Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 93978 |
| ensemblid | ENSG00000205846.4 |
| hgncid | 14556 |
| symbol | CLEC6A |
| name | C-type lectin domain containing 6A |
| refseq_nuc | NM_001007033.2 |
| refseq_prot | NP_001007034.1 |
| ensembl_nuc | ENST00000382073.4 |
| ensembl_prot | ENSP00000371505.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 8455962 |
| end | 8478330 |
| strand | + |
| ver | v1.2 |
| region | chr12:8455962-8478330 |
| region5000 | chr12:8450962-8483330 |
| regionname0 | CLEC6A_chr12_8455962_8478330 |
| regionname5000 | CLEC6A_chr12_8450962_8483330 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 209 | 316 | 77 | 63 | 126 | 12 | 36 | 98 | CLEC6A_chr12_8450962_8483330 | CLEC6A | MMQEQ others(204): Show |
chr12 | 8450962 | 8483330 |
| a0002 | 0/0 | 209 | 9 | 6 | 3 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | MMQEQ others(204): Show |
chr12 | 8450962 | 8483330 |
| a0003 | 0/0 | 209 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | MMQEQ others(204): Show |
chr12 | 8450962 | 8483330 |
| a0004 | 0/0 | 209 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | MMQEQ others(204): Show |
chr12 | 8450962 | 8483330 |
| a0005 | 0/0 | 209 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | MMQEQ others(204): Show |
chr12 | 8450962 | 8483330 |
| a0006 | 0/0 | 199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | MMQEQ others(194): Show |
chr12 | 8450962 | 8483330 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 627 | 316 | 77 | 63 | 126 | 12 | 36 | CLEC6A_chr12_8450962_8483330 | CLEC6A | ATGAT others(622): Show |
chr12 | 8450962 | 8483330 | ||
| a0002c0002 | 0/0 | 627 | 9 | 6 | 3 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | ATGAT others(622): Show |
chr12 | 8450962 | 8483330 | ||
| a0003c0003 | 0/0 | 627 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | ATGAT others(622): Show |
chr12 | 8450962 | 8483330 | ||
| a0004c0004 | 0/0 | 627 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | ATGAT others(622): Show |
chr12 | 8450962 | 8483330 | ||
| a0005c0005 | 0/0 | 627 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | ATGAT others(622): Show |
chr12 | 8450962 | 8483330 | ||
| a0006c0006 | 0/0 | 627 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | ATGAT others(622): Show |
chr12 | 8450962 | 8483330 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1646 | 252 | 43 | 51 | 120 | 9 | 28 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0001c0001t0002 | 0/0 | 1646 | 44 | 18 | 12 | 4 | 3 | 7 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0001c0001t0003 | 0/0 | 1646 | 8 | 8 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0001c0001t0004 | 1/0 | 1646 | 5 | 4 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0001c0001t0006 | 0/0 | 1646 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0001c0001t0008 | 0/0 | 1646 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0001c0001t0009 | 0/0 | 1646 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0001c0001t0010 | 0/0 | 1646 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0001c0001t0011 | 0/0 | 1646 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0002c0002t0002 | 0/0 | 1646 | 9 | 6 | 3 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0003c0003t0005 | 0/0 | 1646 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0003c0003t0007 | 0/0 | 1646 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0004c0004t0005 | 0/0 | 1646 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0005c0005t0001 | 0/0 | 1646 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| a0006c0006t0001 | 0/0 | 1646 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | AATGT others(1641): Show |
chr12 | 8450962 | 8483330 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 55 | 4 | 11 | 29 | 3 | 8 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0002 | 0/1 | 26 | 5 | 2 | 14 | 3 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0004 | 0/0 | 13 | 2 | 7 | 3 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0005 | 0/0 | 11 | 1 | 8 | 0 | 0 | 2 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0006 | 0/0 | 9 | 7 | 2 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0003 | 0/0 | 15 | 6 | 5 | 1 | 0 | 3 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0008 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0034 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0003g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0004g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0006g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0002c0002t0002g0003 | 0/0 | 8 | 5 | 3 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0003c0003t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0003c0003t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0003c0003t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0004c0004t0005g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0005c0005t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| a0006c0006t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0111 | EUR | GBR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | FIN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02257 | hp1 | a0003 | c0003 | t0005 | g0018 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0041 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02630 | hp1 | a0003 | c0003 | t0005 | g0018 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02895 | hp1 | a0005 | c0005 | t0001 | g0002 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02965 | hp1 | a0004 | c0004 | t0005 | g0018 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02965 | hp2 | a0003 | c0003 | t0007 | g0039 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03041 | hp1 | a0005 | c0005 | t0001 | g0002 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03195 | hp1 | a0006 | c0006 | t0001 | g0059 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | YRI | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | YRI | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18953 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19001 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19043 | hp2 | a0003 | c0003 | t0007 | g0040 | AFR | LWK | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ASW | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | ASW | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02109 | hp2 | a0004 | c0004 | t0005 | g0018 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | USA | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0002 | REF | REF | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0107 | REF | REF | CLEC6A_chr12_8450962_8483330 | CLEC6A | chr12 | 8450962 | 8483330 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8457949 | T | A | 1 | a0002 | 9 | HG01168.hp2 HG01169.hp2 HG01993.hp1 others(6): Show |
missense_variant | MODERATE | c.83T>A | p.Ile28Asn | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/6 | 233/1646 | 83/630 | 28/209 | chr12 | 8457949 | |||
| chr12:8457982 | G | C | 2 | a0003 a0004 |
6 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
missense_variant | MODERATE | c.116G>C | p.Cys39Ser | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/6 | 266/1646 | 116/630 | 39/209 | chr12 | 8457982 | |||
| chr12:8459698 | G | C | 1 | a0005 | 2 | HG02895.hp1 HG03041.hp1 |
missense_variant&splice_region_variant | MODERATE | c.223G>C | p.Ala75Pro | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/6 | 373/1646 | 223/630 | 75/209 | chr12 | 8459698 | |||
| chr12:8465590 | G | A | 1 | a0004 | 2 | HG02109.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.330G>A | p.Met110Ile | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/6 | 480/1646 | 330/630 | 110/209 | chr12 | 8465590 | |||
| chr12:8477433 | C | A | 1 | a0006 | 1 | HG03195.hp1 | stop_gained | HIGH | c.599C>A | p.Ser200* | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 749/1646 | 599/630 | 200/209 | chr12 | 8477433 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8455987 | A | G | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(5): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-125A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/6 | chr12 | 8455987 | |||||||
| chr12:8477519 | C | T | 1 | a0001c0001t0006 | 2 | HG02145.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*55C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 55 | chr12 | 8477519 | ||||||
| chr12:8477579 | C | T | 1 | a0001c0001t0008 | 2 | NA18953.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 115 | chr12 | 8477579 | ||||||
| chr12:8477639 | C | T | 3 | a0001c0001t0011 a0003c0003t0005 a0004c0004t0005 |
5 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*175C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 175 | chr12 | 8477639 | ||||||
| chr12:8477640 | G | A | 1 | a0001c0001t0009 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*176G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 176 | chr12 | 8477640 | ||||||
| chr12:8477704 | T | C | 1 | a0001c0001t0003 | 8 | HG02055.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*240T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 240 | chr12 | 8477704 | ||||||
| chr12:8477957 | A | G | 1 | a0001c0001t0010 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*493A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 493 | chr12 | 8477957 | ||||||
| chr12:8478080 | T | C | 3 | a0001c0001t0011 a0003c0003t0005 a0004c0004t0005 |
5 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*616T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 616 | chr12 | 8478080 | ||||||
| chr12:8478111 | A | T | 2 | a0003c0003t0005 a0004c0004t0005 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*647A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 647 | chr12 | 8478111 | ||||||
| chr12:8478202 | T | C | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(6): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*738T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 738 | chr12 | 8478202 | ||||||
| chr12:8478326 | C | T | 1 | a0001c0001t0011 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*862C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 6/6 | 862 | chr12 | 8478326 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8456172 | T | C | 2 | a0003c0003t0007g0039 a0003c0003t0007g0040 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.31+30T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456172 | |||||||
| chr12:8456403 | A | T | 2 | a0003c0003t0007g0039 a0003c0003t0007g0040 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.31+261A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456403 | |||||||
| chr12:8456446 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.31+304A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456446 | |||||||
| chr12:8456531 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+389T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456531 | |||||||
| chr12:8456540 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.31+398G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456540 | |||||||
| chr12:8456615 | A | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.31+473A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456615 | |||||||
| chr12:8456622 | T | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.31+480T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456622 | |||||||
| chr12:8456623 | T | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0043 |
5 | HG01255.hp1 HG02572.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.31+481T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456623 | |||||||
| chr12:8456680 | C | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.31+538C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456680 | |||||||
| chr12:8456691 | A | G | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+549A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456691 | |||||||
| chr12:8456736 | C | T | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+594C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456736 | |||||||
| chr12:8456780 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.31+638C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456780 | |||||||
| chr12:8456793 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.31+651C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456793 | |||||||
| chr12:8456997 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.31+855C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8456997 | |||||||
| chr12:8457078 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.32-820T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457078 | |||||||
| chr12:8457096 | T | C | 4 | a0001c0001t0002g0019 a0001c0001t0002g0108 a0001c0001t0002g0109 others(1): Show |
6 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-802T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457096 | |||||||
| chr12:8457152 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.32-746G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457152 | |||||||
| chr12:8457178 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.32-720C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457178 | |||||||
| chr12:8457199 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(40): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.32-699C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457199 | |||||||
| chr12:8457207 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0009g0041 |
2 | HG02602.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.32-691C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457207 | |||||||
| chr12:8457230 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.32-668G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457230 | |||||||
| chr12:8457249 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.32-649G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457249 | |||||||
| chr12:8457523 | C | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.32-375C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457523 | |||||||
| chr12:8457562 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.32-336C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457562 | |||||||
| chr12:8457627 | C | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.32-271C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457627 | |||||||
| chr12:8457672 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.32-226C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457672 | |||||||
| chr12:8457695 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.32-203T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457695 | |||||||
| chr12:8457721 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.32-177A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457721 | |||||||
| chr12:8457756 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.32-142G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457756 | |||||||
| chr12:8457756 | G | T | 4 | a0003c0003t0005g0018 a0003c0003t0007g0039 a0003c0003t0007g0040 others(1): Show |
6 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-142G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 1/5 | chr12 | 8457756 | |||||||
| chr12:8457994 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02602.hp1 | splice_region_variant&intron_variant | LOW | c.121+7T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8457994 | |||||||
| chr12:8458062 | T | G | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+75T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458062 | |||||||
| chr12:8458135 | T | A | 1 | a0001c0001t0001g0045 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.121+148T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458135 | |||||||
| chr12:8458223 | A | G | 2 | a0003c0003t0007g0039 a0003c0003t0007g0040 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.121+236A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458223 | |||||||
| chr12:8458452 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.121+465A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458452 | |||||||
| chr12:8458484 | A | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.121+497A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458484 | |||||||
| chr12:8458524 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.121+537T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458524 | |||||||
| chr12:8458533 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.121+546G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458533 | |||||||
| chr12:8458580 | G | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.121+593G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458580 | |||||||
| chr12:8458629 | G | T | 1 | a0001c0001t0002g0038 | 2 | HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.121+642G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458629 | |||||||
| chr12:8458832 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.122-765G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458832 | |||||||
| chr12:8458833 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.122-764T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458833 | |||||||
| chr12:8458892 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.122-705T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8458892 | |||||||
| chr12:8459172 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.122-425T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8459172 | |||||||
| chr12:8459236 | T | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG00140.hp2 HG01257.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-361T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8459236 | |||||||
| chr12:8459348 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.122-249C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8459348 | |||||||
| chr12:8459368 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(91): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.122-229A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8459368 | |||||||
| chr12:8459388 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.122-209G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8459388 | |||||||
| chr12:8459448 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.122-149A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 2/5 | chr12 | 8459448 | |||||||
| chr12:8459740 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.223+42G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8459740 | |||||||
| chr12:8459885 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.223+187A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8459885 | |||||||
| chr12:8459888 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.223+190T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8459888 | |||||||
| chr12:8460151 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.223+453C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460151 | |||||||
| chr12:8460195 | A | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.223+497A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460195 | |||||||
| chr12:8460332 | T | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0080 others(3): Show |
17 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.223+634T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460332 | |||||||
| chr12:8460395 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02165.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.223+697T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460395 | |||||||
| chr12:8460483 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.223+785C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460483 | |||||||
| chr12:8460517 | G | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0078 a0001c0001t0001g0084 |
6 | HG00609.hp2 HG02027.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+819G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460517 | |||||||
| chr12:8460556 | G | C | 1 | a0001c0001t0009g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.223+858G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460556 | |||||||
| chr12:8460608 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.223+910A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460608 | |||||||
| chr12:8460709 | G | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0108 a0001c0001t0002g0109 others(1): Show |
6 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1011G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460709 | |||||||
| chr12:8460790 | G | T | 5 | a0001c0001t0009g0041 a0003c0003t0005g0018 a0003c0003t0007g0039 others(2): Show |
7 | HG02109.hp2 HG02257.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1092G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460790 | |||||||
| chr12:8460816 | A | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.223+1118A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460816 | |||||||
| chr12:8460849 | G | A | 5 | a0001c0001t0009g0041 a0003c0003t0005g0018 a0003c0003t0007g0039 others(2): Show |
7 | HG02109.hp2 HG02257.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1151G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460849 | |||||||
| chr12:8460862 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.223+1164G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460862 | |||||||
| chr12:8460880 | G | C | 2 | a0003c0003t0007g0039 a0003c0003t0007g0040 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223+1182G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460880 | |||||||
| chr12:8460931 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.223+1233G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8460931 | |||||||
| chr12:8461095 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0003g0023 |
5 | HG02896.hp1 HG02897.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1397G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461095 | |||||||
| chr12:8461101 | T | C | 2 | a0003c0003t0007g0039 a0003c0003t0007g0040 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223+1403T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461101 | |||||||
| chr12:8461198 | T | C | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.223+1500T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461198 | |||||||
| chr12:8461332 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.223+1634T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461332 | |||||||
| chr12:8461477 | C | T | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+1779C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461477 | |||||||
| chr12:8461548 | G | A | 2 | a0003c0003t0007g0039 a0003c0003t0007g0040 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223+1850G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461548 | |||||||
| chr12:8461579 | G | T | 1 | a0001c0001t0001g0029 | 2 | NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.223+1881G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461579 | |||||||
| chr12:8461642 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.223+1944T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461642 | |||||||
| chr12:8461910 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.223+2212G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461910 | |||||||
| chr12:8461912 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.223+2214C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461912 | |||||||
| chr12:8461950 | C | A | 3 | a0001c0001t0011g0116 a0003c0003t0005g0018 a0004c0004t0005g0018 |
5 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+2252C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461950 | |||||||
| chr12:8461960 | G | T | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.223+2262G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8461960 | |||||||
| chr12:8461981 | GA | G | 1 | a0001c0001t0001g0010 | 7 | NA18961.hp1 NA18977.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.223+2285delA | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 8461981 | ||||||
| chr12:8462056 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.223+2358G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462056 | |||||||
| chr12:8462057 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG00408.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.223+2359C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462057 | |||||||
| chr12:8462073 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.223+2375G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462073 | |||||||
| chr12:8462089 | G | C | 1 | a0001c0001t0003g0023 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.223+2391G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462089 | |||||||
| chr12:8462094 | G | T | 1 | a0001c0001t0001g0010 | 7 | NA18961.hp1 NA18977.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.223+2396G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462094 | |||||||
| chr12:8462172 | C | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.223+2474C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462172 | |||||||
| chr12:8462223 | T | C | 1 | a0001c0001t0009g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.223+2525T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462223 | |||||||
| chr12:8462308 | G | A | 1 | a0003c0003t0007g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.223+2610G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462308 | |||||||
| chr12:8462321 | C | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.223+2623C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462321 | |||||||
| chr12:8462330 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.223+2632G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462330 | |||||||
| chr12:8462355 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.223+2657G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462355 | |||||||
| chr12:8462356 | G | T | 3 | a0001c0001t0011g0116 a0003c0003t0005g0018 a0004c0004t0005g0018 |
5 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+2658G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462356 | |||||||
| chr12:8462390 | C | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.223+2692C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462390 | |||||||
| chr12:8462395 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0055 |
3 | NA18968.hp1 NA19007.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.223+2697C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462395 | |||||||
| chr12:8462438 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | NA18948.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.223+2740G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462438 | |||||||
| chr12:8462442 | A | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.223+2744A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462442 | |||||||
| chr12:8462462 | G | A | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+2764G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462462 | |||||||
| chr12:8462482 | T | C | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.223+2784T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462482 | |||||||
| chr12:8462508 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.223+2810C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462508 | |||||||
| chr12:8462523 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01943.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.223+2825G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462523 | |||||||
| chr12:8462558 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.223+2860T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462558 | |||||||
| chr12:8462592 | C | A | 1 | a0001c0001t0001g0017 | 4 | HG02735.hp2 NA18968.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-2892C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462592 | |||||||
| chr12:8462629 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-2855T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462629 | |||||||
| chr12:8462641 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.224-2843C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462641 | |||||||
| chr12:8462682 | C | A | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-2802C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462682 | |||||||
| chr12:8462846 | C | T | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.224-2638C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8462846 | |||||||
| chr12:8463006 | T | A | 1 | a0001c0001t0001g0011 | 5 | HG00099.hp1 HG01175.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-2478T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463006 | |||||||
| chr12:8463123 | GAACT | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-2358_224-2355d others(6): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 8463123 | ||||||
| chr12:8463213 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-2271C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463213 | |||||||
| chr12:8463306 | T | G | 1 | a0001c0001t0001g0006 | 9 | HG01167.hp1 HG01169.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-2178T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463306 | |||||||
| chr12:8463315 | A | T | 1 | a0002c0002t0002g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.224-2169A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463315 | |||||||
| chr12:8463330 | C | CTA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-2153_224-2152i others(4): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 8463330 | ||||||
| chr12:8463553 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.224-1931T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463553 | |||||||
| chr12:8463796 | G | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-1688G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463796 | |||||||
| chr12:8463806 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-1678C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463806 | |||||||
| chr12:8463840 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-1644C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463840 | |||||||
| chr12:8463856 | AC | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0043 |
4 | HG02572.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-1625delC | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 8463856 | ||||||
| chr12:8463913 | G | C | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-1571G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463913 | |||||||
| chr12:8463954 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.224-1530G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8463954 | |||||||
| chr12:8464012 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.224-1472T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464012 | |||||||
| chr12:8464335 | T | TTC | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.224-1148_224-1147i others(4): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 8464335 | ||||||
| chr12:8464361 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-1123T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464361 | |||||||
| chr12:8464364 | C | G | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.224-1120C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464364 | |||||||
| chr12:8464408 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0081 |
3 | HG01943.hp1 HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.224-1076T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464408 | |||||||
| chr12:8464422 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-1062T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464422 | |||||||
| chr12:8464475 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-1009T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464475 | |||||||
| chr12:8464579 | G | A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0035 a0001c0001t0002g0110 others(1): Show |
13 | HG00642.hp2 HG00738.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.224-905G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464579 | |||||||
| chr12:8464623 | C | A | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-861C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464623 | |||||||
| chr12:8464663 | T | G | 1 | a0006c0006t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.224-821T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464663 | |||||||
| chr12:8464818 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.224-666T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464818 | |||||||
| chr12:8464944 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.224-540C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8464944 | |||||||
| chr12:8465051 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.224-433T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8465051 | |||||||
| chr12:8465161 | G | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.224-323G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8465161 | |||||||
| chr12:8465236 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.224-248A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8465236 | |||||||
| chr12:8465243 | C | CT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.224-228dupT | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 8465243 | ||||||
| chr12:8465272 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.224-212G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8465272 | |||||||
| chr12:8465285 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.224-199C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8465285 | |||||||
| chr12:8465380 | A | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-104A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8465380 | |||||||
| chr12:8465386 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.224-98G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | chr12 | 8465386 | |||||||
| chr12:8465465 | T | TC | 5 | a0001c0001t0004g0037 a0001c0001t0004g0112 a0001c0001t0004g0113 others(2): Show |
6 | HG01884.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-18dupC | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 8465465 | ||||||
| chr12:8465803 | A | G | 3 | a0001c0001t0004g0037 a0001c0001t0004g0112 a0001c0001t0004g0113 |
4 | HG01884.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+174A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8465803 | |||||||
| chr12:8465854 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.369+225G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8465854 | |||||||
| chr12:8465892 | A | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.369+263A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8465892 | |||||||
| chr12:8465967 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+338G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8465967 | |||||||
| chr12:8466246 | G | C | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+617G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466246 | |||||||
| chr12:8466327 | G | A | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.369+698G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466327 | |||||||
| chr12:8466375 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+746T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466375 | |||||||
| chr12:8466441 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+812T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466441 | |||||||
| chr12:8466509 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+880T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466509 | |||||||
| chr12:8466531 | C | G | 1 | a0001c0001t0009g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+902C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466531 | |||||||
| chr12:8466625 | C | G | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.369+996C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466625 | |||||||
| chr12:8466662 | G | GT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1044dupT | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8466662 | ||||||
| chr12:8466694 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1065T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466694 | |||||||
| chr12:8466695 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.369+1066G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466695 | |||||||
| chr12:8466696 | C | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0108 a0001c0001t0002g0109 others(1): Show |
6 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1067C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466696 | |||||||
| chr12:8466716 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.369+1087C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466716 | |||||||
| chr12:8466740 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.369+1111C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466740 | |||||||
| chr12:8466741 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.369+1112T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466741 | |||||||
| chr12:8466742 | G | A | 1 | a0001c0001t0001g0021 | 3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.369+1113G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466742 | |||||||
| chr12:8466748 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1119C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466748 | |||||||
| chr12:8466768 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1139C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466768 | |||||||
| chr12:8466780 | G | T | 1 | a0001c0001t0001g0033 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.369+1151G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466780 | |||||||
| chr12:8466843 | T | TG | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1217dupG | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8466843 | ||||||
| chr12:8466943 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.369+1314C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466943 | |||||||
| chr12:8466966 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1337C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8466966 | |||||||
| chr12:8467022 | C | T | 1 | a0001c0001t0009g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369+1393C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467022 | |||||||
| chr12:8467091 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.369+1462T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467091 | |||||||
| chr12:8467104 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.369+1475A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467104 | |||||||
| chr12:8467196 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1567G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467196 | |||||||
| chr12:8467253 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.369+1624C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467253 | |||||||
| chr12:8467256 | A | G | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1627A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467256 | |||||||
| chr12:8467262 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0010g0019 |
4 | HG02055.hp2 HG02109.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+1633T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467262 | |||||||
| chr12:8467372 | C | T | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.369+1743C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467372 | |||||||
| chr12:8467377 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0089 others(1): Show |
12 | HG00438.hp2 HG01168.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+1748G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467377 | |||||||
| chr12:8467469 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1840A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467469 | |||||||
| chr12:8467538 | C | CA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1910dupA | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8467538 | ||||||
| chr12:8467589 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+1960G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467589 | |||||||
| chr12:8467743 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.369+2114G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467743 | |||||||
| chr12:8467828 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.369+2199T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467828 | |||||||
| chr12:8467855 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.369+2226T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467855 | |||||||
| chr12:8467914 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.369+2285T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467914 | |||||||
| chr12:8467954 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+2325T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467954 | |||||||
| chr12:8467955 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+2326T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467955 | |||||||
| chr12:8467956 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+2327T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8467956 | |||||||
| chr12:8468194 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+2565C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8468194 | |||||||
| chr12:8468204 | A | C | 1 | a0001c0001t0006g0036 | 2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.369+2575A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8468204 | |||||||
| chr12:8468471 | A | G | 5 | a0001c0001t0004g0037 a0001c0001t0004g0112 a0001c0001t0004g0113 others(2): Show |
6 | HG01884.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2842A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8468471 | |||||||
| chr12:8468538 | G | A | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+2909G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8468538 | |||||||
| chr12:8468650 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.369+3021C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8468650 | |||||||
| chr12:8468874 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+3245A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8468874 | |||||||
| chr12:8468929 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.369+3300C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8468929 | |||||||
| chr12:8468937 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.369+3308G>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8468937 | |||||||
| chr12:8469132 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.369+3503A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8469132 | |||||||
| chr12:8469198 | A | T | 1 | a0001c0001t0001g0069 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.369+3569A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8469198 | |||||||
| chr12:8469511 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+3882C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8469511 | |||||||
| chr12:8469671 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
10 | HG02602.hp2 HG04204.hp1 HG06807.hp2 others(7): Show |
intron_variant | MODIFIER | c.369+4042C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8469671 | |||||||
| chr12:8469672 | G | A | 1 | a0006c0006t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.369+4043G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8469672 | |||||||
| chr12:8469892 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+4263A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8469892 | |||||||
| chr12:8469940 | T | G | 3 | a0001c0001t0004g0037 a0001c0001t0004g0112 a0001c0001t0004g0113 |
4 | HG01884.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+4311T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8469940 | |||||||
| chr12:8470003 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+4374A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470003 | |||||||
| chr12:8470066 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.369+4437T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470066 | |||||||
| chr12:8470136 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.369+4507C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470136 | |||||||
| chr12:8470241 | C | A | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.369+4612C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470241 | |||||||
| chr12:8470296 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+4667G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470296 | |||||||
| chr12:8470368 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+4739T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470368 | |||||||
| chr12:8470401 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.369+4772T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470401 | |||||||
| chr12:8470427 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+4798C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470427 | |||||||
| chr12:8470499 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+4870C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470499 | |||||||
| chr12:8470505 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.369+4876A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470505 | |||||||
| chr12:8470637 | T | C | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.369+5008T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470637 | |||||||
| chr12:8470647 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.369+5018A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470647 | |||||||
| chr12:8470665 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.369+5036T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470665 | |||||||
| chr12:8470703 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.369+5074T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470703 | |||||||
| chr12:8470727 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.369+5098T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470727 | |||||||
| chr12:8470874 | A | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.369+5245A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470874 | |||||||
| chr12:8470963 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.370-5162C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8470963 | |||||||
| chr12:8471015 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.370-5110A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471015 | |||||||
| chr12:8471051 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(9): Show |
36 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.370-5074A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471051 | |||||||
| chr12:8471060 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.370-5065T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471060 | |||||||
| chr12:8471169 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0077 |
9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.370-4956A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471169 | |||||||
| chr12:8471190 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.370-4935G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471190 | |||||||
| chr12:8471192 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.370-4933A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471192 | |||||||
| chr12:8471219 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.370-4906G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471219 | |||||||
| chr12:8471253 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.370-4872A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471253 | |||||||
| chr12:8471329 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.370-4796C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471329 | |||||||
| chr12:8471351 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.370-4774G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471351 | |||||||
| chr12:8471495 | A | G | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-4630A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471495 | |||||||
| chr12:8471567 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.370-4558A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471567 | |||||||
| chr12:8471594 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.370-4531T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471594 | |||||||
| chr12:8471899 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.370-4226T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471899 | |||||||
| chr12:8471968 | G | A | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-4157G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8471968 | |||||||
| chr12:8472147 | C | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0108 a0001c0001t0010g0019 |
5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-3978C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8472147 | |||||||
| chr12:8472294 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.370-3831T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8472294 | |||||||
| chr12:8472347 | A | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0101 |
2 | NA18962.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.370-3778A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8472347 | |||||||
| chr12:8472982 | TAGCTCCT others(304): Show |
T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.370-3128_370-2818d others(2): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8472982 | ||||||
| chr12:8472994 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0015 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.370-3123_370-3112d others(14): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8472994 | ||||||
| chr12:8472994 | C | CTTTTTTT others(6): Show |
8 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0015 others(5): Show |
26 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.370-3124_370-3112d others(15): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8472994 | ||||||
| chr12:8472994 | C | CTTTTTTT others(7): Show |
7 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0015 others(4): Show |
17 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.370-3125_370-3112d others(16): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8472994 | ||||||
| chr12:8472994 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0006g0036 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.370-3129_370-3112d others(20): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8472994 | ||||||
| chr12:8472994 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0002g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.370-3112_370-3111i others(23): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8472994 | ||||||
| chr12:8472994 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0002g0019 a0001c0001t0002g0108 a0001c0001t0006g0036 others(1): Show |
5 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-3112_370-3111i others(24): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8472994 | ||||||
| chr12:8473058 | C | T | 1 | a0003c0003t0007g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.370-3067C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473058 | |||||||
| chr12:8473145 | G | A | 2 | a0002c0002t0002g0003 a0002c0002t0002g0114 |
9 | HG01168.hp2 HG01169.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-2980G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473145 | |||||||
| chr12:8473274 | G | A | 1 | a0001c0001t0002g0015 | 5 | HG01884.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-2851G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473274 | |||||||
| chr12:8473444 | A | T | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-2681A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473444 | |||||||
| chr12:8473484 | G | A | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-2641G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473484 | |||||||
| chr12:8473495 | G | A | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-2630G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473495 | |||||||
| chr12:8473541 | A | T | 1 | a0001c0001t0009g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.370-2584A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473541 | |||||||
| chr12:8473588 | A | G | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-2537A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473588 | |||||||
| chr12:8473631 | T | C | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-2494T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473631 | |||||||
| chr12:8473758 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG01168.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.370-2367G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473758 | |||||||
| chr12:8473766 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.370-2359C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473766 | |||||||
| chr12:8473998 | G | T | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-2127G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8473998 | |||||||
| chr12:8474282 | G | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(97): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.370-1843G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8474282 | |||||||
| chr12:8474534 | T | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0093 |
3 | HG00621.hp2 NA18959.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.370-1591T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8474534 | |||||||
| chr12:8474548 | C | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0072 others(1): Show |
8 | HG01952.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-1577C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8474548 | |||||||
| chr12:8474662 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.370-1463C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8474662 | |||||||
| chr12:8474846 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.370-1279A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8474846 | |||||||
| chr12:8474878 | T | C | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-1247T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8474878 | |||||||
| chr12:8474894 | A | T | 17 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0015 others(14): Show |
55 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.370-1231A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8474894 | |||||||
| chr12:8475048 | G | T | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-1077G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475048 | |||||||
| chr12:8475160 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.370-965A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475160 | |||||||
| chr12:8475328 | A | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(93): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.370-797A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475328 | |||||||
| chr12:8475330 | A | C | 3 | a0001c0001t0001g0026 a0001c0001t0002g0015 a0001c0001t0009g0041 |
8 | HG01884.hp2 HG02015.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-795A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475330 | |||||||
| chr12:8475344 | ATG | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(108): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.370-759_370-758del others(2): Show |
CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 8475344 | ||||||
| chr12:8475348 | G | A | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-777G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475348 | |||||||
| chr12:8475418 | G | T | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-707G>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475418 | |||||||
| chr12:8475424 | A | C | 1 | a0001c0001t0001g0093 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.370-701A>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475424 | |||||||
| chr12:8475431 | C | T | 3 | a0001c0001t0011g0116 a0003c0003t0005g0018 a0004c0004t0005g0018 |
5 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-694C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475431 | |||||||
| chr12:8475559 | C | G | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-566C>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475559 | |||||||
| chr12:8475587 | G | A | 1 | a0001c0001t0001g0010 | 7 | NA18961.hp1 NA18977.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.370-538G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475587 | |||||||
| chr12:8475639 | G | A | 2 | a0003c0003t0005g0018 a0004c0004t0005g0018 |
4 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.370-486G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475639 | |||||||
| chr12:8475730 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.370-395C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475730 | |||||||
| chr12:8475786 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.370-339A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475786 | |||||||
| chr12:8475992 | A | T | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.370-133A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 4/5 | chr12 | 8475992 | |||||||
| chr12:8476255 | G | A | 1 | a0001c0001t0009g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485+15G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8476255 | |||||||
| chr12:8476400 | C | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0072 others(1): Show |
8 | HG01952.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.485+160C>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8476400 | |||||||
| chr12:8476481 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.485+241T>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8476481 | |||||||
| chr12:8476492 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.485+252T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8476492 | |||||||
| chr12:8476658 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.485+418C>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8476658 | |||||||
| chr12:8476666 | T | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.485+426T>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8476666 | |||||||
| chr12:8476752 | G | A | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.485+512G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8476752 | |||||||
| chr12:8477043 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.486-277G>A | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8477043 | |||||||
| chr12:8477080 | A | G | 1 | a0001c0001t0011g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.486-240A>G | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8477080 | |||||||
| chr12:8477211 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.486-109A>T | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8477211 | |||||||
| chr12:8477222 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.486-98T>C | CLEC6A | ENSG00000205846.4 | transcript | ENST00000382073.4 | protein_coding | 5/5 | chr12 | 8477222 |