Item | Value |
---|---|
geneid | 8809 |
ensemblid | ENSG00000115604.12 |
hgncid | 5988 |
symbol | IL18R1 |
name | interleukin 18 receptor 1 |
refseq_nuc | NM_003855.5 |
refseq_prot | NP_003846.1 |
ensembl_nuc | ENST00000233957.7 |
ensembl_prot | ENSP00000233957.1 |
mane_status | MANE Select |
chr | chr2 |
start | 102355796 |
end | 102398776 |
strand | + |
ver | v1.2 |
region | chr2:102355796-102398776 |
region5000 | chr2:102350796-102403776 |
regionname0 | IL18R1_chr2_102355796_102398776 |
regionname5000 | IL18R1_chr2_102350796_102403776 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 541 | 356 | 78 | 57 | 163 | 16 | 40 | 130 | IL18R1_chr2_102350796_102403776 | IL18R1 | MNCRE others(536): Show |
chr2 | 102350796 | 102403776 |
a0002 | 0/0 | 541 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | IL18R1_chr2_102350796_102403776 | IL18R1 | MNCRE others(536): Show |
chr2 | 102350796 | 102403776 |
a0003 | 0/0 | 541 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | MNCRE others(536): Show |
chr2 | 102350796 | 102403776 |
a0004 | 0/0 | 541 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | MNCRE others(536): Show |
chr2 | 102350796 | 102403776 |
a0005 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | MNCRE others(536): Show |
chr2 | 102350796 | 102403776 |
a0006 | 0/0 | 541 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | MNCRE others(536): Show |
chr2 | 102350796 | 102403776 |
a0007 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | MNCRE others(536): Show |
chr2 | 102350796 | 102403776 |
a0008 | 0/0 | 541 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | MNCRE others(536): Show |
chr2 | 102350796 | 102403776 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1623 | 235 | 53 | 43 | 95 | 14 | 28 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0001c0002 | 0/0 | 1623 | 108 | 14 | 14 | 66 | 2 | 12 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0001c0003 | 0/0 | 1623 | 11 | 11 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0001c0006 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0001c0011 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0002c0004 | 0/0 | 1623 | 3 | 0 | 0 | 3 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0003c0005 | 0/0 | 1623 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0004c0012 | 0/0 | 1623 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0005c0009 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0006c0007 | 0/0 | 1623 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0007c0008 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 | ||
a0008c0010 | 0/0 | 1623 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | ATGAA others(1618): Show |
chr2 | 102350796 | 102403776 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4149 | 96 | 0 | 19 | 55 | 3 | 17 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0003 | 0/0 | 4149 | 58 | 20 | 7 | 26 | 2 | 3 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0005 | 0/0 | 4150 | 15 | 1 | 6 | 4 | 1 | 3 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0006 | 0/0 | 4150 | 13 | 7 | 3 | 0 | 3 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0007 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0008 | 0/0 | 4133 | 11 | 5 | 5 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4128): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0009 | 0/0 | 4150 | 7 | 0 | 0 | 7 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0010 | 0/0 | 4133 | 6 | 0 | 1 | 0 | 3 | 2 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4128): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0011 | 0/0 | 4149 | 4 | 4 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | AGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0013 | 0/0 | 4151 | 4 | 4 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4146): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0014 | 0/0 | 4135 | 3 | 0 | 0 | 2 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4130): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0015 | 0/0 | 4149 | 3 | 3 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0016 | 0/0 | 4150 | 3 | 3 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0017 | 0/0 | 4150 | 3 | 1 | 2 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0018 | 0/0 | 4151 | 3 | 3 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4146): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0019 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0026 | 0/0 | 4150 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0027 | 0/0 | 4149 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0028 | 0/0 | 4149 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0001t0031 | 0/0 | 4149 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0002 | 0/0 | 4150 | 63 | 8 | 7 | 36 | 2 | 10 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0004 | 0/0 | 4150 | 26 | 1 | 4 | 20 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0012 | 0/0 | 4149 | 3 | 2 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0021 | 0/0 | 4150 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0022 | 0/0 | 4150 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0023 | 0/0 | 4151 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4146): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0024 | 0/0 | 4150 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0025 | 0/0 | 4150 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0029 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4130): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0030 | 0/0 | 4149 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0033 | 0/0 | 4150 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0034 | 0/0 | 4150 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0035 | 0/0 | 4151 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4146): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0036 | 0/0 | 4151 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4146): Show |
chr2 | 102350796 | 102403776 |
a0001c0002t0037 | 0/0 | 4151 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4146): Show |
chr2 | 102350796 | 102403776 |
a0001c0003t0007 | 0/0 | 4149 | 11 | 11 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0006t0001 | 0/0 | 4149 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0001c0011t0001 | 0/0 | 4149 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0002c0004t0001 | 0/0 | 4149 | 3 | 0 | 0 | 3 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0003c0005t0020 | 0/0 | 4150 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0004c0012t0032 | 0/0 | 4150 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0005c0009t0012 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0006c0007t0019 | 0/0 | 4149 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4144): Show |
chr2 | 102350796 | 102403776 |
a0007c0008t0002 | 0/0 | 4150 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
a0008c0010t0002 | 0/0 | 4150 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | GGGAC others(4145): Show |
chr2 | 102350796 | 102403776 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/1 | 11 | 0 | 1 | 6 | 0 | 3 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0024 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0006 | 0/0 | 8 | 0 | 4 | 0 | 2 | 2 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0007 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0006g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0006g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0006g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0006g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0009g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0009g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0009g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0010g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0010g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0010g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0011g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0013g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0013g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0013g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0014g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0014g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0014g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0015g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0016g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0017g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0017g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0018g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0018g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0019g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0026g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0027g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0028g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0001t0031g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0001 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0012g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0012g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0021g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0021g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0022g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0022g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0023g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0023g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0024g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0024g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0025g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0029g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0030g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0033g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0034g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0035g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0036g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0002t0037g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0003t0007g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0003t0007g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0003t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0003t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0003t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0003t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0003t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0003t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0001c0011t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0002c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0003c0005t0020g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0004c0012t0032g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0005c0009t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0006c0007t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0007c0008t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
a0008c0010t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0010 | g0181 | EUR | GBR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | GBR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0147 | EUR | FIN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00323 | hp1 | a0001 | c0001 | t0008 | g0179 | EUR | FIN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00323 | hp2 | a0001 | c0001 | t0006 | g0048 | EUR | FIN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00408 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00558 | hp2 | a0001 | c0002 | t0023 | g0119 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00597 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00621 | hp2 | a0001 | c0006 | t0001 | g0064 | EAS | CHS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0032 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00733 | hp1 | a0001 | c0001 | t0006 | g0048 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0188 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00738 | hp2 | a0001 | c0001 | t0017 | g0037 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01070 | hp1 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0097 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0135 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01175 | hp1 | a0004 | c0012 | t0032 | g0205 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01175 | hp2 | a0001 | c0001 | t0017 | g0141 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0098 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01257 | hp2 | a0001 | c0001 | t0008 | g0183 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01258 | hp1 | a0001 | c0001 | t0008 | g0182 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01261 | hp1 | a0001 | c0002 | t0012 | g0089 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01346 | hp2 | a0001 | c0002 | t0025 | g0011 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01361 | hp1 | a0001 | c0002 | t0004 | g0105 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0184 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01496 | hp2 | a0001 | c0001 | t0010 | g0186 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0212 | EUR | IBS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01516 | hp2 | a0001 | c0001 | t0010 | g0180 | EUR | IBS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0021 | EUR | IBS | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01884 | hp2 | a0001 | c0002 | t0021 | g0101 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01891 | hp2 | a0001 | c0003 | t0007 | g0018 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01943 | hp2 | a0001 | c0002 | t0004 | g0118 | AMR | PEL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01981 | hp2 | a0001 | c0002 | t0030 | g0110 | AMR | PEL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01993 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PEL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02004 | hp2 | a0001 | c0002 | t0004 | g0099 | AMR | PEL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02015 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02027 | hp2 | a0001 | c0001 | t0009 | g0008 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0198 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02132 | hp2 | a0001 | c0002 | t0034 | g0004 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02145 | hp1 | a0001 | c0001 | t0018 | g0204 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0206 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02165 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | CDX | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02257 | hp1 | a0001 | c0003 | t0007 | g0018 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02280 | hp2 | a0001 | c0002 | t0012 | g0088 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0195 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02523 | hp2 | a0001 | c0002 | t0004 | g0033 | EAS | KHV | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02572 | hp2 | a0001 | c0003 | t0007 | g0191 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02602 | hp1 | a0001 | c0001 | t0027 | g0006 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02615 | hp2 | a0001 | c0002 | t0004 | g0124 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02622 | hp1 | a0005 | c0009 | t0012 | g0087 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02647 | hp1 | a0001 | c0003 | t0007 | g0043 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02647 | hp2 | a0006 | c0007 | t0019 | g0083 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0094 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02723 | hp1 | a0001 | c0001 | t0013 | g0208 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0153 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02809 | hp2 | a0001 | c0003 | t0007 | g0189 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02886 | hp1 | a0001 | c0002 | t0035 | g0200 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02886 | hp2 | a0001 | c0002 | t0012 | g0090 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0044 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02965 | hp1 | a0001 | c0003 | t0007 | g0192 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0199 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02970 | hp1 | a0001 | c0003 | t0007 | g0193 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02970 | hp2 | a0001 | c0001 | t0019 | g0075 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02976 | hp1 | a0001 | c0001 | t0015 | g0095 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03130 | hp1 | a0001 | c0001 | t0016 | g0020 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03139 | hp1 | a0001 | c0001 | t0016 | g0020 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03139 | hp2 | a0001 | c0003 | t0007 | g0190 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0203 | AFR | ESN | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | MSL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03209 | hp2 | a0001 | c0002 | t0021 | g0125 | AFR | MSL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03453 | hp1 | a0001 | c0003 | t0007 | g0018 | AFR | MSL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03453 | hp2 | a0001 | c0001 | t0013 | g0201 | AFR | MSL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0044 | AFR | MSL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03490 | hp1 | a0001 | c0001 | t0010 | g0042 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03492 | hp1 | a0001 | c0001 | t0010 | g0042 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03654 | hp2 | a0001 | c0001 | t0031 | g0015 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0121 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0056 | SAS | STU | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03704 | hp2 | a0001 | c0002 | t0033 | g0001 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03710 | hp1 | a0001 | c0001 | t0014 | g0053 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0138 | SAS | PJL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0102 | SAS | BEB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0031 | SAS | STU | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0149 | SAS | STU | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0103 | SAS | BEB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0031 | SAS | STU | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG04228 | hp2 | a0001 | c0002 | t0004 | g0140 | SAS | STU | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | YRI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | YRI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18612 | hp1 | a0007 | c0008 | t0002 | g0113 | EAS | CHB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18612 | hp2 | a0001 | c0002 | t0004 | g0134 | EAS | CHB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | CHB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | YRI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0202 | AFR | YRI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18941 | hp1 | a0001 | c0002 | t0004 | g0123 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18942 | hp1 | a0001 | c0002 | t0037 | g0001 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18942 | hp2 | a0001 | c0001 | t0014 | g0051 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18948 | hp1 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18949 | hp2 | a0001 | c0002 | t0004 | g0011 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18951 | hp1 | a0001 | c0001 | t0009 | g0026 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18951 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18953 | hp1 | a0001 | c0001 | t0009 | g0026 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18954 | hp1 | a0001 | c0002 | t0024 | g0108 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18956 | hp2 | a0001 | c0001 | t0009 | g0055 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18959 | hp1 | a0001 | c0002 | t0004 | g0152 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18960 | hp2 | a0001 | c0002 | t0004 | g0111 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18962 | hp2 | a0008 | c0010 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18966 | hp1 | a0001 | c0001 | t0028 | g0005 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18968 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18973 | hp1 | a0001 | c0002 | t0004 | g0151 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18979 | hp1 | a0001 | c0002 | t0022 | g0133 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18980 | hp1 | a0001 | c0001 | t0014 | g0050 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18983 | hp1 | a0001 | c0002 | t0023 | g0033 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18991 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18993 | hp1 | a0001 | c0002 | t0036 | g0136 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18993 | hp2 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18995 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19002 | hp1 | a0001 | c0002 | t0004 | g0115 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19002 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19003 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19004 | hp1 | a0001 | c0011 | t0001 | g0008 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19004 | hp2 | a0001 | c0002 | t0022 | g0139 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19007 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19011 | hp1 | a0001 | c0002 | t0029 | g0052 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0020 | AFR | LWK | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0197 | AFR | LWK | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19056 | hp1 | a0001 | c0002 | t0024 | g0107 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19060 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19070 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19074 | hp1 | a0001 | c0002 | t0004 | g0117 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19079 | hp1 | a0001 | c0001 | t0009 | g0074 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19086 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | YRI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA19240 | hp2 | a0001 | c0003 | t0007 | g0043 | AFR | YRI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA20129 | hp1 | a0003 | c0005 | t0020 | g0045 | AFR | ASW | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA20129 | hp2 | a0001 | c0001 | t0017 | g0143 | AFR | ASW | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA20752 | hp1 | a0001 | c0001 | t0010 | g0185 | EUR | TSI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0120 | EUR | TSI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA20805 | hp2 | a0001 | c0001 | t0026 | g0037 | EUR | TSI | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0036 | SAS | GIH | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | GIH | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG01123 | hp2 | a0001 | c0001 | t0008 | g0187 | AMR | CLM | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02109 | hp1 | a0003 | c0005 | t0020 | g0045 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02486 | hp1 | a0001 | c0001 | t0015 | g0096 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0196 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0209 | AFR | ACB | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03471 | hp1 | a0001 | c0003 | t0007 | g0194 | AFR | MSL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | USA | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | USA | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | LWK | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0168 | AFR | LWK | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0002 | REF | REF | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0024 | REF | REF | IL18R1_chr2_102350796_102403776 | IL18R1 | chr2 | 102350796 | 102403776 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:102381623 | G | A | 1 | a0003 | 2 | HG02109.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.629G>A | p.Arg210His | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/11 | 1262/4149 | 629/1626 | 210/541 | chr2 | 102381623 | |||
chr2:102381631 | A | G | 1 | a0004 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.637A>G | p.Ile213Val | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/11 | 1270/4149 | 637/1626 | 213/541 | chr2 | 102381631 | |||
chr2:102384967 | A | G | 1 | a0006 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.778A>G | p.Asn260Asp | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/11 | 1411/4149 | 778/1626 | 260/541 | chr2 | 102384967 | |||
chr2:102390194 | C | T | 1 | a0008 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.1088C>T | p.Thr363Met | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/11 | 1721/4149 | 1088/1626 | 363/541 | chr2 | 102390194 | |||
chr2:102394624 | G | A | 1 | a0002 | 3 | NA18991.hp1 NA18993.hp2 NA19086.hp1 |
missense_variant | MODERATE | c.1267G>A | p.Gly423Arg | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/11 | 1900/4149 | 1267/1626 | 423/541 | chr2 | 102394624 | |||
chr2:102396740 | T | G | 1 | a0007 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.1480T>G | p.Ser494Ala | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 2113/4149 | 1480/1626 | 494/541 | chr2 | 102396740 | |||
chr2:102396774 | C | A | 1 | a0005 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1514C>A | p.Ser505Tyr | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 2147/4149 | 1514/1626 | 505/541 | chr2 | 102396774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:102362681 | C | G | 1 | a0001c0003 | 11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
synonymous_variant | LOW | c.21C>G | p.Pro7Pro | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/11 | 654/4149 | 21/1626 | 7/541 | chr2 | 102362681 | |||
chr2:102384885 | C | T | 1 | a0001c0011 | 1 | NA19004.hp1 | synonymous_variant | LOW | c.696C>T | p.Asn232Asn | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/11 | 1329/4149 | 696/1626 | 232/541 | chr2 | 102384885 | |||
chr2:102384942 | C | T | 5 | a0001c0002 a0003c0005 a0005c0009 others(2): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
synonymous_variant | LOW | c.753C>T | p.Phe251Phe | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/11 | 1386/4149 | 753/1626 | 251/541 | chr2 | 102384942 | |||
chr2:102386867 | A | C | 1 | a0001c0006 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.816A>C | p.Pro272Pro | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/11 | 1449/4149 | 816/1626 | 272/541 | chr2 | 102386867 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:102355796 | G | A | 1 | a0001c0001t0011 | 4 | HG02451.hp2 HG02559.hp1 HG02896.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-633G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6865 | chr2 | 102355796 | ||||||
chr2:102355825 | G | A | 1 | a0001c0002t0025 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-604G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6836 | chr2 | 102355825 | ||||||
chr2:102355849 | C | T | 2 | a0001c0002t0024 a0001c0002t0037 |
3 | NA18942.hp1 NA18954.hp1 NA19056.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-580C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | chr2 | 102355849 | |||||||
chr2:102355897 | G | A | 1 | a0001c0001t0026 | 1 | NA20805.hp2 | 5_prime_UTR_variant | MODIFIER | c.-532G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6764 | chr2 | 102355897 | ||||||
chr2:102355933 | G | C | 1 | a0001c0001t0027 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-496G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6728 | chr2 | 102355933 | ||||||
chr2:102355952 | G | A | 1 | a0001c0001t0028 | 1 | NA18966.hp1 | 5_prime_UTR_variant | MODIFIER | c.-477G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6709 | chr2 | 102355952 | ||||||
chr2:102356039 | GGAGCGCC others(9): Show |
G | 4 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0014 others(1): Show |
21 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-376_-361delTGAGAG others(10): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6593 | INFO_REALIGN_3_PRIME | chr2 | 102356039 | |||||
chr2:102356074 | C | T | 2 | a0001c0001t0008 a0001c0001t0010 |
17 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-355C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6587 | chr2 | 102356074 | ||||||
chr2:102356207 | C | CT | 18 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(15): Show |
145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
5_prime_UTR_variant | MODIFIER | c.-207dupT | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6438 | INFO_REALIGN_3_PRIME | chr2 | 102356207 | |||||
chr2:102356207 | C | CTT | 8 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0018 others(5): Show |
16 | HG00558.hp2 HG02145.hp1 HG02559.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-208_-207dupTT | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6438 | INFO_REALIGN_3_PRIME | chr2 | 102356207 | |||||
chr2:102356339 | G | C | 19 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(16): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
5_prime_UTR_variant | MODIFIER | c.-90G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6322 | chr2 | 102356339 | ||||||
chr2:102356347 | G | A | 7 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0016 others(4): Show |
27 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-82G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/11 | 6314 | chr2 | 102356347 | ||||||
chr2:102396948 | C | T | 1 | a0001c0001t0010 | 6 | HG00099.hp1 HG01496.hp2 HG01516.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*62C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 62 | chr2 | 102396948 | ||||||
chr2:102396972 | C | A | 6 | a0001c0002t0004 a0001c0002t0023 a0001c0002t0024 others(3): Show |
33 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*86C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 86 | chr2 | 102396972 | ||||||
chr2:102397290 | G | C | 7 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0017 others(4): Show |
70 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*404G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 404 | chr2 | 102397290 | ||||||
chr2:102397476 | G | C | 1 | a0001c0002t0033 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 590 | chr2 | 102397476 | ||||||
chr2:102397502 | A | C | 14 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0022 others(11): Show |
104 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*616A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 616 | chr2 | 102397502 | ||||||
chr2:102397503 | G | C | 14 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0022 others(11): Show |
104 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*617G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 617 | chr2 | 102397503 | ||||||
chr2:102397842 | T | G | 19 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0012 others(16): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*956T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 956 | chr2 | 102397842 | ||||||
chr2:102397854 | C | A | 3 | a0001c0001t0005 a0001c0001t0031 a0004c0012t0032 |
17 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*968C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 968 | chr2 | 102397854 | ||||||
chr2:102398103 | G | A | 1 | a0001c0002t0034 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1217G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 1217 | chr2 | 102398103 | ||||||
chr2:102398236 | C | T | 38 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(35): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*1350C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 1350 | chr2 | 102398236 | ||||||
chr2:102398537 | G | A | 1 | a0001c0002t0022 | 2 | NA18979.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1651G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 11/11 | 1651 | chr2 | 102398537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:102356498 | A | AAG | 4 | a0001c0001t0014g0050 a0001c0001t0014g0051 a0001c0001t0014g0053 others(1): Show |
4 | HG03710.hp1 NA18942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+112_-29+113dup others(2): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 102356498 | ||||||
chr2:102356515 | A | AGT | 3 | a0001c0001t0006g0021 a0001c0001t0006g0212 a0001c0002t0002g0211 |
5 | HG01070.hp1 HG01071.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+125_-29+126dup others(2): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 102356515 | ||||||
chr2:102356863 | C | T | 1 | a0001c0001t0006g0049 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-29+463C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102356863 | |||||||
chr2:102357318 | C | G | 1 | a0001c0002t0002g0210 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-29+918C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357318 | |||||||
chr2:102357439 | A | G | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-29+1039A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357439 | |||||||
chr2:102357490 | C | CA | 78 | a0001c0001t0001g0054 a0001c0001t0003g0005 a0001c0001t0003g0006 others(75): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-29+1102dupA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 102357490 | ||||||
chr2:102357503 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29+1103G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357503 | |||||||
chr2:102357504 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29+1104A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357504 | |||||||
chr2:102357610 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0156 others(4): Show |
17 | HG00621.hp1 HG02027.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29+1210C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357610 | |||||||
chr2:102357669 | C | T | 85 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(82): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-29+1269C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357669 | |||||||
chr2:102357735 | G | A | 1 | a0001c0001t0006g0049 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-29+1335G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357735 | |||||||
chr2:102357762 | A | T | 18 | a0001c0001t0006g0021 a0001c0001t0006g0046 a0001c0001t0006g0047 others(15): Show |
27 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-29+1362A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357762 | |||||||
chr2:102357868 | G | A | 32 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(29): Show |
61 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-29+1468G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357868 | |||||||
chr2:102357881 | C | CGT | 6 | a0001c0001t0008g0019 a0001c0001t0008g0197 a0001c0001t0008g0198 others(3): Show |
8 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+1496_-29+1497d others(4): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 102357881 | ||||||
chr2:102357911 | A | C | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-29+1511A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357911 | |||||||
chr2:102357957 | G | T | 85 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(82): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-29+1557G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102357957 | |||||||
chr2:102358005 | TA | T | 85 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(82): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-29+1614delA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 102358005 | ||||||
chr2:102358018 | G | T | 3 | a0001c0002t0002g0153 a0001c0002t0002g0154 a0001c0002t0002g0155 |
3 | HG02809.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-29+1618G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358018 | |||||||
chr2:102358304 | G | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-29+1904G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358304 | |||||||
chr2:102358451 | T | G | 1 | a0001c0002t0002g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-29+2051T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358451 | |||||||
chr2:102358518 | C | T | 1 | a0001c0001t0006g0206 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-29+2118C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358518 | |||||||
chr2:102358590 | G | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-29+2190G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358590 | |||||||
chr2:102358667 | C | A | 1 | a0001c0002t0002g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-29+2267C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358667 | |||||||
chr2:102358673 | A | G | 3 | a0001c0001t0011g0044 a0001c0001t0011g0195 a0001c0001t0011g0196 |
4 | HG02451.hp2 HG02559.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+2273A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358673 | |||||||
chr2:102358709 | C | T | 5 | a0001c0003t0007g0190 a0001c0003t0007g0191 a0001c0003t0007g0192 others(2): Show |
5 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+2309C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358709 | |||||||
chr2:102358876 | T | G | 86 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(83): Show |
125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-29+2476T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102358876 | |||||||
chr2:102359141 | C | T | 1 | a0001c0001t0003g0178 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-29+2741C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102359141 | |||||||
chr2:102359142 | G | A | 1 | a0001c0001t0008g0179 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-29+2742G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102359142 | |||||||
chr2:102359437 | A | G | 1 | a0001c0001t0003g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-29+3037A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102359437 | |||||||
chr2:102359712 | G | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-28-2921G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102359712 | |||||||
chr2:102359790 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02015.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.-28-2843C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102359790 | |||||||
chr2:102359981 | G | C | 1 | a0001c0002t0002g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-28-2652G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102359981 | |||||||
chr2:102360078 | G | A | 1 | a0001c0002t0002g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-28-2555G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360078 | |||||||
chr2:102360206 | C | T | 2 | a0001c0002t0004g0151 a0001c0002t0004g0152 |
2 | NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-28-2427C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360206 | |||||||
chr2:102360226 | T | A | 4 | a0001c0001t0014g0050 a0001c0001t0014g0051 a0001c0001t0014g0053 others(1): Show |
4 | HG03710.hp1 NA18942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-2407T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360226 | |||||||
chr2:102360268 | A | T | 4 | a0001c0001t0014g0050 a0001c0001t0014g0051 a0001c0001t0014g0053 others(1): Show |
4 | HG03710.hp1 NA18942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-2365A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360268 | |||||||
chr2:102360418 | C | A | 1 | a0001c0002t0002g0030 | 2 | NA18947.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-28-2215C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360418 | |||||||
chr2:102360555 | G | T | 1 | a0001c0001t0005g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-28-2078G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360555 | |||||||
chr2:102360736 | C | T | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-28-1897C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360736 | |||||||
chr2:102360851 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-28-1782G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360851 | |||||||
chr2:102360912 | C | A | 1 | a0001c0001t0005g0098 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-28-1721C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360912 | |||||||
chr2:102360945 | G | A | 3 | a0001c0001t0011g0044 a0001c0001t0011g0195 a0001c0001t0011g0196 |
4 | HG02451.hp2 HG02559.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1688G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102360945 | |||||||
chr2:102361051 | G | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-28-1582G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361051 | |||||||
chr2:102361077 | A | G | 92 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(89): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-28-1556A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361077 | |||||||
chr2:102361230 | A | T | 1 | a0001c0001t0003g0176 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-28-1403A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361230 | |||||||
chr2:102361251 | G | A | 4 | a0001c0001t0014g0050 a0001c0001t0014g0051 a0001c0001t0014g0053 others(1): Show |
4 | HG03710.hp1 NA18942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1382G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361251 | |||||||
chr2:102361270 | C | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-28-1363C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361270 | |||||||
chr2:102361313 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-28-1320A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361313 | |||||||
chr2:102361494 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-28-1139G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361494 | |||||||
chr2:102361815 | C | CTCCACTG others(70): Show |
1 | a0001c0002t0002g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-28-808_-28-732dup others(77): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 102361815 | ||||||
chr2:102361903 | C | G | 1 | a0001c0002t0002g0148 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-28-730C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361903 | |||||||
chr2:102361940 | A | G | 15 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(12): Show |
20 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28-693A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361940 | |||||||
chr2:102361999 | C | T | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-28-634C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102361999 | |||||||
chr2:102362113 | T | C | 1 | a0005c0009t0012g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-28-520T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102362113 | |||||||
chr2:102362228 | A | AAC | 24 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0016 others(21): Show |
45 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-28-392_-28-391dup others(2): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 102362228 | ||||||
chr2:102362486 | G | A | 2 | a0001c0001t0013g0208 a0001c0001t0018g0209 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-28-147G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102362486 | |||||||
chr2:102362568 | C | T | 92 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(89): Show |
131 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-28-65C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102362568 | |||||||
chr2:102362582 | C | A | 1 | a0001c0001t0013g0199 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28-51C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 1/10 | chr2 | 102362582 | |||||||
chr2:102362981 | T | C | 1 | a0001c0001t0010g0042 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58+263T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102362981 | |||||||
chr2:102363009 | GGA | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0048 a0001c0001t0006g0212 |
6 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+293_58+294delAG | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 102363009 | ||||||
chr2:102363114 | A | T | 1 | a0001c0002t0002g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.58+396A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363114 | |||||||
chr2:102363164 | G | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.58+446G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363164 | |||||||
chr2:102363198 | G | GT | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.58+492dupT | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 102363198 | ||||||
chr2:102363425 | G | A | 1 | a0001c0001t0010g0180 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.58+707G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363425 | |||||||
chr2:102363494 | C | T | 3 | a0001c0001t0003g0040 a0001c0001t0003g0170 a0001c0001t0003g0176 |
4 | NA18979.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+776C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363494 | |||||||
chr2:102363574 | A | G | 1 | a0001c0001t0003g0169 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58+856A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363574 | |||||||
chr2:102363680 | G | A | 5 | a0001c0001t0013g0199 a0001c0001t0013g0201 a0001c0001t0013g0203 others(2): Show |
5 | HG02886.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+962G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363680 | |||||||
chr2:102363686 | CA | C | 18 | a0001c0001t0006g0021 a0001c0001t0006g0046 a0001c0001t0006g0047 others(15): Show |
27 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.58+971delA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 102363686 | ||||||
chr2:102363763 | G | T | 15 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(12): Show |
20 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.58+1045G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363763 | |||||||
chr2:102363771 | T | C | 5 | a0001c0001t0013g0199 a0001c0001t0013g0201 a0001c0001t0013g0203 others(2): Show |
5 | HG02886.hp1 HG02965.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+1053T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363771 | |||||||
chr2:102363775 | G | A | 1 | a0001c0002t0004g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.58+1057G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363775 | |||||||
chr2:102363781 | A | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0084 others(2): Show |
10 | HG00597.hp1 HG00642.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+1063A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363781 | |||||||
chr2:102363794 | G | A | 1 | a0001c0002t0002g0031 | 2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.58+1076G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102363794 | |||||||
chr2:102364083 | C | G | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.58+1365C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364083 | |||||||
chr2:102364130 | A | C | 1 | a0001c0002t0002g0097 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58+1412A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364130 | |||||||
chr2:102364327 | C | T | 1 | a0001c0002t0004g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.58+1609C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364327 | |||||||
chr2:102364398 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.58+1680T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364398 | |||||||
chr2:102364516 | A | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0076 others(8): Show |
16 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.58+1798A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364516 | |||||||
chr2:102364517 | A | G | 21 | a0001c0002t0002g0004 a0001c0002t0002g0030 a0001c0002t0002g0035 others(18): Show |
33 | HG00423.hp1 HG01106.hp2 HG02080.hp1 others(30): Show |
intron_variant | MODIFIER | c.58+1799A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364517 | |||||||
chr2:102364558 | T | G | 14 | a0001c0001t0008g0019 a0001c0001t0008g0179 a0001c0001t0008g0182 others(11): Show |
17 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+1840T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364558 | |||||||
chr2:102364801 | G | A | 3 | a0001c0001t0011g0044 a0001c0001t0011g0195 a0001c0001t0011g0196 |
4 | HG02451.hp2 HG02559.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+2083G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364801 | |||||||
chr2:102364846 | A | G | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.58+2128A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364846 | |||||||
chr2:102364929 | G | A | 1 | a0001c0001t0006g0049 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.58+2211G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102364929 | |||||||
chr2:102365013 | T | A | 1 | a0001c0002t0002g0100 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.58+2295T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365013 | |||||||
chr2:102365094 | C | T | 1 | a0001c0002t0022g0139 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.58+2376C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365094 | |||||||
chr2:102365104 | C | T | 1 | a0001c0001t0011g0196 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+2386C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365104 | |||||||
chr2:102365184 | A | C | 171 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(168): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.58+2466A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365184 | |||||||
chr2:102365186 | G | C | 1 | a0001c0001t0019g0075 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.58+2468G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365186 | |||||||
chr2:102365338 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.59-2487T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365338 | |||||||
chr2:102365345 | G | T | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-2480G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365345 | |||||||
chr2:102365406 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 |
4 | HG02015.hp1 HG02602.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-2419C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365406 | |||||||
chr2:102365431 | T | C | 18 | a0001c0001t0003g0007 a0001c0001t0003g0158 a0001c0001t0003g0159 others(15): Show |
28 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-2394T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365431 | |||||||
chr2:102365436 | T | C | 1 | a0001c0002t0035g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.59-2389T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365436 | |||||||
chr2:102365446 | A | G | 7 | a0001c0001t0015g0094 a0001c0001t0015g0095 a0001c0001t0015g0096 others(4): Show |
7 | HG01261.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-2379A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365446 | |||||||
chr2:102365464 | A | C | 1 | a0001c0001t0005g0147 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.59-2361A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365464 | |||||||
chr2:102365573 | G | T | 28 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0016 others(25): Show |
50 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.59-2252G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365573 | |||||||
chr2:102365634 | C | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.59-2191C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365634 | |||||||
chr2:102365635 | C | T | 1 | a0001c0001t0008g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.59-2190C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365635 | |||||||
chr2:102365763 | C | T | 23 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(20): Show |
28 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.59-2062C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365763 | |||||||
chr2:102365765 | A | T | 1 | a0001c0001t0003g0041 | 2 | HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.59-2060A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365765 | |||||||
chr2:102365816 | C | G | 16 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(13): Show |
21 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.59-2009C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365816 | |||||||
chr2:102365894 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.59-1931G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102365894 | |||||||
chr2:102366006 | C | G | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.59-1819C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366006 | |||||||
chr2:102366025 | T | C | 2 | a0001c0001t0003g0038 a0001c0001t0003g0169 |
3 | HG01167.hp1 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.59-1800T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366025 | |||||||
chr2:102366169 | G | A | 14 | a0001c0001t0008g0019 a0001c0001t0008g0179 a0001c0001t0008g0182 others(11): Show |
17 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-1656G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366169 | |||||||
chr2:102366243 | G | A | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.59-1582G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366243 | |||||||
chr2:102366249 | C | G | 18 | a0001c0001t0008g0019 a0001c0001t0008g0179 a0001c0001t0008g0182 others(15): Show |
21 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-1576C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366249 | |||||||
chr2:102366293 | A | G | 1 | a0006c0007t0019g0083 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.59-1532A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366293 | |||||||
chr2:102366388 | T | C | 1 | a0001c0002t0002g0148 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.59-1437T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366388 | |||||||
chr2:102366416 | T | C | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.59-1409T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366416 | |||||||
chr2:102366500 | T | G | 3 | a0001c0001t0011g0044 a0001c0001t0011g0195 a0001c0001t0011g0196 |
4 | HG02451.hp2 HG02559.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-1325T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366500 | |||||||
chr2:102366787 | C | A | 93 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(90): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.59-1038C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366787 | |||||||
chr2:102366844 | C | A | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.59-981C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366844 | |||||||
chr2:102366963 | T | C | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-862T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102366963 | |||||||
chr2:102367125 | T | C | 1 | a0001c0002t0002g0127 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.59-700T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102367125 | |||||||
chr2:102367474 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-351C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102367474 | |||||||
chr2:102367475 | G | A | 2 | a0001c0001t0016g0020 a0001c0001t0018g0204 |
4 | HG02145.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-350G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102367475 | |||||||
chr2:102367687 | C | G | 1 | a0001c0001t0008g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.59-138C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102367687 | |||||||
chr2:102367819 | T | C | 93 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(90): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
splice_region_variant&intron_variant | LOW | c.59-6T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 2/10 | chr2 | 102367819 | |||||||
chr2:102368164 | C | G | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.302+96C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368164 | |||||||
chr2:102368211 | T | A | 93 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(90): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.302+143T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368211 | |||||||
chr2:102368224 | G | A | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.302+156G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368224 | |||||||
chr2:102368384 | T | C | 1 | a0001c0002t0002g0128 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.302+316T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368384 | |||||||
chr2:102368590 | G | A | 1 | a0001c0002t0021g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.302+522G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368590 | |||||||
chr2:102368617 | G | A | 2 | a0001c0002t0002g0031 a0001c0002t0002g0102 |
3 | HG03942.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.302+549G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368617 | |||||||
chr2:102368671 | G | A | 1 | a0001c0001t0006g0049 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.302+603G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368671 | |||||||
chr2:102368708 | C | A | 1 | a0001c0001t0017g0141 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.302+640C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368708 | |||||||
chr2:102368736 | G | A | 2 | a0001c0001t0005g0017 a0001c0001t0005g0142 |
4 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+668G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368736 | |||||||
chr2:102368742 | G | T | 1 | a0001c0001t0017g0141 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.302+674G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368742 | |||||||
chr2:102368878 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG03669.hp1 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.302+810A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368878 | |||||||
chr2:102368964 | A | G | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.302+896A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102368964 | |||||||
chr2:102369076 | C | A | 1 | a0001c0001t0010g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.302+1008C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369076 | |||||||
chr2:102369186 | GC | G | 170 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(167): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.302+1126delC | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 102369186 | ||||||
chr2:102369261 | C | G | 1 | a0001c0002t0002g0138 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.302+1193C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369261 | |||||||
chr2:102369352 | C | T | 69 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(66): Show |
103 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.302+1284C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369352 | |||||||
chr2:102369354 | G | A | 1 | a0001c0001t0013g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.302+1286G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369354 | |||||||
chr2:102369490 | T | C | 70 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(67): Show |
104 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.302+1422T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369490 | |||||||
chr2:102369520 | T | A | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.302+1452T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369520 | |||||||
chr2:102369694 | G | A | 70 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(67): Show |
104 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.302+1626G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369694 | |||||||
chr2:102369710 | C | T | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.302+1642C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369710 | |||||||
chr2:102369728 | A | G | 18 | a0001c0001t0008g0019 a0001c0001t0008g0179 a0001c0001t0008g0182 others(15): Show |
21 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.302+1660A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369728 | |||||||
chr2:102369762 | G | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.302+1694G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369762 | |||||||
chr2:102369897 | G | A | 4 | a0001c0001t0014g0050 a0001c0001t0014g0051 a0001c0001t0014g0053 others(1): Show |
4 | HG03710.hp1 NA18942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+1829G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369897 | |||||||
chr2:102369915 | G | A | 79 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(76): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.302+1847G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102369915 | |||||||
chr2:102370011 | T | C | 18 | a0001c0001t0008g0019 a0001c0001t0008g0179 a0001c0001t0008g0182 others(15): Show |
21 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.303-1942T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370011 | |||||||
chr2:102370092 | A | T | 4 | a0001c0001t0014g0050 a0001c0001t0014g0051 a0001c0001t0014g0053 others(1): Show |
4 | HG03710.hp1 NA18942.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-1861A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370092 | |||||||
chr2:102370158 | T | C | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.303-1795T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370158 | |||||||
chr2:102370188 | G | A | 1 | a0001c0001t0003g0171 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.303-1765G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370188 | |||||||
chr2:102370430 | T | C | 1 | a0001c0002t0002g0103 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.303-1523T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370430 | |||||||
chr2:102370633 | C | A | 10 | a0001c0001t0008g0179 a0001c0001t0008g0182 a0001c0001t0008g0183 others(7): Show |
11 | HG00099.hp1 HG00323.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.303-1320C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370633 | |||||||
chr2:102370753 | A | G | 14 | a0001c0001t0005g0015 a0001c0001t0005g0036 a0001c0001t0005g0056 others(11): Show |
17 | HG00280.hp2 HG00738.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.303-1200A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370753 | |||||||
chr2:102370804 | A | G | 4 | a0001c0001t0007g0168 a0001c0001t0011g0044 a0001c0001t0011g0195 others(1): Show |
5 | HG02451.hp2 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-1149A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370804 | |||||||
chr2:102370859 | G | T | 1 | a0001c0001t0003g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.303-1094G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370859 | |||||||
chr2:102370901 | A | G | 45 | a0001c0001t0005g0015 a0001c0001t0005g0036 a0001c0001t0005g0056 others(42): Show |
56 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.303-1052A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370901 | |||||||
chr2:102370999 | T | A | 76 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(73): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.303-954T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102370999 | |||||||
chr2:102371025 | T | G | 5 | a0001c0001t0006g0049 a0001c0001t0013g0201 a0001c0001t0013g0208 others(2): Show |
6 | HG02258.hp2 HG02559.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-928T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371025 | |||||||
chr2:102371043 | C | CT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(217): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.303-903dupT | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 102371043 | ||||||
chr2:102371048 | T | TTTTG | 4 | a0001c0001t0006g0021 a0001c0001t0006g0048 a0001c0001t0006g0212 others(1): Show |
7 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-903_303-902ins others(4): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 102371048 | ||||||
chr2:102371066 | G | T | 171 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(168): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.303-887G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371066 | |||||||
chr2:102371090 | C | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0169 |
3 | HG01167.hp1 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.303-863C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371090 | |||||||
chr2:102371119 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0076 others(6): Show |
14 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.303-834C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371119 | |||||||
chr2:102371162 | C | T | 3 | a0001c0001t0013g0208 a0001c0001t0018g0202 a0001c0001t0018g0209 |
3 | HG02559.hp2 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.303-791C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371162 | |||||||
chr2:102371179 | C | T | 1 | a0001c0001t0005g0146 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.303-774C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371179 | |||||||
chr2:102371238 | T | C | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.303-715T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371238 | |||||||
chr2:102371359 | A | G | 2 | a0001c0001t0009g0026 a0001c0001t0009g0074 |
3 | NA18951.hp1 NA18953.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.303-594A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371359 | |||||||
chr2:102371369 | A | G | 1 | a0001c0001t0008g0179 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.303-584A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371369 | |||||||
chr2:102371414 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.303-539A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371414 | |||||||
chr2:102371803 | C | A | 1 | a0001c0002t0004g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.303-150C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371803 | |||||||
chr2:102371807 | G | A | 1 | a0001c0002t0002g0032 | 2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.303-146G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371807 | |||||||
chr2:102371840 | C | A | 2 | a0001c0001t0008g0182 a0001c0001t0008g0183 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.303-113C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371840 | |||||||
chr2:102371918 | G | A | 3 | a0001c0002t0002g0153 a0001c0002t0002g0154 a0001c0002t0002g0155 |
3 | HG02809.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.303-35G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 3/10 | chr2 | 102371918 | |||||||
chr2:102372347 | T | C | 1 | a0001c0001t0005g0036 | 2 | HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.468+229T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102372347 | |||||||
chr2:102372395 | C | T | 1 | a0001c0002t0002g0137 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.468+277C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102372395 | |||||||
chr2:102372503 | C | A | 1 | a0001c0002t0021g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.468+385C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102372503 | |||||||
chr2:102372600 | C | CT | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.468+491dupT | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 102372600 | ||||||
chr2:102372712 | C | G | 1 | a0001c0001t0003g0039 | 2 | NA18977.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.468+594C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102372712 | |||||||
chr2:102372822 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.468+704T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102372822 | |||||||
chr2:102373066 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.468+948G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373066 | |||||||
chr2:102373120 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.468+1002C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373120 | |||||||
chr2:102373225 | C | G | 1 | a0004c0012t0032g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.468+1107C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373225 | |||||||
chr2:102373274 | A | G | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.468+1156A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373274 | |||||||
chr2:102373556 | A | G | 1 | a0001c0001t0003g0167 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.468+1438A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373556 | |||||||
chr2:102373603 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.468+1485A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373603 | |||||||
chr2:102373604 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.468+1486A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373604 | |||||||
chr2:102373611 | TA | T | 78 | a0001c0001t0001g0071 a0001c0002t0002g0001 a0001c0002t0002g0004 others(75): Show |
113 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.468+1503delA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 102373611 | ||||||
chr2:102373706 | G | A | 3 | a0001c0001t0013g0208 a0001c0001t0018g0202 a0001c0001t0018g0209 |
3 | HG02559.hp2 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.468+1588G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373706 | |||||||
chr2:102373722 | A | T | 1 | a0001c0001t0011g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.468+1604A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373722 | |||||||
chr2:102373727 | C | T | 3 | a0001c0002t0004g0105 a0001c0002t0004g0124 a0001c0002t0021g0125 |
3 | HG01361.hp1 HG02615.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.468+1609C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373727 | |||||||
chr2:102373863 | G | A | 1 | a0001c0002t0002g0100 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.468+1745G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102373863 | |||||||
chr2:102374068 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.469-1839C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374068 | |||||||
chr2:102374188 | G | C | 37 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
68 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.469-1719G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374188 | |||||||
chr2:102374287 | G | A | 2 | a0001c0002t0024g0107 a0001c0002t0024g0108 |
2 | NA18954.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.469-1620G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374287 | |||||||
chr2:102374328 | G | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-1579G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374328 | |||||||
chr2:102374460 | T | A | 3 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0167 |
3 | HG01891.hp1 HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.469-1447T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374460 | |||||||
chr2:102374500 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0071 |
3 | HG00140.hp1 HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.469-1407C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374500 | |||||||
chr2:102374531 | C | A | 1 | a0001c0001t0013g0201 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.469-1376C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374531 | |||||||
chr2:102374553 | C | T | 1 | a0001c0002t0002g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.469-1354C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374553 | |||||||
chr2:102374571 | G | A | 1 | a0001c0001t0006g0046 | 2 | HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.469-1336G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374571 | |||||||
chr2:102374596 | A | G | 6 | a0001c0001t0006g0021 a0001c0001t0006g0046 a0001c0001t0006g0047 others(3): Show |
11 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.469-1311A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374596 | |||||||
chr2:102374670 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0076 others(6): Show |
14 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.469-1237C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374670 | |||||||
chr2:102374703 | G | A | 45 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(42): Show |
59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.469-1204G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374703 | |||||||
chr2:102374714 | G | T | 1 | a0003c0005t0020g0045 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.469-1193G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374714 | |||||||
chr2:102374721 | C | T | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.469-1186C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374721 | |||||||
chr2:102374731 | C | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-1176C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374731 | |||||||
chr2:102374753 | A | G | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-1154A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374753 | |||||||
chr2:102374765 | G | A | 1 | a0001c0001t0006g0049 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.469-1142G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374765 | |||||||
chr2:102374769 | C | T | 4 | a0001c0001t0006g0021 a0001c0001t0006g0048 a0001c0001t0006g0212 others(1): Show |
7 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-1138C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374769 | |||||||
chr2:102374777 | CA | C | 78 | a0001c0001t0001g0069 a0001c0001t0005g0142 a0001c0002t0002g0001 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.469-1117delA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 102374777 | ||||||
chr2:102374909 | G | A | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.469-998G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102374909 | |||||||
chr2:102375326 | A | T | 39 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0003g0005 others(36): Show |
70 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.469-581A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102375326 | |||||||
chr2:102375418 | G | T | 1 | a0001c0002t0036g0136 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.469-489G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102375418 | |||||||
chr2:102375450 | G | A | 1 | a0001c0002t0035g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.469-457G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102375450 | |||||||
chr2:102375619 | A | G | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.469-288A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102375619 | |||||||
chr2:102375793 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.469-114A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 4/10 | chr2 | 102375793 | |||||||
chr2:102376215 | T | C | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.625+152T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102376215 | |||||||
chr2:102376346 | G | T | 32 | a0001c0001t0006g0021 a0001c0001t0006g0046 a0001c0001t0006g0047 others(29): Show |
41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.625+283G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102376346 | |||||||
chr2:102376419 | G | A | 1 | a0001c0002t0002g0130 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.625+356G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102376419 | |||||||
chr2:102376579 | G | T | 12 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(9): Show |
17 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.625+516G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102376579 | |||||||
chr2:102376619 | T | C | 1 | a0001c0002t0002g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.625+556T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102376619 | |||||||
chr2:102376701 | A | C | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.625+638A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102376701 | |||||||
chr2:102377015 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.625+952G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102377015 | |||||||
chr2:102377097 | G | A | 3 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 |
6 | HG01891.hp2 HG02257.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+1034G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102377097 | |||||||
chr2:102377491 | T | A | 4 | a0001c0003t0007g0190 a0001c0003t0007g0191 a0001c0003t0007g0192 others(1): Show |
4 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.625+1428T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102377491 | |||||||
chr2:102377596 | A | G | 171 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(168): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.625+1533A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102377596 | |||||||
chr2:102377791 | C | G | 1 | a0001c0001t0006g0049 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.625+1728C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102377791 | |||||||
chr2:102377873 | C | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.625+1810C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102377873 | |||||||
chr2:102378030 | T | C | 2 | a0001c0002t0004g0033 a0001c0002t0023g0033 |
2 | HG02523.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.625+1967T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378030 | |||||||
chr2:102378094 | T | C | 1 | a0001c0001t0001g0025 | 2 | NA18941.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.625+2031T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378094 | |||||||
chr2:102378254 | G | A | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.625+2191G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378254 | |||||||
chr2:102378346 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
5 | HG02015.hp1 HG02602.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.625+2283G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378346 | |||||||
chr2:102378392 | G | A | 3 | a0001c0001t0013g0208 a0001c0001t0018g0202 a0001c0001t0018g0209 |
3 | HG02559.hp2 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.625+2329G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378392 | |||||||
chr2:102378424 | A | G | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.625+2361A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378424 | |||||||
chr2:102378560 | G | A | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.625+2497G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378560 | |||||||
chr2:102378851 | G | A | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.626-2769G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378851 | |||||||
chr2:102378859 | C | T | 5 | a0001c0001t0001g0066 a0001c0002t0012g0088 a0001c0002t0012g0089 others(2): Show |
5 | HG01192.hp2 HG01261.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.626-2761C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102378859 | |||||||
chr2:102379140 | C | G | 37 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
68 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.626-2480C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102379140 | |||||||
chr2:102379182 | G | T | 1 | a0001c0003t0007g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.626-2438G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102379182 | |||||||
chr2:102379444 | C | CA | 49 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0157 others(46): Show |
83 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.626-2154dupA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 102379444 | ||||||
chr2:102379444 | CA | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0077 others(5): Show |
8 | HG01099.hp1 HG01106.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.626-2154delA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 102379444 | ||||||
chr2:102379444 | CAAAAAAA others(5): Show |
C | 45 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(42): Show |
59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.626-2165_626-2154d others(14): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 102379444 | ||||||
chr2:102379562 | C | T | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.626-2058C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102379562 | |||||||
chr2:102379677 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0086 |
3 | HG02080.hp2 NA18955.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.626-1943G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102379677 | |||||||
chr2:102379885 | G | A | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.626-1735G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102379885 | |||||||
chr2:102380047 | C | T | 1 | a0001c0002t0002g0128 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.626-1573C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380047 | |||||||
chr2:102380063 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.626-1557A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380063 | |||||||
chr2:102380154 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.626-1466G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380154 | |||||||
chr2:102380164 | C | CA | 27 | a0001c0002t0002g0004 a0001c0002t0002g0030 a0001c0002t0002g0034 others(24): Show |
40 | HG00423.hp1 HG01106.hp2 HG02080.hp1 others(37): Show |
intron_variant | MODIFIER | c.626-1455dupA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 102380164 | ||||||
chr2:102380274 | G | T | 1 | a0001c0006t0001g0064 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.626-1346G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380274 | |||||||
chr2:102380345 | C | T | 71 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(68): Show |
105 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.626-1275C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380345 | |||||||
chr2:102380412 | C | T | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.626-1208C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380412 | |||||||
chr2:102380478 | G | A | 1 | a0001c0001t0010g0180 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.626-1142G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380478 | |||||||
chr2:102380530 | A | G | 3 | a0001c0001t0013g0208 a0001c0001t0018g0202 a0001c0001t0018g0209 |
3 | HG02559.hp2 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.626-1090A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380530 | |||||||
chr2:102380591 | C | T | 9 | a0001c0001t0003g0006 a0001c0001t0003g0041 a0001c0001t0003g0172 others(6): Show |
19 | HG00099.hp2 HG00741.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.626-1029C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380591 | |||||||
chr2:102380691 | C | T | 1 | a0001c0002t0004g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.626-929C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380691 | |||||||
chr2:102380714 | A | T | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.626-906A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102380714 | |||||||
chr2:102381035 | T | C | 1 | a0001c0001t0003g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.626-585T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102381035 | |||||||
chr2:102381063 | G | A | 1 | a0001c0003t0007g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.626-557G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102381063 | |||||||
chr2:102381260 | G | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.626-360G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102381260 | |||||||
chr2:102381261 | C | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.626-359C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102381261 | |||||||
chr2:102381273 | G | T | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.626-347G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102381273 | |||||||
chr2:102381343 | C | T | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.626-277C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102381343 | |||||||
chr2:102381424 | C | A | 37 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
68 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.626-196C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 5/10 | chr2 | 102381424 | |||||||
chr2:102381755 | A | T | 1 | a0001c0002t0002g0210 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.688+73A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102381755 | |||||||
chr2:102381819 | A | G | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.688+137A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102381819 | |||||||
chr2:102381946 | T | A | 2 | a0001c0002t0002g0014 a0001c0002t0002g0109 |
6 | NA18978.hp1 NA18982.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+264T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102381946 | |||||||
chr2:102381995 | G | A | 1 | a0001c0001t0003g0163 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.688+313G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102381995 | |||||||
chr2:102382038 | C | T | 1 | a0001c0002t0002g0032 | 2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.688+356C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382038 | |||||||
chr2:102382054 | C | G | 2 | a0001c0002t0002g0121 a0001c0002t0002g0122 |
2 | HG02258.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.688+372C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382054 | |||||||
chr2:102382085 | C | T | 1 | a0001c0001t0005g0145 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.688+403C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382085 | |||||||
chr2:102382090 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.688+408C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382090 | |||||||
chr2:102382154 | T | G | 1 | a0001c0001t0005g0147 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.688+472T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382154 | |||||||
chr2:102382254 | G | A | 1 | a0001c0001t0003g0172 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.688+572G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382254 | |||||||
chr2:102382514 | A | C | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.688+832A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382514 | |||||||
chr2:102382605 | T | A | 1 | a0001c0002t0021g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.688+923T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382605 | |||||||
chr2:102382852 | A | G | 73 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(70): Show |
108 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.688+1170A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382852 | |||||||
chr2:102382943 | C | A | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.688+1261C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102382943 | |||||||
chr2:102383039 | T | C | 3 | a0001c0001t0003g0040 a0001c0001t0003g0170 a0001c0001t0003g0176 |
4 | NA18979.hp2 NA18984.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+1357T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102383039 | |||||||
chr2:102383060 | A | G | 45 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(42): Show |
59 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.688+1378A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102383060 | |||||||
chr2:102383477 | T | C | 1 | a0001c0001t0015g0094 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.689-1401T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102383477 | |||||||
chr2:102383492 | T | C | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.689-1386T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102383492 | |||||||
chr2:102383493 | C | T | 12 | a0001c0001t0006g0049 a0001c0001t0013g0208 a0001c0001t0018g0202 others(9): Show |
16 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.689-1385C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102383493 | |||||||
chr2:102383767 | A | C | 1 | a0001c0001t0001g0009 | 7 | NA18945.hp2 NA18975.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.689-1111A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102383767 | |||||||
chr2:102384232 | A | G | 1 | a0001c0002t0022g0133 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.689-646A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102384232 | |||||||
chr2:102384300 | C | T | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.689-578C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102384300 | |||||||
chr2:102384378 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.689-500T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102384378 | |||||||
chr2:102384381 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.689-497T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102384381 | |||||||
chr2:102384388 | T | C | 1 | a0003c0005t0020g0045 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.689-490T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102384388 | |||||||
chr2:102384408 | T | G | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.689-470T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102384408 | |||||||
chr2:102384529 | AATTT | A | 1 | a0001c0001t0008g0019 | 3 | HG02280.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.689-347_689-344del others(4): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 102384529 | ||||||
chr2:102384834 | C | A | 12 | a0001c0001t0006g0049 a0001c0001t0013g0208 a0001c0001t0018g0202 others(9): Show |
16 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.689-44C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102384834 | |||||||
chr2:102384851 | A | G | 4 | a0001c0003t0007g0190 a0001c0003t0007g0191 a0001c0003t0007g0192 others(1): Show |
4 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.689-27A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 6/10 | chr2 | 102384851 | |||||||
chr2:102385001 | A | G | 1 | a0001c0002t0002g0120 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.809+3A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385001 | |||||||
chr2:102385130 | C | A | 1 | a0001c0002t0002g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.809+132C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385130 | |||||||
chr2:102385138 | A | G | 20 | a0001c0001t0007g0168 a0001c0001t0008g0179 a0001c0001t0008g0182 others(17): Show |
22 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.809+140A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385138 | |||||||
chr2:102385190 | C | T | 12 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(9): Show |
17 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.809+192C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385190 | |||||||
chr2:102385317 | G | C | 1 | a0001c0003t0007g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.809+319G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385317 | |||||||
chr2:102385523 | C | T | 1 | a0001c0002t0002g0103 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.809+525C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385523 | |||||||
chr2:102385734 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.809+736G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385734 | |||||||
chr2:102385935 | A | G | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.810-926A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385935 | |||||||
chr2:102385981 | G | C | 1 | a0001c0002t0002g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.810-880G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102385981 | |||||||
chr2:102386180 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.810-681C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102386180 | |||||||
chr2:102386235 | T | C | 1 | a0001c0002t0002g0148 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.810-626T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102386235 | |||||||
chr2:102386375 | C | T | 1 | a0001c0001t0008g0019 | 3 | HG02280.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.810-486C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102386375 | |||||||
chr2:102386434 | G | A | 1 | a0001c0001t0008g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.810-427G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102386434 | |||||||
chr2:102386526 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.810-335C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102386526 | |||||||
chr2:102386574 | A | C | 4 | a0001c0001t0006g0021 a0001c0001t0006g0048 a0001c0001t0006g0212 others(1): Show |
7 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.810-287A>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102386574 | |||||||
chr2:102386583 | T | C | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.810-278T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102386583 | |||||||
chr2:102386805 | C | A | 46 | a0001c0002t0002g0001 a0001c0002t0002g0011 a0001c0002t0002g0014 others(43): Show |
67 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.810-56C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 7/10 | chr2 | 102386805 | |||||||
chr2:102387018 | T | G | 1 | a0001c0003t0007g0194 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.949+18T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387018 | |||||||
chr2:102387054 | G | A | 1 | a0001c0001t0006g0049 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.949+54G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387054 | |||||||
chr2:102387090 | C | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG00438.hp2 HG00621.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.949+90C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387090 | |||||||
chr2:102387242 | G | A | 1 | a0001c0002t0002g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.949+242G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387242 | |||||||
chr2:102387249 | G | A | 12 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(9): Show |
17 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.949+249G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387249 | |||||||
chr2:102387496 | G | C | 3 | a0001c0001t0013g0208 a0001c0001t0018g0202 a0001c0001t0018g0209 |
3 | HG02559.hp2 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.949+496G>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387496 | |||||||
chr2:102387501 | C | A | 37 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
68 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.949+501C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387501 | |||||||
chr2:102387546 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.949+546G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387546 | |||||||
chr2:102387680 | C | G | 2 | a0001c0002t0002g0129 a0001c0002t0002g0132 |
2 | NA19000.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.949+680C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102387680 | |||||||
chr2:102388064 | A | AACATGCA others(15): Show |
1 | a0001c0002t0023g0119 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.949+1068_949+1089d others(24): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 102388064 | ||||||
chr2:102388333 | T | G | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.949+1333T>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102388333 | |||||||
chr2:102388425 | G | T | 1 | a0001c0001t0008g0187 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.949+1425G>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102388425 | |||||||
chr2:102388498 | T | C | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.949+1498T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102388498 | |||||||
chr2:102388693 | C | A | 2 | a0001c0001t0008g0019 a0001c0001t0008g0197 |
4 | HG02280.hp1 HG03540.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.950-1363C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102388693 | |||||||
chr2:102388870 | A | G | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.950-1186A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102388870 | |||||||
chr2:102389035 | T | A | 1 | a0003c0005t0020g0045 | 2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.950-1021T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389035 | |||||||
chr2:102389187 | T | A | 1 | a0001c0002t0004g0115 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.950-869T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389187 | |||||||
chr2:102389207 | C | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0169 |
3 | HG01167.hp1 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.950-849C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389207 | |||||||
chr2:102389382 | T | A | 1 | a0001c0001t0008g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.950-674T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389382 | |||||||
chr2:102389588 | C | A | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.950-468C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389588 | |||||||
chr2:102389644 | A | G | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.950-412A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389644 | |||||||
chr2:102389717 | C | T | 1 | a0001c0002t0035g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.950-339C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389717 | |||||||
chr2:102389784 | C | T | 1 | a0001c0001t0003g0165 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.950-272C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389784 | |||||||
chr2:102389927 | A | G | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.950-129A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389927 | |||||||
chr2:102389988 | C | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.950-68C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102389988 | |||||||
chr2:102390036 | T | C | 1 | a0001c0001t0009g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.950-20T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 8/10 | chr2 | 102390036 | |||||||
chr2:102390484 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1111+267G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102390484 | |||||||
chr2:102390591 | C | T | 22 | a0001c0002t0002g0004 a0001c0002t0002g0030 a0001c0002t0002g0035 others(19): Show |
34 | HG00423.hp1 HG01106.hp2 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.1111+374C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102390591 | |||||||
chr2:102390760 | T | C | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1111+543T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102390760 | |||||||
chr2:102390761 | G | A | 1 | a0001c0001t0008g0184 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1111+544G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102390761 | |||||||
chr2:102390804 | G | A | 1 | a0001c0003t0007g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1111+587G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102390804 | |||||||
chr2:102390839 | A | G | 1 | a0001c0001t0015g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1111+622A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102390839 | |||||||
chr2:102390934 | C | CAAAA | 59 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(56): Show |
98 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1111+730_1111+733d others(6): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102390934 | ||||||
chr2:102390934 | C | CAAAAA | 17 | a0001c0001t0003g0159 a0001c0001t0003g0164 a0001c0001t0006g0021 others(14): Show |
24 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1111+729_1111+733d others(7): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102390934 | ||||||
chr2:102390934 | C | CAAAAAA | 16 | a0001c0001t0006g0049 a0001c0001t0007g0168 a0001c0001t0008g0182 others(13): Show |
19 | HG00099.hp1 HG00735.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1111+728_1111+733d others(8): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102390934 | ||||||
chr2:102390934 | C | CAAAAAAA others(4): Show |
5 | a0001c0002t0002g0122 a0001c0002t0002g0155 a0001c0002t0004g0118 others(2): Show |
5 | HG01943.hp2 HG02258.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+723_1111+733d others(13): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102390934 | ||||||
chr2:102390934 | C | CAAAAAAA others(5): Show |
53 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0014 others(50): Show |
82 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1111+722_1111+733d others(14): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102390934 | ||||||
chr2:102390934 | C | CAAAAAAA others(6): Show |
17 | a0001c0002t0002g0011 a0001c0002t0002g0031 a0001c0002t0002g0035 others(14): Show |
22 | HG01261.hp1 HG01346.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.1111+721_1111+733d others(15): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102390934 | ||||||
chr2:102390934 | C | CAAAAAAA others(7): Show |
3 | a0001c0002t0012g0088 a0001c0002t0035g0200 a0003c0005t0020g0045 |
4 | HG02109.hp1 HG02280.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+720_1111+733d others(16): Show |
IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102390934 | ||||||
chr2:102390951 | G | A | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1111+734G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102390951 | |||||||
chr2:102391107 | T | C | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1111+890T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391107 | |||||||
chr2:102391163 | A | G | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1111+946A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391163 | |||||||
chr2:102391232 | G | GC | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1111+1021dupC | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102391232 | ||||||
chr2:102391234 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1111+1017C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391234 | |||||||
chr2:102391255 | G | A | 1 | a0001c0002t0004g0134 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1111+1038G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391255 | |||||||
chr2:102391277 | T | C | 2 | a0001c0002t0002g0154 a0001c0002t0002g0155 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111+1060T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391277 | |||||||
chr2:102391333 | A | T | 1 | a0001c0002t0012g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1111+1116A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391333 | |||||||
chr2:102391395 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1111+1178C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391395 | |||||||
chr2:102391416 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1111+1199A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391416 | |||||||
chr2:102391577 | A | G | 9 | a0001c0001t0003g0005 a0001c0001t0003g0040 a0001c0001t0003g0164 others(6): Show |
18 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.1111+1360A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391577 | |||||||
chr2:102391627 | A | G | 5 | a0001c0003t0007g0190 a0001c0003t0007g0191 a0001c0003t0007g0192 others(2): Show |
5 | HG02572.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111+1410A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391627 | |||||||
chr2:102391660 | C | T | 1 | a0001c0002t0035g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1111+1443C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391660 | |||||||
chr2:102391910 | AT | A | 10 | a0001c0001t0006g0049 a0001c0001t0013g0208 a0001c0003t0007g0018 others(7): Show |
14 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111+1697delT | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102391910 | ||||||
chr2:102391917 | G | A | 1 | a0001c0002t0030g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1111+1700G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102391917 | |||||||
chr2:102392139 | A | T | 1 | a0001c0001t0006g0206 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1111+1922A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392139 | |||||||
chr2:102392166 | G | A | 1 | a0001c0002t0002g0116 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1111+1949G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392166 | |||||||
chr2:102392208 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1111+1991A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392208 | |||||||
chr2:102392250 | T | C | 172 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(169): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1111+2033T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392250 | |||||||
chr2:102392254 | C | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1111+2037C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392254 | |||||||
chr2:102392420 | A | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0069 others(1): Show |
15 | HG00408.hp2 NA18953.hp2 NA18959.hp2 others(12): Show |
intron_variant | MODIFIER | c.1112-2049A>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392420 | |||||||
chr2:102392509 | C | G | 78 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(75): Show |
113 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1112-1960C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392509 | |||||||
chr2:102392748 | A | G | 1 | a0001c0002t0002g0109 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1112-1721A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392748 | |||||||
chr2:102392894 | C | G | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1112-1575C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392894 | |||||||
chr2:102392952 | A | G | 4 | a0001c0001t0003g0006 a0001c0001t0003g0172 a0001c0001t0003g0174 others(1): Show |
11 | HG00099.hp2 HG00741.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112-1517A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102392952 | |||||||
chr2:102393077 | C | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1112-1392C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102393077 | |||||||
chr2:102393135 | G | A | 2 | a0001c0002t0002g0031 a0001c0002t0002g0102 |
3 | HG03942.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1112-1334G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102393135 | |||||||
chr2:102393202 | G | A | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1112-1267G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102393202 | |||||||
chr2:102393270 | GA | G | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1112-1197delA | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 102393270 | ||||||
chr2:102393319 | A | G | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1112-1150A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102393319 | |||||||
chr2:102393369 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1112-1100T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102393369 | |||||||
chr2:102393434 | A | G | 39 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(36): Show |
70 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1112-1035A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102393434 | |||||||
chr2:102393648 | T | A | 1 | a0001c0001t0013g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1112-821T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102393648 | |||||||
chr2:102393933 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0065 others(2): Show |
16 | HG00408.hp2 HG00423.hp2 NA18953.hp2 others(13): Show |
intron_variant | MODIFIER | c.1112-536T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102393933 | |||||||
chr2:102394034 | T | A | 2 | a0001c0002t0002g0121 a0001c0002t0002g0122 |
2 | HG02258.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1112-435T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102394034 | |||||||
chr2:102394070 | G | A | 71 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(68): Show |
105 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1112-399G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102394070 | |||||||
chr2:102394128 | C | A | 72 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(69): Show |
107 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1112-341C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102394128 | |||||||
chr2:102394234 | C | T | 2 | a0001c0002t0012g0089 a0001c0002t0012g0090 |
2 | HG01261.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1112-235C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102394234 | |||||||
chr2:102394452 | C | T | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1112-17C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 9/10 | chr2 | 102394452 | |||||||
chr2:102394726 | A | G | 1 | a0001c0001t0014g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1270+99A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102394726 | |||||||
chr2:102394775 | G | A | 5 | a0001c0002t0012g0088 a0001c0002t0012g0089 a0001c0002t0012g0090 others(2): Show |
5 | HG01261.hp1 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+148G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102394775 | |||||||
chr2:102394777 | T | C | 94 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(91): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1270+150T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102394777 | |||||||
chr2:102394843 | C | T | 8 | a0001c0003t0007g0018 a0001c0003t0007g0043 a0001c0003t0007g0189 others(5): Show |
11 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1270+216C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102394843 | |||||||
chr2:102394869 | G | A | 12 | a0001c0001t0005g0015 a0001c0001t0005g0017 a0001c0001t0005g0036 others(9): Show |
17 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1270+242G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102394869 | |||||||
chr2:102394915 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0070 |
6 | HG00609.hp2 NA18961.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1270+288A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102394915 | |||||||
chr2:102395092 | C | T | 77 | a0001c0001t0006g0021 a0001c0001t0006g0046 a0001c0001t0006g0047 others(74): Show |
116 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1270+465C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395092 | |||||||
chr2:102395095 | A | G | 1 | a0001c0002t0004g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1270+468A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395095 | |||||||
chr2:102395146 | G | A | 1 | a0001c0002t0004g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1270+519G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395146 | |||||||
chr2:102395181 | GT | G | 11 | a0001c0001t0006g0049 a0001c0001t0013g0208 a0001c0002t0035g0200 others(8): Show |
15 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1270+562delT | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 102395181 | ||||||
chr2:102395189 | T | A | 1 | a0001c0001t0008g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1270+562T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395189 | |||||||
chr2:102395315 | G | A | 1 | a0001c0001t0013g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1270+688G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395315 | |||||||
chr2:102395360 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1270+733T>C | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395360 | |||||||
chr2:102395412 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1270+785T>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395412 | |||||||
chr2:102395678 | G | A | 1 | a0001c0001t0010g0185 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1271-853G>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395678 | |||||||
chr2:102395777 | C | G | 10 | a0001c0001t0006g0049 a0001c0001t0013g0208 a0001c0003t0007g0018 others(7): Show |
14 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1271-754C>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102395777 | |||||||
chr2:102396214 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0065 others(80): Show |
129 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1271-317C>T | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102396214 | |||||||
chr2:102396321 | C | A | 39 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(36): Show |
70 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1271-210C>A | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102396321 | |||||||
chr2:102396442 | A | G | 7 | a0001c0001t0006g0021 a0001c0001t0006g0046 a0001c0001t0006g0047 others(4): Show |
12 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1271-89A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102396442 | |||||||
chr2:102396467 | A | G | 10 | a0001c0001t0006g0049 a0001c0001t0013g0208 a0001c0003t0007g0018 others(7): Show |
14 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1271-64A>G | IL18R1 | ENSG00000115604.12 | transcript | ENST00000233957.7 | protein_coding | 10/10 | chr2 | 102396467 |