Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 170482 |
| ensemblid | ENSG00000198178.11 |
| hgncid | 13258 |
| symbol | CLEC4C |
| name | C-type lectin domain family 4 member C |
| refseq_nuc | NM_001371390.1 |
| refseq_prot | NP_001358319.1 |
| ensembl_nuc | ENST00000360345.8 |
| ensembl_prot | ENSP00000353500.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 7729383 |
| end | 7747375 |
| strand | - |
| ver | v1.2 |
| region | chr12:7729383-7747375 |
| region5000 | chr12:7724383-7752375 |
| regionname0 | CLEC4C_chr12_7729383_7747375 |
| regionname5000 | CLEC4C_chr12_7724383_7752375 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 213 | 336 | 80 | 45 | 161 | 9 | 39 | 127 | CLEC4C_chr12_7724383_7752375 | CLEC4C | MVPEE others(208): Show |
chr12 | 7724383 | 7752375 |
| a0002 | 0/0 | 213 | 94 | 3 | 32 | 47 | 5 | 7 | 39 | CLEC4C_chr12_7724383_7752375 | CLEC4C | MVPEE others(208): Show |
chr12 | 7724383 | 7752375 |
| a0003 | 0/0 | 213 | 15 | 12 | 3 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | MVPEE others(208): Show |
chr12 | 7724383 | 7752375 |
| a0004 | 0/0 | 213 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | MVPEE others(208): Show |
chr12 | 7724383 | 7752375 |
| a0005 | 0/0 | 213 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | MVPEE others(208): Show |
chr12 | 7724383 | 7752375 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 639 | 334 | 78 | 45 | 161 | 9 | 39 | CLEC4C_chr12_7724383_7752375 | CLEC4C | ATGGT others(634): Show |
chr12 | 7724383 | 7752375 | ||
| a0001c0005 | 0/0 | 639 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | ATGGT others(634): Show |
chr12 | 7724383 | 7752375 | ||
| a0002c0002 | 0/0 | 639 | 94 | 3 | 32 | 47 | 5 | 7 | CLEC4C_chr12_7724383_7752375 | CLEC4C | ATGGT others(634): Show |
chr12 | 7724383 | 7752375 | ||
| a0003c0003 | 0/0 | 639 | 15 | 12 | 3 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | ATGGT others(634): Show |
chr12 | 7724383 | 7752375 | ||
| a0004c0004 | 0/0 | 639 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | ATGGT others(634): Show |
chr12 | 7724383 | 7752375 | ||
| a0005c0006 | 0/0 | 639 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | ATGGT others(634): Show |
chr12 | 7724383 | 7752375 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 882 | 68 | 21 | 1 | 38 | 0 | 7 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(877): Show |
chr12 | 7724383 | 7752375 |
| a0001c0001t0002 | 0/0 | 874 | 93 | 15 | 23 | 38 | 6 | 11 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(869): Show |
chr12 | 7724383 | 7752375 |
| a0001c0001t0003 | 0/1 | 874 | 75 | 10 | 5 | 54 | 1 | 4 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(869): Show |
chr12 | 7724383 | 7752375 |
| a0001c0001t0004 | 0/0 | 890 | 65 | 26 | 7 | 20 | 1 | 11 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(885): Show |
chr12 | 7724383 | 7752375 |
| a0001c0001t0005 | 0/0 | 882 | 26 | 1 | 8 | 10 | 1 | 6 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(877): Show |
chr12 | 7724383 | 7752375 |
| a0001c0001t0006 | 0/0 | 882 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(877): Show |
chr12 | 7724383 | 7752375 |
| a0001c0001t0007 | 0/0 | 890 | 3 | 2 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(885): Show |
chr12 | 7724383 | 7752375 |
| a0001c0001t0009 | 0/0 | 874 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(869): Show |
chr12 | 7724383 | 7752375 |
| a0001c0005t0008 | 0/0 | 882 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(877): Show |
chr12 | 7724383 | 7752375 |
| a0002c0002t0001 | 0/0 | 882 | 94 | 3 | 32 | 47 | 5 | 7 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(877): Show |
chr12 | 7724383 | 7752375 |
| a0003c0003t0002 | 0/0 | 874 | 15 | 12 | 3 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(869): Show |
chr12 | 7724383 | 7752375 |
| a0004c0004t0002 | 0/0 | 874 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(869): Show |
chr12 | 7724383 | 7752375 |
| a0004c0004t0010 | 0/0 | 866 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(861): Show |
chr12 | 7724383 | 7752375 |
| a0005c0006t0006 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | GAAGT others(877): Show |
chr12 | 7724383 | 7752375 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 14 | 0 | 0 | 12 | 0 | 2 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0214 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0002 | 0/0 | 22 | 2 | 0 | 14 | 3 | 3 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0008 | 0/0 | 9 | 1 | 7 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0013 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0014 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0036 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0003 | 0/0 | 19 | 6 | 0 | 12 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0012 | 0/0 | 7 | 1 | 0 | 4 | 0 | 2 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0028 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0006 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0011 | 0/0 | 8 | 0 | 2 | 2 | 0 | 4 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0016 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0010 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0029 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0006g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0005t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0001c0005t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0001 | 0/0 | 27 | 0 | 13 | 9 | 3 | 2 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0005 | 0/0 | 10 | 1 | 0 | 9 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0003c0003t0002g0009 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0003c0003t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0003c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0003c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0003c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0003c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0003c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0004c0004t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0004c0004t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| a0005c0006t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | GBR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | GBR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0029 | EUR | FIN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0048 | EUR | FIN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0232 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0237 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01109 | hp2 | a0003 | c0003 | t0002 | g0009 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0126 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01169 | hp2 | a0003 | c0003 | t0002 | g0109 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0234 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0110 | EUR | IBS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0112 | EUR | IBS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0150 | EUR | IBS | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0090 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0228 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02055 | hp1 | a0003 | c0003 | t0002 | g0073 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | CDX | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | PEL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02615 | hp2 | a0004 | c0004 | t0010 | g0178 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02622 | hp2 | a0003 | c0003 | t0002 | g0071 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02647 | hp2 | a0001 | c0005 | t0008 | g0226 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0009 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0156 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0239 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02818 | hp2 | a0003 | c0003 | t0002 | g0009 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02886 | hp2 | a0005 | c0006 | t0006 | g0055 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02895 | hp1 | a0003 | c0003 | t0002 | g0108 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02896 | hp1 | a0003 | c0003 | t0002 | g0009 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02897 | hp2 | a0003 | c0003 | t0002 | g0009 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02922 | hp1 | a0004 | c0004 | t0002 | g0179 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02970 | hp2 | a0003 | c0003 | t0002 | g0009 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0091 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03225 | hp1 | a0003 | c0003 | t0002 | g0106 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03453 | hp2 | a0003 | c0003 | t0002 | g0009 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03486 | hp1 | a0001 | c0005 | t0008 | g0227 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0236 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0081 | SAS | BEB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0230 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0238 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18522 | hp1 | a0003 | c0003 | t0002 | g0009 | AFR | YRI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | YRI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18612 | hp1 | a0001 | c0001 | t0009 | g0054 | EAS | CHB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | YRI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | LWK | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | LWK | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20129 | hp1 | a0003 | c0003 | t0002 | g0009 | AFR | ASW | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ASW | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0025 | EUR | TSI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | GIH | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0051 | SAS | GIH | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | MSL | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | USA | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | USA | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | USA | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | USA | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | LWK | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0190 | REF | REF | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0214 | REF | REF | CLEC4C_chr12_7724383_7752375 | CLEC4C | chr12 | 7724383 | 7752375 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7729384 | G | A | 1 | a0001 | 3 | HG01952.hp1 HG02723.hp2 HG03041.hp1 |
splice_region_variant | LOW | c.*212C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | chr12 | 7729384 | |||||||
| chr12:7737444 | G | T | 1 | a0003 | 15 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
missense_variant | MODERATE | c.366C>A | p.Asn122Lys | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/6 | 393/882 | 366/642 | 122/213 | chr12 | 7737444 | |||
| chr12:7741460 | G | A | 1 | a0002 | 94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
missense_variant | MODERATE | c.196C>T | p.Pro66Ser | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/6 | 223/882 | 196/642 | 66/213 | chr12 | 7741460 | |||
| chr12:7741484 | A | C | 1 | a0004 | 2 | HG02615.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.172T>G | p.Leu58Val | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/6 | 199/882 | 172/642 | 58/213 | chr12 | 7741484 | |||
| chr12:7741511 | T | C | 1 | a0005 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.145A>G | p.Ser49Gly | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/6 | 172/882 | 145/642 | 49/213 | chr12 | 7741511 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7737480 | G | A | 1 | a0001c0005 | 2 | HG02647.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.330C>T | p.Asn110Asn | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/6 | 357/882 | 330/642 | 110/213 | chr12 | 7737480 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7729399 | A | C | 1 | a0001c0001t0003 | 74 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*197T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | 197 | chr12 | 7729399 | ||||||
| chr12:7729406 | G | GAATGAAT others(1): Show |
2 | a0001c0001t0004 a0001c0001t0007 |
68 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*182_*189dupTATTCA others(2): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | 189 | chr12 | 7729406 | ||||||
| chr12:7729406 | GAATGAAT others(1): Show |
G | 5 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(2): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*182_*189delTATTCA others(2): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | 182 | chr12 | 7729406 | ||||||
| chr12:7729406 | GAATGAAT others(9): Show |
G | 1 | a0004c0004t0010 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*174_*189delTATTCA others(10): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | 174 | chr12 | 7729406 | ||||||
| chr12:7729442 | G | A | 1 | a0001c0001t0005 | 26 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*154C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | 154 | chr12 | 7729442 | ||||||
| chr12:7729457 | T | C | 3 | a0001c0001t0006 a0001c0005t0008 a0005c0006t0006 |
6 | HG02647.hp2 HG02886.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*139A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | 139 | chr12 | 7729457 | ||||||
| chr12:7729508 | C | T | 1 | a0001c0001t0009 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | 88 | chr12 | 7729508 | ||||||
| chr12:7729524 | A | G | 2 | a0001c0001t0006 a0005c0006t0006 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*72T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 6/6 | 72 | chr12 | 7729524 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:7729746 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG01891.hp1 | splice_region_variant&intron_variant | LOW | c.498-6T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7729746 | |||||||
| chr12:7729951 | C | T | 2 | a0001c0001t0005g0228 a0001c0001t0005g0230 |
2 | HG02015.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.498-211G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7729951 | |||||||
| chr12:7729959 | C | G | 1 | a0001c0001t0004g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.498-219G>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7729959 | |||||||
| chr12:7729973 | T | C | 50 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(47): Show |
86 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.498-233A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7729973 | |||||||
| chr12:7730006 | A | C | 133 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0062 others(130): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.498-266T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730006 | |||||||
| chr12:7730099 | A | T | 39 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0026 others(36): Show |
74 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.498-359T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730099 | |||||||
| chr12:7730174 | C | T | 1 | a0001c0001t0004g0064 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.498-434G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730174 | |||||||
| chr12:7730244 | T | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.498-504A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730244 | |||||||
| chr12:7730354 | T | TA | 15 | a0001c0001t0005g0010 a0001c0001t0005g0029 a0001c0001t0005g0051 others(12): Show |
26 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.497+442dupT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730354 | |||||||
| chr12:7730383 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0168 others(6): Show |
13 | HG00558.hp2 HG02056.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+414C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730383 | |||||||
| chr12:7730499 | G | A | 116 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(113): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.497+298C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730499 | |||||||
| chr12:7730597 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0168 others(6): Show |
13 | HG00558.hp2 HG02056.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+200T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730597 | |||||||
| chr12:7730639 | T | TA | 42 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0062 others(39): Show |
59 | HG00280.hp1 HG00558.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.497+157dupT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730639 | |||||||
| chr12:7730639 | TA | T | 8 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0002g0084 others(5): Show |
8 | HG01081.hp2 HG01169.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.497+157delT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730639 | |||||||
| chr12:7730674 | C | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0168 others(6): Show |
13 | HG00558.hp2 HG02056.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.497+123G>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730674 | |||||||
| chr12:7730742 | C | A | 1 | a0001c0001t0006g0042 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.497+55G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 5/5 | chr12 | 7730742 | |||||||
| chr12:7731078 | A | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-166T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7731078 | |||||||
| chr12:7731239 | G | T | 1 | a0001c0001t0007g0090 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.382-327C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7731239 | |||||||
| chr12:7731254 | G | A | 30 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0062 others(27): Show |
45 | HG00280.hp1 HG00558.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.382-342C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7731254 | |||||||
| chr12:7731261 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0221 |
2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.382-349T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7731261 | |||||||
| chr12:7731755 | A | G | 44 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0003g0003 others(41): Show |
79 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.382-843T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7731755 | |||||||
| chr12:7732002 | ATGAACAC others(3): Show |
A | 1 | a0001c0001t0004g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.382-1100_382-1091d others(12): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732002 | |||||||
| chr12:7732018 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382-1106G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732018 | |||||||
| chr12:7732075 | G | T | 15 | a0001c0001t0005g0010 a0001c0001t0005g0029 a0001c0001t0005g0051 others(12): Show |
26 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-1163C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732075 | |||||||
| chr12:7732120 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.382-1208G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732120 | |||||||
| chr12:7732180 | A | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382-1268T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732180 | |||||||
| chr12:7732350 | AT | A | 8 | a0001c0001t0005g0029 a0001c0001t0005g0051 a0001c0001t0005g0231 others(5): Show |
11 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-1439delA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732350 | |||||||
| chr12:7732363 | A | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382-1451T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732363 | |||||||
| chr12:7732413 | GTGATCTC others(1534): Show |
G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382-3042_382-1502d others(2): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732413 | |||||||
| chr12:7732487 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.382-1575C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732487 | |||||||
| chr12:7732494 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.382-1582G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732494 | |||||||
| chr12:7732514 | G | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0016 a0001c0001t0004g0020 others(6): Show |
22 | HG00438.hp2 HG00597.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.382-1602C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732514 | |||||||
| chr12:7732787 | C | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0043 others(55): Show |
126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.382-1875G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732787 | |||||||
| chr12:7732798 | C | T | 236 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(233): Show |
442 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(439): Show |
intron_variant | MODIFIER | c.382-1886G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732798 | |||||||
| chr12:7732818 | G | A | 12 | a0001c0001t0004g0006 a0001c0001t0004g0016 a0001c0001t0004g0019 others(9): Show |
27 | HG00438.hp2 HG00597.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.382-1906C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732818 | |||||||
| chr12:7732851 | AG | A | 31 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0062 others(28): Show |
47 | HG00280.hp1 HG00558.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.382-1940delC | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732851 | |||||||
| chr12:7732881 | G | A | 1 | a0001c0001t0005g0236 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.382-1969C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7732881 | |||||||
| chr12:7733056 | G | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0043 others(55): Show |
126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.382-2144C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733056 | |||||||
| chr12:7733093 | G | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(87): Show |
174 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.382-2181C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733093 | |||||||
| chr12:7733341 | G | A | 3 | a0001c0001t0006g0042 a0001c0001t0006g0164 a0005c0006t0006g0055 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2429C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733341 | |||||||
| chr12:7733342 | C | A | 3 | a0001c0001t0006g0042 a0001c0001t0006g0164 a0005c0006t0006g0055 |
4 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2430G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733342 | |||||||
| chr12:7733433 | T | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.382-2521A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733433 | |||||||
| chr12:7733481 | C | CT | 13 | a0001c0001t0001g0082 a0001c0001t0002g0002 a0001c0001t0002g0014 others(10): Show |
16 | HG00673.hp2 HG01934.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.382-2570dupA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733481 | |||||||
| chr12:7733481 | C | CTT | 64 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0043 others(61): Show |
145 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.382-2571_382-2570d others(4): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733481 | |||||||
| chr12:7733481 | C | CTTT | 7 | a0001c0001t0004g0006 a0001c0001t0004g0056 a0001c0001t0004g0081 others(4): Show |
7 | HG02056.hp1 HG03225.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-2572_382-2570d others(5): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733481 | |||||||
| chr12:7733567 | C | T | 2 | a0001c0001t0004g0094 a0001c0001t0004g0095 |
2 | HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.382-2655G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733567 | |||||||
| chr12:7733568 | G | A | 2 | a0001c0001t0005g0051 a0001c0001t0005g0234 |
2 | HG01167.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.382-2656C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733568 | |||||||
| chr12:7733648 | A | ATTTTTTG others(190): Show |
1 | a0001c0001t0002g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.382-2737_382-2736i others(199): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733648 | |||||||
| chr12:7733648 | A | ATTTTTTG others(191): Show |
1 | a0001c0001t0002g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-2737_382-2736i others(200): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733648 | |||||||
| chr12:7733672 | G | A | 1 | a0001c0001t0003g0185 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.382-2760C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733672 | |||||||
| chr12:7733683 | A | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0107 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.382-2771T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733683 | |||||||
| chr12:7733685 | A | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0107 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.382-2773T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733685 | |||||||
| chr12:7733703 | A | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0107 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.382-2791T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733703 | |||||||
| chr12:7733716 | T | C | 2 | a0001c0001t0002g0014 a0001c0001t0002g0107 |
2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.382-2804A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733716 | |||||||
| chr12:7733855 | G | A | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
65 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.382-2943C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733855 | |||||||
| chr12:7733990 | TCAAG | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0031 a0001c0001t0002g0102 others(2): Show |
14 | HG01106.hp2 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.382-3082_382-3079d others(6): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7733990 | |||||||
| chr12:7734016 | C | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.382-3104G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734016 | |||||||
| chr12:7734026 | G | A | 1 | a0002c0002t0001g0135 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.382-3114C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734026 | |||||||
| chr12:7734080 | GA | G | 34 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(31): Show |
65 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.382-3169delT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734080 | |||||||
| chr12:7734081 | A | G | 1 | a0001c0001t0004g0092 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.382-3169T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734081 | |||||||
| chr12:7734085 | G | T | 1 | a0005c0006t0006g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.382-3173C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734085 | |||||||
| chr12:7734136 | G | A | 12 | a0001c0001t0004g0006 a0001c0001t0004g0016 a0001c0001t0004g0020 others(9): Show |
26 | HG00438.hp2 HG00597.hp1 HG02132.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-3224C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734136 | |||||||
| chr12:7734222 | C | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+3207G>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734222 | |||||||
| chr12:7734233 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+3196G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734233 | |||||||
| chr12:7734297 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.381+3132C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734297 | |||||||
| chr12:7734414 | T | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(53): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.381+3015A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734414 | |||||||
| chr12:7734437 | T | C | 1 | a0001c0001t0005g0237 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.381+2992A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734437 | |||||||
| chr12:7734466 | A | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2963T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734466 | |||||||
| chr12:7734552 | A | AT | 112 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0165 others(109): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.381+2876dupA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734552 | |||||||
| chr12:7734552 | AT | A | 8 | a0001c0001t0001g0158 a0001c0001t0001g0209 a0001c0001t0001g0222 others(5): Show |
8 | HG03195.hp2 NA18951.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+2876delA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734552 | |||||||
| chr12:7734587 | C | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2842G>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734587 | |||||||
| chr12:7734601 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2828G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734601 | |||||||
| chr12:7734674 | G | A | 3 | a0002c0002t0001g0023 a0002c0002t0001g0136 a0002c0002t0001g0143 |
5 | HG00741.hp1 HG01496.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+2755C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734674 | |||||||
| chr12:7734697 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2732A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734697 | |||||||
| chr12:7734713 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2716A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734713 | |||||||
| chr12:7734744 | C | T | 40 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0026 others(37): Show |
75 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.381+2685G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734744 | |||||||
| chr12:7734747 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.381+2682G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734747 | |||||||
| chr12:7734748 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.381+2681T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734748 | |||||||
| chr12:7734915 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2514G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734915 | |||||||
| chr12:7734966 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.381+2463G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7734966 | |||||||
| chr12:7735104 | G | C | 1 | a0001c0001t0001g0175 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.381+2325C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735104 | |||||||
| chr12:7735116 | A | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2313T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735116 | |||||||
| chr12:7735134 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.381+2295C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735134 | |||||||
| chr12:7735322 | G | GTAAAACC others(6): Show |
1 | a0001c0001t0001g0207 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.381+2094_381+2106d others(15): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735322 | |||||||
| chr12:7735364 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.381+2065C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735364 | |||||||
| chr12:7735372 | A | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2057T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735372 | |||||||
| chr12:7735373 | G | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+2056C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735373 | |||||||
| chr12:7735376 | G | A | 5 | a0001c0001t0005g0029 a0001c0001t0005g0231 a0001c0001t0005g0232 others(2): Show |
7 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+2053C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735376 | |||||||
| chr12:7735417 | C | T | 40 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0026 others(37): Show |
75 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.381+2012G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735417 | |||||||
| chr12:7735447 | A | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1982T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735447 | |||||||
| chr12:7735472 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.381+1957G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735472 | |||||||
| chr12:7735484 | T | C | 4 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+1945A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735484 | |||||||
| chr12:7735506 | G | GA | 36 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0036 others(33): Show |
49 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.381+1922dupT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735506 | |||||||
| chr12:7735506 | G | GAA | 47 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0082 others(44): Show |
112 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.381+1921_381+1922d others(4): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735506 | |||||||
| chr12:7735506 | G | GAAA | 10 | a0001c0001t0001g0027 a0001c0001t0001g0176 a0002c0002t0001g0038 others(7): Show |
13 | HG00423.hp2 HG01175.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.381+1920_381+1922d others(5): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735506 | |||||||
| chr12:7735506 | GA | G | 12 | a0001c0001t0001g0018 a0001c0001t0001g0172 a0001c0001t0001g0173 others(9): Show |
15 | HG00558.hp1 HG00558.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.381+1922delT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735506 | |||||||
| chr12:7735517 | A | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1912T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735517 | |||||||
| chr12:7735534 | C | T | 40 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0026 others(37): Show |
75 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.381+1895G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735534 | |||||||
| chr12:7735588 | C | T | 2 | a0001c0001t0002g0127 a0001c0001t0002g0128 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.381+1841G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735588 | |||||||
| chr12:7735646 | A | G | 1 | a0001c0001t0004g0081 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.381+1783T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735646 | |||||||
| chr12:7735704 | C | CTG | 60 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0043 others(57): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.381+1724_381+1725i others(4): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735704 | |||||||
| chr12:7735708 | G | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1721C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735708 | |||||||
| chr12:7735728 | A | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1701T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735728 | |||||||
| chr12:7735734 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1695A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735734 | |||||||
| chr12:7735821 | C | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1608G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735821 | |||||||
| chr12:7735959 | A | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0043 others(55): Show |
126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.381+1470T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7735959 | |||||||
| chr12:7736006 | A | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1423T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736006 | |||||||
| chr12:7736170 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1259A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736170 | |||||||
| chr12:7736197 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1232G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736197 | |||||||
| chr12:7736198 | G | A | 1 | a0001c0001t0003g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.381+1231C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736198 | |||||||
| chr12:7736202 | G | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1227C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736202 | |||||||
| chr12:7736237 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1192G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736237 | |||||||
| chr12:7736239 | TGCCATTG others(15): Show |
T | 1 | a0001c0001t0003g0193 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.381+1168_381+1189d others(24): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736239 | |||||||
| chr12:7736315 | A | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+1114T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736315 | |||||||
| chr12:7736440 | T | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+989A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736440 | |||||||
| chr12:7736525 | T | A | 1 | a0001c0001t0003g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.381+904A>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736525 | |||||||
| chr12:7736600 | G | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+829C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736600 | |||||||
| chr12:7736674 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+755G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736674 | |||||||
| chr12:7736691 | G | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+738C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736691 | |||||||
| chr12:7736772 | G | A | 1 | a0001c0001t0002g0035 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.381+657C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736772 | |||||||
| chr12:7736809 | A | C | 99 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(96): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.381+620T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736809 | |||||||
| chr12:7736819 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+610A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736819 | |||||||
| chr12:7736904 | A | G | 5 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0001c0001t0002g0099 others(2): Show |
5 | HG02040.hp2 NA18954.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+525T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736904 | |||||||
| chr12:7736955 | A | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+474T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736955 | |||||||
| chr12:7736997 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.381+432C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7736997 | |||||||
| chr12:7737002 | A | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+427T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737002 | |||||||
| chr12:7737060 | G | A | 40 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0026 others(37): Show |
75 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.381+369C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737060 | |||||||
| chr12:7737081 | A | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+348T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737081 | |||||||
| chr12:7737118 | C | A | 1 | a0001c0005t0008g0226 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.381+311G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737118 | |||||||
| chr12:7737232 | A | C | 3 | a0001c0005t0008g0226 a0001c0005t0008g0227 a0002c0002t0001g0151 |
3 | HG01192.hp1 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.381+197T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737232 | |||||||
| chr12:7737307 | T | G | 1 | a0002c0002t0001g0153 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.381+122A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737307 | |||||||
| chr12:7737324 | G | GT | 8 | a0001c0001t0002g0084 a0001c0001t0002g0110 a0001c0001t0004g0088 others(5): Show |
8 | HG01515.hp1 HG02056.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+104dupA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737324 | |||||||
| chr12:7737324 | GT | G | 52 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0165 others(49): Show |
91 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.381+104delA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737324 | |||||||
| chr12:7737381 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.381+48A>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 4/5 | chr12 | 7737381 | |||||||
| chr12:7737598 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.236-24C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7737598 | |||||||
| chr12:7737847 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.236-273C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7737847 | |||||||
| chr12:7737882 | A | C | 4 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-308T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7737882 | |||||||
| chr12:7737953 | C | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0043 others(55): Show |
126 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.236-379G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7737953 | |||||||
| chr12:7738003 | AAAGACAA others(7): Show |
A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-443_236-430del others(14): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738003 | |||||||
| chr12:7738090 | G | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-516C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738090 | |||||||
| chr12:7738180 | T | G | 64 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0043 others(61): Show |
133 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.236-606A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738180 | |||||||
| chr12:7738183 | C | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-609G>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738183 | |||||||
| chr12:7738262 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.236-688G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738262 | |||||||
| chr12:7738263 | G | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-689C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738263 | |||||||
| chr12:7738344 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-770G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738344 | |||||||
| chr12:7738347 | G | A | 1 | a0001c0001t0007g0093 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.236-773C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738347 | |||||||
| chr12:7738374 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-800G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738374 | |||||||
| chr12:7738634 | A | G | 69 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(66): Show |
141 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.236-1060T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738634 | |||||||
| chr12:7738754 | A | G | 93 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(90): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.236-1180T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738754 | |||||||
| chr12:7738810 | A | G | 170 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(167): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.236-1236T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738810 | |||||||
| chr12:7738879 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.236-1305A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738879 | |||||||
| chr12:7738895 | T | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-1321A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738895 | |||||||
| chr12:7738919 | C | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(21): Show |
44 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.236-1345G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738919 | |||||||
| chr12:7738956 | T | TC | 13 | a0001c0001t0001g0083 a0001c0001t0001g0171 a0001c0001t0001g0177 others(10): Show |
13 | HG00642.hp1 HG01192.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-1383dupG | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738956 | |||||||
| chr12:7738962 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-1388G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7738962 | |||||||
| chr12:7739030 | G | A | 2 | a0001c0001t0004g0215 a0001c0001t0004g0223 |
2 | HG00738.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.236-1456C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739030 | |||||||
| chr12:7739052 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.236-1478T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739052 | |||||||
| chr12:7739095 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.236-1521T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739095 | |||||||
| chr12:7739197 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-1623A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739197 | |||||||
| chr12:7739199 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.236-1625C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739199 | |||||||
| chr12:7739206 | G | A | 1 | a0001c0001t0004g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.236-1632C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739206 | |||||||
| chr12:7739217 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.236-1643T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739217 | |||||||
| chr12:7739234 | T | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-1660A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739234 | |||||||
| chr12:7739237 | G | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-1663C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739237 | |||||||
| chr12:7739238 | G | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-1664C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739238 | |||||||
| chr12:7739257 | T | C | 44 | a0001c0005t0008g0226 a0001c0005t0008g0227 a0002c0002t0001g0001 others(41): Show |
96 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.236-1683A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739257 | |||||||
| chr12:7739301 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.236-1727G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739301 | |||||||
| chr12:7739390 | G | C | 3 | a0001c0001t0003g0045 a0001c0001t0003g0184 a0001c0001t0003g0188 |
4 | NA18963.hp2 NA18968.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-1816C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739390 | |||||||
| chr12:7739400 | C | T | 1 | a0003c0003t0002g0106 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.236-1826G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739400 | |||||||
| chr12:7739406 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-1832A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739406 | |||||||
| chr12:7739430 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.236-1856A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739430 | |||||||
| chr12:7739444 | T | TAA | 4 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-1871_236-1870i others(4): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739444 | |||||||
| chr12:7739445 | T | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-1871A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739445 | |||||||
| chr12:7739461 | TC | T | 40 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0026 others(37): Show |
75 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.236-1888delG | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739461 | |||||||
| chr12:7739516 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG02300.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.235+1905G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739516 | |||||||
| chr12:7739517 | G | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.235+1904C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739517 | |||||||
| chr12:7739548 | G | C | 1 | a0001c0005t0008g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.235+1873C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739548 | |||||||
| chr12:7739690 | CT | C | 45 | a0001c0001t0001g0165 a0001c0005t0008g0226 a0001c0005t0008g0227 others(42): Show |
97 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.235+1730delA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739690 | |||||||
| chr12:7739711 | A | G | 1 | a0001c0001t0004g0063 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.235+1710T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739711 | |||||||
| chr12:7739846 | A | AT | 66 | a0001c0001t0001g0181 a0001c0001t0002g0002 a0001c0001t0002g0008 others(63): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.235+1574dupA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739846 | |||||||
| chr12:7739846 | A | ATT | 6 | a0001c0001t0002g0033 a0001c0001t0002g0052 a0001c0001t0002g0068 others(3): Show |
7 | HG03225.hp1 HG03486.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+1573_235+1574d others(4): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739846 | |||||||
| chr12:7739996 | G | A | 16 | a0001c0001t0001g0229 a0001c0001t0005g0010 a0001c0001t0005g0029 others(13): Show |
27 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.235+1425C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7739996 | |||||||
| chr12:7740020 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.235+1401C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740020 | |||||||
| chr12:7740152 | G | A | 223 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(220): Show |
428 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(425): Show |
intron_variant | MODIFIER | c.235+1269C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740152 | |||||||
| chr12:7740206 | G | A | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.235+1215C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740206 | |||||||
| chr12:7740329 | G | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0218 |
3 | HG02145.hp1 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.235+1092C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740329 | |||||||
| chr12:7740341 | G | A | 12 | a0001c0001t0004g0006 a0001c0001t0004g0016 a0001c0001t0004g0019 others(9): Show |
27 | HG00438.hp2 HG00597.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.235+1080C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740341 | |||||||
| chr12:7740465 | C | T | 45 | a0001c0001t0001g0165 a0001c0005t0008g0226 a0001c0005t0008g0227 others(42): Show |
97 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.235+956G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740465 | |||||||
| chr12:7740470 | C | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.235+951G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740470 | |||||||
| chr12:7740529 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.235+892C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740529 | |||||||
| chr12:7740561 | C | A | 3 | a0001c0001t0001g0165 a0001c0005t0008g0226 a0001c0005t0008g0227 |
3 | HG02647.hp2 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.235+860G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740561 | |||||||
| chr12:7740601 | C | T | 238 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(235): Show |
444 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(441): Show |
intron_variant | MODIFIER | c.235+820G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740601 | |||||||
| chr12:7740650 | G | A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(53): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.235+771C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740650 | |||||||
| chr12:7740841 | G | A | 16 | a0001c0001t0001g0229 a0001c0001t0005g0010 a0001c0001t0005g0029 others(13): Show |
27 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.235+580C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740841 | |||||||
| chr12:7740847 | AT | A | 45 | a0001c0001t0003g0202 a0001c0005t0008g0226 a0001c0005t0008g0227 others(42): Show |
97 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.235+573delA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740847 | |||||||
| chr12:7740864 | G | A | 1 | a0002c0002t0001g0137 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.235+557C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740864 | |||||||
| chr12:7740954 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG02300.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.235+467G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740954 | |||||||
| chr12:7740989 | T | C | 165 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(162): Show |
315 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.235+432A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7740989 | |||||||
| chr12:7741027 | G | A | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.235+394C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741027 | |||||||
| chr12:7741041 | C | T | 4 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+380G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741041 | |||||||
| chr12:7741064 | G | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(21): Show |
44 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.235+357C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741064 | |||||||
| chr12:7741074 | C | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(21): Show |
44 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.235+347G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741074 | |||||||
| chr12:7741079 | C | T | 1 | a0001c0001t0004g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.235+342G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741079 | |||||||
| chr12:7741119 | C | T | 1 | a0001c0001t0005g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.235+302G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741119 | |||||||
| chr12:7741124 | G | A | 16 | a0001c0001t0001g0229 a0001c0001t0005g0010 a0001c0001t0005g0029 others(13): Show |
27 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.235+297C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741124 | |||||||
| chr12:7741217 | C | T | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.235+204G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741217 | |||||||
| chr12:7741371 | G | A | 1 | a0001c0001t0004g0064 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.235+50C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741371 | |||||||
| chr12:7741389 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 |
4 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+32C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 3/5 | chr12 | 7741389 | |||||||
| chr12:7741536 | GA | G | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
splice_region_variant&intron_variant | LOW | c.125-6delT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741536 | |||||||
| chr12:7741592 | C | G | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-61G>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741592 | |||||||
| chr12:7741596 | C | T | 18 | a0001c0001t0004g0007 a0001c0001t0004g0011 a0001c0001t0004g0032 others(15): Show |
34 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-65G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741596 | |||||||
| chr12:7741600 | T | G | 1 | a0001c0001t0001g0224 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.125-69A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741600 | |||||||
| chr12:7741783 | C | T | 38 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(35): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.125-252G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741783 | |||||||
| chr12:7741819 | G | A | 32 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(29): Show |
63 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.125-288C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741819 | |||||||
| chr12:7741907 | G | C | 18 | a0001c0001t0004g0007 a0001c0001t0004g0011 a0001c0001t0004g0032 others(15): Show |
34 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-376C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741907 | |||||||
| chr12:7741915 | G | A | 3 | a0001c0001t0004g0067 a0001c0001t0004g0094 a0001c0001t0004g0095 |
3 | HG01257.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.125-384C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741915 | |||||||
| chr12:7741939 | A | T | 221 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(218): Show |
426 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(423): Show |
intron_variant | MODIFIER | c.125-408T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741939 | |||||||
| chr12:7741966 | A | T | 4 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-435T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741966 | |||||||
| chr12:7741974 | C | T | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-443G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741974 | |||||||
| chr12:7741982 | T | C | 1 | a0002c0002t0001g0144 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.125-451A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741982 | |||||||
| chr12:7741999 | C | T | 1 | a0001c0001t0004g0088 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.125-468G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7741999 | |||||||
| chr12:7742020 | C | CAA | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-491_125-490dup others(2): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742020 | |||||||
| chr12:7742180 | CA | C | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-650delT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742180 | |||||||
| chr12:7742217 | T | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0013 others(53): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.125-686A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742217 | |||||||
| chr12:7742230 | C | T | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-699G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742230 | |||||||
| chr12:7742248 | C | T | 30 | a0001c0001t0004g0006 a0001c0001t0004g0007 a0001c0001t0004g0011 others(27): Show |
61 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.125-717G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742248 | |||||||
| chr12:7742380 | G | GCA | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(21): Show |
44 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.125-851_125-850dup others(2): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742380 | |||||||
| chr12:7742390 | G | T | 4 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 others(1): Show |
5 | HG02886.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-859C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742390 | |||||||
| chr12:7742462 | G | C | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-931C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742462 | |||||||
| chr12:7742511 | G | GA | 58 | a0001c0001t0001g0043 a0001c0001t0001g0165 a0001c0001t0001g0207 others(55): Show |
105 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.125-981dupT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742511 | |||||||
| chr12:7742511 | G | GAA | 7 | a0001c0001t0003g0189 a0001c0001t0003g0198 a0001c0001t0003g0199 others(4): Show |
7 | HG01192.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-982_125-981dup others(2): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742511 | |||||||
| chr12:7742511 | GAAA | G | 37 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(34): Show |
89 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.125-983_125-981del others(3): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742511 | |||||||
| chr12:7742648 | A | C | 41 | a0001c0001t0002g0161 a0001c0001t0003g0003 a0001c0001t0003g0012 others(38): Show |
76 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.125-1117T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742648 | |||||||
| chr12:7742716 | A | AG | 4 | a0001c0001t0001g0037 a0001c0001t0001g0053 a0001c0001t0001g0077 others(1): Show |
5 | HG01243.hp2 HG01891.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-1186dupC | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742716 | |||||||
| chr12:7742730 | G | A | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-1199C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742730 | |||||||
| chr12:7742737 | G | A | 1 | a0001c0001t0005g0237 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.125-1206C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742737 | |||||||
| chr12:7742779 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0043 others(8): Show |
27 | HG02132.hp1 HG03688.hp1 HG04228.hp2 others(24): Show |
intron_variant | MODIFIER | c.125-1248G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742779 | |||||||
| chr12:7742809 | AAAAATAA others(6): Show |
A | 1 | a0001c0001t0003g0201 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.125-1291_125-1279d others(15): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742809 | |||||||
| chr12:7742810 | A | AAAAT | 46 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0044 others(43): Show |
75 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.125-1283_125-1280d others(6): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742810 | |||||||
| chr12:7742810 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0002g0002 a0001c0001t0002g0075 a0001c0001t0002g0225 others(1): Show |
4 | HG02055.hp2 HG02723.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1287_125-1280d others(10): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742810 | |||||||
| chr12:7742810 | AAAAT | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(42): Show |
65 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.125-1283_125-1280d others(6): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742810 | |||||||
| chr12:7742810 | AAAATAAA others(1): Show |
A | 18 | a0001c0001t0001g0229 a0001c0001t0003g0198 a0001c0001t0003g0211 others(15): Show |
29 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-1287_125-1280d others(10): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742810 | |||||||
| chr12:7742810 | AAAATAAA others(5): Show |
A | 42 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(39): Show |
77 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.125-1291_125-1280d others(14): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742810 | |||||||
| chr12:7742810 | AAAATAAA others(9): Show |
A | 1 | a0002c0002t0001g0017 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.125-1295_125-1280d others(18): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742810 | |||||||
| chr12:7742810 | AAAATAAA others(13): Show |
A | 46 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 others(43): Show |
98 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.125-1299_125-1280d others(22): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742810 | |||||||
| chr12:7742844 | A | G | 1 | a0001c0001t0003g0191 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.125-1313T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742844 | |||||||
| chr12:7742930 | A | G | 2 | a0002c0002t0001g0133 a0002c0002t0001g0140 |
2 | HG01261.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.125-1399T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7742930 | |||||||
| chr12:7743032 | T | A | 1 | a0001c0001t0004g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.125-1501A>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743032 | |||||||
| chr12:7743032 | T | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(63): Show |
138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.125-1501A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743032 | |||||||
| chr12:7743092 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.125-1561G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743092 | |||||||
| chr12:7743148 | T | A | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-1617A>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743148 | |||||||
| chr12:7743201 | G | T | 1 | a0001c0005t0008g0226 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.125-1670C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743201 | |||||||
| chr12:7743208 | C | T | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-1677G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743208 | |||||||
| chr12:7743226 | G | A | 1 | a0002c0002t0001g0039 | 2 | NA18950.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.125-1695C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743226 | |||||||
| chr12:7743334 | G | A | 6 | a0001c0001t0004g0011 a0001c0001t0004g0076 a0001c0001t0004g0117 others(3): Show |
13 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.125-1803C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743334 | |||||||
| chr12:7743334 | G | T | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-1803C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743334 | |||||||
| chr12:7743379 | CTTT | C | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-1851_125-1849d others(5): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743379 | |||||||
| chr12:7743395 | C | T | 1 | a0001c0001t0003g0202 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.125-1864G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743395 | |||||||
| chr12:7743396 | T | C | 1 | a0001c0001t0003g0202 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.125-1865A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743396 | |||||||
| chr12:7743509 | T | C | 237 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(234): Show |
443 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(440): Show |
intron_variant | MODIFIER | c.125-1978A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743509 | |||||||
| chr12:7743529 | C | T | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-1998G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743529 | |||||||
| chr12:7743534 | G | A | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-2003C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743534 | |||||||
| chr12:7743546 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(21): Show |
44 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.125-2015C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743546 | |||||||
| chr12:7743562 | A | AT | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.125-2032dupA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743562 | |||||||
| chr12:7743638 | C | T | 1 | a0002c0002t0001g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.125-2107G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743638 | |||||||
| chr12:7743674 | T | C | 1 | a0001c0001t0003g0203 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.125-2143A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743674 | |||||||
| chr12:7743760 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 |
4 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-2229C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743760 | |||||||
| chr12:7743831 | C | T | 163 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(160): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.125-2300G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743831 | |||||||
| chr12:7743837 | AC | A | 2 | a0001c0001t0003g0048 a0001c0001t0003g0206 |
3 | HG00323.hp2 HG01074.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.125-2307delG | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743837 | |||||||
| chr12:7743853 | G | T | 12 | a0001c0001t0004g0006 a0001c0001t0004g0016 a0001c0001t0004g0019 others(9): Show |
27 | HG00438.hp2 HG00597.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.125-2322C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743853 | |||||||
| chr12:7743968 | C | A | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+2363G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7743968 | |||||||
| chr12:7744009 | G | A | 41 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(38): Show |
93 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.124+2322C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744009 | |||||||
| chr12:7744037 | C | A | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+2294G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744037 | |||||||
| chr12:7744059 | T | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(63): Show |
138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.124+2272A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744059 | |||||||
| chr12:7744074 | G | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(21): Show |
44 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.124+2257C>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744074 | |||||||
| chr12:7744189 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(21): Show |
44 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.124+2142T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744189 | |||||||
| chr12:7744287 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.124+2044C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744287 | |||||||
| chr12:7744411 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02109.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+1920A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744411 | |||||||
| chr12:7744575 | T | A | 1 | a0001c0001t0004g0081 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.124+1756A>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744575 | |||||||
| chr12:7744577 | CTTTG | C | 16 | a0001c0001t0001g0229 a0001c0001t0005g0010 a0001c0001t0005g0029 others(13): Show |
27 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.124+1750_124+1753d others(6): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744577 | |||||||
| chr12:7744588 | T | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(63): Show |
138 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.124+1743A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744588 | |||||||
| chr12:7744748 | G | A | 2 | a0001c0001t0003g0003 a0001c0001t0003g0049 |
4 | HG02027.hp2 HG02071.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+1583C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744748 | |||||||
| chr12:7744812 | A | T | 16 | a0001c0001t0001g0229 a0001c0001t0005g0010 a0001c0001t0005g0029 others(13): Show |
27 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.124+1519T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744812 | |||||||
| chr12:7744881 | C | CTGGGA | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+1449_124+1450i others(7): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744881 | |||||||
| chr12:7744883 | C | T | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+1448G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744883 | |||||||
| chr12:7744896 | C | A | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124+1435G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744896 | |||||||
| chr12:7744930 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 |
4 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+1401A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744930 | |||||||
| chr12:7744932 | T | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0183 a0001c0001t0003g0204 |
4 | NA18951.hp1 NA18983.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+1399A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7744932 | |||||||
| chr12:7745029 | A | T | 1 | a0001c0001t0002g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.124+1302T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745029 | |||||||
| chr12:7745129 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.124+1202T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745129 | |||||||
| chr12:7745139 | C | T | 42 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+1192G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745139 | |||||||
| chr12:7745164 | G | A | 2 | a0001c0001t0002g0084 a0001c0001t0003g0122 |
2 | HG00639.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.124+1167C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745164 | |||||||
| chr12:7745171 | G | T | 2 | a0001c0001t0002g0085 a0001c0001t0002g0086 |
2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.124+1160C>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745171 | |||||||
| chr12:7745203 | A | G | 1 | a0005c0006t0006g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124+1128T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745203 | |||||||
| chr12:7745300 | A | G | 1 | a0001c0001t0004g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124+1031T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745300 | |||||||
| chr12:7745302 | C | T | 16 | a0001c0001t0001g0229 a0001c0001t0005g0010 a0001c0001t0005g0029 others(13): Show |
27 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.124+1029G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745302 | |||||||
| chr12:7745424 | C | CT | 18 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(15): Show |
20 | HG00558.hp2 HG01074.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.124+906dupA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745424 | |||||||
| chr12:7745424 | C | CTT | 97 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(94): Show |
228 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.124+905_124+906dup others(2): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745424 | |||||||
| chr12:7745424 | C | CTTT | 46 | a0001c0001t0001g0043 a0001c0001t0001g0077 a0001c0001t0001g0079 others(43): Show |
69 | HG00140.hp2 HG00597.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.124+904_124+906dup others(3): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745424 | |||||||
| chr12:7745424 | C | CTTTT | 5 | a0001c0001t0001g0062 a0002c0002t0001g0017 a0002c0002t0001g0131 others(2): Show |
8 | HG00408.hp2 HG02109.hp2 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+903_124+906dup others(4): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745424 | |||||||
| chr12:7745424 | CT | C | 35 | a0001c0001t0001g0229 a0001c0001t0002g0200 a0001c0001t0003g0003 others(32): Show |
68 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.124+906delA | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745424 | |||||||
| chr12:7745424 | CTT | C | 12 | a0001c0001t0005g0010 a0001c0001t0005g0029 a0001c0001t0005g0051 others(9): Show |
23 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.124+905_124+906del others(2): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745424 | |||||||
| chr12:7745424 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0130 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.124+895_124+906del others(12): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745424 | |||||||
| chr12:7745596 | C | T | 41 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0015 others(38): Show |
93 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.124+735G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745596 | |||||||
| chr12:7745712 | C | A | 2 | a0001c0001t0003g0047 a0001c0001t0003g0212 |
3 | NA18953.hp1 NA18969.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.124+619G>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745712 | |||||||
| chr12:7745712 | C | T | 42 | a0001c0001t0004g0148 a0002c0002t0001g0001 a0002c0002t0001g0005 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.124+619G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745712 | |||||||
| chr12:7745724 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 |
4 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+607G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745724 | |||||||
| chr12:7745725 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.124+606C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745725 | |||||||
| chr12:7745736 | T | G | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124+595A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745736 | |||||||
| chr12:7745827 | A | T | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124+504T>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745827 | |||||||
| chr12:7745837 | A | G | 42 | a0001c0001t0004g0148 a0002c0002t0001g0001 a0002c0002t0001g0005 others(39): Show |
94 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.124+494T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745837 | |||||||
| chr12:7745853 | T | G | 1 | a0001c0001t0002g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.124+478A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745853 | |||||||
| chr12:7745916 | G | A | 41 | a0001c0001t0004g0148 a0002c0002t0001g0001 a0002c0002t0001g0005 others(38): Show |
93 | HG00408.hp1 HG00408.hp2 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.124+415C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745916 | |||||||
| chr12:7745931 | C | T | 4 | a0002c0002t0001g0015 a0002c0002t0001g0059 a0002c0002t0001g0060 others(1): Show |
8 | HG00408.hp1 HG02040.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+400G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745931 | |||||||
| chr12:7745938 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0005g0238 a0001c0001t0006g0042 others(1): Show |
5 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+393C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745938 | |||||||
| chr12:7745943 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.124+388G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745943 | |||||||
| chr12:7745982 | A | G | 1 | a0001c0001t0003g0166 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.124+349T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745982 | |||||||
| chr12:7745997 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0006g0042 a0001c0001t0006g0164 |
4 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+334G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7745997 | |||||||
| chr12:7746014 | A | G | 1 | a0002c0002t0001g0058 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.124+317T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746014 | |||||||
| chr12:7746019 | C | T | 1 | a0002c0002t0001g0058 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.124+312G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746019 | |||||||
| chr12:7746026 | T | C | 9 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0150 others(6): Show |
13 | HG01099.hp2 HG01123.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.124+305A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746026 | |||||||
| chr12:7746032 | A | G | 6 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0163 others(3): Show |
10 | HG02572.hp2 HG02647.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.124+299T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746032 | |||||||
| chr12:7746039 | A | C | 3 | a0001c0001t0004g0019 a0001c0001t0004g0056 a0001c0001t0004g0057 |
5 | HG02572.hp2 HG02647.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+292T>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746039 | |||||||
| chr12:7746132 | A | G | 1 | a0001c0001t0005g0228 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.124+199T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746132 | |||||||
| chr12:7746139 | C | T | 1 | a0005c0006t0006g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124+192G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746139 | |||||||
| chr12:7746193 | G | A | 2 | a0001c0001t0003g0048 a0001c0001t0003g0206 |
3 | HG00323.hp2 HG01074.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.124+138C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746193 | |||||||
| chr12:7746201 | G | A | 1 | a0001c0001t0004g0157 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.124+130C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746201 | |||||||
| chr12:7746213 | C | CA | 19 | a0001c0001t0001g0050 a0001c0001t0001g0207 a0001c0001t0001g0208 others(16): Show |
21 | HG02071.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.124+117dupT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746213 | |||||||
| chr12:7746213 | CA | C | 7 | a0001c0001t0001g0158 a0001c0001t0002g0161 a0001c0001t0003g0026 others(4): Show |
9 | HG00423.hp1 HG02083.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+117delT | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746213 | |||||||
| chr12:7746213 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.124+108_124+117del others(10): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746213 | |||||||
| chr12:7746213 | CAAAAAAA others(5): Show |
C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124+106_124+117del others(12): Show |
CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746213 | |||||||
| chr12:7746228 | A | G | 138 | a0001c0001t0001g0037 a0001c0001t0001g0053 a0001c0001t0001g0062 others(135): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.124+103T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 2/5 | chr12 | 7746228 | |||||||
| chr12:7746764 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.32-341A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 1/5 | chr12 | 7746764 | |||||||
| chr12:7746823 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.32-400A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 1/5 | chr12 | 7746823 | |||||||
| chr12:7746855 | A | G | 227 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0027 others(224): Show |
433 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(430): Show |
intron_variant | MODIFIER | c.32-432T>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 1/5 | chr12 | 7746855 | |||||||
| chr12:7746877 | T | G | 1 | a0001c0001t0002g0225 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31+441A>C | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 1/5 | chr12 | 7746877 | |||||||
| chr12:7747051 | T | C | 2 | a0001c0005t0008g0226 a0001c0005t0008g0227 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.31+267A>G | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 1/5 | chr12 | 7747051 | |||||||
| chr12:7747107 | G | A | 16 | a0001c0001t0001g0229 a0001c0001t0005g0010 a0001c0001t0005g0029 others(13): Show |
27 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.31+211C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 1/5 | chr12 | 7747107 | |||||||
| chr12:7747112 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.31+206G>A | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 1/5 | chr12 | 7747112 | |||||||
| chr12:7747119 | G | A | 1 | a0002c0002t0001g0241 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.31+199C>T | CLEC4C | ENSG00000198178.11 | transcript | ENST00000360345.8 | protein_coding | 1/5 | chr12 | 7747119 |