Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 348174 |
| ensemblid | ENSG00000157322.18 |
| hgncid | 30388 |
| symbol | CLEC18A |
| name | C-type lectin domain family 18 member A |
| refseq_nuc | NM_001370523.4 |
| refseq_prot | NP_001357452.1 |
| ensembl_nuc | ENST00000288040.11 |
| ensembl_prot | ENSP00000288040.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 69951334 |
| end | 69963986 |
| strand | + |
| ver | v1.2 |
| region | chr16:69951334-69963986 |
| region5000 | chr16:69946334-69968986 |
| regionname0 | CLEC18A_chr16_69951334_69963986 |
| regionname5000 | CLEC18A_chr16_69946334_69968986 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 446 | 128 | 44 | 9 | 65 | 1 | 9 | 45 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0002 | 0/0 | 446 | 87 | 12 | 16 | 43 | 3 | 13 | 25 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0003 | 1/0 | 446 | 49 | 2 | 22 | 5 | 5 | 14 | 4 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0004 | 0/0 | 446 | 34 | 0 | 14 | 18 | 0 | 2 | 16 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0005 | 0/0 | 446 | 17 | 0 | 5 | 11 | 0 | 1 | 8 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0006 | 0/0 | 446 | 17 | 0 | 0 | 14 | 0 | 3 | 14 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0007 | 0/0 | 446 | 10 | 1 | 4 | 0 | 2 | 3 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0008 | 0/0 | 446 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0009 | 0/0 | 446 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0010 | 0/0 | 445 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(440): Show |
chr16 | 69946334 | 69968986 |
| a0011 | 0/0 | 446 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0012 | 0/0 | 446 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0013 | 0/0 | 446 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0014 | 0/0 | 446 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0015 | 0/0 | 446 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0016 | 0/0 | 446 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0017 | 0/0 | 446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0018 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0019 | 0/0 | 446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0020 | 0/0 | 446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0021 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0022 | 0/0 | 446 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0023 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0024 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0025 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0026 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0027 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| a0028 | 0/0 | 446 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | MLHPE others(441): Show |
chr16 | 69946334 | 69968986 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1338 | 118 | 35 | 9 | 64 | 1 | 9 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0001c0008 | 0/0 | 1338 | 7 | 7 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0001c0024 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0001c0032 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0001c0035 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0002c0002 | 0/0 | 1338 | 86 | 12 | 16 | 42 | 3 | 13 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0002c0033 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0003c0003 | 1/0 | 1338 | 49 | 2 | 22 | 5 | 5 | 14 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0004c0004 | 0/0 | 1338 | 32 | 0 | 14 | 16 | 0 | 2 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0004c0013 | 0/0 | 1338 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0005c0006 | 0/0 | 1338 | 17 | 0 | 5 | 11 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0006c0005 | 0/0 | 1338 | 17 | 0 | 0 | 14 | 0 | 3 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0007c0007 | 0/0 | 1338 | 9 | 0 | 4 | 0 | 2 | 3 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0007c0027 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0008c0009 | 0/0 | 1338 | 6 | 0 | 0 | 6 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0009c0010 | 0/0 | 1338 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0010c0011 | 0/0 | 1335 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1330): Show |
chr16 | 69946334 | 69968986 | ||
| a0011c0023 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0011c0028 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0012c0015 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0013c0014 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0014c0016 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0015c0012 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0016c0017 | 0/0 | 1338 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0017c0019 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0018c0036 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0019c0022 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0020c0020 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0021c0031 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0022c0030 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0023c0034 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0024c0026 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0025c0025 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0026c0018 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0027c0021 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 | ||
| a0028c0029 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | ATGCT others(1333): Show |
chr16 | 69946334 | 69968986 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1749 | 59 | 33 | 4 | 20 | 0 | 2 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0001t0002 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0001t0004 | 0/0 | 1749 | 43 | 0 | 5 | 31 | 1 | 6 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0001t0005 | 0/0 | 1749 | 13 | 1 | 0 | 11 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0001t0011 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0001t0015 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0008t0001 | 0/0 | 1749 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0008t0007 | 0/0 | 1749 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0008t0009 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0024t0001 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0032t0001 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0001c0035t0001 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0002c0002t0001 | 0/0 | 1749 | 86 | 12 | 16 | 42 | 3 | 13 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0002c0033t0001 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0003c0003t0002 | 1/0 | 1749 | 49 | 2 | 22 | 5 | 5 | 14 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0004c0004t0003 | 0/0 | 1749 | 31 | 0 | 14 | 15 | 0 | 2 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0004c0004t0014 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0004c0013t0003 | 0/0 | 1749 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0005c0006t0001 | 0/0 | 1749 | 17 | 0 | 5 | 11 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0006c0005t0001 | 0/0 | 1749 | 13 | 0 | 0 | 10 | 0 | 3 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0006c0005t0004 | 0/0 | 1749 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0006c0005t0009 | 0/0 | 1749 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0007c0007t0003 | 0/0 | 1749 | 9 | 0 | 4 | 0 | 2 | 3 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0007c0027t0003 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0008c0009t0006 | 0/0 | 1749 | 6 | 0 | 0 | 6 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0009c0010t0001 | 0/0 | 1749 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0010c0011t0008 | 0/0 | 1746 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1741): Show |
chr16 | 69946334 | 69968986 |
| a0011c0023t0003 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0011c0028t0003 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0012c0015t0001 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0013c0014t0001 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0014c0016t0010 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0015c0012t0001 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0016c0017t0001 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0017c0019t0003 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0018c0036t0001 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0019c0022t0006 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0020c0020t0001 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0021c0031t0001 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0022c0030t0001 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0023c0034t0013 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0024c0026t0006 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0025c0025t0012 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0026c0018t0004 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0027c0021t0003 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| a0028c0029t0016 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | GTGCA others(1744): Show |
chr16 | 69946334 | 69968986 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0012 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0006 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0009 | 0/0 | 7 | 0 | 4 | 0 | 1 | 2 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0019 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0005g0008 | 0/0 | 9 | 1 | 0 | 7 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0005g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0011g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0001t0015g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0008t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0008t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0008t0007g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0008t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0024t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0032t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0001c0035t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0004 | 0/0 | 14 | 1 | 3 | 10 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0011 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0017 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0021 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0002c0033t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0001 | 0/0 | 18 | 0 | 4 | 5 | 3 | 6 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0005 | 1/0 | 13 | 1 | 8 | 0 | 1 | 2 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0013 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0003c0003t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0016 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0004t0014g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0013t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0004c0013t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0005c0006t0001g0003 | 0/0 | 12 | 0 | 5 | 6 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0005c0006t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0005c0006t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0005c0006t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0005c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0005c0006t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0006c0005t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0006c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0006c0005t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0006c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0006c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0006c0005t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0006c0005t0009g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0007t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0007c0027t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0008c0009t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0008c0009t0006g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0008c0009t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0008c0009t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0008c0009t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0009c0010t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0009c0010t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0009c0010t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0010c0011t0008g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0011c0023t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0011c0028t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0012c0015t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0012c0015t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0013c0014t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0014c0016t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0014c0016t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0015c0012t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0016c0017t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0016c0017t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0017c0019t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0018c0036t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0019c0022t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0020c0020t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0021c0031t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0022c0030t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0023c0034t0013g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0024c0026t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0025c0025t0012g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0026c0018t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0027c0021t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| a0028c0029t0016g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0163 | EUR | GBR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00099 | hp2 | a0003 | c0003 | t0002 | g0005 | EUR | GBR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0120 | EUR | GBR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0185 | EUR | GBR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00408 | hp2 | a0005 | c0006 | t0001 | g0003 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00438 | hp2 | a0008 | c0009 | t0006 | g0118 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00609 | hp1 | a0004 | c0004 | t0003 | g0040 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00639 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00642 | hp1 | a0007 | c0007 | t0003 | g0162 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00673 | hp1 | a0001 | c0001 | t0015 | g0015 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | CHS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00733 | hp1 | a0003 | c0003 | t0002 | g0187 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00733 | hp2 | a0005 | c0006 | t0001 | g0003 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0013 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00741 | hp1 | a0003 | c0003 | t0002 | g0190 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG00741 | hp2 | a0004 | c0004 | t0003 | g0040 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01070 | hp1 | a0004 | c0004 | t0003 | g0042 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01070 | hp2 | a0003 | c0003 | t0002 | g0013 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01071 | hp1 | a0003 | c0003 | t0002 | g0194 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0013 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01074 | hp1 | a0004 | c0004 | t0003 | g0132 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01081 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01099 | hp1 | a0017 | c0019 | t0003 | g0140 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01099 | hp2 | a0005 | c0006 | t0001 | g0003 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01109 | hp2 | a0007 | c0007 | t0003 | g0174 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01167 | hp1 | a0004 | c0004 | t0003 | g0131 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0061 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01168 | hp1 | a0007 | c0007 | t0003 | g0152 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01168 | hp2 | a0004 | c0004 | t0003 | g0042 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01169 | hp1 | a0007 | c0007 | t0003 | g0153 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01192 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01243 | hp2 | a0003 | c0003 | t0002 | g0047 | AMR | PUR | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01255 | hp1 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01255 | hp2 | a0004 | c0004 | t0003 | g0126 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01257 | hp2 | a0003 | c0003 | t0002 | g0013 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0013 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01261 | hp2 | a0004 | c0004 | t0003 | g0041 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01346 | hp2 | a0004 | c0004 | t0003 | g0043 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01358 | hp1 | a0005 | c0006 | t0001 | g0003 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01361 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01361 | hp2 | a0004 | c0004 | t0003 | g0147 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01433 | hp1 | a0003 | c0003 | t0002 | g0005 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01515 | hp1 | a0003 | c0003 | t0002 | g0001 | EUR | IBS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01515 | hp2 | a0007 | c0007 | t0003 | g0173 | EUR | IBS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01516 | hp1 | a0003 | c0003 | t0002 | g0001 | EUR | IBS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01884 | hp1 | a0009 | c0010 | t0001 | g0035 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01891 | hp2 | a0018 | c0036 | t0001 | g0181 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01928 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01934 | hp1 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01943 | hp1 | a0019 | c0022 | t0006 | g0141 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01943 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01952 | hp2 | a0004 | c0004 | t0003 | g0016 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01975 | hp1 | a0004 | c0004 | t0003 | g0043 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01975 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01978 | hp2 | a0005 | c0006 | t0001 | g0003 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01981 | hp1 | a0005 | c0006 | t0001 | g0003 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01981 | hp2 | a0011 | c0028 | t0003 | g0154 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01993 | hp1 | a0004 | c0004 | t0003 | g0139 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01993 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02055 | hp2 | a0001 | c0008 | t0001 | g0192 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02056 | hp2 | a0008 | c0009 | t0006 | g0119 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02129 | hp2 | a0005 | c0006 | t0001 | g0003 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02135 | hp2 | a0005 | c0006 | t0001 | g0003 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02145 | hp1 | a0009 | c0010 | t0001 | g0176 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02148 | hp1 | a0003 | c0003 | t0002 | g0048 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02148 | hp2 | a0004 | c0004 | t0003 | g0041 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CDX | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | CDX | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CDX | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | CDX | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02258 | hp2 | a0001 | c0008 | t0007 | g0029 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02273 | hp1 | a0003 | c0003 | t0002 | g0005 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02273 | hp2 | a0020 | c0020 | t0001 | g0142 | AMR | PEL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02451 | hp1 | a0012 | c0015 | t0001 | g0059 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02451 | hp2 | a0003 | c0003 | t0002 | g0184 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | KHV | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0125 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02622 | hp2 | a0013 | c0014 | t0001 | g0046 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02647 | hp1 | a0001 | c0008 | t0009 | g0193 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02647 | hp2 | a0014 | c0016 | t0010 | g0101 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02683 | hp1 | a0003 | c0003 | t0002 | g0001 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0189 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02698 | hp2 | a0003 | c0003 | t0002 | g0188 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02717 | hp1 | a0015 | c0012 | t0001 | g0044 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02723 | hp1 | a0010 | c0011 | t0008 | g0025 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02735 | hp1 | a0004 | c0004 | t0003 | g0127 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02735 | hp2 | a0003 | c0003 | t0002 | g0005 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0060 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02738 | hp2 | a0007 | c0007 | t0003 | g0151 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02809 | hp2 | a0016 | c0017 | t0001 | g0113 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02818 | hp1 | a0010 | c0011 | t0008 | g0025 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02895 | hp1 | a0016 | c0017 | t0001 | g0179 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02965 | hp1 | a0021 | c0031 | t0001 | g0057 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0075 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03017 | hp1 | a0006 | c0005 | t0001 | g0166 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0049 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03139 | hp1 | a0001 | c0008 | t0001 | g0049 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03239 | hp2 | a0022 | c0030 | t0001 | g0081 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03453 | hp1 | a0009 | c0010 | t0001 | g0071 | AFR | MSL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03486 | hp2 | a0010 | c0011 | t0008 | g0025 | AFR | MSL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03492 | hp1 | a0003 | c0003 | t0002 | g0001 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03492 | hp2 | a0003 | c0003 | t0002 | g0183 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03516 | hp1 | a0001 | c0008 | t0007 | g0029 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03540 | hp1 | a0015 | c0012 | t0001 | g0044 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0099 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0001 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0021 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03704 | hp2 | a0007 | c0007 | t0003 | g0175 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03710 | hp2 | a0007 | c0007 | t0003 | g0150 | SAS | PJL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03831 | hp1 | a0003 | c0003 | t0002 | g0005 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03831 | hp2 | a0003 | c0003 | t0002 | g0001 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03834 | hp1 | a0006 | c0005 | t0001 | g0114 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03834 | hp2 | a0003 | c0003 | t0002 | g0001 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03927 | hp2 | a0004 | c0004 | t0003 | g0133 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0048 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04115 | hp1 | a0006 | c0005 | t0001 | g0079 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0017 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04184 | hp1 | a0005 | c0006 | t0001 | g0003 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | BEB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0047 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04204 | hp1 | a0003 | c0003 | t0002 | g0182 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0095 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | STU | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18747 | hp1 | a0004 | c0004 | t0003 | g0135 | EAS | CHB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | CHB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18939 | hp2 | a0004 | c0004 | t0003 | g0016 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18940 | hp2 | a0004 | c0004 | t0003 | g0144 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18943 | hp1 | a0004 | c0004 | t0003 | g0137 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18943 | hp2 | a0023 | c0034 | t0013 | g0186 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18946 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18946 | hp2 | a0005 | c0006 | t0001 | g0112 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18947 | hp2 | a0024 | c0026 | t0006 | g0038 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18948 | hp2 | a0004 | c0004 | t0003 | g0130 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18954 | hp2 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18957 | hp1 | a0006 | c0005 | t0004 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18957 | hp2 | a0004 | c0004 | t0003 | g0055 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18960 | hp2 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18963 | hp1 | a0006 | c0005 | t0009 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18964 | hp1 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18964 | hp2 | a0004 | c0004 | t0003 | g0138 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18966 | hp1 | a0004 | c0004 | t0003 | g0149 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18968 | hp1 | a0005 | c0006 | t0001 | g0108 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18970 | hp1 | a0004 | c0004 | t0014 | g0148 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18970 | hp2 | a0008 | c0009 | t0006 | g0039 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18971 | hp1 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18972 | hp1 | a0005 | c0006 | t0001 | g0106 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18972 | hp2 | a0004 | c0004 | t0003 | g0134 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18973 | hp2 | a0025 | c0025 | t0012 | g0088 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18975 | hp1 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18975 | hp2 | a0026 | c0018 | t0004 | g0028 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18977 | hp2 | a0004 | c0004 | t0003 | g0128 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18979 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18980 | hp1 | a0005 | c0006 | t0001 | g0109 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18981 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18986 | hp2 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18988 | hp1 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18989 | hp2 | a0008 | c0009 | t0006 | g0038 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18991 | hp1 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18991 | hp2 | a0004 | c0004 | t0003 | g0031 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18993 | hp1 | a0005 | c0006 | t0001 | g0003 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18993 | hp2 | a0001 | c0024 | t0001 | g0146 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18994 | hp2 | a0004 | c0013 | t0003 | g0056 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19000 | hp1 | a0002 | c0033 | t0001 | g0024 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19001 | hp2 | a0006 | c0005 | t0009 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19002 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19007 | hp1 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19009 | hp2 | a0011 | c0023 | t0003 | g0143 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19012 | hp1 | a0004 | c0013 | t0003 | g0031 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19030 | hp1 | a0001 | c0032 | t0001 | g0089 | AFR | LWK | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19043 | hp1 | a0012 | c0015 | t0001 | g0159 | AFR | LWK | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19055 | hp2 | a0004 | c0004 | t0003 | g0016 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19057 | hp1 | a0004 | c0004 | t0003 | g0016 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19057 | hp2 | a0006 | c0005 | t0001 | g0070 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19064 | hp1 | a0005 | c0006 | t0001 | g0003 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19067 | hp1 | a0006 | c0005 | t0004 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19068 | hp2 | a0005 | c0006 | t0001 | g0003 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19072 | hp2 | a0008 | c0009 | t0006 | g0117 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19075 | hp1 | a0005 | c0006 | t0001 | g0107 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19080 | hp2 | a0006 | c0005 | t0001 | g0002 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19086 | hp2 | a0027 | c0021 | t0003 | g0136 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19090 | hp1 | a0004 | c0004 | t0003 | g0145 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20129 | hp1 | a0014 | c0016 | t0010 | g0102 | AFR | ASW | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ASW | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20752 | hp1 | a0007 | c0007 | t0003 | g0155 | EUR | TSI | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20752 | hp2 | a0003 | c0003 | t0002 | g0001 | EUR | TSI | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20805 | hp1 | a0028 | c0029 | t0016 | g0196 | EUR | TSI | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | TSI | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20905 | hp1 | a0003 | c0003 | t0002 | g0001 | SAS | GIH | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | GIH | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG01123 | hp2 | a0004 | c0004 | t0003 | g0129 | AMR | CLM | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02109 | hp2 | a0009 | c0010 | t0001 | g0035 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02559 | hp1 | a0001 | c0008 | t0007 | g0029 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG02559 | hp2 | a0007 | c0027 | t0003 | g0072 | AFR | ACB | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03471 | hp1 | a0013 | c0014 | t0001 | g0046 | AFR | MSL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| HG06807 | hp2 | a0001 | c0035 | t0001 | g0076 | AFR | USA | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA18955 | hp2 | a0008 | c0009 | t0006 | g0039 | EAS | JPT | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20300 | hp1 | a0003 | c0003 | t0002 | g0005 | AFR | USA | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | USA | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | LWK | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | LWK | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0002 | g0005 | REF | REF | CLEC18A_chr16_69946334_69968986 | CLEC18A | chr16 | 69946334 | 69968986 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69951395 | G | A | 1 | a0026 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.29G>A | p.Arg10Gln | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/12 | 62/1749 | 29/1341 | 10/446 | chr16 | 69951395 | |||
| chr16:69951407 | T | C | 1 | a0015 | 2 | HG02717.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.41T>C | p.Leu14Pro | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/12 | 74/1749 | 41/1341 | 14/446 | chr16 | 69951407 | |||
| chr16:69951436 | G | A | 1 | a0017 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.70G>A | p.Ala24Thr | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/12 | 103/1749 | 70/1341 | 24/446 | chr16 | 69951436 | |||
| chr16:69952080 | G | A | 2 | a0006 a0025 |
18 | HG03017.hp1 HG03834.hp1 HG04115.hp1 others(15): Show |
missense_variant | MODERATE | c.170G>A | p.Arg57His | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/12 | 203/1749 | 170/1341 | 57/446 | chr16 | 69952080 | |||
| chr16:69954389 | C | T | 2 | a0018 a0028 |
2 | HG01891.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.272C>T | p.Thr91Ile | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 305/1749 | 272/1341 | 91/446 | chr16 | 69954389 | |||
| chr16:69954412 | G | A | 1 | a0013 | 2 | HG02622.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.295G>A | p.Gly99Ser | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 328/1749 | 295/1341 | 99/446 | chr16 | 69954412 | |||
| chr16:69954416 | T | C | 10 | a0004 a0007 a0008 others(7): Show |
58 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(55): Show |
missense_variant | MODERATE | c.299T>C | p.Leu100Pro | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 332/1749 | 299/1341 | 100/446 | chr16 | 69954416 | |||
| chr16:69954425 | C | A | 1 | a0024 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.308C>A | p.Thr103Asn | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 341/1749 | 308/1341 | 103/446 | chr16 | 69954425 | |||
| chr16:69954455 | T | A | 1 | a0022 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.338T>A | p.Leu113Gln | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 371/1749 | 338/1341 | 113/446 | chr16 | 69954455 | |||
| chr16:69954470 | T | C | 26 | a0001 a0002 a0004 others(23): Show |
329 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(326): Show |
missense_variant | MODERATE | c.353T>C | p.Val118Ala | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 386/1749 | 353/1341 | 118/446 | chr16 | 69954470 | |||
| chr16:69954526 | G | A | 1 | a0012 | 2 | HG02451.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.409G>A | p.Ala137Thr | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 442/1749 | 409/1341 | 137/446 | chr16 | 69954526 | |||
| chr16:69954560 | C | G | 4 | a0008 a0011 a0018 others(1): Show |
10 | HG00438.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
missense_variant | MODERATE | c.443C>G | p.Thr148Ser | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 476/1749 | 443/1341 | 148/446 | chr16 | 69954560 | |||
| chr16:69954569 | C | T | 5 | a0002 a0005 a0006 others(2): Show |
123 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(120): Show |
missense_variant | MODERATE | c.452C>T | p.Thr151Met | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 485/1749 | 452/1341 | 151/446 | chr16 | 69954569 | |||
| chr16:69959006 | C | T | 4 | a0008 a0018 a0019 others(1): Show |
9 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(6): Show |
missense_variant | MODERATE | c.521C>T | p.Ala174Val | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 4/12 | 554/1749 | 521/1341 | 174/446 | chr16 | 69959006 | |||
| chr16:69959038 | A | G | 7 | a0008 a0009 a0014 others(4): Show |
17 | HG00438.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
missense_variant&splice_region_variant | MODERATE | c.553A>G | p.Arg185Gly | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 4/12 | 586/1749 | 553/1341 | 185/446 | chr16 | 69959038 | |||
| chr16:69959491 | G | A | 1 | a0014 | 2 | HG02647.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.586G>A | p.Val196Ile | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 5/12 | 619/1749 | 586/1341 | 196/446 | chr16 | 69959491 | |||
| chr16:69960400 | G | A | 1 | a0021 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.812G>A | p.Gly271Asp | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/12 | 845/1749 | 812/1341 | 271/446 | chr16 | 69960400 | |||
| chr16:69960402 | C | T | 1 | a0010 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.814C>T | p.Arg272Trp | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/12 | 847/1749 | 814/1341 | 272/446 | chr16 | 69960402 | |||
| chr16:69960413 | G | C | 2 | a0010 a0018 |
4 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.825G>C | p.Glu275Asp | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/12 | 858/1749 | 825/1341 | 275/446 | chr16 | 69960413 | |||
| chr16:69960886 | G | A | 3 | a0010 a0016 a0018 |
6 | HG01891.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
missense_variant | MODERATE | c.919G>A | p.Asp307Asn | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/12 | 952/1749 | 919/1341 | 307/446 | chr16 | 69960886 | |||
| chr16:69960939 | G | C | 2 | a0010 a0018 |
4 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.972G>C | p.Arg324Ser | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/12 | 1005/1749 | 972/1341 | 324/446 | chr16 | 69960939 | |||
| chr16:69961595 | G | A | 1 | a0025 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.994G>A | p.Gly332Arg | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/12 | 1027/1749 | 994/1341 | 332/446 | chr16 | 69961595 | |||
| chr16:69961618 | C | A | 1 | a0005 | 17 | HG00408.hp2 HG00733.hp2 HG01099.hp2 others(14): Show |
missense_variant | MODERATE | c.1017C>A | p.Ser339Arg | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/12 | 1050/1749 | 1017/1341 | 339/446 | chr16 | 69961618 | |||
| chr16:69961655 | C | T | 4 | a0004 a0011 a0017 others(1): Show |
38 | HG00609.hp1 HG00741.hp2 HG01070.hp1 others(35): Show |
missense_variant | MODERATE | c.1054C>T | p.Arg352Cys | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/12 | 1087/1749 | 1054/1341 | 352/446 | chr16 | 69961655 | |||
| chr16:69961680 | T | C | 2 | a0023 a0027 |
2 | NA18943.hp2 NA19086.hp2 |
missense_variant | MODERATE | c.1079T>C | p.Ile360Thr | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/12 | 1112/1749 | 1079/1341 | 360/446 | chr16 | 69961680 | |||
| chr16:69962015 | CCTT | C | 1 | a0010 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
conservative_inframe_deletion | MODERATE | c.1144_1146delTTC | p.Phe382del | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/12 | 1177/1749 | 1144/1341 | 382/446 | INFO_REALIGN_3_PRIME | chr16 | 69962015 | ||
| chr16:69962051 | C | G | 1 | a0018 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1178C>G | p.Thr393Ser | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/12 | 1211/1749 | 1178/1341 | 393/446 | chr16 | 69962051 | |||
| chr16:69963025 | G | A | 7 | a0004 a0007 a0011 others(4): Show |
51 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(48): Show |
missense_variant | MODERATE | c.1261G>A | p.Asp421Asn | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/12 | 1294/1749 | 1261/1341 | 421/446 | chr16 | 69963025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69951480 | G | A | 7 | a0001c0024 a0004c0004 a0007c0007 others(4): Show |
46 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(43): Show |
synonymous_variant | LOW | c.114G>A | p.Pro38Pro | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/12 | 147/1749 | 114/1341 | 38/446 | chr16 | 69951480 | |||
| chr16:69954357 | G | A | 13 | a0004c0004 a0004c0013 a0007c0007 others(10): Show |
58 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(55): Show |
synonymous_variant | LOW | c.240G>A | p.Gln80Gln | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 273/1749 | 240/1341 | 80/446 | chr16 | 69954357 | |||
| chr16:69954456 | A | G | 17 | a0001c0008 a0001c0035 a0004c0004 others(14): Show |
70 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(67): Show |
synonymous_variant | LOW | c.339A>G | p.Leu113Leu | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 372/1749 | 339/1341 | 113/446 | chr16 | 69954456 | |||
| chr16:69954480 | C | T | 1 | a0028c0029 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.363C>T | p.Val121Val | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 396/1749 | 363/1341 | 121/446 | chr16 | 69954480 | |||
| chr16:69954570 | G | A | 5 | a0008c0009 a0011c0023 a0011c0028 others(2): Show |
10 | HG00438.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
synonymous_variant | LOW | c.453G>A | p.Thr151Thr | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/12 | 486/1749 | 453/1341 | 151/446 | chr16 | 69954570 | |||
| chr16:69958944 | C | T | 2 | a0001c0032 a0001c0035 |
2 | HG06807.hp2 NA19030.hp1 |
splice_region_variant&synonymous_variant | LOW | c.459C>T | p.Leu153Leu | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 4/12 | 492/1749 | 459/1341 | 153/446 | chr16 | 69958944 | |||
| chr16:69959574 | G | C | 1 | a0002c0033 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.669G>C | p.Gly223Gly | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 5/12 | 702/1749 | 669/1341 | 223/446 | chr16 | 69959574 | |||
| chr16:69959779 | T | C | 3 | a0008c0009 a0019c0022 a0024c0026 |
8 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(5): Show |
synonymous_variant | LOW | c.717T>C | p.His239His | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/12 | 750/1749 | 717/1341 | 239/446 | chr16 | 69959779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69951344 | C | T | 1 | a0028c0029t0016 | 1 | NA20805.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/12 | 23 | chr16 | 69951344 | ||||||
| chr16:69951352 | G | A | 6 | a0001c0001t0004 a0001c0001t0011 a0001c0008t0007 others(3): Show |
52 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-15G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/12 | 15 | chr16 | 69951352 | ||||||
| chr16:69963634 | G | C | 5 | a0001c0008t0007 a0008c0009t0006 a0010c0011t0008 others(2): Show |
14 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 12/12 | 23 | chr16 | 69963634 | ||||||
| chr16:69963669 | T | C | 4 | a0001c0001t0005 a0001c0001t0011 a0014c0016t0010 others(1): Show |
17 | HG00544.hp2 HG02015.hp1 HG02647.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*58T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 12/12 | 58 | chr16 | 69963669 | ||||||
| chr16:69963703 | T | C | 17 | a0001c0008t0007 a0004c0004t0003 a0004c0004t0014 others(14): Show |
66 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*92T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 12/12 | 92 | chr16 | 69963703 | ||||||
| chr16:69963816 | C | T | 4 | a0004c0004t0014 a0008c0009t0006 a0019c0022t0006 others(1): Show |
9 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 12/12 | 205 | chr16 | 69963816 | ||||||
| chr16:69963822 | G | A | 2 | a0001c0008t0009 a0006c0005t0009 |
3 | HG02647.hp1 NA18963.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*211G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 12/12 | 211 | chr16 | 69963822 | ||||||
| chr16:69963862 | G | A | 2 | a0014c0016t0010 a0025c0025t0012 |
3 | HG02647.hp2 NA18973.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*251G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 12/12 | 251 | chr16 | 69963862 | ||||||
| chr16:69963877 | G | A | 1 | a0001c0001t0015 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 12/12 | 266 | chr16 | 69963877 | ||||||
| chr16:69963960 | A | G | 28 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(25): Show |
266 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*349A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 12/12 | 349 | chr16 | 69963960 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69951532 | C | T | 2 | a0002c0002t0001g0195 a0028c0029t0016g0196 |
2 | NA19007.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.124+42C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951532 | |||||||
| chr16:69951642 | T | C | 1 | a0001c0001t0004g0050 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.124+152T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951642 | |||||||
| chr16:69951718 | G | A | 180 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(177): Show |
313 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.124+228G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951718 | |||||||
| chr16:69951743 | A | AC | 156 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(153): Show |
275 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.124+253_124+254ins others(1): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951743 | |||||||
| chr16:69951747 | G | A | 1 | a0003c0003t0002g0182 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.124+257G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951747 | |||||||
| chr16:69951773 | G | A | 1 | a0007c0007t0003g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.125-262G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951773 | |||||||
| chr16:69951786 | A | G | 40 | a0001c0024t0001g0146 a0004c0004t0003g0016 a0004c0004t0003g0040 others(37): Show |
48 | HG00609.hp1 HG00741.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.125-249A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951786 | |||||||
| chr16:69951813 | C | G | 1 | a0007c0007t0003g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.125-222C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951813 | |||||||
| chr16:69951839 | C | T | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.125-196C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951839 | |||||||
| chr16:69951863 | G | A | 4 | a0002c0002t0001g0018 a0002c0002t0001g0051 a0002c0002t0001g0052 others(1): Show |
6 | HG02155.hp2 NA18941.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-172G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69951863 | |||||||
| chr16:69952025 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0121 a0001c0001t0001g0122 others(8): Show |
13 | HG00544.hp1 HG00673.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.125-10C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 1/11 | chr16 | 69952025 | |||||||
| chr16:69952139 | C | G | 1 | a0002c0002t0001g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.216+13C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952139 | |||||||
| chr16:69952173 | C | T | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01981.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.216+47C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952173 | |||||||
| chr16:69952174 | G | A | 1 | a0001c0008t0007g0029 | 3 | HG02258.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.216+48G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952174 | |||||||
| chr16:69952235 | G | A | 1 | a0004c0004t0003g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.216+109G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952235 | |||||||
| chr16:69952262 | T | C | 48 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(45): Show |
68 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.216+136T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952262 | |||||||
| chr16:69952283 | G | T | 1 | a0003c0003t0002g0194 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.216+157G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952283 | |||||||
| chr16:69952303 | A | G | 193 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(190): Show |
331 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.216+177A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952303 | |||||||
| chr16:69952357 | G | A | 1 | a0002c0002t0001g0058 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.216+231G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952357 | |||||||
| chr16:69952399 | T | C | 35 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0004g0006 others(32): Show |
62 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.216+273T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952399 | |||||||
| chr16:69952468 | C | G | 1 | a0002c0002t0001g0120 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.216+342C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952468 | |||||||
| chr16:69952524 | G | A | 6 | a0008c0009t0006g0038 a0008c0009t0006g0117 a0008c0009t0006g0118 others(3): Show |
6 | HG00438.hp2 HG01981.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+398G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952524 | |||||||
| chr16:69952534 | C | T | 119 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(116): Show |
227 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.216+408C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952534 | |||||||
| chr16:69952576 | G | T | 6 | a0001c0001t0001g0158 a0001c0001t0002g0008 a0001c0001t0005g0008 others(3): Show |
15 | HG00544.hp2 HG02015.hp1 HG03139.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+450G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952576 | |||||||
| chr16:69952582 | G | C | 1 | a0002c0002t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.216+456G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952582 | |||||||
| chr16:69952645 | G | A | 7 | a0001c0001t0001g0158 a0001c0001t0002g0008 a0001c0001t0005g0008 others(4): Show |
16 | HG00544.hp2 HG02015.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.216+519G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952645 | |||||||
| chr16:69952663 | A | G | 57 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0002g0008 others(54): Show |
75 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.216+537A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952663 | |||||||
| chr16:69952695 | T | G | 1 | a0004c0004t0003g0128 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.216+569T>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952695 | |||||||
| chr16:69952722 | C | T | 3 | a0001c0008t0001g0049 a0001c0008t0001g0192 a0001c0008t0009g0193 |
4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+596C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952722 | |||||||
| chr16:69952729 | C | A | 3 | a0009c0010t0001g0071 a0009c0010t0001g0176 a0018c0036t0001g0181 |
3 | HG01891.hp2 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.216+603C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952729 | |||||||
| chr16:69952730 | C | T | 50 | a0001c0001t0001g0115 a0001c0001t0001g0158 a0001c0001t0002g0008 others(47): Show |
66 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.216+604C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952730 | |||||||
| chr16:69952733 | C | A | 50 | a0001c0001t0001g0115 a0001c0001t0001g0158 a0001c0001t0002g0008 others(47): Show |
66 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.216+607C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952733 | |||||||
| chr16:69952744 | C | A | 4 | a0001c0008t0007g0029 a0009c0010t0001g0071 a0009c0010t0001g0176 others(1): Show |
6 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+618C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952744 | |||||||
| chr16:69952806 | G | T | 1 | a0001c0008t0009g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.216+680G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952806 | |||||||
| chr16:69952848 | C | T | 8 | a0001c0001t0001g0158 a0001c0001t0002g0008 a0001c0001t0005g0008 others(5): Show |
17 | HG00544.hp2 HG02015.hp1 HG03139.hp2 others(14): Show |
intron_variant | MODIFIER | c.216+722C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952848 | |||||||
| chr16:69952855 | A | G | 195 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(192): Show |
346 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.216+729A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952855 | |||||||
| chr16:69952860 | C | T | 5 | a0009c0010t0001g0035 a0009c0010t0001g0071 a0009c0010t0001g0176 others(2): Show |
6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+734C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952860 | |||||||
| chr16:69952891 | G | A | 161 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(158): Show |
273 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.216+765G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952891 | |||||||
| chr16:69952936 | G | C | 192 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
329 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.216+810G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69952936 | |||||||
| chr16:69953108 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(6): Show |
20 | HG01243.hp1 HG01433.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.216+982C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953108 | |||||||
| chr16:69953126 | G | A | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.216+1000G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953126 | |||||||
| chr16:69953144 | C | A | 1 | a0003c0003t0002g0184 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.216+1018C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953144 | |||||||
| chr16:69953147 | C | T | 1 | a0001c0001t0005g0037 | 2 | NA19080.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.216+1021C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953147 | |||||||
| chr16:69953172 | G | A | 1 | a0002c0002t0001g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.216+1046G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953172 | |||||||
| chr16:69953215 | C | T | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.216+1089C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953215 | |||||||
| chr16:69953233 | G | A | 1 | a0002c0002t0001g0075 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.217-1101G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953233 | |||||||
| chr16:69953255 | G | A | 8 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(5): Show |
9 | HG00438.hp2 HG01891.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-1079G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953255 | |||||||
| chr16:69953474 | C | T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(34): Show |
68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.217-860C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953474 | |||||||
| chr16:69953537 | T | C | 1 | a0001c0008t0007g0029 | 3 | HG02258.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.217-797T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953537 | |||||||
| chr16:69953582 | G | A | 1 | a0002c0002t0001g0105 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.217-752G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953582 | |||||||
| chr16:69953591 | A | C | 1 | a0002c0002t0001g0096 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.217-743A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953591 | |||||||
| chr16:69953633 | A | ATG | 51 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(48): Show |
59 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.217-701_217-700ins others(2): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953633 | |||||||
| chr16:69953675 | C | T | 51 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(48): Show |
59 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.217-659C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953675 | |||||||
| chr16:69953681 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.217-653G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953681 | |||||||
| chr16:69953706 | T | C | 42 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(39): Show |
49 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.217-628T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953706 | |||||||
| chr16:69953746 | C | T | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.217-588C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953746 | |||||||
| chr16:69953756 | A | T | 1 | a0004c0004t0003g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.217-578A>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953756 | |||||||
| chr16:69953764 | G | A | 1 | a0012c0015t0001g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.217-570G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953764 | |||||||
| chr16:69953812 | C | CA | 123 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(120): Show |
253 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.217-502dupA | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 69953812 | ||||||
| chr16:69953812 | C | CAA | 9 | a0001c0001t0004g0060 a0001c0035t0001g0076 a0002c0002t0001g0051 others(6): Show |
9 | HG00642.hp2 HG01928.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-503_217-502dup others(2): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 69953812 | ||||||
| chr16:69953812 | C | CAAA | 36 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(33): Show |
43 | HG00609.hp1 HG00741.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.217-504_217-502dup others(3): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 69953812 | ||||||
| chr16:69953812 | CAA | C | 5 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0119 others(2): Show |
6 | HG01981.hp2 HG02056.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.217-503_217-502del others(2): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr16 | 69953812 | ||||||
| chr16:69953848 | G | A | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01981.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.217-486G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953848 | |||||||
| chr16:69953861 | C | T | 49 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(46): Show |
57 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.217-473C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953861 | |||||||
| chr16:69953884 | G | A | 3 | a0001c0001t0001g0156 a0001c0008t0001g0192 a0028c0029t0016g0196 |
3 | HG02055.hp2 HG03130.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.217-450G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953884 | |||||||
| chr16:69953894 | G | A | 1 | a0003c0003t0002g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.217-440G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953894 | |||||||
| chr16:69953917 | G | A | 1 | a0002c0002t0001g0080 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.217-417G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953917 | |||||||
| chr16:69953918 | C | T | 2 | a0001c0001t0001g0156 a0003c0003t0002g0184 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.217-416C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69953918 | |||||||
| chr16:69954036 | C | T | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01981.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.217-298C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69954036 | |||||||
| chr16:69954075 | C | T | 1 | a0001c0001t0004g0161 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.217-259C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69954075 | |||||||
| chr16:69954079 | T | C | 192 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
329 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.217-255T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 2/11 | chr16 | 69954079 | |||||||
| chr16:69954599 | T | C | 13 | a0002c0002t0001g0011 a0002c0002t0001g0021 a0008c0009t0006g0038 others(10): Show |
21 | HG00438.hp2 HG00639.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.456+26T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954599 | |||||||
| chr16:69954631 | G | T | 3 | a0001c0001t0001g0027 a0002c0002t0001g0093 a0028c0029t0016g0196 |
5 | HG01884.hp2 HG02818.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+58G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954631 | |||||||
| chr16:69954701 | C | CT | 7 | a0001c0001t0004g0066 a0001c0001t0004g0067 a0002c0002t0001g0091 others(4): Show |
7 | HG00438.hp2 HG02135.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.456+142dupT | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69954701 | ||||||
| chr16:69954732 | C | G | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+159C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954732 | |||||||
| chr16:69954739 | C | G | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+166C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954739 | |||||||
| chr16:69954743 | G | A | 1 | a0004c0004t0003g0147 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.456+170G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954743 | |||||||
| chr16:69954764 | C | G | 1 | a0018c0036t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.456+191C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954764 | |||||||
| chr16:69954793 | G | A | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+220G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954793 | |||||||
| chr16:69954810 | A | C | 143 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(140): Show |
272 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.456+237A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954810 | |||||||
| chr16:69954889 | G | A | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+316G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954889 | |||||||
| chr16:69954909 | A | C | 50 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(47): Show |
58 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.456+336A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954909 | |||||||
| chr16:69954935 | A | G | 1 | a0003c0003t0002g0013 | 5 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.456+362A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954935 | |||||||
| chr16:69954980 | A | G | 2 | a0003c0003t0002g0188 a0028c0029t0016g0196 |
2 | HG02698.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.456+407A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954980 | |||||||
| chr16:69954983 | A | C | 1 | a0002c0002t0001g0090 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.456+410A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69954983 | |||||||
| chr16:69955032 | C | G | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+459C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955032 | |||||||
| chr16:69955061 | T | C | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+488T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955061 | |||||||
| chr16:69955069 | C | T | 2 | a0007c0007t0003g0152 a0007c0007t0003g0153 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.456+496C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955069 | |||||||
| chr16:69955074 | C | T | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+501C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955074 | |||||||
| chr16:69955153 | A | T | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+580A>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955153 | |||||||
| chr16:69955210 | T | C | 16 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(13): Show |
27 | HG00438.hp2 HG01243.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.456+637T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955210 | |||||||
| chr16:69955240 | T | C | 15 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(12): Show |
26 | HG00438.hp2 HG01243.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.456+667T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955240 | |||||||
| chr16:69955274 | A | G | 8 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(5): Show |
9 | HG00438.hp2 HG01981.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+701A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955274 | |||||||
| chr16:69955349 | A | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(13): Show |
27 | HG00438.hp2 HG01243.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.456+776A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955349 | |||||||
| chr16:69955373 | C | T | 1 | a0001c0032t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.456+800C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955373 | |||||||
| chr16:69955374 | A | G | 192 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
329 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.456+801A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955374 | |||||||
| chr16:69955419 | C | T | 1 | a0001c0001t0004g0065 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.456+846C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955419 | |||||||
| chr16:69955451 | A | G | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+878A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955451 | |||||||
| chr16:69955484 | G | A | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+911G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955484 | |||||||
| chr16:69955498 | G | A | 1 | a0001c0035t0001g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.456+925G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955498 | |||||||
| chr16:69955537 | GAT | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(6): Show |
16 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.456+966_456+967del others(2): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69955537 | ||||||
| chr16:69955554 | C | T | 11 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(8): Show |
13 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.456+981C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955554 | |||||||
| chr16:69955601 | C | G | 10 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(7): Show |
11 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+1028C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955601 | |||||||
| chr16:69955628 | G | A | 192 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
329 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.456+1055G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955628 | |||||||
| chr16:69955719 | A | C | 122 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(119): Show |
236 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.456+1146A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955719 | |||||||
| chr16:69955783 | CTGAT | C | 184 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(181): Show |
320 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.456+1211_456+1214d others(6): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955783 | |||||||
| chr16:69955829 | G | A | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+1256G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955829 | |||||||
| chr16:69955863 | C | T | 4 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0018c0036t0001g0181 others(1): Show |
4 | HG01891.hp2 NA18944.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+1290C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955863 | |||||||
| chr16:69955864 | G | A | 1 | a0004c0004t0003g0129 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.456+1291G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955864 | |||||||
| chr16:69955920 | T | C | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+1347T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955920 | |||||||
| chr16:69955973 | C | T | 18 | a0002c0002t0001g0002 a0002c0002t0001g0024 a0002c0002t0001g0045 others(15): Show |
31 | HG00140.hp1 HG00621.hp1 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.456+1400C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955973 | |||||||
| chr16:69955974 | G | A | 41 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(38): Show |
48 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.456+1401G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69955974 | |||||||
| chr16:69956048 | T | C | 2 | a0018c0036t0001g0181 a0028c0029t0016g0196 |
2 | HG01891.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.456+1475T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956048 | |||||||
| chr16:69956066 | C | A | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+1493C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956066 | |||||||
| chr16:69956091 | A | G | 1 | a0018c0036t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.456+1518A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956091 | |||||||
| chr16:69956180 | G | A | 184 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(181): Show |
320 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.456+1607G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956180 | |||||||
| chr16:69956247 | C | T | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+1674C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956247 | |||||||
| chr16:69956297 | T | G | 1 | a0002c0002t0001g0082 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.456+1724T>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956297 | |||||||
| chr16:69956358 | A | AT | 167 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(164): Show |
301 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(298): Show |
intron_variant | MODIFIER | c.456+1800dupT | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69956358 | ||||||
| chr16:69956358 | A | ATT | 5 | a0001c0001t0004g0064 a0002c0002t0001g0034 a0002c0002t0001g0087 others(2): Show |
6 | HG00408.hp1 HG01074.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.456+1799_456+1800d others(4): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69956358 | ||||||
| chr16:69956358 | A | ATTT | 8 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(5): Show |
9 | HG00438.hp2 HG01981.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+1798_456+1800d others(5): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69956358 | ||||||
| chr16:69956379 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.456+1806G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956379 | |||||||
| chr16:69956396 | C | T | 1 | a0001c0001t0004g0020 | 3 | NA18947.hp1 NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.456+1823C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956396 | |||||||
| chr16:69956404 | A | G | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.456+1831A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956404 | |||||||
| chr16:69956458 | C | G | 1 | a0007c0027t0003g0072 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.456+1885C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956458 | |||||||
| chr16:69956465 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0165 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.456+1892C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956465 | |||||||
| chr16:69956519 | C | T | 1 | a0028c0029t0016g0196 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.456+1946C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956519 | |||||||
| chr16:69956559 | C | T | 1 | a0002c0002t0001g0034 | 2 | HG01074.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.456+1986C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956559 | |||||||
| chr16:69956607 | C | T | 9 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(6): Show |
10 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.456+2034C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956607 | |||||||
| chr16:69956609 | T | C | 192 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
329 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.456+2036T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956609 | |||||||
| chr16:69956637 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.456+2064T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956637 | |||||||
| chr16:69956692 | G | C | 1 | a0006c0005t0001g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.456+2119G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956692 | |||||||
| chr16:69956705 | C | G | 1 | a0018c0036t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.456+2132C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956705 | |||||||
| chr16:69956716 | T | G | 40 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(37): Show |
47 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.456+2143T>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956716 | |||||||
| chr16:69956828 | C | T | 2 | a0001c0032t0001g0089 a0001c0035t0001g0076 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.457-2114C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956828 | |||||||
| chr16:69956931 | G | T | 22 | a0001c0001t0001g0062 a0002c0002t0001g0002 a0002c0002t0001g0024 others(19): Show |
35 | HG00140.hp1 HG00621.hp1 HG02015.hp2 others(32): Show |
intron_variant | MODIFIER | c.457-2011G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956931 | |||||||
| chr16:69956955 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.457-1987C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69956955 | |||||||
| chr16:69957005 | C | T | 2 | a0004c0004t0003g0139 a0017c0019t0003g0140 |
2 | HG01099.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.457-1937C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957005 | |||||||
| chr16:69957049 | C | A | 2 | a0001c0001t0001g0062 a0028c0029t0016g0196 |
2 | HG03225.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.457-1893C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957049 | |||||||
| chr16:69957060 | T | A | 3 | a0001c0001t0001g0062 a0005c0006t0001g0109 a0028c0029t0016g0196 |
3 | HG03225.hp1 NA18980.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.457-1882T>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957060 | |||||||
| chr16:69957109 | C | T | 2 | a0001c0008t0001g0049 a0001c0008t0001g0192 |
3 | HG02055.hp2 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.457-1833C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957109 | |||||||
| chr16:69957139 | G | GT | 19 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(16): Show |
27 | HG00438.hp2 HG00738.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.457-1797dupT | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69957139 | ||||||
| chr16:69957249 | T | A | 2 | a0001c0001t0001g0062 a0028c0029t0016g0196 |
2 | HG03225.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.457-1693T>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957249 | |||||||
| chr16:69957276 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.457-1666C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957276 | |||||||
| chr16:69957403 | G | T | 192 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
329 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.457-1539G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957403 | |||||||
| chr16:69957579 | C | G | 153 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(150): Show |
280 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.457-1363C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957579 | |||||||
| chr16:69957636 | A | G | 10 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(7): Show |
11 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.457-1306A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69957636 | |||||||
| chr16:69958248 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(4): Show |
17 | HG01243.hp1 HG01433.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.457-694G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958248 | |||||||
| chr16:69958412 | T | G | 49 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(46): Show |
57 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.457-530T>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958412 | |||||||
| chr16:69958465 | C | T | 2 | a0014c0016t0010g0101 a0014c0016t0010g0102 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.457-477C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958465 | |||||||
| chr16:69958533 | T | C | 3 | a0002c0002t0001g0110 a0014c0016t0010g0101 a0014c0016t0010g0102 |
3 | HG02027.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.457-409T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958533 | |||||||
| chr16:69958548 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.457-394A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958548 | |||||||
| chr16:69958563 | G | C | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.457-379G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958563 | |||||||
| chr16:69958576 | G | T | 184 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(181): Show |
320 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.457-366G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958576 | |||||||
| chr16:69958604 | G | GGCATGGT others(7): Show |
3 | a0002c0002t0001g0105 a0014c0016t0010g0101 a0014c0016t0010g0102 |
3 | HG01952.hp1 HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.457-336_457-335ins others(14): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69958604 | ||||||
| chr16:69958604 | G | GGCATGGT others(7): Show |
181 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(178): Show |
317 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.457-336_457-335ins others(14): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69958604 | ||||||
| chr16:69958661 | G | A | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.457-281G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958661 | |||||||
| chr16:69958671 | G | A | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.457-271G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958671 | |||||||
| chr16:69958734 | AAAAT | A | 170 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(167): Show |
293 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.457-177_457-174del others(4): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69958734 | ||||||
| chr16:69958734 | AAAATAAA others(1): Show |
A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(9): Show |
24 | HG01243.hp1 HG01433.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.457-181_457-174del others(8): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr16 | 69958734 | ||||||
| chr16:69958766 | T | A | 3 | a0002c0002t0001g0195 a0014c0016t0010g0101 a0014c0016t0010g0102 |
3 | HG02647.hp2 NA19007.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.457-176T>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958766 | |||||||
| chr16:69958770 | C | G | 1 | a0018c0036t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.457-172C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958770 | |||||||
| chr16:69958833 | C | G | 17 | a0001c0001t0001g0121 a0001c0001t0004g0006 a0001c0001t0004g0014 others(14): Show |
32 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.457-109C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958833 | |||||||
| chr16:69958838 | G | A | 2 | a0014c0016t0010g0101 a0014c0016t0010g0102 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.457-104G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958838 | |||||||
| chr16:69958860 | C | G | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.457-82C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958860 | |||||||
| chr16:69958861 | A | G | 9 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(6): Show |
10 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.457-81A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958861 | |||||||
| chr16:69958913 | G | A | 41 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(38): Show |
48 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.457-29G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958913 | |||||||
| chr16:69958926 | CCT | C | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.457-15_457-14delCT | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 3/11 | chr16 | 69958926 | |||||||
| chr16:69959057 | C | T | 2 | a0014c0016t0010g0101 a0014c0016t0010g0102 |
2 | HG02647.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.554+18C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 4/11 | chr16 | 69959057 | |||||||
| chr16:69959233 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
19 | HG01243.hp1 HG01433.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.554+194G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 4/11 | chr16 | 69959233 | |||||||
| chr16:69959380 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0033 others(6): Show |
23 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.555-80G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 4/11 | chr16 | 69959380 | |||||||
| chr16:69959383 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0033 others(6): Show |
23 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.555-77C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 4/11 | chr16 | 69959383 | |||||||
| chr16:69959402 | T | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0033 others(6): Show |
23 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.555-58T>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 4/11 | chr16 | 69959402 | |||||||
| chr16:69959702 | A | C | 3 | a0010c0011t0008g0025 a0014c0016t0010g0101 a0014c0016t0010g0102 |
5 | HG02647.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-37A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 5/11 | chr16 | 69959702 | |||||||
| chr16:69959723 | C | T | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.677-16C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 5/11 | chr16 | 69959723 | |||||||
| chr16:69959904 | T | C | 1 | a0004c0004t0003g0144 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.784+58T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69959904 | |||||||
| chr16:69959905 | G | T | 1 | a0004c0004t0003g0144 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.784+59G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69959905 | |||||||
| chr16:69959906 | C | A | 1 | a0004c0004t0003g0144 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.784+60C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69959906 | |||||||
| chr16:69959911 | C | G | 1 | a0004c0004t0003g0144 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.784+65C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69959911 | |||||||
| chr16:69959998 | C | G | 6 | a0001c0008t0007g0029 a0004c0004t0003g0138 a0010c0011t0008g0025 others(3): Show |
10 | HG01099.hp1 HG01891.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+152C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69959998 | |||||||
| chr16:69960018 | A | G | 70 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(67): Show |
126 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.784+172A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960018 | |||||||
| chr16:69960051 | A | G | 4 | a0004c0004t0003g0138 a0010c0011t0008g0025 a0018c0036t0001g0181 others(1): Show |
6 | HG01891.hp2 HG01943.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+205A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960051 | |||||||
| chr16:69960079 | G | A | 2 | a0002c0002t0001g0011 a0022c0030t0001g0081 |
7 | HG00639.hp2 HG01106.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+233G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960079 | |||||||
| chr16:69960091 | T | C | 40 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(37): Show |
47 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.784+245T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960091 | |||||||
| chr16:69960148 | C | A | 6 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(3): Show |
7 | HG00438.hp2 HG02056.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.785-225C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960148 | |||||||
| chr16:69960230 | T | C | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-143T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960230 | |||||||
| chr16:69960231 | C | T | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-142C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960231 | |||||||
| chr16:69960232 | G | A | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-141G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960232 | |||||||
| chr16:69960233 | G | T | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-140G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960233 | |||||||
| chr16:69960235 | A | C | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-138A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960235 | |||||||
| chr16:69960236 | GCCTTGGT others(4): Show |
G | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-136_785-126del others(11): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960236 | |||||||
| chr16:69960249 | C | A | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-124C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960249 | |||||||
| chr16:69960251 | G | A | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-122G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960251 | |||||||
| chr16:69960255 | A | C | 79 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0004 others(76): Show |
138 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.785-118A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960255 | |||||||
| chr16:69960261 | G | T | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.785-112G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960261 | |||||||
| chr16:69960304 | C | CT | 2 | a0010c0011t0008g0025 a0018c0036t0001g0181 |
4 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.785-68dupT | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr16 | 69960304 | ||||||
| chr16:69960306 | C | T | 2 | a0010c0011t0008g0025 a0018c0036t0001g0181 |
4 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.785-67C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960306 | |||||||
| chr16:69960321 | G | A | 2 | a0010c0011t0008g0025 a0018c0036t0001g0181 |
4 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.785-52G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960321 | |||||||
| chr16:69960354 | C | T | 1 | a0018c0036t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.785-19C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 6/11 | chr16 | 69960354 | |||||||
| chr16:69960511 | C | T | 40 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(37): Show |
47 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.877+46C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | chr16 | 69960511 | |||||||
| chr16:69960645 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.877+180A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | chr16 | 69960645 | |||||||
| chr16:69960656 | AT | A | 13 | a0002c0002t0001g0164 a0004c0004t0003g0137 a0005c0006t0001g0112 others(10): Show |
14 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.878-178delT | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 69960656 | ||||||
| chr16:69960656 | ATT | A | 178 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(175): Show |
314 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.878-179_878-178del others(2): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr16 | 69960656 | ||||||
| chr16:69960701 | T | G | 1 | a0023c0034t0013g0186 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.878-144T>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | chr16 | 69960701 | |||||||
| chr16:69960708 | T | C | 2 | a0001c0008t0001g0049 a0001c0008t0001g0192 |
3 | HG02055.hp2 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.878-137T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | chr16 | 69960708 | |||||||
| chr16:69960710 | G | A | 189 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(186): Show |
326 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.878-135G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | chr16 | 69960710 | |||||||
| chr16:69960808 | T | C | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.878-37T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | chr16 | 69960808 | |||||||
| chr16:69960829 | G | A | 41 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(38): Show |
48 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.878-16G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 7/11 | chr16 | 69960829 | |||||||
| chr16:69960954 | G | A | 1 | a0002c0002t0001g0163 | 1 | HG00099.hp1 | splice_region_variant&intron_variant | LOW | c.984+3G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69960954 | |||||||
| chr16:69960960 | C | T | 2 | a0010c0011t0008g0025 a0018c0036t0001g0181 |
4 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.984+9C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69960960 | |||||||
| chr16:69960979 | A | G | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.984+28A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69960979 | |||||||
| chr16:69960981 | C | T | 3 | a0014c0016t0010g0101 a0014c0016t0010g0102 a0025c0025t0012g0088 |
3 | HG02647.hp2 NA18973.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.984+30C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69960981 | |||||||
| chr16:69960996 | G | T | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.984+45G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69960996 | |||||||
| chr16:69960999 | A | T | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.984+48A>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69960999 | |||||||
| chr16:69961042 | C | A | 192 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(189): Show |
329 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.984+91C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961042 | |||||||
| chr16:69961044 | C | T | 2 | a0010c0011t0008g0025 a0018c0036t0001g0181 |
4 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.984+93C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961044 | |||||||
| chr16:69961045 | G | A | 3 | a0014c0016t0010g0101 a0014c0016t0010g0102 a0025c0025t0012g0088 |
3 | HG02647.hp2 NA18973.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.984+94G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961045 | |||||||
| chr16:69961088 | G | A | 2 | a0016c0017t0001g0113 a0016c0017t0001g0179 |
2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.984+137G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961088 | |||||||
| chr16:69961158 | A | G | 1 | a0001c0008t0009g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.984+207A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961158 | |||||||
| chr16:69961260 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.984+309G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961260 | |||||||
| chr16:69961277 | A | G | 10 | a0001c0001t0004g0100 a0008c0009t0006g0038 a0008c0009t0006g0039 others(7): Show |
13 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.985-309A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961277 | |||||||
| chr16:69961298 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.985-288A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961298 | |||||||
| chr16:69961305 | T | C | 13 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(10): Show |
16 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.985-281T>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961305 | |||||||
| chr16:69961336 | C | G | 1 | a0014c0016t0010g0102 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.985-250C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961336 | |||||||
| chr16:69961376 | G | A | 9 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(6): Show |
12 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.985-210G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961376 | |||||||
| chr16:69961387 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.985-199C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961387 | |||||||
| chr16:69961393 | C | T | 16 | a0001c0001t0001g0033 a0001c0032t0001g0089 a0001c0035t0001g0076 others(13): Show |
20 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.985-193C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961393 | |||||||
| chr16:69961394 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.985-192G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961394 | |||||||
| chr16:69961419 | G | A | 1 | a0022c0030t0001g0081 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.985-167G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961419 | |||||||
| chr16:69961460 | G | A | 1 | a0002c0002t0001g0167 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.985-126G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961460 | |||||||
| chr16:69961515 | G | A | 9 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(6): Show |
12 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.985-71G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961515 | |||||||
| chr16:69961522 | G | C | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.985-64G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961522 | |||||||
| chr16:69961529 | G | T | 1 | a0002c0002t0001g0168 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.985-57G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961529 | |||||||
| chr16:69961542 | G | C | 5 | a0001c0032t0001g0089 a0001c0035t0001g0076 a0014c0016t0010g0101 others(2): Show |
5 | HG02647.hp2 HG06807.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.985-44G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961542 | |||||||
| chr16:69961554 | C | A | 186 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(183): Show |
323 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(320): Show |
intron_variant | MODIFIER | c.985-32C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 8/11 | chr16 | 69961554 | |||||||
| chr16:69961719 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18980.hp2 | splice_region_variant&intron_variant | LOW | c.1114+4A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/11 | chr16 | 69961719 | |||||||
| chr16:69961738 | G | T | 2 | a0001c0001t0004g0067 a0001c0001t0004g0068 |
2 | NA18940.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1114+23G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/11 | chr16 | 69961738 | |||||||
| chr16:69961760 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(135): Show |
265 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1114+45A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/11 | chr16 | 69961760 | |||||||
| chr16:69961812 | C | G | 5 | a0002c0002t0001g0024 a0002c0002t0001g0045 a0002c0002t0001g0168 others(2): Show |
7 | HG00621.hp1 HG02015.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+97C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/11 | chr16 | 69961812 | |||||||
| chr16:69961829 | C | T | 1 | a0002c0002t0001g0052 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1114+114C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/11 | chr16 | 69961829 | |||||||
| chr16:69961857 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1115-131C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/11 | chr16 | 69961857 | |||||||
| chr16:69961873 | A | G | 180 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(177): Show |
314 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.1115-115A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/11 | chr16 | 69961873 | |||||||
| chr16:69961908 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(14): Show |
25 | HG00438.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1115-80C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 9/11 | chr16 | 69961908 | |||||||
| chr16:69962134 | G | A | 10 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(7): Show |
14 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.1211+50G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962134 | |||||||
| chr16:69962141 | G | A | 40 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(37): Show |
47 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1211+57G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962141 | |||||||
| chr16:69962144 | G | GC | 16 | a0001c0001t0004g0060 a0002c0002t0001g0168 a0007c0007t0003g0151 others(13): Show |
18 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.1211+66dupC | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 69962144 | ||||||
| chr16:69962156 | G | A | 3 | a0014c0016t0010g0101 a0014c0016t0010g0102 a0025c0025t0012g0088 |
3 | HG02647.hp2 NA18973.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1211+72G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962156 | |||||||
| chr16:69962226 | C | T | 35 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(32): Show |
66 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1211+142C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962226 | |||||||
| chr16:69962270 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0022 others(12): Show |
40 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1211+186G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962270 | |||||||
| chr16:69962282 | A | AC | 13 | a0003c0003t0002g0183 a0008c0009t0006g0038 a0008c0009t0006g0039 others(10): Show |
16 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1211+199dupC | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr16 | 69962282 | ||||||
| chr16:69962300 | C | T | 2 | a0004c0004t0003g0042 a0004c0004t0003g0043 |
4 | HG01070.hp1 HG01168.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1211+216C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962300 | |||||||
| chr16:69962343 | G | GC | 53 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(50): Show |
63 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1211+259_1211+260i others(3): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962343 | |||||||
| chr16:69962343 | G | GCTGTGAC others(6888): Show |
1 | a0004c0004t0003g0144 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1211+259_1211+260i others(6897): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962343 | |||||||
| chr16:69962356 | C | T | 13 | a0004c0004t0003g0144 a0008c0009t0006g0038 a0008c0009t0006g0039 others(10): Show |
16 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1211+272C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962356 | |||||||
| chr16:69962384 | G | C | 54 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(51): Show |
64 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1211+300G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962384 | |||||||
| chr16:69962518 | C | T | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1211+434C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962518 | |||||||
| chr16:69962550 | A | G | 49 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(46): Show |
59 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1212-426A>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962550 | |||||||
| chr16:69962579 | G | T | 9 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(6): Show |
12 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1212-397G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962579 | |||||||
| chr16:69962583 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1212-393C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962583 | |||||||
| chr16:69962634 | C | T | 8 | a0004c0004t0003g0144 a0008c0009t0006g0038 a0008c0009t0006g0039 others(5): Show |
9 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1212-342C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962634 | |||||||
| chr16:69962635 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1212-341G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962635 | |||||||
| chr16:69962639 | T | TCTTGCCT others(6): Show |
1 | a0003c0003t0002g0183 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1212-337_1212-336i others(15): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962639 | |||||||
| chr16:69962653 | C | G | 146 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(143): Show |
274 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.1212-323C>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962653 | |||||||
| chr16:69962693 | G | A | 136 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(133): Show |
263 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.1212-283G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962693 | |||||||
| chr16:69962721 | G | A | 45 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0040 others(42): Show |
52 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.1212-255G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962721 | |||||||
| chr16:69962779 | G | C | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0104 |
3 | HG02055.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1212-197G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962779 | |||||||
| chr16:69962783 | C | A | 1 | a0023c0034t0013g0186 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1212-193C>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962783 | |||||||
| chr16:69962835 | G | C | 4 | a0001c0001t0001g0191 a0001c0008t0001g0049 a0001c0008t0001g0192 others(1): Show |
5 | HG02055.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-141G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962835 | |||||||
| chr16:69962836 | G | A | 1 | a0001c0008t0007g0029 | 3 | HG02258.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1212-140G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962836 | |||||||
| chr16:69962848 | G | A | 48 | a0001c0008t0007g0029 a0004c0004t0003g0016 a0004c0004t0003g0031 others(45): Show |
59 | HG00609.hp1 HG00642.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.1212-128G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962848 | |||||||
| chr16:69962865 | G | T | 1 | a0010c0011t0008g0025 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1212-111G>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962865 | |||||||
| chr16:69962883 | C | T | 2 | a0010c0011t0008g0025 a0018c0036t0001g0181 |
4 | HG01891.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1212-93C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962883 | |||||||
| chr16:69962928 | G | GA | 15 | a0004c0004t0003g0042 a0004c0004t0003g0144 a0008c0009t0006g0038 others(12): Show |
19 | HG00438.hp2 HG01070.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1212-48_1212-47ins others(1): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6885): Show |
1 | a0007c0007t0003g0175 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6892): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6886): Show |
1 | a0007c0007t0003g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6893): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6878): Show |
1 | a0007c0007t0003g0173 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6885): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(13778): Show |
1 | a0017c0019t0003g0140 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(13785): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6886): Show |
1 | a0004c0004t0003g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6893): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6885): Show |
3 | a0004c0004t0003g0055 a0004c0004t0003g0132 a0004c0004t0003g0137 |
3 | HG01074.hp1 NA18943.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1212-48_1212-47ins others(6892): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6886): Show |
1 | a0007c0007t0003g0150 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6893): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6886): Show |
1 | a0004c0004t0003g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6893): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6886): Show |
14 | a0004c0004t0003g0016 a0004c0004t0003g0031 a0004c0004t0003g0043 others(11): Show |
18 | HG00642.hp1 HG01109.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1212-48_1212-47ins others(6893): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(13775): Show |
1 | a0004c0004t0003g0133 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(13782): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6882): Show |
2 | a0004c0004t0003g0127 a0004c0004t0003g0129 |
2 | HG01123.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1212-48_1212-47ins others(6889): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6888): Show |
1 | a0004c0004t0003g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6895): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6887): Show |
4 | a0004c0004t0003g0040 a0004c0004t0003g0130 a0011c0023t0003g0143 others(1): Show |
5 | HG00609.hp1 HG00741.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1212-48_1212-47ins others(6894): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6883): Show |
1 | a0007c0007t0003g0151 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6890): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6888): Show |
1 | a0004c0004t0003g0145 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6895): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6885): Show |
1 | a0004c0004t0003g0131 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(6892): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(13786): Show |
1 | a0004c0004t0003g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1212-48_1212-47ins others(13793): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962928 | G | GATCCCTG others(6886): Show |
3 | a0004c0004t0003g0041 a0004c0004t0003g0138 a0011c0028t0003g0154 |
4 | HG01261.hp2 HG01981.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212-48_1212-47ins others(6893): Show |
CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962928 | |||||||
| chr16:69962965 | A | C | 15 | a0002c0002t0001g0111 a0005c0006t0001g0107 a0008c0009t0006g0038 others(12): Show |
18 | HG00438.hp2 HG01891.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.1212-11A>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 10/11 | chr16 | 69962965 | |||||||
| chr16:69963082 | G | C | 7 | a0008c0009t0006g0038 a0008c0009t0006g0039 a0008c0009t0006g0117 others(4): Show |
8 | HG00438.hp2 HG01943.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1303+15G>C | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963082 | |||||||
| chr16:69963102 | C | T | 3 | a0014c0016t0010g0101 a0014c0016t0010g0102 a0025c0025t0012g0088 |
3 | HG02647.hp2 NA18973.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1303+35C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963102 | |||||||
| chr16:69963243 | C | T | 1 | a0004c0004t0003g0042 | 2 | HG01070.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1303+176C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963243 | |||||||
| chr16:69963246 | C | T | 2 | a0004c0004t0003g0042 a0023c0034t0013g0186 |
3 | HG01070.hp1 HG01168.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1303+179C>T | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963246 | |||||||
| chr16:69963347 | T | G | 9 | a0001c0001t0004g0100 a0002c0002t0001g0023 a0002c0002t0001g0087 others(6): Show |
12 | HG01070.hp1 HG01168.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1304-227T>G | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963347 | |||||||
| chr16:69963466 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1304-108G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963466 | |||||||
| chr16:69963501 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0027 others(6): Show |
22 | HG01243.hp1 HG01433.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1304-73G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963501 | |||||||
| chr16:69963508 | G | A | 4 | a0014c0016t0010g0101 a0014c0016t0010g0102 a0023c0034t0013g0186 others(1): Show |
4 | HG02647.hp2 NA18943.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1304-66G>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963508 | |||||||
| chr16:69963529 | T | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0022 others(12): Show |
40 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.1304-45T>A | CLEC18A | ENSG00000157322.18 | transcript | ENST00000288040.11 | protein_coding | 11/11 | chr16 | 69963529 |