0012 | 0/0 | 5273 | 4 | 1 | 1 | 0 | 1 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0018 | 0/0 | 5275 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0029 | 0/0 | 5272 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5267): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0030 | 0/0 | 5275 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0031 | 0/0 | 5248 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5243): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0034 | 0/0 | 5275 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0035 | 0/0 | 5275 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0002c0002t0036 | 0/0 | 5275 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0002c0007t0024 | 0/0 | 5274 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5269): Show |
chr12 | 9664713 | 9704553 |
| a0002c0007t0047 | 0/0 | 5274 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5269): Show |
chr12 | 9664713 | 9704553 |
| a0003c0003t0003 | 0/0 | 5271 | 28 | 19 | 7 | 0 | 1 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0003c0003t0007 | 0/0 | 5273 | 6 | 6 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0003c0003t0016 | 0/0 | 5271 | 2 | 1 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0003c0003t0056 | 0/0 | 5271 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0003c0003t0057 | 0/0 | 5271 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0003c0003t0058 | 0/0 | 5271 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0003c0003t0059 | 0/0 | 5271 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0003c0004t0002 | 0/0 | 5273 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0003c0004t0005 | 0/0 | 5275 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0003c0004t0009 | 0/0 | 5266 | 5 | 5 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5261): Show |
chr12 | 9664713 | 9704553 |
| a0003c0004t0010 | 0/0 | 5273 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0003c0004t0014 | 0/0 | 5271 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5266): Show |
chr12 | 9664713 | 9704553 |
| a0003c0004t0023 | 0/0 | 5277 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5272): Show |
chr12 | 9664713 | 9704553 |
| a0003c0004t0027 | 0/0 | 5273 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0004c0005t0001 | 0/0 | 5275 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0004c0005t0008 | 0/0 | 5270 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5265): Show |
chr12 | 9664713 | 9704553 |
| a0004c0005t0028 | 0/0 | 5275 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0004c0005t0037 | 0/0 | 5275 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| a0005c0008t0002 | 0/0 | 5273 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5268): Show |
chr12 | 9664713 | 9704553 |
| a0005c0008t0053 | 0/0 | 5275 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | ACTCA others(5270): Show |
chr12 | 9664713 | 9704553 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0001 | 0/0 | 28 | 2 | 6 | 18 | 0 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 2 | 2 | 1 | 3 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0005g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0005g0032 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0010g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0011g0001 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0011g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0011g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0013g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0013g0128 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0014g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0014g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0015g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0015g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0017g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0019g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0020g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0020g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0021g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0022g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0022g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0025g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0026g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0026g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0032g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0033g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0038g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0039g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0040g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0041g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0042g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0043g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0044g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0045g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0046g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0048g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0049g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0050g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0051g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0052g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0054g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0001t0055g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0006t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0006t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0006t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0006t0016g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0001c0006t0016g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0002 | 0/0 | 11 | 0 | 1 | 8 | 1 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0003 | 0/0 | 12 | 2 | 4 | 3 | 1 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0005 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0008g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0008g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0012g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0012g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0012g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0018g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0018g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0029g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0030g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0031g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0034g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0035g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0002t0036g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0007t0024g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0007t0024g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0002c0007t0047g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0016g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0016g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0056g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0057g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0058g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0003t0059g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0009g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0014g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0023g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0023g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0027g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0003c0004t0027g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0004c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0004c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0004c0005t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0004c0005t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0004c0005t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0004c0005t0028g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0004c0005t0037g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0005c0008t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| a0005c0008t0053g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0037 | EUR | GBR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00140 | hp1 | a0004 | c0005 | t0028 | g0061 | EUR | GBR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | GBR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00280 | hp1 | a0003 | c0004 | t0005 | g0129 | EUR | FIN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00280 | hp2 | a0002 | c0002 | t0012 | g0027 | EUR | FIN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0196 | EUR | FIN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00438 | hp1 | a0001 | c0001 | t0026 | g0209 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00438 | hp2 | a0002 | c0002 | t0018 | g0002 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00609 | hp1 | a0001 | c0001 | t0045 | g0001 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00642 | hp2 | a0003 | c0003 | t0003 | g0019 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00733 | hp2 | a0003 | c0004 | t0027 | g0148 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00735 | hp2 | a0003 | c0004 | t0027 | g0149 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00738 | hp1 | a0001 | c0001 | t0040 | g0004 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00738 | hp2 | a0003 | c0003 | t0059 | g0135 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01070 | hp2 | a0001 | c0001 | t0021 | g0022 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01071 | hp2 | a0001 | c0001 | t0021 | g0022 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01074 | hp2 | a0003 | c0003 | t0003 | g0138 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01081 | hp2 | a0002 | c0002 | t0031 | g0003 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01109 | hp2 | a0003 | c0003 | t0003 | g0018 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01167 | hp1 | a0003 | c0003 | t0003 | g0133 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01168 | hp1 | a0002 | c0002 | t0008 | g0005 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01168 | hp2 | a0001 | c0001 | t0010 | g0029 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01169 | hp1 | a0001 | c0001 | t0010 | g0029 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01255 | hp1 | a0003 | c0003 | t0003 | g0144 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01256 | hp1 | a0003 | c0004 | t0002 | g0001 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01257 | hp2 | a0003 | c0003 | t0003 | g0163 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01346 | hp2 | a0001 | c0001 | t0041 | g0001 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01496 | hp1 | a0001 | c0001 | t0051 | g0203 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01884 | hp1 | a0003 | c0004 | t0009 | g0028 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01884 | hp2 | a0003 | c0003 | t0003 | g0035 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01891 | hp1 | a0003 | c0003 | t0003 | g0018 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01928 | hp2 | a0001 | c0001 | t0011 | g0004 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01934 | hp1 | a0003 | c0003 | t0003 | g0137 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01952 | hp1 | a0001 | c0001 | t0019 | g0123 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01952 | hp2 | a0001 | c0001 | t0011 | g0011 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01978 | hp2 | a0001 | c0001 | t0011 | g0001 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02055 | hp1 | a0001 | c0001 | t0014 | g0115 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02055 | hp2 | a0001 | c0001 | t0020 | g0030 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02083 | hp2 | a0002 | c0002 | t0018 | g0072 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02132 | hp1 | a0002 | c0002 | t0030 | g0087 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02145 | hp1 | a0003 | c0003 | t0003 | g0134 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02145 | hp2 | a0001 | c0001 | t0022 | g0168 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02148 | hp2 | a0003 | c0003 | t0016 | g0142 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | CDX | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | CDX | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0114 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02257 | hp2 | a0001 | c0001 | t0020 | g0030 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02273 | hp1 | a0001 | c0001 | t0011 | g0178 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02280 | hp1 | a0003 | c0004 | t0009 | g0110 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02280 | hp2 | a0003 | c0003 | t0007 | g0158 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02300 | hp1 | a0002 | c0002 | t0029 | g0075 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02451 | hp1 | a0002 | c0002 | t0034 | g0080 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02451 | hp2 | a0003 | c0004 | t0014 | g0132 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02523 | hp1 | a0002 | c0002 | t0036 | g0002 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02572 | hp1 | a0004 | c0005 | t0001 | g0105 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02572 | hp2 | a0003 | c0004 | t0010 | g0119 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02602 | hp1 | a0002 | c0002 | t0012 | g0102 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0032 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02615 | hp2 | a0001 | c0006 | t0003 | g0045 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02622 | hp1 | a0003 | c0003 | t0007 | g0159 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02622 | hp2 | a0003 | c0003 | t0058 | g0034 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02630 | hp1 | a0003 | c0003 | t0007 | g0040 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02630 | hp2 | a0003 | c0004 | t0009 | g0028 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02647 | hp1 | a0003 | c0003 | t0016 | g0145 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02647 | hp2 | a0003 | c0003 | t0003 | g0020 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02683 | hp2 | a0001 | c0001 | t0050 | g0001 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02698 | hp2 | a0001 | c0006 | t0016 | g0033 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02717 | hp1 | a0003 | c0003 | t0056 | g0179 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02717 | hp2 | a0003 | c0003 | t0003 | g0020 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0031 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02723 | hp2 | a0003 | c0003 | t0003 | g0139 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02735 | hp1 | a0001 | c0001 | t0052 | g0183 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0155 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02809 | hp1 | a0003 | c0003 | t0003 | g0020 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02809 | hp2 | a0001 | c0001 | t0039 | g0017 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02886 | hp1 | a0003 | c0004 | t0023 | g0152 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0121 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02895 | hp2 | a0002 | c0002 | t0008 | g0024 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02922 | hp2 | a0003 | c0003 | t0007 | g0157 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02965 | hp1 | a0004 | c0005 | t0008 | g0073 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02965 | hp2 | a0001 | c0001 | t0038 | g0109 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02976 | hp2 | a0003 | c0003 | t0003 | g0018 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03041 | hp1 | a0001 | c0001 | t0033 | g0122 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0023 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03098 | hp1 | a0004 | c0005 | t0037 | g0103 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03098 | hp2 | a0003 | c0003 | t0003 | g0162 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0113 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0035 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03195 | hp2 | a0003 | c0004 | t0010 | g0118 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03209 | hp1 | a0001 | c0001 | t0019 | g0125 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03209 | hp2 | a0001 | c0006 | t0007 | g0040 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03225 | hp1 | a0003 | c0003 | t0003 | g0019 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03225 | hp2 | a0001 | c0001 | t0020 | g0126 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03239 | hp1 | a0003 | c0003 | t0003 | g0143 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03453 | hp1 | a0003 | c0004 | t0023 | g0007 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03453 | hp2 | a0001 | c0001 | t0017 | g0023 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03486 | hp1 | a0001 | c0006 | t0003 | g0045 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03486 | hp2 | a0004 | c0005 | t0001 | g0108 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03491 | hp1 | a0002 | c0007 | t0024 | g0052 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03491 | hp2 | a0001 | c0001 | t0025 | g0050 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03492 | hp2 | a0001 | c0001 | t0025 | g0050 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03516 | hp1 | a0004 | c0005 | t0008 | g0176 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0124 | AFR | ESN | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03540 | hp1 | a0003 | c0003 | t0057 | g0044 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03540 | hp2 | a0001 | c0006 | t0003 | g0181 | AFR | GWD | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03579 | hp1 | a0001 | c0001 | t0014 | g0131 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0127 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03669 | hp2 | a0002 | c0007 | t0047 | g0052 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0153 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03831 | hp1 | a0001 | c0001 | t0043 | g0147 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03834 | hp2 | a0001 | c0001 | t0042 | g0100 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03927 | hp2 | a0002 | c0007 | t0024 | g0193 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | STU | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04115 | hp2 | a0001 | c0006 | t0016 | g0140 | SAS | STU | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04199 | hp1 | a0001 | c0001 | t0049 | g0011 | SAS | STU | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0090 | SAS | STU | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | STU | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | STU | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0069 | SAS | STU | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18522 | hp1 | a0001 | c0001 | t0032 | g0055 | AFR | YRI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18522 | hp2 | a0003 | c0003 | t0003 | g0019 | AFR | YRI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18612 | hp2 | a0001 | c0001 | t0048 | g0221 | EAS | CHB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18747 | hp1 | a0001 | c0001 | t0054 | g0001 | EAS | CHB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | CHB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18906 | hp1 | a0003 | c0004 | t0009 | g0112 | AFR | YRI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0130 | AFR | YRI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18970 | hp2 | a0002 | c0002 | t0018 | g0174 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18971 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18972 | hp2 | a0001 | c0001 | t0026 | g0046 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18988 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0216 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18993 | hp1 | a0005 | c0008 | t0002 | g0185 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19004 | hp2 | a0001 | c0001 | t0046 | g0006 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19030 | hp1 | a0003 | c0003 | t0003 | g0161 | AFR | LWK | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19030 | hp2 | a0003 | c0003 | t0003 | g0180 | AFR | LWK | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | LWK | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19043 | hp2 | a0004 | c0005 | t0001 | g0104 | AFR | LWK | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19068 | hp1 | a0005 | c0008 | t0053 | g0184 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19072 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19077 | hp2 | a0001 | c0001 | t0015 | g0011 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19081 | hp1 | a0001 | c0001 | t0044 | g0190 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19085 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA19240 | hp2 | a0002 | c0002 | t0008 | g0024 | AFR | YRI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA20129 | hp1 | a0003 | c0003 | t0003 | g0034 | AFR | ASW | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ASW | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA20752 | hp1 | a0002 | c0002 | t0035 | g0002 | EUR | TSI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA20752 | hp2 | a0003 | c0003 | t0003 | g0136 | EUR | TSI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0056 | EUR | TSI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | TSI | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG01123 | hp2 | a0002 | c0002 | t0012 | g0101 | AMR | CLM | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0031 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0033 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02486 | hp1 | a0003 | c0004 | t0009 | g0111 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02486 | hp2 | a0003 | c0004 | t0010 | g0120 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02559 | hp1 | a0003 | c0003 | t0003 | g0141 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG02559 | hp2 | a0002 | c0002 | t0008 | g0005 | AFR | ACB | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03471 | hp1 | a0003 | c0003 | t0003 | g0160 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG03471 | hp2 | a0003 | c0003 | t0007 | g0044 | AFR | MSL | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG06807 | hp1 | a0002 | c0002 | t0012 | g0027 | AFR | USA | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| HG06807 | hp2 | a0003 | c0003 | t0007 | g0156 | AFR | USA | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA20300 | hp1 | a0001 | c0001 | t0022 | g0167 | AFR | USA | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0001 | AFR | USA | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | LWK | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| NA21309 | hp2 | a0003 | c0003 | t0003 | g0146 | AFR | LWK | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0055 | g0212 | REF | REF | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0128 | REF | REF | CLEC2D_chr12_9664713_9704553 | CLEC2D | chr12 | 9664713 | 9704553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9669791 | C | G | 2 | a0003 a0004 |
62 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(59): Show |
missense_variant | MODERATE | c.57C>G | p.Asn19Lys | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/5 | 79/5277 | 57/576 | 19/191 | chr12 | 9669791 | |||
| chr12:9680928 | C | G | 2 | a0002 a0004 |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
missense_variant | MODERATE | c.67C>G | p.Leu23Val | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/5 | 89/5277 | 67/576 | 23/191 | chr12 | 9680928 | |||
| chr12:9681003 | A | G | 1 | a0005 | 2 | NA18993.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.142A>G | p.Ile48Val | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/5 | 164/5277 | 142/576 | 48/191 | chr12 | 9681003 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9681032 | C | T | 4 | a0001c0006 a0002c0002 a0003c0003 others(1): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
splice_region_variant&synonymous_variant | LOW | c.171C>T | p.Ser57Ser | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/5 | 193/5277 | 171/576 | 57/191 | chr12 | 9681032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9669721 | A | T | 1 | a0001c0001t0011 | 6 | HG01109.hp1 HG01928.hp2 HG01952.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/5 | 14 | chr12 | 9669721 | ||||||
| chr12:9695212 | A | G | 9 | a0001c0006t0003 a0001c0006t0007 a0001c0006t0016 others(6): Show |
45 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*338A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 338 | chr12 | 9695212 | ||||||
| chr12:9695394 | C | T | 10 | a0001c0006t0003 a0001c0006t0007 a0001c0006t0016 others(7): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*520C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 520 | chr12 | 9695394 | ||||||
| chr12:9695410 | G | C | 1 | a0004c0005t0028 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*536G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 536 | chr12 | 9695410 | ||||||
| chr12:9695583 | C | T | 2 | a0001c0006t0016 a0003c0003t0016 |
4 | HG02148.hp2 HG02647.hp1 HG02698.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*709C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 709 | chr12 | 9695583 | ||||||
| chr12:9695721 | A | G | 1 | a0003c0003t0059 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*847A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 847 | chr12 | 9695721 | ||||||
| chr12:9695749 | G | C | 1 | a0001c0001t0021 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*875G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 875 | chr12 | 9695749 | ||||||
| chr12:9695779 | G | A | 1 | a0002c0002t0029 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 905 | chr12 | 9695779 | ||||||
| chr12:9695788 | T | G | 1 | a0002c0002t0030 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*914T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 914 | chr12 | 9695788 | ||||||
| chr12:9695834 | A | G | 1 | a0001c0001t0020 | 3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*960A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 960 | chr12 | 9695834 | ||||||
| chr12:9695842 | CTT | C | 1 | a0002c0002t0012 | 4 | HG00280.hp2 HG01123.hp2 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*969_*970delTT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 969 | chr12 | 9695842 | ||||||
| chr12:9695843 | T | TTGC | 24 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(21): Show |
142 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*981_*983dupCTG | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 984 | INFO_REALIGN_3_PRIME | chr12 | 9695843 | |||||
| chr12:9695843 | T | TTGCTGC | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0019 others(3): Show |
12 | HG01081.hp1 HG01952.hp1 HG01978.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*978_*983dupCTGCTG | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 984 | INFO_REALIGN_3_PRIME | chr12 | 9695843 | |||||
| chr12:9695843 | T | TTTCTGC | 1 | a0001c0001t0004 | 11 | HG00099.hp2 HG01070.hp1 HG01099.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*970_*971insTCTGCT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 971 | INFO_REALIGN_3_PRIME | chr12 | 9695843 | |||||
| chr12:9695855 | CTGA | C | 2 | a0002c0002t0029 a0003c0004t0027 |
3 | HG00733.hp2 HG00735.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*997_*999delTGA | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 997 | INFO_REALIGN_3_PRIME | chr12 | 9695855 | |||||
| chr12:9695855 | CTGATGAT others(20): Show |
C | 1 | a0002c0002t0031 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*994_*1020delTGATG others(22): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 994 | INFO_REALIGN_3_PRIME | chr12 | 9695855 | |||||
| chr12:9695858 | A | C | 45 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(42): Show |
225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*984A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 984 | chr12 | 9695858 | ||||||
| chr12:9695861 | A | C | 22 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0015 others(19): Show |
136 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*987A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 987 | chr12 | 9695861 | ||||||
| chr12:9695868 | TGATGAA | T | 1 | a0001c0001t0017 | 3 | HG03041.hp2 HG03130.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1000_*1005delAGAT others(2): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1000 | INFO_REALIGN_3_PRIME | chr12 | 9695868 | |||||
| chr12:9695871 | T | A | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0019 others(3): Show |
23 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*997T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 997 | chr12 | 9695871 | ||||||
| chr12:9695874 | A | T | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0019 others(3): Show |
23 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1000A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1000 | chr12 | 9695874 | ||||||
| chr12:9695874 | AGAT | A | 2 | a0001c0001t0022 a0002c0002t0008 |
3 | HG01168.hp1 HG02145.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1018_*1020delTGA | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1018 | INFO_REALIGN_3_PRIME | chr12 | 9695874 | |||||
| chr12:9695877 | T | A | 1 | a0001c0001t0017 | 3 | HG03041.hp2 HG03130.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1003T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1003 | chr12 | 9695877 | ||||||
| chr12:9695882 | A | G | 1 | a0001c0001t0054 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1008A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1008 | chr12 | 9695882 | ||||||
| chr12:9695902 | G | A | 1 | a0002c0002t0018 | 3 | HG00438.hp2 HG02083.hp2 NA18970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1028G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1028 | chr12 | 9695902 | ||||||
| chr12:9695916 | G | A | 1 | a0001c0001t0032 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1042G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1042 | chr12 | 9695916 | ||||||
| chr12:9696052 | A | G | 3 | a0001c0001t0004 a0001c0001t0042 a0003c0004t0023 |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1178A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1178 | chr12 | 9696052 | ||||||
| chr12:9696164 | A | G | 1 | a0001c0001t0041 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1290 | chr12 | 9696164 | ||||||
| chr12:9696272 | T | C | 1 | a0003c0003t0057 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1398T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1398 | chr12 | 9696272 | ||||||
| chr12:9696287 | A | G | 26 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0010 others(23): Show |
149 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1413A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1413 | chr12 | 9696287 | ||||||
| chr12:9696542 | ATAAAG | A | 2 | a0002c0002t0008 a0004c0005t0008 |
6 | HG01168.hp1 HG02559.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1673_*1677delGTAA others(1): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1673 | INFO_REALIGN_3_PRIME | chr12 | 9696542 | |||||
| chr12:9696543 | TAAAGTA | T | 12 | a0001c0001t0001 a0002c0002t0001 a0002c0002t0012 others(9): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1673_*1678delGTAA others(2): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1673 | INFO_REALIGN_3_PRIME | chr12 | 9696543 | |||||
| chr12:9696543 | TAAAGTAA | T | 2 | a0002c0002t0001 a0002c0002t0034 |
6 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1673_*1679delGTAA others(3): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1673 | INFO_REALIGN_3_PRIME | chr12 | 9696543 | |||||
| chr12:9696548 | TA | T | 47 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(44): Show |
230 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1689delA | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1689 | INFO_REALIGN_3_PRIME | chr12 | 9696548 | |||||
| chr12:9696606 | G | A | 1 | a0001c0001t0017 | 3 | HG03041.hp2 HG03130.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1732G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1732 | chr12 | 9696606 | ||||||
| chr12:9696619 | G | A | 1 | a0001c0001t0044 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1745G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1745 | chr12 | 9696619 | ||||||
| chr12:9696679 | C | T | 24 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(21): Show |
143 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*1805C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 1805 | chr12 | 9696679 | ||||||
| chr12:9696886 | C | G | 1 | a0004c0005t0037 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2012C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2012 | chr12 | 9696886 | ||||||
| chr12:9696952 | G | A | 5 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0033 others(2): Show |
22 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2078G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2078 | chr12 | 9696952 | ||||||
| chr12:9696981 | G | C | 1 | a0001c0001t0038 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2107G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2107 | chr12 | 9696981 | ||||||
| chr12:9697036 | CAT | C | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(56): Show |
349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*2178_*2179delTA | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2178 | INFO_REALIGN_3_PRIME | chr12 | 9697036 | |||||
| chr12:9697049 | ATAT | A | 3 | a0001c0001t0004 a0001c0001t0042 a0003c0004t0023 |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2176_*2178delTAT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2176 | chr12 | 9697049 | ||||||
| chr12:9697051 | AT | A | 2 | a0001c0001t0019 a0001c0001t0033 |
4 | HG01952.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2178delT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2178 | chr12 | 9697051 | ||||||
| chr12:9697052 | T | A | 1 | a0001c0001t0022 | 2 | HG02145.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2178T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2178 | chr12 | 9697052 | ||||||
| chr12:9697052 | TAA | T | 3 | a0001c0001t0026 a0001c0006t0007 a0003c0003t0007 |
8 | HG00438.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2183_*2184delAA | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2183 | INFO_REALIGN_3_PRIME | chr12 | 9697052 | |||||
| chr12:9697059 | T | A | 1 | a0005c0008t0053 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2185T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2185 | chr12 | 9697059 | ||||||
| chr12:9697215 | G | A | 1 | a0002c0002t0034 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2341G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2341 | chr12 | 9697215 | ||||||
| chr12:9697280 | G | A | 1 | a0001c0001t0045 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2406G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2406 | chr12 | 9697280 | ||||||
| chr12:9697294 | A | C | 1 | a0001c0001t0040 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2420A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2420 | chr12 | 9697294 | ||||||
| chr12:9697370 | C | T | 1 | a0001c0001t0052 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2496C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2496 | chr12 | 9697370 | ||||||
| chr12:9697439 | G | T | 1 | a0003c0003t0058 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2565G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2565 | chr12 | 9697439 | ||||||
| chr12:9697440 | A | G | 1 | a0001c0001t0025 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2566A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2566 | chr12 | 9697440 | ||||||
| chr12:9697535 | A | G | 1 | a0001c0001t0004 | 15 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2661A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2661 | chr12 | 9697535 | ||||||
| chr12:9697541 | CTG | C | 16 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0022 others(13): Show |
59 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2677_*2678delGT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2677 | INFO_REALIGN_3_PRIME | chr12 | 9697541 | |||||
| chr12:9697591 | G | A | 3 | a0001c0001t0004 a0001c0001t0042 a0003c0004t0023 |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2717G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2717 | chr12 | 9697591 | ||||||
| chr12:9697719 | TA | T | 47 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(44): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*2855delA | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2855 | INFO_REALIGN_3_PRIME | chr12 | 9697719 | |||||
| chr12:9697840 | T | G | 1 | a0001c0001t0048 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2966T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 2966 | chr12 | 9697840 | ||||||
| chr12:9697919 | C | CCACA | 6 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0020 others(3): Show |
25 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3048_*3051dupCACA | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3052 | INFO_REALIGN_3_PRIME | chr12 | 9697919 | |||||
| chr12:9697934 | G | T | 4 | a0001c0001t0009 a0001c0001t0014 a0003c0004t0009 others(1): Show |
10 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3060G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3060 | chr12 | 9697934 | ||||||
| chr12:9697987 | A | C | 10 | a0001c0006t0003 a0001c0006t0007 a0001c0006t0016 others(7): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*3113A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3113 | chr12 | 9697987 | ||||||
| chr12:9697995 | A | G | 1 | a0002c0007t0047 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3121A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3121 | chr12 | 9697995 | ||||||
| chr12:9698090 | ATATTT | A | 2 | a0001c0001t0009 a0003c0004t0009 |
6 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3218_*3222delATTT others(1): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3218 | INFO_REALIGN_3_PRIME | chr12 | 9698090 | |||||
| chr12:9698313 | G | C | 16 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0022 others(13): Show |
59 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3439G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3439 | chr12 | 9698313 | ||||||
| chr12:9698389 | C | T | 1 | a0002c0002t0036 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3515C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3515 | chr12 | 9698389 | ||||||
| chr12:9698427 | T | A | 26 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0010 others(23): Show |
149 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*3553T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3553 | chr12 | 9698427 | ||||||
| chr12:9698637 | C | T | 6 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0022 others(3): Show |
13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3763C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3763 | chr12 | 9698637 | ||||||
| chr12:9698678 | T | G | 1 | a0001c0001t0033 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3804T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3804 | chr12 | 9698678 | ||||||
| chr12:9698697 | A | G | 1 | a0001c0001t0051 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3823A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3823 | chr12 | 9698697 | ||||||
| chr12:9698702 | T | A | 1 | a0001c0001t0049 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3828T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3828 | chr12 | 9698702 | ||||||
| chr12:9698778 | C | T | 1 | a0005c0008t0053 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3904C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3904 | chr12 | 9698778 | ||||||
| chr12:9698786 | T | C | 1 | a0001c0001t0042 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3912T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 3912 | chr12 | 9698786 | ||||||
| chr12:9699113 | T | C | 1 | a0001c0001t0015 | 4 | NA18971.hp2 NA18988.hp2 NA19077.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4239T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 4239 | chr12 | 9699113 | ||||||
| chr12:9699203 | C | A | 2 | a0001c0001t0010 a0003c0004t0010 |
6 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4329C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 4329 | chr12 | 9699203 | ||||||
| chr12:9699212 | G | T | 18 | a0001c0001t0001 a0001c0001t0050 a0002c0002t0001 others(15): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*4338G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 4338 | chr12 | 9699212 | ||||||
| chr12:9699229 | A | AT | 6 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0020 others(3): Show |
25 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4357dupT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 4358 | INFO_REALIGN_3_PRIME | chr12 | 9699229 | |||||
| chr12:9699310 | A | G | 3 | a0001c0001t0004 a0001c0001t0042 a0003c0004t0023 |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4436A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 4436 | chr12 | 9699310 | ||||||
| chr12:9699333 | C | A | 21 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(18): Show |
139 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*4459C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 4459 | chr12 | 9699333 | ||||||
| chr12:9699419 | T | C | 1 | a0002c0002t0035 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4545T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 5/5 | 4545 | chr12 | 9699419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9669894 | T | C | 1 | a0001c0001t0032g0055 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.61+99T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9669894 | |||||||
| chr12:9670028 | ATAAGGT | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(100): Show |
171 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.61+238_61+243delGT others(4): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9670028 | ||||||
| chr12:9670095 | A | G | 2 | a0001c0001t0022g0167 a0001c0001t0022g0168 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61+300A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670095 | |||||||
| chr12:9670135 | T | A | 1 | a0001c0001t0002g0169 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.61+340T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670135 | |||||||
| chr12:9670136 | A | T | 1 | a0002c0002t0001g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.61+341A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670136 | |||||||
| chr12:9670143 | C | T | 1 | a0002c0002t0001g0165 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.61+348C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670143 | |||||||
| chr12:9670280 | A | AAT | 21 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(18): Show |
29 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.61+499_61+500dupTA | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9670280 | ||||||
| chr12:9670289 | A | G | 1 | a0001c0001t0005g0164 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.61+494A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670289 | |||||||
| chr12:9670356 | A | G | 138 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(135): Show |
212 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.61+561A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670356 | |||||||
| chr12:9670544 | G | A | 91 | a0001c0001t0001g0063 a0001c0001t0009g0114 a0001c0001t0014g0113 others(88): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.61+749G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670544 | |||||||
| chr12:9670549 | G | T | 2 | a0001c0001t0022g0167 a0001c0001t0022g0168 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61+754G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670549 | |||||||
| chr12:9670582 | G | C | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+787G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670582 | |||||||
| chr12:9670615 | G | A | 1 | a0002c0002t0008g0024 | 2 | HG02895.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.61+820G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670615 | |||||||
| chr12:9670678 | T | A | 84 | a0001c0001t0001g0063 a0001c0001t0042g0100 a0002c0002t0001g0002 others(81): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.61+883T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670678 | |||||||
| chr12:9670838 | G | A | 1 | a0001c0001t0011g0178 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.61+1043G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670838 | |||||||
| chr12:9670890 | T | C | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+1095T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670890 | |||||||
| chr12:9670923 | A | T | 7 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(4): Show |
8 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+1128A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670923 | |||||||
| chr12:9670957 | G | A | 246 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(243): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.61+1162G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9670957 | |||||||
| chr12:9671050 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.61+1255C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671050 | |||||||
| chr12:9671108 | C | G | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.61+1313C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671108 | |||||||
| chr12:9671263 | C | G | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.61+1468C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671263 | |||||||
| chr12:9671272 | G | A | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+1477G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671272 | |||||||
| chr12:9671345 | T | C | 4 | a0003c0003t0003g0180 a0003c0003t0007g0044 a0003c0003t0056g0179 others(1): Show |
4 | HG02717.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+1550T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671345 | |||||||
| chr12:9671377 | C | G | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+1582C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671377 | |||||||
| chr12:9671436 | G | A | 234 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(231): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.61+1641G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671436 | |||||||
| chr12:9671472 | G | A | 38 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(35): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.61+1677G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671472 | |||||||
| chr12:9671472 | G | C | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+1677G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671472 | |||||||
| chr12:9671477 | C | T | 1 | a0002c0002t0001g0107 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.61+1682C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671477 | |||||||
| chr12:9671483 | C | G | 246 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(243): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.61+1688C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671483 | |||||||
| chr12:9671499 | C | A | 3 | a0002c0002t0001g0056 a0002c0002t0001g0057 a0002c0002t0001g0058 |
3 | HG02683.hp1 NA20805.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.61+1704C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671499 | |||||||
| chr12:9671542 | T | G | 84 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(81): Show |
143 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.61+1747T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671542 | |||||||
| chr12:9671697 | A | T | 1 | a0002c0002t0001g0106 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.61+1902A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671697 | |||||||
| chr12:9671928 | T | C | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0182 others(1): Show |
5 | NA18952.hp2 NA18972.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+2133T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671928 | |||||||
| chr12:9671931 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.61+2136G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9671931 | |||||||
| chr12:9672013 | T | C | 1 | a0001c0001t0052g0183 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.61+2218T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672013 | |||||||
| chr12:9672177 | AAGAG | A | 235 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(232): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.61+2389_61+2392del others(4): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9672177 | ||||||
| chr12:9672392 | T | C | 13 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(10): Show |
19 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.61+2597T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672392 | |||||||
| chr12:9672435 | C | T | 1 | a0001c0001t0002g0224 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.61+2640C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672435 | |||||||
| chr12:9672450 | C | A | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.61+2655C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672450 | |||||||
| chr12:9672480 | C | T | 2 | a0001c0001t0022g0167 a0001c0001t0022g0168 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.61+2685C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672480 | |||||||
| chr12:9672521 | G | A | 2 | a0005c0008t0002g0185 a0005c0008t0053g0184 |
2 | NA18993.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.61+2726G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672521 | |||||||
| chr12:9672608 | G | A | 1 | a0001c0001t0017g0023 | 3 | HG03041.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.61+2813G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672608 | |||||||
| chr12:9672868 | G | A | 1 | a0001c0001t0002g0186 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.61+3073G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672868 | |||||||
| chr12:9672930 | C | G | 1 | a0001c0001t0002g0223 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.61+3135C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9672930 | |||||||
| chr12:9673052 | A | G | 3 | a0004c0005t0001g0104 a0004c0005t0001g0105 a0004c0005t0037g0103 |
3 | HG02572.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.61+3257A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673052 | |||||||
| chr12:9673057 | A | G | 9 | a0001c0001t0010g0029 a0001c0001t0010g0121 a0001c0001t0019g0123 others(6): Show |
10 | HG01168.hp2 HG01169.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+3262A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673057 | |||||||
| chr12:9673133 | G | A | 1 | a0001c0001t0006g0187 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.61+3338G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673133 | |||||||
| chr12:9673143 | A | T | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.61+3348A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673143 | |||||||
| chr12:9673300 | A | G | 1 | a0003c0003t0003g0163 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.61+3505A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673300 | |||||||
| chr12:9673373 | G | A | 212 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(209): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.61+3578G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673373 | |||||||
| chr12:9673426 | T | C | 34 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(31): Show |
42 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.61+3631T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673426 | |||||||
| chr12:9673468 | C | T | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+3673C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673468 | |||||||
| chr12:9673470 | G | A | 2 | a0002c0002t0001g0059 a0002c0002t0001g0060 |
2 | NA18994.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.61+3675G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673470 | |||||||
| chr12:9673546 | C | T | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+3751C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673546 | |||||||
| chr12:9673650 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0021g0022 |
3 | HG01070.hp2 HG01071.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.61+3855A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673650 | |||||||
| chr12:9673683 | C | T | 3 | a0002c0002t0012g0027 a0002c0002t0012g0101 a0002c0002t0012g0102 |
4 | HG00280.hp2 HG01123.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+3888C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673683 | |||||||
| chr12:9673790 | C | T | 1 | a0001c0001t0038g0109 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.61+3995C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673790 | |||||||
| chr12:9673812 | G | C | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+4017G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9673812 | |||||||
| chr12:9673930 | T | TC | 9 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.61+4141dupC | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9673930 | ||||||
| chr12:9674105 | G | A | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+4310G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9674105 | |||||||
| chr12:9674150 | C | T | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+4355C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9674150 | |||||||
| chr12:9674186 | G | C | 212 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(209): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.61+4391G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9674186 | |||||||
| chr12:9674322 | G | A | 1 | a0001c0001t0002g0188 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.61+4527G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9674322 | |||||||
| chr12:9674543 | T | G | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+4748T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9674543 | |||||||
| chr12:9674763 | T | A | 23 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(20): Show |
30 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.61+4968T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9674763 | |||||||
| chr12:9674891 | A | G | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+5096A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9674891 | |||||||
| chr12:9675003 | G | A | 4 | a0003c0003t0003g0180 a0003c0003t0007g0044 a0003c0003t0056g0179 others(1): Show |
4 | HG02717.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+5208G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9675003 | |||||||
| chr12:9675191 | C | CTTT | 9 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(6): Show |
15 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+5412_61+5414dup others(3): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9675191 | ||||||
| chr12:9675191 | CT | C | 178 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(175): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.61+5414delT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9675191 | ||||||
| chr12:9675279 | C | T | 4 | a0001c0001t0002g0053 a0001c0001t0002g0169 a0003c0003t0003g0161 others(1): Show |
5 | HG03098.hp2 NA18940.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+5484C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9675279 | |||||||
| chr12:9675356 | C | T | 3 | a0001c0001t0005g0017 a0001c0001t0005g0130 a0001c0001t0039g0017 |
4 | HG01993.hp1 HG02809.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+5561C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9675356 | |||||||
| chr12:9675357 | G | A | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.61+5562G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9675357 | |||||||
| chr12:9675702 | T | C | 1 | a0004c0005t0028g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.62-5221T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9675702 | |||||||
| chr12:9675813 | A | C | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-5110A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9675813 | |||||||
| chr12:9675831 | T | G | 89 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(86): Show |
150 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.62-5092T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9675831 | |||||||
| chr12:9675849 | T | C | 14 | a0001c0006t0007g0040 a0003c0003t0003g0018 a0003c0003t0003g0020 others(11): Show |
18 | HG00738.hp2 HG01109.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.62-5074T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9675849 | |||||||
| chr12:9676133 | T | C | 2 | a0003c0004t0027g0148 a0003c0004t0027g0149 |
2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.62-4790T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9676133 | |||||||
| chr12:9676266 | A | T | 1 | a0001c0001t0048g0221 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.62-4657A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9676266 | |||||||
| chr12:9676419 | T | C | 12 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(9): Show |
13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.62-4504T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9676419 | |||||||
| chr12:9676431 | T | C | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-4492T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9676431 | |||||||
| chr12:9676842 | A | T | 89 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(86): Show |
150 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.62-4081A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9676842 | |||||||
| chr12:9676861 | A | G | 34 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(31): Show |
42 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.62-4062A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9676861 | |||||||
| chr12:9676893 | T | C | 1 | a0003c0003t0003g0136 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.62-4030T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9676893 | |||||||
| chr12:9676970 | T | C | 38 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(35): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.62-3953T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9676970 | |||||||
| chr12:9677005 | C | T | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG01175.hp2 HG01192.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.62-3918C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9677005 | |||||||
| chr12:9677043 | AT | A | 130 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0009g0114 others(127): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.62-3867delT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9677043 | ||||||
| chr12:9677043 | ATT | A | 5 | a0001c0001t0002g0189 a0002c0002t0001g0025 a0002c0002t0001g0064 others(2): Show |
6 | HG00609.hp2 HG01261.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3868_62-3867del others(2): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9677043 | ||||||
| chr12:9677157 | C | T | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.62-3766C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9677157 | |||||||
| chr12:9677203 | T | A | 2 | a0002c0002t0001g0025 a0002c0002t0001g0106 |
3 | HG00423.hp2 HG00609.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.62-3720T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9677203 | |||||||
| chr12:9677347 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.62-3576T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9677347 | |||||||
| chr12:9677606 | A | C | 1 | a0001c0001t0014g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.62-3317A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9677606 | |||||||
| chr12:9677707 | CT | C | 15 | a0001c0001t0004g0007 a0001c0001t0004g0039 a0001c0001t0004g0116 others(12): Show |
20 | HG01099.hp2 HG01243.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.62-3195delT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9677707 | ||||||
| chr12:9677707 | CTT | C | 98 | a0001c0001t0001g0063 a0001c0001t0002g0217 a0001c0001t0002g0222 others(95): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.62-3196_62-3195del others(2): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9677707 | ||||||
| chr12:9677707 | CTTT | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(119): Show |
189 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.62-3197_62-3195del others(3): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9677707 | ||||||
| chr12:9677707 | CTTTT | C | 8 | a0001c0001t0002g0036 a0001c0001t0002g0048 a0001c0001t0002g0182 others(5): Show |
10 | HG00323.hp1 HG02071.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-3198_62-3195del others(4): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9677707 | ||||||
| chr12:9677713 | T | C | 1 | a0003c0004t0014g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.62-3210T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9677713 | |||||||
| chr12:9677729 | A | T | 3 | a0001c0001t0005g0032 a0001c0001t0005g0164 a0003c0004t0005g0129 |
4 | HG00280.hp1 HG01891.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-3194A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9677729 | |||||||
| chr12:9678011 | A | C | 224 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(221): Show |
344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.62-2912A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678011 | |||||||
| chr12:9678013 | A | G | 224 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(221): Show |
344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.62-2910A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678013 | |||||||
| chr12:9678080 | A | G | 2 | a0001c0001t0002g0215 a0001c0001t0002g0217 |
2 | NA19076.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.62-2843A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678080 | |||||||
| chr12:9678082 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.62-2841C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678082 | |||||||
| chr12:9678102 | G | A | 224 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(221): Show |
344 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.62-2821G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678102 | |||||||
| chr12:9678142 | G | A | 5 | a0001c0001t0010g0029 a0001c0001t0010g0121 a0003c0004t0010g0118 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-2781G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678142 | |||||||
| chr12:9678168 | C | T | 1 | a0003c0003t0059g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.62-2755C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678168 | |||||||
| chr12:9678208 | C | T | 5 | a0003c0003t0003g0034 a0003c0003t0003g0035 a0003c0003t0003g0146 others(2): Show |
6 | HG01884.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-2715C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678208 | |||||||
| chr12:9678304 | T | G | 1 | a0002c0002t0001g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.62-2619T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678304 | |||||||
| chr12:9678447 | TAA | T | 11 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(8): Show |
17 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.62-2473_62-2472del others(2): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 9678447 | ||||||
| chr12:9678550 | T | C | 1 | a0001c0001t0014g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.62-2373T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678550 | |||||||
| chr12:9678568 | C | A | 1 | a0001c0001t0002g0021 | 3 | HG01361.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.62-2355C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678568 | |||||||
| chr12:9678725 | C | T | 12 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(9): Show |
13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.62-2198C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678725 | |||||||
| chr12:9678782 | C | G | 1 | a0001c0001t0002g0197 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.62-2141C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9678782 | |||||||
| chr12:9679009 | A | C | 1 | a0001c0001t0009g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.62-1914A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9679009 | |||||||
| chr12:9679061 | C | A | 1 | a0002c0002t0001g0070 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.62-1862C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9679061 | |||||||
| chr12:9679236 | T | C | 38 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(35): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.62-1687T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9679236 | |||||||
| chr12:9679363 | C | G | 84 | a0001c0001t0042g0100 a0002c0002t0001g0002 a0002c0002t0001g0003 others(81): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.62-1560C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9679363 | |||||||
| chr12:9679440 | T | C | 223 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(220): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.62-1483T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9679440 | |||||||
| chr12:9679643 | A | C | 6 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0003c0004t0009g0028 others(3): Show |
7 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-1280A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9679643 | |||||||
| chr12:9679825 | G | A | 223 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(220): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.62-1098G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9679825 | |||||||
| chr12:9679853 | C | A | 1 | a0001c0001t0002g0198 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.62-1070C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9679853 | |||||||
| chr12:9680091 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.62-832T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680091 | |||||||
| chr12:9680123 | C | T | 1 | a0001c0001t0002g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.62-800C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680123 | |||||||
| chr12:9680226 | C | T | 223 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(220): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.62-697C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680226 | |||||||
| chr12:9680286 | T | C | 222 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(219): Show |
342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.62-637T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680286 | |||||||
| chr12:9680384 | A | G | 223 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(220): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.62-539A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680384 | |||||||
| chr12:9680603 | G | A | 1 | a0003c0003t0003g0138 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.62-320G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680603 | |||||||
| chr12:9680683 | T | A | 1 | a0003c0004t0014g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.62-240T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680683 | |||||||
| chr12:9680688 | C | T | 1 | a0002c0002t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.62-235C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680688 | |||||||
| chr12:9680802 | A | G | 38 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(35): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.62-121A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680802 | |||||||
| chr12:9680830 | A | G | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.62-93A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 1/4 | chr12 | 9680830 | |||||||
| chr12:9681169 | T | A | 1 | a0002c0002t0001g0071 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.172+136T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681169 | |||||||
| chr12:9681226 | A | T | 2 | a0001c0001t0022g0167 a0001c0001t0022g0168 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.172+193A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681226 | |||||||
| chr12:9681248 | G | C | 1 | a0001c0001t0013g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.172+215G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681248 | |||||||
| chr12:9681287 | T | C | 211 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(208): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.172+254T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681287 | |||||||
| chr12:9681333 | G | A | 1 | a0001c0001t0002g0199 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.172+300G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681333 | |||||||
| chr12:9681613 | A | AT | 130 | a0001c0001t0002g0006 a0001c0001t0002g0186 a0001c0001t0002g0189 others(127): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.172+581dupT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9681613 | ||||||
| chr12:9681749 | C | T | 81 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(78): Show |
137 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.172+716C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681749 | |||||||
| chr12:9681798 | A | G | 92 | a0001c0001t0002g0006 a0001c0001t0002g0186 a0001c0001t0002g0189 others(89): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.172+765A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681798 | |||||||
| chr12:9681885 | A | C | 29 | a0002c0002t0001g0005 a0002c0002t0001g0015 a0002c0002t0001g0016 others(26): Show |
45 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.172+852A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681885 | |||||||
| chr12:9681971 | C | G | 223 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(220): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.172+938C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681971 | |||||||
| chr12:9681981 | A | G | 1 | a0003c0004t0009g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.172+948A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9681981 | |||||||
| chr12:9682158 | G | A | 223 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(220): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.172+1125G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682158 | |||||||
| chr12:9682290 | C | A | 1 | a0002c0002t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.172+1257C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682290 | |||||||
| chr12:9682330 | A | T | 1 | a0002c0002t0012g0027 | 2 | HG00280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.172+1297A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682330 | |||||||
| chr12:9682375 | T | C | 3 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0003c0003t0003g0139 |
4 | HG02615.hp2 HG02723.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+1342T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682375 | |||||||
| chr12:9682418 | C | T | 211 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(208): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.172+1385C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682418 | |||||||
| chr12:9682534 | A | G | 1 | a0003c0003t0003g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.172+1501A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682534 | |||||||
| chr12:9682557 | C | T | 1 | a0001c0001t0004g0039 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.172+1524C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682557 | |||||||
| chr12:9682573 | G | A | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+1540G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682573 | |||||||
| chr12:9682786 | G | T | 2 | a0001c0001t0002g0192 a0001c0001t0002g0213 |
2 | HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.172+1753G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682786 | |||||||
| chr12:9682995 | C | G | 1 | a0002c0002t0001g0172 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.172+1962C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9682995 | |||||||
| chr12:9683004 | G | A | 1 | a0001c0001t0014g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.172+1971G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683004 | |||||||
| chr12:9683123 | T | G | 1 | a0001c0001t0032g0055 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.172+2090T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683123 | |||||||
| chr12:9683317 | AGTTTGTT others(6): Show |
A | 2 | a0001c0001t0002g0211 a0002c0002t0001g0064 |
2 | HG01261.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.172+2296_172+2308d others(15): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9683317 | ||||||
| chr12:9683320 | TTGTTTTT others(4): Show |
T | 2 | a0001c0001t0002g0210 a0001c0001t0014g0131 |
2 | HG01123.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.172+2289_172+2299d others(13): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9683320 | ||||||
| chr12:9683323 | TTTTTTGT others(5): Show |
T | 157 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(154): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.172+2296_172+2307d others(14): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9683323 | ||||||
| chr12:9683324 | TTTTTGTG others(4): Show |
T | 23 | a0001c0001t0002g0004 a0001c0001t0002g0022 a0001c0001t0002g0051 others(20): Show |
26 | HG00099.hp1 HG00423.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.172+2296_172+2306d others(13): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9683324 | ||||||
| chr12:9683325 | TTTTGTGT others(3): Show |
T | 30 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(27): Show |
35 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.172+2296_172+2305d others(12): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9683325 | ||||||
| chr12:9683326 | TTTGTGTT others(2): Show |
T | 10 | a0001c0001t0014g0115 a0001c0006t0016g0033 a0001c0006t0016g0140 others(7): Show |
11 | HG00642.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+2296_172+2304d others(11): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9683326 | ||||||
| chr12:9683329 | G | T | 23 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(20): Show |
31 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.172+2296G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683329 | |||||||
| chr12:9683335 | G | GTTT | 6 | a0001c0001t0010g0029 a0001c0001t0010g0121 a0001c0001t0019g0125 others(3): Show |
7 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.172+2319_172+2321d others(5): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9683335 | ||||||
| chr12:9683335 | G | T | 2 | a0001c0001t0002g0210 a0001c0001t0014g0131 |
2 | HG01123.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.172+2302G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683335 | |||||||
| chr12:9683339 | T | G | 16 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(13): Show |
22 | HG00099.hp2 HG00423.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.172+2306T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683339 | |||||||
| chr12:9683340 | T | G | 81 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0003 others(78): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.172+2307T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683340 | |||||||
| chr12:9683341 | T | G | 1 | a0002c0002t0001g0064 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.172+2308T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683341 | |||||||
| chr12:9683343 | T | G | 1 | a0001c0001t0004g0154 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.172+2310T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683343 | |||||||
| chr12:9683409 | G | A | 2 | a0001c0001t0002g0200 a0001c0001t0044g0190 |
2 | NA19079.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.172+2376G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683409 | |||||||
| chr12:9683447 | C | T | 2 | a0001c0001t0022g0167 a0001c0001t0022g0168 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.172+2414C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683447 | |||||||
| chr12:9683464 | T | G | 1 | a0001c0001t0002g0201 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.172+2431T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683464 | |||||||
| chr12:9683537 | G | C | 223 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(220): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.172+2504G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683537 | |||||||
| chr12:9683886 | G | GT | 108 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(105): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.172+2866dupT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 9683886 | ||||||
| chr12:9683967 | A | C | 1 | a0001c0001t0002g0224 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.172+2934A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9683967 | |||||||
| chr12:9684185 | T | C | 1 | a0002c0002t0001g0225 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.172+3152T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9684185 | |||||||
| chr12:9684460 | G | C | 1 | a0002c0002t0001g0074 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.172+3427G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9684460 | |||||||
| chr12:9684628 | G | A | 246 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(243): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.173-3274G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9684628 | |||||||
| chr12:9684785 | T | C | 1 | a0002c0002t0029g0075 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.173-3117T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9684785 | |||||||
| chr12:9684901 | G | A | 5 | a0001c0001t0010g0029 a0001c0001t0010g0121 a0003c0004t0010g0118 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.173-3001G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9684901 | |||||||
| chr12:9684926 | A | G | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-2976A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9684926 | |||||||
| chr12:9685087 | T | C | 1 | a0001c0001t0038g0109 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-2815T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685087 | |||||||
| chr12:9685393 | A | G | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.173-2509A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685393 | |||||||
| chr12:9685402 | T | C | 138 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(135): Show |
210 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.173-2500T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685402 | |||||||
| chr12:9685420 | C | G | 1 | a0001c0001t0002g0227 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.173-2482C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685420 | |||||||
| chr12:9685456 | G | C | 42 | a0001c0001t0005g0017 a0001c0001t0005g0130 a0001c0001t0017g0023 others(39): Show |
53 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.173-2446G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685456 | |||||||
| chr12:9685508 | C | T | 1 | a0003c0003t0003g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.173-2394C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685508 | |||||||
| chr12:9685588 | C | G | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.173-2314C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685588 | |||||||
| chr12:9685625 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.173-2277G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685625 | |||||||
| chr12:9685941 | C | T | 1 | a0003c0003t0003g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.173-1961C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9685941 | |||||||
| chr12:9686219 | C | A | 4 | a0003c0003t0003g0180 a0003c0003t0007g0044 a0003c0003t0056g0179 others(1): Show |
4 | HG02717.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-1683C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686219 | |||||||
| chr12:9686275 | A | C | 1 | a0002c0002t0029g0075 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.173-1627A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686275 | |||||||
| chr12:9686313 | G | T | 1 | a0001c0001t0002g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.173-1589G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686313 | |||||||
| chr12:9686320 | C | G | 85 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(82): Show |
144 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.173-1582C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686320 | |||||||
| chr12:9686397 | A | C | 246 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(243): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.173-1505A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686397 | |||||||
| chr12:9686597 | A | G | 1 | a0002c0002t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.173-1305A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686597 | |||||||
| chr12:9686780 | A | G | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.173-1122A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686780 | |||||||
| chr12:9686803 | T | C | 1 | a0003c0003t0003g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.173-1099T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686803 | |||||||
| chr12:9686809 | G | T | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.173-1093G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686809 | |||||||
| chr12:9686844 | C | T | 5 | a0001c0001t0010g0029 a0001c0001t0010g0121 a0003c0004t0010g0118 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.173-1058C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686844 | |||||||
| chr12:9686849 | A | C | 236 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(233): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.173-1053A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9686849 | |||||||
| chr12:9687090 | T | A | 3 | a0002c0002t0001g0091 a0002c0002t0001g0092 a0002c0002t0001g0093 |
3 | HG00558.hp1 HG02056.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.173-812T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687090 | |||||||
| chr12:9687149 | A | G | 1 | a0003c0004t0005g0129 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.173-753A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687149 | |||||||
| chr12:9687207 | A | G | 1 | a0002c0002t0001g0089 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.173-695A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687207 | |||||||
| chr12:9687222 | A | G | 1 | a0002c0002t0001g0062 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.173-680A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687222 | |||||||
| chr12:9687241 | T | C | 12 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(9): Show |
13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.173-661T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687241 | |||||||
| chr12:9687442 | C | T | 85 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0005 others(82): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.173-460C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687442 | |||||||
| chr12:9687494 | C | T | 2 | a0001c0001t0022g0167 a0001c0001t0022g0168 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.173-408C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687494 | |||||||
| chr12:9687524 | G | A | 1 | a0001c0001t0051g0203 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.173-378G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687524 | |||||||
| chr12:9687640 | A | G | 11 | a0001c0006t0007g0040 a0003c0003t0003g0020 a0003c0003t0003g0160 others(8): Show |
13 | HG01257.hp2 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.173-262A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687640 | |||||||
| chr12:9687641 | T | C | 1 | a0001c0001t0014g0113 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.173-261T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687641 | |||||||
| chr12:9687744 | G | A | 4 | a0002c0002t0001g0065 a0002c0002t0001g0076 a0002c0002t0001g0077 others(1): Show |
4 | NA18948.hp1 NA18981.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.173-158G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687744 | |||||||
| chr12:9687802 | T | G | 1 | a0002c0002t0001g0079 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.173-100T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 2/4 | chr12 | 9687802 | |||||||
| chr12:9688125 | C | T | 1 | a0003c0003t0016g0142 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.357+39C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688125 | |||||||
| chr12:9688177 | T | A | 84 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(81): Show |
145 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.357+91T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688177 | |||||||
| chr12:9688190 | A | AT | 53 | a0001c0001t0002g0011 a0001c0001t0002g0047 a0001c0001t0002g0051 others(50): Show |
63 | HG00280.hp2 HG00621.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.357+128dupT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9688190 | ||||||
| chr12:9688190 | A | ATT | 7 | a0001c0001t0010g0029 a0001c0001t0026g0209 a0002c0002t0001g0171 others(4): Show |
8 | HG00438.hp1 HG00733.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.357+127_357+128dup others(2): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9688190 | ||||||
| chr12:9688190 | A | ATTT | 27 | a0001c0001t0010g0121 a0001c0006t0007g0040 a0003c0003t0003g0018 others(24): Show |
33 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.357+126_357+128dup others(3): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9688190 | ||||||
| chr12:9688190 | A | ATTTT | 10 | a0001c0006t0003g0045 a0001c0006t0016g0033 a0003c0003t0003g0033 others(7): Show |
12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.357+125_357+128dup others(4): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9688190 | ||||||
| chr12:9688190 | AT | A | 9 | a0001c0001t0002g0049 a0001c0001t0002g0189 a0001c0001t0020g0030 others(6): Show |
12 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.357+128delT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9688190 | ||||||
| chr12:9688190 | ATTTTTTT others(1): Show |
A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
19 | HG00099.hp2 HG00609.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.357+121_357+128del others(8): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9688190 | ||||||
| chr12:9688278 | A | C | 1 | a0002c0002t0001g0088 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.357+192A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688278 | |||||||
| chr12:9688330 | A | G | 89 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0003 others(86): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.357+244A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688330 | |||||||
| chr12:9688368 | G | A | 89 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0003 others(86): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.357+282G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688368 | |||||||
| chr12:9688525 | C | T | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+439C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688525 | |||||||
| chr12:9688561 | A | G | 1 | a0002c0002t0029g0075 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.357+475A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688561 | |||||||
| chr12:9688586 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.357+500G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688586 | |||||||
| chr12:9688661 | A | C | 1 | a0001c0001t0010g0121 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.357+575A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688661 | |||||||
| chr12:9688723 | TAATAA | T | 84 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(81): Show |
145 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.357+645_357+649del others(5): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9688723 | ||||||
| chr12:9688735 | A | G | 84 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(81): Show |
145 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.357+649A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688735 | |||||||
| chr12:9688768 | G | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+682G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688768 | |||||||
| chr12:9688924 | G | A | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.357+838G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9688924 | |||||||
| chr12:9689071 | G | A | 246 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(243): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.357+985G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689071 | |||||||
| chr12:9689136 | G | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+1050G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689136 | |||||||
| chr12:9689184 | A | G | 1 | a0003c0003t0007g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.357+1098A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689184 | |||||||
| chr12:9689273 | T | C | 9 | a0001c0001t0010g0029 a0001c0001t0010g0121 a0001c0001t0019g0123 others(6): Show |
10 | HG01168.hp2 HG01169.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.357+1187T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689273 | |||||||
| chr12:9689319 | T | A | 89 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0003 others(86): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.357+1233T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689319 | |||||||
| chr12:9689408 | A | G | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+1322A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689408 | |||||||
| chr12:9689409 | G | A | 1 | a0003c0004t0014g0132 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.357+1323G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689409 | |||||||
| chr12:9689412 | T | C | 24 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(21): Show |
31 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.357+1326T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689412 | |||||||
| chr12:9689438 | A | G | 1 | a0003c0004t0027g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.357+1352A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689438 | |||||||
| chr12:9689461 | G | T | 1 | a0002c0002t0001g0083 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.357+1375G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689461 | |||||||
| chr12:9689517 | C | T | 1 | a0001c0001t0002g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.357+1431C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689517 | |||||||
| chr12:9689639 | G | C | 3 | a0001c0001t0017g0023 a0003c0004t0027g0148 a0003c0004t0027g0149 |
5 | HG00733.hp2 HG00735.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.357+1553G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689639 | |||||||
| chr12:9689739 | A | C | 1 | a0001c0001t0033g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357+1653A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689739 | |||||||
| chr12:9689911 | G | A | 1 | a0003c0004t0009g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.357+1825G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9689911 | |||||||
| chr12:9690000 | A | G | 4 | a0001c0001t0019g0123 a0001c0001t0019g0124 a0001c0001t0019g0125 others(1): Show |
4 | HG01952.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+1914A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690000 | |||||||
| chr12:9690086 | CAG | C | 5 | a0001c0001t0010g0029 a0001c0001t0010g0121 a0003c0004t0010g0118 others(2): Show |
6 | HG01168.hp2 HG01169.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+2006_357+2007d others(4): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9690086 | ||||||
| chr12:9690150 | A | G | 4 | a0001c0001t0002g0010 a0001c0001t0002g0194 a0001c0001t0002g0208 others(1): Show |
7 | NA18951.hp2 NA18969.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+2064A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690150 | |||||||
| chr12:9690197 | G | C | 11 | a0001c0006t0007g0040 a0003c0003t0003g0020 a0003c0003t0003g0160 others(8): Show |
13 | HG01257.hp2 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.357+2111G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690197 | |||||||
| chr12:9690231 | A | G | 1 | a0001c0001t0033g0122 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.357+2145A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690231 | |||||||
| chr12:9690307 | T | A | 38 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(35): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.357+2221T>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690307 | |||||||
| chr12:9690425 | G | C | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.357+2339G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690425 | |||||||
| chr12:9690574 | T | C | 24 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0009 others(21): Show |
40 | HG00323.hp2 HG00438.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.358-2254T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690574 | |||||||
| chr12:9690635 | CAT | C | 10 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.358-2189_358-2188d others(4): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9690635 | ||||||
| chr12:9690657 | A | T | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.358-2171A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690657 | |||||||
| chr12:9690768 | G | T | 38 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(35): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.358-2060G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690768 | |||||||
| chr12:9690799 | C | A | 86 | a0001c0001t0001g0063 a0002c0002t0001g0002 a0002c0002t0001g0003 others(83): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.358-2029C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690799 | |||||||
| chr12:9690817 | A | T | 247 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(244): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.358-2011A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690817 | |||||||
| chr12:9690848 | C | T | 1 | a0002c0002t0018g0174 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.358-1980C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690848 | |||||||
| chr12:9690923 | A | C | 1 | a0001c0001t0002g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.358-1905A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9690923 | |||||||
| chr12:9691033 | T | C | 2 | a0001c0001t0022g0167 a0001c0001t0022g0168 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.358-1795T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691033 | |||||||
| chr12:9691037 | A | G | 2 | a0003c0003t0007g0156 a0003c0003t0007g0157 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.358-1791A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691037 | |||||||
| chr12:9691086 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.358-1742C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691086 | |||||||
| chr12:9691137 | A | G | 81 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0006 others(78): Show |
140 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.358-1691A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691137 | |||||||
| chr12:9691219 | A | ATC | 162 | a0001c0001t0001g0063 a0001c0001t0004g0007 a0001c0001t0004g0037 others(159): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.358-1608_358-1607i others(4): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9691219 | ||||||
| chr12:9691290 | G | T | 1 | a0001c0001t0032g0055 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.358-1538G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691290 | |||||||
| chr12:9691381 | T | C | 15 | a0002c0002t0001g0012 a0002c0002t0001g0041 a0002c0002t0001g0079 others(12): Show |
18 | HG00597.hp2 HG02015.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.358-1447T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691381 | |||||||
| chr12:9691442 | C | A | 1 | a0002c0002t0001g0074 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.358-1386C>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691442 | |||||||
| chr12:9691491 | T | TTAAAAA | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.358-1333_358-1332i others(8): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 9691491 | ||||||
| chr12:9691575 | G | A | 5 | a0001c0001t0002g0053 a0001c0001t0002g0169 a0001c0001t0002g0206 others(2): Show |
6 | HG00673.hp1 NA18940.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-1253G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691575 | |||||||
| chr12:9691642 | C | T | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.358-1186C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691642 | |||||||
| chr12:9691772 | A | G | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.358-1056A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691772 | |||||||
| chr12:9691817 | A | G | 1 | a0001c0001t0020g0030 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.358-1011A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691817 | |||||||
| chr12:9691930 | A | G | 2 | a0002c0002t0001g0064 a0002c0002t0001g0095 |
2 | HG00642.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.358-898A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691930 | |||||||
| chr12:9691959 | C | T | 38 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(35): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.358-869C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691959 | |||||||
| chr12:9691960 | G | A | 2 | a0001c0001t0022g0167 a0001c0001t0022g0168 |
2 | HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.358-868G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691960 | |||||||
| chr12:9691985 | A | G | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.358-843A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9691985 | |||||||
| chr12:9692099 | T | C | 252 | a0001c0001t0001g0063 a0001c0001t0002g0001 a0001c0001t0002g0004 others(249): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.358-729T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692099 | |||||||
| chr12:9692103 | T | C | 2 | a0001c0001t0014g0113 a0002c0002t0001g0082 |
2 | HG02015.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.358-725T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692103 | |||||||
| chr12:9692128 | G | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0169 a0001c0001t0002g0206 |
4 | HG00673.hp1 NA18940.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-700G>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692128 | |||||||
| chr12:9692136 | G | A | 1 | a0001c0001t0025g0050 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.358-692G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692136 | |||||||
| chr12:9692140 | G | A | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.358-688G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692140 | |||||||
| chr12:9692276 | C | T | 24 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(21): Show |
31 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.358-552C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692276 | |||||||
| chr12:9692326 | A | T | 38 | a0001c0006t0003g0045 a0001c0006t0003g0181 a0001c0006t0007g0040 others(35): Show |
46 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.358-502A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692326 | |||||||
| chr12:9692361 | A | G | 3 | a0001c0001t0017g0023 a0003c0004t0027g0148 a0003c0004t0027g0149 |
5 | HG00733.hp2 HG00735.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-467A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692361 | |||||||
| chr12:9692422 | T | C | 12 | a0001c0001t0004g0007 a0001c0001t0004g0037 a0001c0001t0004g0038 others(9): Show |
18 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.358-406T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692422 | |||||||
| chr12:9692629 | A | G | 12 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(9): Show |
13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.358-199A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692629 | |||||||
| chr12:9692739 | G | C | 3 | a0002c0002t0001g0066 a0002c0002t0001g0081 a0002c0002t0001g0084 |
3 | NA18946.hp2 NA18977.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.358-89G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692739 | |||||||
| chr12:9692776 | A | G | 1 | a0002c0002t0001g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.358-52A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692776 | |||||||
| chr12:9692788 | A | T | 9 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.358-40A>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 3/4 | chr12 | 9692788 | |||||||
| chr12:9693107 | C | G | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG01175.hp2 HG01192.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.461+176C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9693107 | |||||||
| chr12:9693483 | T | C | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.461+552T>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9693483 | |||||||
| chr12:9693586 | A | G | 1 | a0001c0001t0014g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.461+655A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9693586 | |||||||
| chr12:9693684 | T | G | 1 | a0001c0001t0004g0155 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.461+753T>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9693684 | |||||||
| chr12:9693731 | G | C | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.461+800G>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9693731 | |||||||
| chr12:9693829 | A | C | 3 | a0002c0002t0001g0016 a0002c0002t0001g0068 a0002c0002t0001g0098 |
5 | NA18956.hp2 NA18991.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.461+898A>C | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9693829 | |||||||
| chr12:9693925 | C | G | 152 | a0001c0001t0001g0063 a0001c0001t0002g0205 a0001c0001t0009g0114 others(149): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.462-835C>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9693925 | |||||||
| chr12:9693969 | C | CT | 13 | a0001c0001t0005g0032 a0001c0001t0005g0130 a0001c0001t0013g0031 others(10): Show |
17 | HG01257.hp2 HG01891.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.462-765dupT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 9693969 | ||||||
| chr12:9693969 | CT | C | 98 | a0001c0001t0001g0063 a0001c0001t0009g0114 a0001c0001t0014g0113 others(95): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.462-765delT | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 9693969 | ||||||
| chr12:9693969 | CTT | C | 18 | a0001c0001t0002g0004 a0001c0001t0002g0022 a0001c0001t0002g0051 others(15): Show |
27 | HG00099.hp1 HG00738.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.462-766_462-765del others(2): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 9693969 | ||||||
| chr12:9693969 | CTTT | C | 73 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0011 others(70): Show |
122 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.462-767_462-765del others(3): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 9693969 | ||||||
| chr12:9693969 | CTTTT | C | 7 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0208 others(4): Show |
14 | HG00099.hp2 HG00673.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.462-768_462-765del others(4): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 9693969 | ||||||
| chr12:9693969 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0020g0030 a0001c0001t0020g0126 |
3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.462-776_462-765del others(12): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 9693969 | ||||||
| chr12:9693969 | CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0001g0091 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.462-778_462-765del others(14): Show |
CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 9693969 | ||||||
| chr12:9694067 | G | A | 1 | a0003c0003t0003g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.462-693G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9694067 | |||||||
| chr12:9694130 | G | A | 2 | a0003c0003t0003g0018 a0003c0003t0003g0134 |
4 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.462-630G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9694130 | |||||||
| chr12:9694231 | G | A | 9 | a0001c0001t0010g0029 a0001c0001t0010g0121 a0001c0001t0019g0123 others(6): Show |
10 | HG01168.hp2 HG01169.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.462-529G>A | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9694231 | |||||||
| chr12:9694537 | C | T | 49 | a0001c0001t0009g0114 a0001c0001t0014g0113 a0001c0001t0014g0115 others(46): Show |
58 | HG00642.hp2 HG00738.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.462-223C>T | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9694537 | |||||||
| chr12:9694686 | A | G | 1 | a0003c0004t0010g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.462-74A>G | CLEC2D | ENSG00000069493.15 | transcript | ENST00000290855.11 | protein_coding | 4/4 | chr12 | 9694686 |