Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8807 |
| ensemblid | ENSG00000115607.10 |
| hgncid | 5989 |
| symbol | IL18RAP |
| name | interleukin 18 receptor accessory protein |
| refseq_nuc | NM_001393487.1 |
| refseq_prot | NP_001380416.1 |
| ensembl_nuc | ENST00000687160.1 |
| ensembl_prot | ENSP00000510345.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 102423160 |
| end | 102452565 |
| strand | + |
| ver | v1.2 |
| region | chr2:102423160-102452565 |
| region5000 | chr2:102418160-102457565 |
| regionname0 | IL18RAP_chr2_102423160_102452565 |
| regionname5000 | IL18RAP_chr2_102418160_102457565 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 599 | 403 | 92 | 65 | 185 | 15 | 44 | 156 | IL18RAP_chr2_102418160_102457565 | IL18RAP | MLCLG others(594): Show |
chr2 | 102418160 | 102457565 |
| a0002 | 0/0 | 599 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | MLCLG others(594): Show |
chr2 | 102418160 | 102457565 |
| a0003 | 0/0 | 599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | MLCLG others(594): Show |
chr2 | 102418160 | 102457565 |
| a0004 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | MLCLG others(594): Show |
chr2 | 102418160 | 102457565 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1797 | 384 | 76 | 65 | 183 | 14 | 44 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 | ||
| a0001c0002 | 0/0 | 1797 | 15 | 15 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 | ||
| a0001c0003 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 | ||
| a0001c0004 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 | ||
| a0001c0005 | 0/0 | 1797 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 | ||
| a0001c0008 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 | ||
| a0002c0009 | 0/0 | 1797 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 | ||
| a0003c0006 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 | ||
| a0004c0007 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | ATGCT others(1792): Show |
chr2 | 102418160 | 102457565 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2302 | 252 | 69 | 35 | 115 | 7 | 26 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0001c0001t0002 | 1/1 | 2302 | 118 | 2 | 25 | 68 | 3 | 18 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0001c0001t0003 | 0/0 | 2302 | 14 | 5 | 5 | 0 | 4 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0001c0002t0001 | 0/0 | 2302 | 15 | 15 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0001c0003t0001 | 0/0 | 2302 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0001c0004t0002 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0001c0005t0004 | 0/0 | 2302 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0001c0008t0001 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0002c0009t0001 | 0/0 | 2302 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0003c0006t0001 | 0/0 | 2302 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| a0004c0007t0001 | 0/0 | 2302 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | CCATT others(2297): Show |
chr2 | 102418160 | 102457565 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 39 | 3 | 6 | 28 | 1 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0003 | 0/0 | 18 | 1 | 0 | 17 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0005 | 0/0 | 16 | 12 | 0 | 4 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0006 | 0/0 | 12 | 4 | 3 | 0 | 2 | 3 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0002 | 0/0 | 38 | 0 | 1 | 29 | 0 | 8 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0004 | 0/0 | 16 | 0 | 1 | 14 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0007 | 0/0 | 8 | 0 | 7 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0003g0009 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0004t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0005t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0001c0008t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0002c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0003c0006t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| a0004c0007t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00140 | hp1 | a0002 | c0009 | t0001 | g0001 | EUR | GBR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | GBR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0148 | EUR | FIN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0126 | EUR | FIN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01361 | hp2 | a0003 | c0006 | t0001 | g0025 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0127 | EUR | IBS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02080 | hp2 | a0004 | c0007 | t0001 | g0003 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | STU | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | YRI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18944 | hp1 | a0001 | c0008 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19062 | hp2 | a0001 | c0004 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | YRI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ASW | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0129 | EUR | TSI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA20805 | hp1 | a0001 | c0005 | t0004 | g0023 | EUR | TSI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | TSI | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | MSL | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | USA | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | USA | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0152 | REF | REF | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0158 | REF | REF | IL18RAP_chr2_102418160_102457565 | IL18RAP | chr2 | 102418160 | 102457565 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102424242 | A | G | 1 | a0002 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.407A>G | p.Asp136Gly | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/10 | 525/2302 | 407/1800 | 136/599 | chr2 | 102424242 | |||
| chr2:102445316 | G | A | 1 | a0003 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1048G>A | p.Val350Ile | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/10 | 1166/2302 | 1048/1800 | 350/599 | chr2 | 102445316 | |||
| chr2:102450917 | C | A | 1 | a0004 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1280C>A | p.Ser427Tyr | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/10 | 1398/2302 | 1280/1800 | 427/599 | chr2 | 102450917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102423283 | C | T | 1 | a0001c0002 | 15 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
synonymous_variant | LOW | c.6C>T | p.Leu2Leu | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/10 | 124/2302 | 6/1800 | 2/599 | chr2 | 102423283 | |||
| chr2:102424399 | G | A | 1 | a0001c0003 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.564G>A | p.Ala188Ala | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/10 | 682/2302 | 564/1800 | 188/599 | chr2 | 102424399 | |||
| chr2:102443204 | G | A | 1 | a0001c0004 | 1 | NA19062.hp2 | synonymous_variant | LOW | c.801G>A | p.Lys267Lys | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/10 | 919/2302 | 801/1800 | 267/599 | chr2 | 102443204 | |||
| chr2:102443229 | C | A | 1 | a0001c0005 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.826C>A | p.Arg276Arg | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/10 | 944/2302 | 826/1800 | 276/599 | chr2 | 102443229 | |||
| chr2:102450945 | C | T | 1 | a0001c0008 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.1308C>T | p.Ser436Ser | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/10 | 1426/2302 | 1308/1800 | 436/599 | chr2 | 102450945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102423226 | C | A | 1 | a0001c0001t0003 | 14 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-52C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/10 | 52 | chr2 | 102423226 | ||||||
| chr2:102452258 | G | A | 1 | a0001c0005t0004 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*77G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 10/10 | 77 | chr2 | 102452258 | ||||||
| chr2:102452327 | G | A | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0001 others(6): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*146G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 10/10 | 146 | chr2 | 102452327 | ||||||
| chr2:102452374 | T | A | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0001 others(6): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*193T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 10/10 | 193 | chr2 | 102452374 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102423403 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0052 |
7 | NA18961.hp2 NA18964.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+56G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423403 | |||||||
| chr2:102423413 | C | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.70+66C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423413 | |||||||
| chr2:102423469 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.70+122G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423469 | |||||||
| chr2:102423470 | G | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.70+123G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423470 | |||||||
| chr2:102423514 | A | T | 1 | a0001c0001t0001g0024 | 3 | HG01167.hp2 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.70+167A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423514 | |||||||
| chr2:102423587 | A | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(82): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.71-224A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423587 | |||||||
| chr2:102423699 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
10 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-112A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423699 | |||||||
| chr2:102423707 | C | A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0032 others(8): Show |
18 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.71-104C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423707 | |||||||
| chr2:102423717 | A | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(82): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.71-94A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423717 | |||||||
| chr2:102423721 | C | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18989.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.71-90C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423721 | |||||||
| chr2:102423722 | T | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.71-89T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423722 | |||||||
| chr2:102423787 | T | TG | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.71-23dupG | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 102423787 | ||||||
| chr2:102423789 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.71-22C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 1/9 | chr2 | 102423789 | |||||||
| chr2:102424157 | A | G | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 |
3 | NA18991.hp1 NA18993.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.395+22A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 2/9 | chr2 | 102424157 | |||||||
| chr2:102424468 | CTTCATGG others(4): Show |
C | 1 | a0001c0001t0001g0053 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.579+62_579+72delGC others(9): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102424468 | ||||||
| chr2:102424485 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(61): Show |
134 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.579+71G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102424485 | |||||||
| chr2:102424493 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.579+79G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102424493 | |||||||
| chr2:102424535 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.579+121C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102424535 | |||||||
| chr2:102424707 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(70): Show |
143 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.579+293T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102424707 | |||||||
| chr2:102424794 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.579+380A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102424794 | |||||||
| chr2:102424818 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.579+404C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102424818 | |||||||
| chr2:102424925 | A | G | 1 | a0001c0001t0002g0142 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.579+511A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102424925 | |||||||
| chr2:102424983 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.579+569A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102424983 | |||||||
| chr2:102425081 | C | G | 1 | a0001c0001t0002g0170 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.579+667C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102425081 | |||||||
| chr2:102425096 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.579+682C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102425096 | |||||||
| chr2:102425304 | T | C | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01261.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+890T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102425304 | |||||||
| chr2:102425315 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.579+901C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102425315 | |||||||
| chr2:102425519 | T | TCAATAAA others(280): Show |
1 | a0001c0001t0001g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579+1109_579+1395d others(289): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102425519 | ||||||
| chr2:102425941 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.579+1527A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102425941 | |||||||
| chr2:102426146 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.579+1732T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426146 | |||||||
| chr2:102426252 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.579+1838G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426252 | |||||||
| chr2:102426298 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.579+1884A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426298 | |||||||
| chr2:102426316 | C | T | 1 | a0001c0001t0002g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.579+1902C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426316 | |||||||
| chr2:102426361 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.579+1947C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426361 | |||||||
| chr2:102426431 | A | AT | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.579+2024dupT | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102426431 | ||||||
| chr2:102426505 | A | C | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.579+2091A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426505 | |||||||
| chr2:102426565 | T | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0001t0001g0143 others(9): Show |
18 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+2151T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426565 | |||||||
| chr2:102426640 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.579+2226C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426640 | |||||||
| chr2:102426850 | TA | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.579+2438delA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102426850 | ||||||
| chr2:102426860 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.579+2446C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102426860 | |||||||
| chr2:102427244 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.579+2830T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427244 | |||||||
| chr2:102427279 | T | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(54): Show |
120 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.579+2865T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427279 | |||||||
| chr2:102427333 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.579+2919G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427333 | |||||||
| chr2:102427379 | C | A | 1 | a0001c0001t0001g0047 | 2 | HG00558.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.579+2965C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427379 | |||||||
| chr2:102427407 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.579+2993G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427407 | |||||||
| chr2:102427521 | G | A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0035 others(17): Show |
31 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.579+3107G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427521 | |||||||
| chr2:102427715 | T | G | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.579+3301T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427715 | |||||||
| chr2:102427750 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.579+3336T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427750 | |||||||
| chr2:102427959 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.579+3545C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427959 | |||||||
| chr2:102427980 | CT | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(98): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.579+3581delT | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102427980 | ||||||
| chr2:102427984 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.579+3570T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102427984 | |||||||
| chr2:102428127 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.579+3713G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428127 | |||||||
| chr2:102428243 | G | A | 2 | a0001c0001t0001g0103 a0001c0002t0001g0113 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.579+3829G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428243 | |||||||
| chr2:102428379 | G | GT | 26 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0035 others(23): Show |
43 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.579+3978dupT | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102428379 | ||||||
| chr2:102428379 | G | GTT | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(44): Show |
96 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.579+3977_579+3978d others(4): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102428379 | ||||||
| chr2:102428379 | GT | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0025 others(62): Show |
127 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.579+3978delT | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102428379 | ||||||
| chr2:102428443 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.579+4029A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428443 | |||||||
| chr2:102428560 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.579+4146A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428560 | |||||||
| chr2:102428632 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.579+4218A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428632 | |||||||
| chr2:102428660 | C | T | 1 | a0001c0002t0001g0040 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.579+4246C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428660 | |||||||
| chr2:102428685 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0086 |
3 | HG02630.hp1 HG03130.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.579+4271A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428685 | |||||||
| chr2:102428721 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.579+4307G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428721 | |||||||
| chr2:102428733 | A | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(82): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.579+4319A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102428733 | |||||||
| chr2:102429032 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.579+4618G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102429032 | |||||||
| chr2:102429427 | C | G | 11 | a0001c0001t0001g0143 a0001c0002t0001g0016 a0001c0002t0001g0034 others(8): Show |
16 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+5013C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102429427 | |||||||
| chr2:102429441 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0110 a0001c0001t0001g0119 |
4 | HG02280.hp1 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+5027T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102429441 | |||||||
| chr2:102429631 | CT | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.579+5222delT | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102429631 | ||||||
| chr2:102429744 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0131 |
5 | HG00323.hp1 HG00735.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+5330C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102429744 | |||||||
| chr2:102429754 | T | G | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.579+5340T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102429754 | |||||||
| chr2:102429830 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.579+5416T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102429830 | |||||||
| chr2:102430092 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.579+5678G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430092 | |||||||
| chr2:102430365 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0191 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.579+5951A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430365 | |||||||
| chr2:102430420 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.579+6006G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430420 | |||||||
| chr2:102430492 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.579+6078A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430492 | |||||||
| chr2:102430538 | T | C | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01261.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+6124T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430538 | |||||||
| chr2:102430574 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.579+6160G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430574 | |||||||
| chr2:102430595 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.579+6181A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430595 | |||||||
| chr2:102430714 | C | T | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01261.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+6300C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430714 | |||||||
| chr2:102430791 | A | T | 1 | a0001c0001t0002g0140 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.579+6377A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102430791 | |||||||
| chr2:102431072 | T | C | 5 | a0001c0001t0003g0009 a0001c0001t0003g0126 a0001c0001t0003g0127 others(2): Show |
9 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-6140T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431072 | |||||||
| chr2:102431146 | T | C | 1 | a0001c0001t0001g0017 | 3 | HG02486.hp1 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.580-6066T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431146 | |||||||
| chr2:102431339 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.580-5873T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431339 | |||||||
| chr2:102431342 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(62): Show |
128 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.580-5870C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431342 | |||||||
| chr2:102431526 | C | T | 1 | a0001c0001t0002g0021 | 3 | HG00639.hp2 HG01192.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.580-5686C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431526 | |||||||
| chr2:102431583 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.580-5629C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431583 | |||||||
| chr2:102431643 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.580-5569C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431643 | |||||||
| chr2:102431648 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(19): Show |
43 | HG00423.hp2 HG00673.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.580-5564C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431648 | |||||||
| chr2:102431697 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(56): Show |
122 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.580-5515G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431697 | |||||||
| chr2:102431747 | C | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.580-5465C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431747 | |||||||
| chr2:102431782 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.580-5430T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431782 | |||||||
| chr2:102431792 | CTAT | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.580-5414_580-5412d others(5): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102431792 | ||||||
| chr2:102431957 | C | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.580-5255C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431957 | |||||||
| chr2:102431971 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.580-5241A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431971 | |||||||
| chr2:102431977 | A | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.580-5235A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102431977 | |||||||
| chr2:102432007 | T | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.580-5205T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432007 | |||||||
| chr2:102432120 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.580-5092G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432120 | |||||||
| chr2:102432197 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.580-5015C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432197 | |||||||
| chr2:102432275 | G | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0018 a0001c0001t0003g0112 others(4): Show |
13 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-4937G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432275 | |||||||
| chr2:102432278 | G | A | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(36): Show |
63 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.580-4934G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432278 | |||||||
| chr2:102432320 | C | T | 5 | a0001c0001t0003g0009 a0001c0001t0003g0126 a0001c0001t0003g0127 others(2): Show |
9 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-4892C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432320 | |||||||
| chr2:102432377 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.580-4835C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432377 | |||||||
| chr2:102432466 | T | C | 1 | a0001c0001t0001g0048 | 2 | NA18952.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.580-4746T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432466 | |||||||
| chr2:102432577 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.580-4635A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432577 | |||||||
| chr2:102432610 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.580-4602G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432610 | |||||||
| chr2:102432614 | A | G | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.580-4598A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432614 | |||||||
| chr2:102432833 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.580-4379G>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432833 | |||||||
| chr2:102432958 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.580-4254C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102432958 | |||||||
| chr2:102433055 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.580-4157C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433055 | |||||||
| chr2:102433069 | T | C | 1 | a0001c0002t0001g0039 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.580-4143T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433069 | |||||||
| chr2:102433077 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.580-4135T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433077 | |||||||
| chr2:102433405 | G | A | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.580-3807G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433405 | |||||||
| chr2:102433416 | G | A | 1 | a0001c0003t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.580-3796G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433416 | |||||||
| chr2:102433450 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.580-3762A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433450 | |||||||
| chr2:102433597 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.580-3615G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433597 | |||||||
| chr2:102433628 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0108 others(1): Show |
6 | HG01123.hp2 HG01175.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-3584C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433628 | |||||||
| chr2:102433767 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.580-3445A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433767 | |||||||
| chr2:102433890 | T | A | 1 | a0001c0001t0001g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.580-3322T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433890 | |||||||
| chr2:102433930 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.580-3282C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433930 | |||||||
| chr2:102433998 | T | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.580-3214T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102433998 | |||||||
| chr2:102434008 | T | G | 1 | a0001c0001t0002g0149 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.580-3204T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434008 | |||||||
| chr2:102434051 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.580-3161C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434051 | |||||||
| chr2:102434109 | T | C | 3 | a0001c0001t0002g0144 a0001c0001t0002g0150 a0001c0001t0002g0151 |
3 | HG01256.hp2 HG01258.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.580-3103T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434109 | |||||||
| chr2:102434313 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.580-2899A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434313 | |||||||
| chr2:102434337 | C | G | 1 | a0001c0001t0003g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.580-2875C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434337 | |||||||
| chr2:102434395 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.580-2817T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434395 | |||||||
| chr2:102434402 | A | AATG | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(62): Show |
128 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.580-2808_580-2807i others(5): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102434402 | ||||||
| chr2:102434441 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.580-2771G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434441 | |||||||
| chr2:102434465 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.580-2747A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434465 | |||||||
| chr2:102434556 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.580-2656G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434556 | |||||||
| chr2:102434684 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(53): Show |
119 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.580-2528A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434684 | |||||||
| chr2:102434811 | G | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01261.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-2401G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434811 | |||||||
| chr2:102434949 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.580-2263G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102434949 | |||||||
| chr2:102435014 | TA | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(103): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.580-2188delA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102435014 | ||||||
| chr2:102435055 | T | C | 1 | a0001c0003t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.580-2157T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435055 | |||||||
| chr2:102435098 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(62): Show |
128 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.580-2114T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435098 | |||||||
| chr2:102435099 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.580-2113A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435099 | |||||||
| chr2:102435132 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-2080C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435132 | |||||||
| chr2:102435246 | A | T | 10 | a0001c0001t0001g0143 a0001c0002t0001g0016 a0001c0002t0001g0034 others(7): Show |
14 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.580-1966A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435246 | |||||||
| chr2:102435321 | G | A | 1 | a0001c0001t0002g0019 | 3 | HG00140.hp2 HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.580-1891G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435321 | |||||||
| chr2:102435414 | T | C | 1 | a0001c0002t0001g0040 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.580-1798T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435414 | |||||||
| chr2:102435506 | G | C | 1 | a0001c0001t0001g0024 | 3 | HG01167.hp2 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.580-1706G>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435506 | |||||||
| chr2:102435578 | G | C | 11 | a0001c0001t0001g0143 a0001c0002t0001g0016 a0001c0002t0001g0034 others(8): Show |
16 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-1634G>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435578 | |||||||
| chr2:102435594 | G | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0083 |
2 | HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.580-1618G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435594 | |||||||
| chr2:102435746 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.580-1466C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435746 | |||||||
| chr2:102435833 | C | G | 1 | a0001c0001t0002g0166 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.580-1379C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102435833 | |||||||
| chr2:102435843 | AT | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(99): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.580-1353delT | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102435843 | ||||||
| chr2:102435843 | ATT | A | 11 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(8): Show |
11 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-1354_580-1353d others(4): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102435843 | ||||||
| chr2:102436218 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-994G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436218 | |||||||
| chr2:102436247 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.580-965G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436247 | |||||||
| chr2:102436256 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.580-956C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436256 | |||||||
| chr2:102436324 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.580-888A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436324 | |||||||
| chr2:102436345 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.580-867T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436345 | |||||||
| chr2:102436356 | C | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.580-856C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436356 | |||||||
| chr2:102436535 | G | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.580-677G>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436535 | |||||||
| chr2:102436617 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.580-595C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436617 | |||||||
| chr2:102436681 | GA | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.580-523delA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102436681 | ||||||
| chr2:102436698 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.580-514C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436698 | |||||||
| chr2:102436756 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.580-456C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436756 | |||||||
| chr2:102436805 | A | ATG | 62 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(59): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.580-393_580-392dup others(2): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102436805 | ||||||
| chr2:102436819 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.580-393G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436819 | |||||||
| chr2:102436819 | G | GTA | 2 | a0001c0002t0001g0039 a0001c0003t0001g0098 |
3 | HG01884.hp1 HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.580-381_580-380dup others(2): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102436819 | ||||||
| chr2:102436819 | G | GTGTA | 11 | a0001c0001t0001g0143 a0001c0001t0001g0188 a0001c0001t0001g0191 others(8): Show |
14 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.580-392_580-391ins others(4): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102436819 | ||||||
| chr2:102436833 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.580-379G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436833 | |||||||
| chr2:102436837 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(61): Show |
127 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.580-375G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436837 | |||||||
| chr2:102436839 | A | ATATATAT others(1): Show |
4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-371_580-370ins others(8): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102436839 | ||||||
| chr2:102436839 | A | ATATGTAT others(1): Show |
4 | a0001c0001t0001g0059 a0001c0001t0001g0083 a0001c0001t0001g0100 others(1): Show |
4 | HG00408.hp2 HG02132.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-371_580-370ins others(8): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102436839 | ||||||
| chr2:102436839 | A | ATG | 10 | a0001c0001t0001g0143 a0001c0002t0001g0016 a0001c0002t0001g0034 others(7): Show |
13 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-372_580-371ins others(2): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102436839 | ||||||
| chr2:102436839 | A | ATGTATG | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(52): Show |
118 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.580-372_580-371ins others(6): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 102436839 | ||||||
| chr2:102436842 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.580-370C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436842 | |||||||
| chr2:102436925 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.580-287T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102436925 | |||||||
| chr2:102437064 | A | T | 1 | a0001c0001t0001g0038 | 2 | HG03710.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.580-148A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102437064 | |||||||
| chr2:102437175 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.580-37T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 3/9 | chr2 | 102437175 | |||||||
| chr2:102437614 | A | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.730+252A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102437614 | |||||||
| chr2:102437672 | C | T | 2 | a0001c0002t0001g0039 a0001c0002t0001g0040 |
4 | HG02258.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+310C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102437672 | |||||||
| chr2:102437960 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(35): Show |
84 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.730+598T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102437960 | |||||||
| chr2:102437989 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.730+627G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102437989 | |||||||
| chr2:102438096 | G | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.730+734G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438096 | |||||||
| chr2:102438117 | T | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0036 others(11): Show |
24 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.730+755T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438117 | |||||||
| chr2:102438307 | G | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.730+945G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438307 | |||||||
| chr2:102438343 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.730+981T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438343 | |||||||
| chr2:102438513 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18968.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.730+1151A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438513 | |||||||
| chr2:102438589 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.730+1227C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438589 | |||||||
| chr2:102438649 | C | G | 1 | a0001c0001t0002g0164 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.730+1287C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438649 | |||||||
| chr2:102438788 | A | C | 1 | a0001c0001t0003g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.730+1426A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438788 | |||||||
| chr2:102438789 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.730+1427A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438789 | |||||||
| chr2:102438807 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.730+1445C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438807 | |||||||
| chr2:102438851 | A | G | 1 | a0001c0001t0003g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.730+1489A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438851 | |||||||
| chr2:102438872 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.730+1510T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438872 | |||||||
| chr2:102438874 | C | A | 3 | a0001c0001t0003g0130 a0001c0002t0001g0039 a0001c0002t0001g0040 |
5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+1512C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438874 | |||||||
| chr2:102438960 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.730+1598G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102438960 | |||||||
| chr2:102439018 | A | G | 9 | a0001c0001t0001g0143 a0001c0002t0001g0016 a0001c0002t0001g0034 others(6): Show |
12 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.730+1656A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439018 | |||||||
| chr2:102439048 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.730+1686A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439048 | |||||||
| chr2:102439150 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
6 | HG02451.hp2 HG02559.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+1788G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439150 | |||||||
| chr2:102439174 | G | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0186 a0001c0001t0001g0192 others(1): Show |
5 | HG00738.hp1 HG01175.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.730+1812G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439174 | |||||||
| chr2:102439184 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.730+1822G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439184 | |||||||
| chr2:102439201 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.730+1839C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439201 | |||||||
| chr2:102439351 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.731-1961G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439351 | |||||||
| chr2:102439401 | G | A | 9 | a0001c0001t0001g0143 a0001c0002t0001g0016 a0001c0002t0001g0034 others(6): Show |
12 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.731-1911G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439401 | |||||||
| chr2:102439544 | C | T | 3 | a0001c0001t0003g0130 a0001c0002t0001g0039 a0001c0002t0001g0040 |
5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1768C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439544 | |||||||
| chr2:102439636 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.731-1676A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439636 | |||||||
| chr2:102439667 | A | T | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(36): Show |
63 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.731-1645A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439667 | |||||||
| chr2:102439780 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.731-1532A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439780 | |||||||
| chr2:102439846 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.731-1466G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102439846 | |||||||
| chr2:102440033 | A | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(71): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.731-1279A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440033 | |||||||
| chr2:102440056 | A | G | 1 | a0001c0001t0003g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.731-1256A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440056 | |||||||
| chr2:102440074 | A | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(53): Show |
119 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.731-1238A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440074 | |||||||
| chr2:102440313 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.731-999C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440313 | |||||||
| chr2:102440429 | A | G | 1 | a0001c0002t0001g0016 | 3 | HG01891.hp2 HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.731-883A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440429 | |||||||
| chr2:102440436 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.731-876G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440436 | |||||||
| chr2:102440555 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.731-757G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440555 | |||||||
| chr2:102440583 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0035 others(24): Show |
44 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.731-729G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440583 | |||||||
| chr2:102440586 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.731-726T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440586 | |||||||
| chr2:102440596 | T | C | 3 | a0001c0001t0003g0130 a0001c0002t0001g0039 a0001c0002t0001g0040 |
5 | HG02145.hp2 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-716T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440596 | |||||||
| chr2:102440627 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.731-685C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440627 | |||||||
| chr2:102440641 | GGA | G | 9 | a0001c0001t0001g0143 a0001c0002t0001g0016 a0001c0002t0001g0034 others(6): Show |
12 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.731-662_731-661del others(2): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 102440641 | ||||||
| chr2:102440699 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.731-613C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440699 | |||||||
| chr2:102440791 | G | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.731-521G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440791 | |||||||
| chr2:102440903 | T | C | 7 | a0001c0001t0003g0009 a0001c0001t0003g0018 a0001c0001t0003g0112 others(4): Show |
13 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.731-409T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440903 | |||||||
| chr2:102440994 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.731-318G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102440994 | |||||||
| chr2:102441041 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.731-271G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102441041 | |||||||
| chr2:102441075 | G | T | 1 | a0001c0001t0002g0138 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.731-237G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102441075 | |||||||
| chr2:102441208 | G | A | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(36): Show |
63 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.731-104G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102441208 | |||||||
| chr2:102441239 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.731-73T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102441239 | |||||||
| chr2:102441246 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.731-66A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102441246 | |||||||
| chr2:102441257 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0186 a0001c0001t0001g0192 others(1): Show |
5 | HG00738.hp1 HG01175.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-55A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102441257 | |||||||
| chr2:102441287 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.731-25A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 4/9 | chr2 | 102441287 | |||||||
| chr2:102441432 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0175 others(5): Show |
20 | HG00099.hp1 HG00741.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.796+55A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102441432 | |||||||
| chr2:102441482 | G | T | 1 | a0001c0001t0003g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.796+105G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102441482 | |||||||
| chr2:102441744 | C | T | 1 | a0001c0001t0002g0163 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.796+367C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102441744 | |||||||
| chr2:102441748 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(71): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.796+371C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102441748 | |||||||
| chr2:102441836 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.796+459C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102441836 | |||||||
| chr2:102441868 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.796+491G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102441868 | |||||||
| chr2:102441888 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0121 others(3): Show |
9 | HG02451.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.796+511A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102441888 | |||||||
| chr2:102441891 | GA | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(75): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.796+525delA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 102441891 | ||||||
| chr2:102442005 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.796+628C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442005 | |||||||
| chr2:102442019 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.796+642A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442019 | |||||||
| chr2:102442201 | C | A | 1 | a0001c0001t0001g0022 | 3 | HG02717.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.796+824C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442201 | |||||||
| chr2:102442307 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.797-893T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442307 | |||||||
| chr2:102442343 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.797-857C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442343 | |||||||
| chr2:102442350 | T | G | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.797-850T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442350 | |||||||
| chr2:102442453 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.797-747G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442453 | |||||||
| chr2:102442517 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.797-683T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442517 | |||||||
| chr2:102442562 | G | A | 2 | a0001c0001t0001g0025 a0003c0006t0001g0025 |
2 | HG01361.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.797-638G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442562 | |||||||
| chr2:102442745 | A | AT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.797-448dupT | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 102442745 | ||||||
| chr2:102442769 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.797-431A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442769 | |||||||
| chr2:102442770 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.797-430C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442770 | |||||||
| chr2:102442771 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.797-429A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442771 | |||||||
| chr2:102442777 | T | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.797-423T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442777 | |||||||
| chr2:102442865 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.797-335G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442865 | |||||||
| chr2:102442991 | A | T | 1 | a0001c0002t0001g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.797-209A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 5/9 | chr2 | 102442991 | |||||||
| chr2:102443349 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.920+26T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443349 | |||||||
| chr2:102443474 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18989.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.920+151G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443474 | |||||||
| chr2:102443492 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.920+169G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443492 | |||||||
| chr2:102443527 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.920+204C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443527 | |||||||
| chr2:102443564 | T | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.920+241T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443564 | |||||||
| chr2:102443571 | G | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
13 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.920+248G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443571 | |||||||
| chr2:102443579 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.920+256C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443579 | |||||||
| chr2:102443632 | T | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0032 others(8): Show |
18 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.920+309T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443632 | |||||||
| chr2:102443728 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.920+405G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443728 | |||||||
| chr2:102443733 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.920+410G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443733 | |||||||
| chr2:102443739 | A | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.920+416A>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443739 | |||||||
| chr2:102443840 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(70): Show |
139 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.920+517T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443840 | |||||||
| chr2:102443841 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.920+518G>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443841 | |||||||
| chr2:102443853 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.920+530A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102443853 | |||||||
| chr2:102444058 | A | G | 1 | a0001c0001t0003g0130 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.920+735A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444058 | |||||||
| chr2:102444298 | G | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0112 |
4 | HG02572.hp2 HG02922.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-891G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444298 | |||||||
| chr2:102444310 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.921-879A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444310 | |||||||
| chr2:102444358 | C | G | 2 | a0001c0002t0001g0039 a0001c0002t0001g0040 |
4 | HG02258.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-831C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444358 | |||||||
| chr2:102444388 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.921-801G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444388 | |||||||
| chr2:102444391 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(54): Show |
120 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.921-798G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444391 | |||||||
| chr2:102444404 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.921-785C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444404 | |||||||
| chr2:102444602 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18968.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.921-587T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444602 | |||||||
| chr2:102444687 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.921-502G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444687 | |||||||
| chr2:102444725 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.921-464C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444725 | |||||||
| chr2:102444781 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.921-408T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444781 | |||||||
| chr2:102444826 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(65): Show |
134 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.921-363G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102444826 | |||||||
| chr2:102445051 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.921-138A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 6/9 | chr2 | 102445051 | |||||||
| chr2:102445491 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1072+151A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102445491 | |||||||
| chr2:102445656 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1072+316A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102445656 | |||||||
| chr2:102445715 | A | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(36): Show |
63 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.1072+375A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102445715 | |||||||
| chr2:102445820 | TA | T | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1072+492delA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 102445820 | ||||||
| chr2:102445822 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1072+482A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102445822 | |||||||
| chr2:102445946 | C | T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0035 others(24): Show |
44 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1072+606C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102445946 | |||||||
| chr2:102446294 | T | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(71): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1073-776T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446294 | |||||||
| chr2:102446354 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1073-716C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446354 | |||||||
| chr2:102446420 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1073-650C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446420 | |||||||
| chr2:102446466 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1073-604C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446466 | |||||||
| chr2:102446477 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1073-593T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446477 | |||||||
| chr2:102446503 | C | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG01261.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1073-567C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446503 | |||||||
| chr2:102446534 | T | G | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | NA18956.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1073-536T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446534 | |||||||
| chr2:102446597 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1073-473C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446597 | |||||||
| chr2:102446753 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1073-317C>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446753 | |||||||
| chr2:102446780 | T | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(74): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1073-290T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446780 | |||||||
| chr2:102446795 | C | CA | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(75): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1073-258dupA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 102446795 | ||||||
| chr2:102446795 | CA | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG01256.hp2 HG02622.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1073-258delA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 102446795 | ||||||
| chr2:102446853 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1073-217C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446853 | |||||||
| chr2:102446856 | A | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
4 | HG03710.hp1 NA18942.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073-214A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446856 | |||||||
| chr2:102446909 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1073-161G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446909 | |||||||
| chr2:102446965 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1073-105A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446965 | |||||||
| chr2:102446972 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1073-98T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102446972 | |||||||
| chr2:102447014 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1073-56G>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102447014 | |||||||
| chr2:102447029 | C | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0018 a0001c0001t0003g0112 others(4): Show |
13 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1073-41C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102447029 | |||||||
| chr2:102447060 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0050 a0001c0001t0001g0175 others(5): Show |
20 | HG00099.hp1 HG00741.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1073-10G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 7/9 | chr2 | 102447060 | |||||||
| chr2:102447395 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0106 |
5 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210+188C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447395 | |||||||
| chr2:102447427 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0147 |
4 | NA18999.hp2 NA19003.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210+220C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447427 | |||||||
| chr2:102447458 | G | A | 1 | a0001c0002t0001g0039 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1210+251G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447458 | |||||||
| chr2:102447555 | T | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0193 |
3 | HG00741.hp2 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1210+348T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447555 | |||||||
| chr2:102447614 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1210+407A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447614 | |||||||
| chr2:102447652 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1210+445G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447652 | |||||||
| chr2:102447706 | T | TTATG | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(30): Show |
77 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1210+519_1210+522d others(6): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102447706 | ||||||
| chr2:102447706 | T | TTATGTAT others(1): Show |
12 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0032 others(9): Show |
19 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.1210+515_1210+522d others(10): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102447706 | ||||||
| chr2:102447722 | G | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1210+515G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447722 | |||||||
| chr2:102447726 | G | GTATGTAT others(1): Show |
29 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0035 others(26): Show |
47 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1210+522_1210+523i others(10): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102447726 | ||||||
| chr2:102447726 | G | T | 16 | a0001c0001t0001g0058 a0001c0001t0001g0084 a0001c0001t0001g0092 others(13): Show |
16 | HG00423.hp2 HG01261.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1210+519G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447726 | |||||||
| chr2:102447730 | T | G | 1 | a0001c0001t0002g0044 | 2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1210+523T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447730 | |||||||
| chr2:102447785 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1210+578C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447785 | |||||||
| chr2:102447804 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1210+597T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447804 | |||||||
| chr2:102447880 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1210+673G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102447880 | |||||||
| chr2:102448043 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
219 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1210+836A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448043 | |||||||
| chr2:102448051 | T | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
219 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1210+844T>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448051 | |||||||
| chr2:102448052 | G | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
219 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1210+845G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448052 | |||||||
| chr2:102448293 | A | T | 1 | a0001c0001t0003g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1210+1086A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448293 | |||||||
| chr2:102448419 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1210+1212G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448419 | |||||||
| chr2:102448464 | A | G | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(39): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1210+1257A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448464 | |||||||
| chr2:102448522 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1210+1315T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448522 | |||||||
| chr2:102448602 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1210+1395G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448602 | |||||||
| chr2:102448645 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1210+1438G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448645 | |||||||
| chr2:102448669 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1210+1462G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448669 | |||||||
| chr2:102448907 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(66): Show |
135 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1210+1700G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448907 | |||||||
| chr2:102448952 | C | A | 1 | a0001c0001t0002g0157 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1210+1745C>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448952 | |||||||
| chr2:102448960 | C | CA | 19 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0064 others(16): Show |
39 | HG00408.hp1 HG00423.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1210+1777dupA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102448960 | ||||||
| chr2:102448960 | CA | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(49): Show |
98 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1210+1777delA | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102448960 | ||||||
| chr2:102448960 | CAA | C | 42 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(39): Show |
68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1210+1776_1210+177 others(6): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102448960 | ||||||
| chr2:102448990 | C | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0018 a0001c0001t0003g0112 others(4): Show |
13 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1210+1783C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102448990 | |||||||
| chr2:102449007 | A | G | 3 | a0001c0001t0002g0144 a0001c0001t0002g0150 a0001c0001t0002g0151 |
3 | HG01256.hp2 HG01258.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1210+1800A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449007 | |||||||
| chr2:102449043 | C | T | 1 | a0001c0002t0001g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1211-1805C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449043 | |||||||
| chr2:102449062 | A | AG | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1211-1786_1211-178 others(5): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449062 | |||||||
| chr2:102449087 | G | A | 47 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(44): Show |
73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1211-1761G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449087 | |||||||
| chr2:102449122 | G | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0018 a0001c0001t0003g0112 others(4): Show |
13 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1211-1726G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449122 | |||||||
| chr2:102449126 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1211-1722G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449126 | |||||||
| chr2:102449184 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1211-1664C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449184 | |||||||
| chr2:102449287 | A | T | 1 | a0001c0002t0001g0040 | 2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1211-1561A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449287 | |||||||
| chr2:102449448 | T | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(148): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1211-1400T>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449448 | |||||||
| chr2:102449603 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1211-1245A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449603 | |||||||
| chr2:102449672 | G | A | 47 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(44): Show |
73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1211-1176G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449672 | |||||||
| chr2:102449775 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(192): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1211-1073G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449775 | |||||||
| chr2:102449886 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1211-962C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449886 | |||||||
| chr2:102449957 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1211-891C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449957 | |||||||
| chr2:102449970 | T | C | 1 | a0001c0002t0001g0039 | 2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1211-878T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102449970 | |||||||
| chr2:102450024 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1211-824A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102450024 | |||||||
| chr2:102450139 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1211-709G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102450139 | |||||||
| chr2:102450206 | A | ATGAAAAC others(103): Show |
1 | a0001c0001t0001g0168 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1211-636_1211-635i others(112): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102450206 | ||||||
| chr2:102450206 | A | ATGAAAAT others(103): Show |
46 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0007 others(43): Show |
117 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1211-633_1211-632i others(112): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102450206 | ||||||
| chr2:102450206 | A | ATGAAAAT others(103): Show |
1 | a0001c0001t0001g0088 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1211-633_1211-632i others(112): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102450206 | ||||||
| chr2:102450206 | A | ATGAAAAT others(107): Show |
1 | a0001c0001t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1211-633_1211-632i others(116): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102450206 | ||||||
| chr2:102450206 | A | ATGAAAAT others(103): Show |
1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1211-633_1211-632i others(112): Show |
IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 102450206 | ||||||
| chr2:102450253 | A | G | 1 | a0001c0002t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1211-595A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102450253 | |||||||
| chr2:102450304 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0099 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1211-544G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102450304 | |||||||
| chr2:102450398 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
214 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1211-450A>G | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102450398 | |||||||
| chr2:102450683 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(66): Show |
135 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1211-165G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 8/9 | chr2 | 102450683 | |||||||
| chr2:102451146 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1384+125T>C | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451146 | |||||||
| chr2:102451298 | A | T | 1 | a0001c0001t0002g0145 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1384+277A>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451298 | |||||||
| chr2:102451363 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0029 others(21): Show |
46 | HG00423.hp2 HG00673.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1384+342C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451363 | |||||||
| chr2:102451402 | C | T | 47 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(44): Show |
73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1385-364C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451402 | |||||||
| chr2:102451403 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1385-363G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451403 | |||||||
| chr2:102451409 | G | A | 47 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(44): Show |
73 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1385-357G>A | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451409 | |||||||
| chr2:102451443 | G | T | 1 | a0001c0001t0002g0045 | 2 | NA18959.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1385-323G>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451443 | |||||||
| chr2:102451470 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(32): Show |
79 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1385-296C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451470 | |||||||
| chr2:102451696 | C | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0018 a0001c0001t0003g0112 others(4): Show |
13 | HG00323.hp2 HG00733.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1385-70C>T | IL18RAP | ENSG00000115607.10 | transcript | ENST00000687160.1 | protein_coding | 9/9 | chr2 | 102451696 |