| geneid | 78989 |
|---|---|
| ensemblid | ENSG00000118004.18 |
| hgncid | 17213 |
| symbol | COLEC11 |
| name | collectin subfamily member 11 |
| refseq_nuc | NM_024027.5 |
| refseq_prot | NP_076932.1 |
| ensembl_nuc | ENST00000349077.9 |
| ensembl_prot | ENSP00000339168.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 3595112 |
| end | 3644644 |
| strand | + |
| ver | v1.2 |
| region | chr2:3595112-3644644 |
| region5000 | chr2:3590112-3649644 |
| regionname0 | COLEC11_chr2_3595112_3644644 |
| regionname5000 | COLEC11_chr2_3590112_3649644 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 271 | 284 | 22 | 67 | 144 | 15 | 34 | 108 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002 | 0/0 | 271 | 86 | 70 | 7 | 4 | 1 | 4 | 3 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0003 | 0/0 | 271 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0004 | 0/0 | 271 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0005 | 0/0 | 271 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0006 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0007 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 816 | 280 | 21 | 67 | 144 | 15 | 31 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0002 | 0/0 | 816 | 50 | 46 | 3 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0003 | 0/0 | 816 | 13 | 2 | 3 | 4 | 1 | 3 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0004 | 0/0 | 816 | 9 | 9 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0005 | 0/0 | 816 | 8 | 8 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0006 | 0/0 | 816 | 6 | 5 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0007 | 0/0 | 816 | 3 | 1 | 0 | 0 | 0 | 2 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0008 | 0/0 | 816 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0009 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0010 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0011 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0012 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0013 | 0/0 | 816 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0014 | 0/0 | 816 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| c0015 | 0/0 | 816 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 610 | 366 | 91 | 74 | 146 | 16 | 37 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| t0002 | 0/0 | 610 | 7 | 7 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| t0003 | 0/0 | 610 | 3 | 0 | 0 | 3 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| t0004 | 0/0 | 610 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| t0005 | 0/0 | 610 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 816 | 280 | 21 | 67 | 144 | 15 | 31 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0001c0007 | 0/0 | 816 | 3 | 1 | 0 | 0 | 0 | 2 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0001c0014 | 0/0 | 816 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0002 | 0/0 | 816 | 50 | 46 | 3 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0003 | 0/0 | 816 | 13 | 2 | 3 | 4 | 1 | 3 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0004 | 0/0 | 816 | 9 | 9 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0005 | 0/0 | 816 | 8 | 8 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0006 | 0/0 | 816 | 6 | 5 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0003c0009 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0003c0010 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0003c0012 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0004c0008 | 0/0 | 816 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0005c0011 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0006c0013 | 0/0 | 816 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0007c0015 | 0/0 | 816 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1425 | 275 | 21 | 67 | 140 | 15 | 30 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0001c0001t0003 | 0/0 | 1425 | 3 | 0 | 0 | 3 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0001c0001t0004 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0001c0001t0005 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0001c0007t0001 | 0/0 | 1425 | 3 | 1 | 0 | 0 | 0 | 2 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0001c0014t0001 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0002t0001 | 0/0 | 1425 | 50 | 46 | 3 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0003t0001 | 0/0 | 1425 | 13 | 2 | 3 | 4 | 1 | 3 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0004t0001 | 0/0 | 1425 | 9 | 9 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0005t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0005t0002 | 0/0 | 1425 | 7 | 7 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0002c0006t0001 | 0/0 | 1425 | 6 | 5 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0003c0009t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0003c0010t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0003c0012t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0004c0008t0001 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0005c0011t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0006c0013t0001 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| a0007c0015t0001 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | copy fasta | chr2 | 3590112 | 3649644 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0007t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0007t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0007t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0014t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0003c0009t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0003c0010t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0003c0012t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0004c0008t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0004c0008t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0005c0011t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0006c0013t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0007c0015t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | FIN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0352 | EUR | FIN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0334 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01099 | hp2 | a0002 | c0006 | t0001 | g0199 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01361 | hp2 | a0002 | c0003 | t0001 | g0024 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01884 | hp1 | a0005 | c0011 | t0001 | g0032 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01884 | hp2 | a0003 | c0010 | t0001 | g0357 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0221 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0223 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02015 | hp2 | a0006 | c0013 | t0001 | g0260 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0053 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02055 | hp1 | a0002 | c0005 | t0002 | g0183 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02145 | hp2 | a0002 | c0004 | t0001 | g0289 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02451 | hp1 | a0002 | c0004 | t0001 | g0231 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02572 | hp2 | a0003 | c0012 | t0001 | g0358 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02622 | hp1 | a0002 | c0005 | t0002 | g0181 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02622 | hp2 | a0002 | c0006 | t0001 | g0333 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0347 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0191 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02647 | hp2 | a0002 | c0004 | t0001 | g0322 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02683 | hp2 | a0001 | c0007 | t0001 | g0259 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02717 | hp2 | a0004 | c0008 | t0001 | g0043 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0327 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0217 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0324 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02895 | hp2 | a0002 | c0004 | t0001 | g0246 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02896 | hp1 | a0002 | c0005 | t0002 | g0211 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02897 | hp1 | a0002 | c0005 | t0002 | g0212 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0310 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0326 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02970 | hp1 | a0002 | c0005 | t0002 | g0348 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02970 | hp2 | a0002 | c0006 | t0001 | g0200 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02976 | hp2 | a0002 | c0005 | t0002 | g0018 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0359 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0127 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03098 | hp2 | a0002 | c0006 | t0001 | g0329 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0302 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03195 | hp1 | a0003 | c0009 | t0001 | g0356 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03195 | hp2 | a0004 | c0008 | t0001 | g0225 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0309 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03209 | hp2 | a0002 | c0004 | t0001 | g0214 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03225 | hp1 | a0002 | c0006 | t0001 | g0315 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0286 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0277 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0040 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0317 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0314 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0186 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03834 | hp2 | a0001 | c0007 | t0001 | g0135 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04115 | hp2 | a0001 | c0014 | t0001 | g0156 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0171 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | CHB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0197 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18977 | hp1 | a0007 | c0015 | t0001 | g0159 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0363 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0341 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0233 | EUR | TSI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | GIH | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02486 | hp2 | a0002 | c0006 | t0001 | g0031 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0263 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0318 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03471 | hp2 | a0002 | c0005 | t0002 | g0182 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | USA | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0313 | AFR | USA | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | USA | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | USA | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA21309 | hp1 | a0002 | c0005 | t0001 | g0362 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA21309 | hp2 | a0001 | c0007 | t0001 | g0224 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0274 | REF | REF | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0138 | REF | REF | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:3595166
|
C | T | 1 | a0001 | 1 | HG03017.hp2 | splice_region_variant | LOW | c.-29C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/7 | chr2 | 3595166 | ||||||
| chr2:3604363
|
T | C | 2 | a0003a0005 | 4 | HG01884.hp1 HG01884.hp2 HG02572.hp2 others(1): Show |
missense_variant | MODERATE | c.23T>C | p.Val8Ala | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/7 | 106/1425 | 23/816 | 8/271 | chr2 | 3604363 | ||
| chr2:3613349
|
C | T | 1 | a0007 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.169C>T | p.Arg57Trp | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/7 | 252/1425 | 169/816 | 57/271 | chr2 | 3613349 | ||
| chr2:3613371
|
C | T | 1 | a0004 | 2 | HG02717.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.191C>T | p.Thr64Met | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/7 | 274/1425 | 191/816 | 64/271 | chr2 | 3613371 | ||
| chr2:3643452
|
T | C | 1 | a0006 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.337T>C | p.Cys113Arg | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/7 | 420/1425 | 337/816 | 113/271 | chr2 | 3643452 | ||
| chr2:3643958
|
A | G | 2 | a0002a0003 | 89 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(86): Show |
missense_variant | MODERATE | c.656A>G | p.His219Arg | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 7/7 | 739/1425 | 656/816 | 219/271 | chr2 | 3643958 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:3637573
|
T | C | 2 | a0001c0007a0002c0003 | 16 | HG00741.hp1 HG01361.hp2 HG02004.hp2 others(13): Show |
synonymous_variant | LOW | c.243T>C | p.Arg81Arg | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/7 | 326/1425 | 243/816 | 81/271 | chr2 | 3637573 | ||
| chr2:3637585
|
T | C | 4 | a0002c0005a0002c0006a0003c0009others(1): Show | 16 | HG01099.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
synonymous_variant | LOW | c.255T>C | p.Ile85Ile | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/7 | 338/1425 | 255/816 | 85/271 | chr2 | 3637585 | ||
| chr2:3643475
|
G | A | 1 | a0002c0004 | 9 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
synonymous_variant | LOW | c.360G>A | p.Lys120Lys | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/7 | 443/1425 | 360/816 | 120/271 | chr2 | 3643475 | ||
| chr2:3643481
|
C | T | 2 | a0002c0006a0003c0010 | 7 | HG01099.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
synonymous_variant | LOW | c.366C>T | p.Ile122Ile | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/7 | 449/1425 | 366/816 | 122/271 | chr2 | 3643481 | ||
| chr2:3643848
|
C | T | 1 | a0001c0014 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.546C>T | p.Asp182Asp | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 7/7 | 629/1425 | 546/816 | 182/271 | chr2 | 3643848 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:3595125
|
G | C | 1 | a0001c0001t0004 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/7 | 9216 | chr2 | 3595125 | |||||
| chr2:3595126
|
C | G | 1 | a0001c0001t0004 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/7 | 9215 | chr2 | 3595126 | |||||
| chr2:3644140
|
T | C | 1 | a0002c0005t0002 | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*22T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 7/7 | 22 | chr2 | 3644140 | |||||
| chr2:3644422
|
A | G | 1 | a0001c0001t0003 | 3 | HG02027.hp1 HG02080.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*304A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 7/7 | 304 | chr2 | 3644422 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:3595303
|
A | G | 1 | a0001c0001t0001g0365 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-27+135A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595303 | ||||||
| chr2:3595387
|
A | G | 1 | a0001c0001t0001g0364 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-27+219A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595387 | ||||||
| chr2:3595428
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-27+260T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595428 | ||||||
| chr2:3595492
|
G | A | 1 | a0002c0002t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-27+324G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595492 | ||||||
| chr2:3595559
|
G | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 18 | HG00140.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27+391G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595559 | ||||||
| chr2:3595587
|
C | G | 1 | a0002c0002t0001g0363 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-27+419C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595587 | ||||||
| chr2:3595796
|
C | T | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-27+628C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595796 | ||||||
| chr2:3595868
|
C | T | 1 | a0001c0001t0001g0361 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-27+700C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595868 | ||||||
| chr2:3595902
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00408.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-27+734T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595902 | ||||||
| chr2:3595947
|
T | C | 5 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0037others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+779T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595947 | ||||||
| chr2:3595992
|
C | T | 1 | a0001c0001t0001g0360 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-27+824C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3595992 | ||||||
| chr2:3596337
|
A | AT | 189 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(186): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-27+1186dupT | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 3596337 | |||||
| chr2:3596337
|
A | T | 1 | a0001c0001t0001g0359 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-27+1169A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3596337 | ||||||
| chr2:3596337
|
AT | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0042a0002c0002t0001g0044others(3): Show | 6 | HG02717.hp2 HG02809.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27+1186delT | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 3596337 | |||||
| chr2:3596393
|
A | G | 1 | a0003c0012t0001g0358 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-27+1225A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3596393 | ||||||
| chr2:3596495
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-27+1327C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3596495 | ||||||
| chr2:3596745
|
C | T | 6 | a0001c0001t0001g0201a0002c0002t0001g0044a0002c0005t0001g0362others(3): Show | 6 | HG01099.hp2 HG02145.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27+1577C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3596745 | ||||||
| chr2:3596816
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-27+1648G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3596816 | ||||||
| chr2:3596891
|
C | T | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-27+1723C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3596891 | ||||||
| chr2:3597005
|
C | T | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 14 | HG00140.hp2 HG00733.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27+1837C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597005 | ||||||
| chr2:3597173
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 88 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-27+2005T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597173 | ||||||
| chr2:3597349
|
A | C | 8 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0196others(5): Show | 8 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27+2181A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597349 | ||||||
| chr2:3597420
|
G | A | 19 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(16): Show | 19 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+2252G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597420 | ||||||
| chr2:3597488
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-27+2320T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597488 | ||||||
| chr2:3597506
|
A | G | 1 | a0001c0001t0001g0355 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-27+2338A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597506 | ||||||
| chr2:3597565
|
C | A | 23 | a0001c0001t0001g0203a0001c0001t0001g0264a0001c0001t0001g0265others(20): Show | 23 | HG00738.hp2 HG01099.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-27+2397C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597565 | ||||||
| chr2:3597569
|
G | A | 1 | a0002c0004t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+2401G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597569 | ||||||
| chr2:3597674
|
T | TA | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0064others(16): Show | 19 | HG00733.hp1 HG01123.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.-27+2520dupA | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 3597674 | |||||
| chr2:3597686
|
A | AC | 6 | a0001c0001t0001g0013a0001c0001t0001g0350a0001c0001t0001g0351others(3): Show | 7 | HG00323.hp1 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27+2518_-27+2519i others(3): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597686 | ||||||
| chr2:3597827
|
C | A | 3 | a0002c0002t0001g0065a0002c0002t0001g0302a0002c0002t0001g0363 | 3 | HG02615.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-27+2659C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597827 | ||||||
| chr2:3597839
|
C | T | 106 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(103): Show | 109 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.-27+2671C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597839 | ||||||
| chr2:3597865
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-27+2697G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597865 | ||||||
| chr2:3597981
|
G | A | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-27+2813G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3597981 | ||||||
| chr2:3598004
|
C | T | 3 | a0001c0001t0001g0201a0002c0002t0001g0044a0002c0006t0001g0200 | 3 | HG02145.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-27+2836C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598004 | ||||||
| chr2:3598038
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0349 | 2 | HG00099.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-27+2870C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598038 | ||||||
| chr2:3598136
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-27+2968A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598136 | ||||||
| chr2:3598332
|
T | A | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-27+3164T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598332 | ||||||
| chr2:3598364
|
C | G | 4 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0006t0001g0031others(1): Show | 4 | HG01884.hp1 HG02486.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+3196C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598364 | ||||||
| chr2:3598437
|
C | T | 1 | a0002c0004t0001g0263 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-27+3269C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598437 | ||||||
| chr2:3598521
|
A | G | 1 | a0003c0010t0001g0357 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-27+3353A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598521 | ||||||
| chr2:3598533
|
C | A | 1 | a0001c0001t0001g0312 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-27+3365C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598533 | ||||||
| chr2:3598549
|
T | C | 45 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(42): Show | 46 | HG00323.hp1 HG00609.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-27+3381T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598549 | ||||||
| chr2:3598555
|
C | G | 107 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(104): Show | 110 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(107): Show |
intron_variant | MODIFIER | c.-27+3387C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598555 | ||||||
| chr2:3598555
|
C | T | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 29 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.-27+3387C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598555 | ||||||
| chr2:3598613
|
C | T | 1 | a0002c0005t0002g0348 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-27+3445C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598613 | ||||||
| chr2:3598636
|
T | C | 104 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0019others(101): Show | 107 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(104): Show |
intron_variant | MODIFIER | c.-27+3468T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598636 | ||||||
| chr2:3598639
|
G | A | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-27+3471G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598639 | ||||||
| chr2:3598676
|
C | CGGGTGAG others(107): Show |
3 | a0002c0002t0001g0065a0002c0002t0001g0302a0002c0002t0001g0363 | 3 | HG02615.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-27+3610_-27+3611i others(116): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 3598676 | |||||
| chr2:3598739
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-27+3571T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598739 | ||||||
| chr2:3598799
|
G | A | 6 | a0002c0002t0001g0313a0002c0002t0001g0314a0002c0002t0001g0316others(3): Show | 6 | HG01099.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27+3631G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598799 | ||||||
| chr2:3599022
|
A | G | 5 | a0002c0002t0001g0313a0002c0002t0001g0314a0002c0002t0001g0316others(2): Show | 5 | HG02109.hp1 HG02572.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+3854A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599022 | ||||||
| chr2:3599058
|
A | AG | 233 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-27+3890_-27+3891i others(3): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599058 | ||||||
| chr2:3599082
|
T | C | 1 | a0002c0002t0001g0191 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-27+3914T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599082 | ||||||
| chr2:3599176
|
T | C | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-27+4008T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599176 | ||||||
| chr2:3599252
|
C | T | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-27+4084C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599252 | ||||||
| chr2:3599390
|
G | A | 23 | a0001c0001t0001g0203a0001c0001t0001g0264a0001c0001t0001g0265others(20): Show | 23 | HG00738.hp2 HG01099.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-27+4222G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599390 | ||||||
| chr2:3599527
|
C | T | 32 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(29): Show | 33 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-27+4359C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599527 | ||||||
| chr2:3599765
|
C | G | 11 | a0001c0001t0001g0346a0002c0002t0001g0189a0002c0002t0001g0190others(8): Show | 11 | HG01099.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26-4550C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599765 | ||||||
| chr2:3599954
|
G | A | 1 | a0002c0002t0001g0065 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-26-4361G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599954 | ||||||
| chr2:3599998
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-26-4317G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599998 | ||||||
| chr2:3600001
|
C | T | 25 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 26 | HG00323.hp1 HG00733.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-26-4314C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600001 | ||||||
| chr2:3600010
|
T | TGGATCAT others(6): Show |
1 | a0001c0001t0001g0178 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-26-4304_-26-4292d others(15): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 3600010 | |||||
| chr2:3600037
|
C | A | 1 | a0002c0002t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-26-4278C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600037 | ||||||
| chr2:3600045
|
C | T | 1 | a0002c0006t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-26-4270C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600045 | ||||||
| chr2:3600103
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-26-4212C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600103 | ||||||
| chr2:3600143
|
G | A | 32 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(29): Show | 33 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-26-4172G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600143 | ||||||
| chr2:3600222
|
G | C | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-26-4093G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600222 | ||||||
| chr2:3600234
|
C | CA | 61 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(58): Show | 62 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-26-4064dupA | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 3600234 | |||||
| chr2:3600260
|
CAA | C | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 29 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.-26-4052_-26-4051d others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 3600260 | |||||
| chr2:3600300
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-26-4015G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600300 | ||||||
| chr2:3600371
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-26-3944A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600371 | ||||||
| chr2:3600381
|
C | T | 1 | a0002c0003t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-26-3934C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600381 | ||||||
| chr2:3600505
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0052a0002c0003t0001g0051 | 4 | NA18947.hp2 NA18984.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-3810A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600505 | ||||||
| chr2:3600596
|
C | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(230): Show | 242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-26-3719C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600596 | ||||||
| chr2:3600729
|
TAGACCTC others(3): Show |
T | 1 | a0001c0001t0001g0250 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-26-3584_-26-3575d others(12): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 3600729 | |||||
| chr2:3600773
|
T | C | 1 | a0002c0004t0001g0317 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-26-3542T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600773 | ||||||
| chr2:3600806
|
T | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(181): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.-26-3509T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600806 | ||||||
| chr2:3600939
|
G | A | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-26-3376G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600939 | ||||||
| chr2:3600960
|
G | A | 6 | a0001c0001t0001g0068a0002c0002t0001g0016a0002c0002t0001g0179others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26-3355G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3600960 | ||||||
| chr2:3601068
|
C | T | 2 | a0001c0001t0001g0319a0002c0002t0001g0318 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-26-3247C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601068 | ||||||
| chr2:3601107
|
G | A | 1 | a0002c0002t0001g0035 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-26-3208G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601107 | ||||||
| chr2:3601147
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-26-3168A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601147 | ||||||
| chr2:3601167
|
C | A | 94 | a0001c0001t0001g0012a0001c0001t0001g0074a0001c0001t0001g0185others(91): Show | 96 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.-26-3148C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601167 | ||||||
| chr2:3601609
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-26-2706T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601609 | ||||||
| chr2:3601614
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(59): Show | 67 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.-26-2701C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601614 | ||||||
| chr2:3601651
|
C | G | 16 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(13): Show | 16 | HG00738.hp2 HG01099.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.-26-2664C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601651 | ||||||
| chr2:3601729
|
G | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 98 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-26-2586G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601729 | ||||||
| chr2:3601730
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-26-2585C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601730 | ||||||
| chr2:3601733
|
G | A | 27 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0077others(24): Show | 28 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.-26-2582G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601733 | ||||||
| chr2:3601751
|
C | T | 3 | a0001c0001t0001g0201a0002c0002t0001g0044a0002c0006t0001g0200 | 3 | HG02145.hp1 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-26-2564C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601751 | ||||||
| chr2:3601836
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-26-2479G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601836 | ||||||
| chr2:3601866
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-26-2449G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601866 | ||||||
| chr2:3602001
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-26-2314C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602001 | ||||||
| chr2:3602093
|
G | A | 4 | a0002c0002t0001g0180a0002c0005t0002g0181a0002c0005t0002g0182others(1): Show | 4 | HG02055.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-2222G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602093 | ||||||
| chr2:3602196
|
A | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0284a0001c0001t0004g0174 | 3 | HG00438.hp1 HG02698.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-26-2119A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602196 | ||||||
| chr2:3602203
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-26-2112A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602203 | ||||||
| chr2:3602277
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-26-2038C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602277 | ||||||
| chr2:3602339
|
G | C | 8 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0323others(5): Show | 9 | HG02257.hp1 HG02647.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26-1976G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602339 | ||||||
| chr2:3602402
|
T | C | 2 | a0002c0002t0001g0347a0002c0004t0001g0286 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-26-1913T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602402 | ||||||
| chr2:3602578
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-26-1737C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602578 | ||||||
| chr2:3602599
|
C | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-1716C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602599 | ||||||
| chr2:3602662
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 92 | HG00408.hp2 HG00438.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-26-1653G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602662 | ||||||
| chr2:3602739
|
G | A | 24 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(21): Show | 25 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-26-1576G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602739 | ||||||
| chr2:3602741
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-26-1574C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602741 | ||||||
| chr2:3602749
|
C | G | 1 | a0001c0001t0001g0172 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-26-1566C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602749 | ||||||
| chr2:3602765
|
C | T | 10 | a0001c0001t0001g0319a0002c0002t0001g0180a0002c0004t0001g0231others(7): Show | 10 | HG01884.hp2 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-1550C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602765 | ||||||
| chr2:3602766
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-26-1549G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602766 | ||||||
| chr2:3602817
|
A | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(151): Show | 161 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-26-1498A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602817 | ||||||
| chr2:3602877
|
G | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0247a0001c0001t0001g0248others(7): Show | 10 | HG00639.hp1 HG01074.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-1438G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3602877 | ||||||
| chr2:3603154
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-26-1161G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603154 | ||||||
| chr2:3603175
|
T | C | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-26-1140T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603175 | ||||||
| chr2:3603183
|
G | A | 1 | a0002c0006t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-26-1132G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603183 | ||||||
| chr2:3603330
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-26-985T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603330 | ||||||
| chr2:3603336
|
T | G | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-26-979T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603336 | ||||||
| chr2:3603503
|
C | T | 7 | a0002c0002t0001g0044a0002c0002t0001g0180a0002c0004t0001g0231others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-812C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603503 | ||||||
| chr2:3603545
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-26-770G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603545 | ||||||
| chr2:3603555
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-26-760G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603555 | ||||||
| chr2:3603631
|
G | T | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-26-684G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603631 | ||||||
| chr2:3603635
|
C | T | 11 | a0001c0001t0001g0061a0002c0002t0001g0001a0002c0002t0001g0016others(8): Show | 12 | HG00639.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-26-680C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603635 | ||||||
| chr2:3603726
|
C | T | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-26-589C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603726 | ||||||
| chr2:3603764
|
G | A | 3 | a0001c0001t0001g0061a0002c0003t0001g0171a0006c0013t0001g0260 | 3 | HG00639.hp1 HG02015.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-26-551G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603764 | ||||||
| chr2:3603805
|
G | A | 2 | a0001c0001t0001g0026a0002c0002t0001g0313 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-26-510G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603805 | ||||||
| chr2:3603841
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-26-474G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603841 | ||||||
| chr2:3603867
|
C | T | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-26-448C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603867 | ||||||
| chr2:3603912
|
T | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(18): Show | 22 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.-26-403T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3603912 | ||||||
| chr2:3604012
|
C | T | 2 | a0002c0005t0002g0211a0002c0005t0002g0212 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-303C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3604012 | ||||||
| chr2:3604051
|
C | T | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-26-264C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3604051 | ||||||
| chr2:3604056
|
C | T | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-26-259C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3604056 | ||||||
| chr2:3604083
|
C | T | 19 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(16): Show | 22 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-26-232C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3604083 | ||||||
| chr2:3604270
|
C | T | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-26-45C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3604270 | ||||||
| chr2:3604513
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.130+43G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604513 | ||||||
| chr2:3604570
|
C | G | 4 | a0003c0009t0001g0356a0003c0010t0001g0357a0003c0012t0001g0358others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+100C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604570 | ||||||
| chr2:3604690
|
T | C | 1 | a0002c0006t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.130+220T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604690 | ||||||
| chr2:3604701
|
C | T | 10 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(7): Show | 10 | HG00408.hp2 HG00735.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+231C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604701 | ||||||
| chr2:3604708
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.130+238C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604708 | ||||||
| chr2:3604765
|
C | A | 1 | a0002c0002t0001g0189 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130+295C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604765 | ||||||
| chr2:3604782
|
G | C | 1 | a0002c0006t0001g0333 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.130+312G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604782 | ||||||
| chr2:3604794
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+324T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604794 | ||||||
| chr2:3604966
|
T | A | 1 | a0001c0001t0001g0109 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.130+496T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3604966 | ||||||
| chr2:3605026
|
G | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(276): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.130+556G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605026 | ||||||
| chr2:3605193
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.130+723C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605193 | ||||||
| chr2:3605240
|
G | T | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.130+770G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605240 | ||||||
| chr2:3605254
|
C | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(205): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.130+784C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605254 | ||||||
| chr2:3605266
|
C | T | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.130+796C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605266 | ||||||
| chr2:3605274
|
C | T | 281 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(278): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.130+804C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605274 | ||||||
| chr2:3605279
|
A | AGGGGAGT others(24): Show |
1 | a0002c0003t0001g0053 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.130+901_130+931dup others(31): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605279 | |||||
| chr2:3605279
|
AGGGGAGT others(24): Show |
A | 2 | a0001c0001t0001g0232a0001c0001t0001g0319 | 2 | HG01243.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.130+901_130+931del others(31): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605279 | |||||
| chr2:3605289
|
C | CGTGGGTG others(175): Show |
1 | a0001c0001t0001g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.130+930_130+931ins others(182): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605289 | |||||
| chr2:3605309
|
CG | C | 4 | a0001c0001t0001g0305a0002c0002t0001g0029a0002c0002t0001g0030others(1): Show | 4 | HG02818.hp1 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+844delG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605309 | |||||
| chr2:3605310
|
G | GGGGGAGT others(384): Show |
2 | a0002c0003t0001g0171a0006c0013t0001g0260 | 2 | HG02015.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.130+900_130+901ins others(391): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605310 | |||||
| chr2:3605317
|
T | TCACGTGG others(115): Show |
1 | a0002c0004t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.130+900_130+901ins others(122): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605317 | |||||
| chr2:3605339
|
GC | G | 3 | a0002c0006t0001g0199a0003c0009t0001g0356a0003c0010t0001g0357 | 3 | HG01099.hp2 HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.130+870delC | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605339 | ||||||
| chr2:3605341
|
G | A | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.130+871G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605341 | ||||||
| chr2:3605360
|
CGAGGAGG others(203): Show |
C | 1 | a0001c0001t0001g0239 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.130+900_130+1109de others(1): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605360 | |||||
| chr2:3605366
|
GGGGGCGG others(53): Show |
G | 3 | a0002c0002t0001g0189a0002c0002t0001g0190a0005c0011t0001g0032 | 3 | HG01884.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.130+901_130+960del others(60): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605366 | |||||
| chr2:3605370
|
GC | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0073a0002c0002t0001g0027others(3): Show | 6 | HG00639.hp1 HG03130.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+901delC | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605370 | ||||||
| chr2:3605371
|
C | A | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(221): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.130+901C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605371 | ||||||
| chr2:3605371
|
CG | C | 6 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0044others(3): Show | 6 | HG02809.hp1 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+906delG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605371 | |||||
| chr2:3605372
|
G | A | 6 | a0001c0001t0001g0061a0001c0001t0001g0073a0002c0002t0001g0027others(3): Show | 6 | HG00639.hp1 HG03130.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+902G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605372 | ||||||
| chr2:3605372
|
G | C | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.130+902G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605372 | ||||||
| chr2:3605372
|
G | GGGGAGTC others(86): Show |
223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(220): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.130+905_130+906ins others(93): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605372 | |||||
| chr2:3605372
|
G | GGGGAGTC others(87): Show |
1 | a0001c0001t0001g0141 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.130+905_130+906ins others(94): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605372 | |||||
| chr2:3605379
|
T | TCATGTGG others(336): Show |
2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.130+911_130+912ins others(343): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605379 | |||||
| chr2:3605391
|
C | T | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(221): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.130+921C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605391 | ||||||
| chr2:3605396
|
A | AGGGGCGG others(120): Show |
4 | a0002c0002t0001g0027a0002c0002t0001g0193a0002c0002t0001g0302others(1): Show | 4 | HG03130.hp2 NA19030.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+930_130+931ins others(127): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605396 | |||||
| chr2:3605396
|
A | AGGGGGCG others(244): Show |
2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.130+931_130+932ins others(251): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605396 | |||||
| chr2:3605397
|
GGGGGAGG others(22): Show |
G | 39 | a0001c0001t0001g0060a0001c0001t0001g0137a0001c0001t0001g0195others(36): Show | 39 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.130+980_130+1008de others(30): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605397 | |||||
| chr2:3605401
|
G | GC | 10 | a0001c0001t0001g0077a0001c0001t0001g0192a0001c0001t0001g0330others(7): Show | 10 | HG01109.hp2 HG02015.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+931_130+932ins others(1): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605401 | ||||||
| chr2:3605402
|
A | C | 1 | a0001c0001t0001g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.130+932A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605402 | ||||||
| chr2:3605402
|
A | G | 10 | a0001c0001t0001g0077a0001c0001t0001g0192a0001c0001t0001g0330others(7): Show | 10 | HG01109.hp2 HG02015.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+932A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605402 | ||||||
| chr2:3605406
|
G | GC | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(220): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.130+936_130+937ins others(1): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605406 | ||||||
| chr2:3605407
|
A | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(221): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.130+937A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605407 | ||||||
| chr2:3605409
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(221): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.130+939T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605409 | ||||||
| chr2:3605409
|
T | TCATGTGG others(90): Show |
1 | a0001c0001t0001g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.130+941_130+942ins others(97): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605409 | |||||
| chr2:3605421
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.130+951C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605421 | ||||||
| chr2:3605421
|
CGAGGAGG others(51): Show |
C | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.130+961_130+1018de others(59): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605421 | |||||
| chr2:3605426
|
A | AG | 11 | a0001c0001t0001g0320a0001c0001t0001g0321a0002c0002t0001g0027others(8): Show | 11 | HG01884.hp2 HG02015.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+960dupG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605426 | |||||
| chr2:3605426
|
A | AGGCGGGG others(27): Show |
225 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(222): Show | 232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.130+958_130+959ins others(34): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605426 | |||||
| chr2:3605426
|
A | AGGGGCGG others(339): Show |
1 | a0003c0012t0001g0358 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+960_130+961ins others(346): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605426 | |||||
| chr2:3605426
|
A | AGGGGGAG others(152): Show |
1 | a0001c0001t0001g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.130+960_130+961ins others(159): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605426 | |||||
| chr2:3605426
|
A | AGGGGGAG others(123): Show |
1 | a0001c0001t0001g0293 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.130+960_130+961ins others(130): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605426 | |||||
| chr2:3605426
|
A | AGGGGGCG others(387): Show |
1 | a0001c0001t0001g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.130+960_130+961ins others(394): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605426 | |||||
| chr2:3605430
|
G | GGAGGGGA others(87): Show |
1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.130+960_130+961ins others(94): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605430 | ||||||
| chr2:3605430
|
G | GGC | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+960_130+961ins others(2): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605430 | ||||||
| chr2:3605431
|
A | G | 5 | a0001c0001t0001g0192a0001c0001t0001g0330a0001c0001t0001g0346others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+961A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605431 | ||||||
| chr2:3605441
|
C | CGTGGGTG others(23): Show |
1 | a0001c0001t0001g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.130+989_130+990ins others(30): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605441 | |||||
| chr2:3605441
|
C | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(223): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.130+971C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605441 | ||||||
| chr2:3605460
|
A | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+990A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605460 | ||||||
| chr2:3605479
|
T | C | 5 | a0001c0001t0001g0192a0001c0001t0001g0330a0001c0001t0001g0346others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+1009T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605479 | ||||||
| chr2:3605484
|
AG | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1019delG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605484 | |||||
| chr2:3605493
|
G | A | 236 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.130+1023G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605493 | ||||||
| chr2:3605494
|
GC | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1025delC | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605494 | ||||||
| chr2:3605496
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1026G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605496 | ||||||
| chr2:3605498
|
C | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1028C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605498 | ||||||
| chr2:3605510
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1040T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605510 | ||||||
| chr2:3605519
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.130+1049G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605519 | ||||||
| chr2:3605523
|
G | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1053G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605523 | ||||||
| chr2:3605524
|
A | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1054A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605524 | ||||||
| chr2:3605539
|
T | G | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1069T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605539 | ||||||
| chr2:3605539
|
T | TTGG | 130 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(127): Show | 134 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.130+1071_130+1072i others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605539 | |||||
| chr2:3605540
|
T | TGCC | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1071_130+1072i others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605540 | |||||
| chr2:3605540
|
T | TGGTGAGG others(26): Show |
152 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(149): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.130+1071_130+1072i others(35): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605540 | |||||
| chr2:3605543
|
T | G | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(283): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.130+1073T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605543 | ||||||
| chr2:3605543
|
T | TGAG | 17 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(14): Show | 18 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.130+1075_130+1077d others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605543 | |||||
| chr2:3605551
|
A | AG | 4 | a0001c0001t0001g0192a0001c0001t0001g0346a0002c0003t0001g0277others(1): Show | 4 | HG02145.hp2 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+1085dupG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605551 | |||||
| chr2:3605570
|
T | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(321): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.130+1100T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605570 | ||||||
| chr2:3605575
|
A | AG | 4 | a0002c0002t0001g0027a0002c0002t0001g0193a0002c0002t0001g0302others(1): Show | 4 | HG03130.hp2 NA19030.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+1109dupG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3605575 | |||||
| chr2:3605689
|
C | T | 236 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.130+1219C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605689 | ||||||
| chr2:3605692
|
T | G | 1 | a0002c0002t0001g0314 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+1222T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605692 | ||||||
| chr2:3605763
|
C | T | 2 | a0002c0002t0001g0302a0002c0002t0001g0363 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.130+1293C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605763 | ||||||
| chr2:3605986
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(249): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.130+1516A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605986 | ||||||
| chr2:3606208
|
C | G | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.130+1738C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606208 | ||||||
| chr2:3606223
|
G | C | 3 | a0001c0001t0001g0320a0001c0001t0001g0321a0003c0012t0001g0358 | 3 | HG02257.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130+1753G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606223 | ||||||
| chr2:3606252
|
C | A | 26 | a0001c0001t0001g0060a0001c0001t0001g0137a0001c0001t0001g0195others(23): Show | 26 | HG00140.hp1 HG01070.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.130+1782C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606252 | ||||||
| chr2:3606254
|
T | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(280): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.130+1784T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606254 | ||||||
| chr2:3606298
|
G | A | 51 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0137others(48): Show | 51 | HG00140.hp1 HG00639.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.130+1828G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606298 | ||||||
| chr2:3606453
|
G | T | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.130+1983G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606453 | ||||||
| chr2:3606464
|
C | T | 2 | a0001c0001t0001g0026a0002c0002t0001g0313 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.130+1994C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606464 | ||||||
| chr2:3606473
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.130+2003T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606473 | ||||||
| chr2:3606517
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0153a0001c0001t0001g0173others(1): Show | 4 | HG02027.hp1 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+2047C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606517 | ||||||
| chr2:3606592
|
C | T | 1 | a0002c0002t0001g0222 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.130+2122C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606592 | ||||||
| chr2:3606600
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(237): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.130+2130T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606600 | ||||||
| chr2:3606700
|
C | T | 124 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(121): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.130+2230C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606700 | ||||||
| chr2:3606732
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0001g0323 | 2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.130+2262G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606732 | ||||||
| chr2:3606740
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.130+2270G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606740 | ||||||
| chr2:3606842
|
G | A | 1 | a0003c0012t0001g0358 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+2372G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3606842 | ||||||
| chr2:3607004
|
C | T | 1 | a0002c0005t0002g0348 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+2534C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607004 | ||||||
| chr2:3607013
|
C | T | 27 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0137others(24): Show | 27 | HG00140.hp1 HG00609.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.130+2543C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607013 | ||||||
| chr2:3607063
|
C | T | 1 | a0002c0004t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.130+2593C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607063 | ||||||
| chr2:3607081
|
C | A | 1 | a0001c0001t0001g0305 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.130+2611C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607081 | ||||||
| chr2:3607094
|
C | T | 90 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(87): Show | 95 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.130+2624C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607094 | ||||||
| chr2:3607105
|
A | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0238 | 2 | HG00741.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.130+2635A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607105 | ||||||
| chr2:3607194
|
G | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(261): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.130+2724G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607194 | ||||||
| chr2:3607266
|
A | T | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.130+2796A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607266 | ||||||
| chr2:3607449
|
C | CTTTTTT | 8 | a0001c0001t0001g0049a0001c0001t0001g0064a0001c0001t0001g0114others(5): Show | 9 | NA18948.hp2 NA18964.hp1 NA18992.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+2989_130+2994d others(8): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3607449 | |||||
| chr2:3607449
|
C | CTTTTTTT | 184 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(181): Show | 189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.130+2988_130+2994d others(9): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3607449 | |||||
| chr2:3607449
|
C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0015a0001c0001t0001g0089a0001c0001t0001g0107others(15): Show | 18 | HG00735.hp2 HG01106.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.130+2987_130+2994d others(10): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3607449 | |||||
| chr2:3607449
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0061a0002c0002t0001g0302a0002c0002t0001g0316others(4): Show | 7 | HG00639.hp1 HG02004.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+2986_130+2994d others(11): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3607449 | |||||
| chr2:3607449
|
C | CTTTTTTT others(3): Show |
2 | a0002c0003t0001g0334a0005c0011t0001g0032 | 2 | HG00741.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.130+2985_130+2994d others(12): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3607449 | |||||
| chr2:3607451
|
T | C | 34 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(31): Show | 36 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.130+2981T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607451 | ||||||
| chr2:3607678
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.130+3208A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607678 | ||||||
| chr2:3607684
|
C | T | 23 | a0001c0001t0001g0060a0001c0001t0001g0137a0001c0001t0001g0184others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.130+3214C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607684 | ||||||
| chr2:3607685
|
G | A | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.130+3215G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607685 | ||||||
| chr2:3607737
|
A | C | 276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(273): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.130+3267A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607737 | ||||||
| chr2:3607750
|
A | G | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.130+3280A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607750 | ||||||
| chr2:3607762
|
T | G | 276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(273): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.130+3292T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607762 | ||||||
| chr2:3607763
|
T | A | 276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(273): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.130+3293T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607763 | ||||||
| chr2:3607831
|
G | A | 23 | a0001c0001t0001g0060a0001c0001t0001g0137a0001c0001t0001g0184others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.130+3361G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607831 | ||||||
| chr2:3607901
|
A | G | 3 | a0002c0002t0001g0035a0002c0002t0001g0062a0002c0006t0001g0315 | 3 | HG02683.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+3431A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607901 | ||||||
| chr2:3607917
|
T | C | 276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(273): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.130+3447T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607917 | ||||||
| chr2:3607991
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.130+3521C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607991 | ||||||
| chr2:3607992
|
G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0142a0001c0001t0001g0264others(1): Show | 4 | NA18960.hp1 NA18967.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+3522G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607992 | ||||||
| chr2:3608059
|
C | T | 8 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0038others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+3589C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608059 | ||||||
| chr2:3608153
|
C | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(223): Show | 232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.130+3683C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608153 | ||||||
| chr2:3608178
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.130+3708G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608178 | ||||||
| chr2:3608215
|
C | T | 287 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(284): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.130+3745C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608215 | ||||||
| chr2:3608232
|
G | A | 276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(273): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.130+3762G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608232 | ||||||
| chr2:3608265
|
T | A | 276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(273): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.130+3795T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608265 | ||||||
| chr2:3608394
|
G | A | 1 | a0002c0002t0001g0314 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.130+3924G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608394 | ||||||
| chr2:3608406
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.130+3936T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608406 | ||||||
| chr2:3608412
|
AC | A | 6 | a0001c0001t0001g0061a0002c0003t0001g0171a0002c0003t0001g0223others(3): Show | 6 | HG00639.hp1 HG00741.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+3943delC | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608412 | ||||||
| chr2:3608495
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.130+4025A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608495 | ||||||
| chr2:3608536
|
A | G | 1 | a0001c0001t0001g0351 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.130+4066A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608536 | ||||||
| chr2:3608565
|
G | A | 23 | a0001c0001t0001g0060a0001c0001t0001g0137a0001c0001t0001g0184others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.130+4095G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608565 | ||||||
| chr2:3608572
|
C | T | 3 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0327 | 3 | HG02818.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.130+4102C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608572 | ||||||
| chr2:3608589
|
G | A | 3 | a0001c0001t0001g0192a0002c0003t0001g0277a0002c0004t0001g0289 | 3 | HG02145.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.130+4119G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608589 | ||||||
| chr2:3608654
|
C | T | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.130+4184C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608654 | ||||||
| chr2:3608903
|
G | C | 8 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0038others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-4408G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608903 | ||||||
| chr2:3608971
|
C | T | 1 | a0002c0002t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-4340C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608971 | ||||||
| chr2:3608986
|
A | G | 1 | a0003c0012t0001g0358 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.131-4325A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608986 | ||||||
| chr2:3609013
|
G | A | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.131-4298G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609013 | ||||||
| chr2:3609115
|
G | A | 3 | a0002c0002t0001g0035a0002c0002t0001g0062a0002c0006t0001g0315 | 3 | HG02683.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.131-4196G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609115 | ||||||
| chr2:3609301
|
T | C | 5 | a0002c0002t0001g0027a0002c0002t0001g0035a0002c0002t0001g0062others(2): Show | 5 | HG02683.hp1 HG03225.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-4010T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609301 | ||||||
| chr2:3609306
|
GTC | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-4001_131-4000d others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609306 | |||||
| chr2:3609315
|
C | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(24): Show | 29 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.131-3996C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609315 | ||||||
| chr2:3609347
|
CTTTGA | C | 31 | a0001c0001t0001g0020a0001c0001t0001g0060a0001c0001t0001g0137others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.131-3960_131-3956d others(7): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609347 | |||||
| chr2:3609348
|
TTTGA | T | 126 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.131-3960_131-3957d others(6): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609348 | |||||
| chr2:3609349
|
TTGA | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0047others(76): Show | 81 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.131-3960_131-3958d others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609349 | |||||
| chr2:3609350
|
TGA | T | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0075others(6): Show | 10 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-3960_131-3959d others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609350 | ||||||
| chr2:3609351
|
G | T | 9 | a0001c0001t0001g0061a0002c0002t0001g0302a0002c0002t0001g0363others(6): Show | 9 | HG00639.hp1 HG00741.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-3960G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609351 | ||||||
| chr2:3609352
|
A | AT | 7 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0237others(4): Show | 7 | NA18522.hp2 NA18940.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-3925dupT | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609352 | |||||
| chr2:3609352
|
A | C | 9 | a0001c0001t0001g0061a0002c0002t0001g0302a0002c0002t0001g0363others(6): Show | 9 | HG00639.hp1 HG00741.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-3959A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609352 | ||||||
| chr2:3609352
|
A | T | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.131-3959A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609352 | ||||||
| chr2:3609352
|
AT | A | 25 | a0001c0001t0001g0023a0001c0001t0001g0066a0001c0001t0001g0068others(22): Show | 25 | HG00140.hp2 HG00738.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.131-3925delT | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609352 | |||||
| chr2:3609352
|
ATT | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(12): Show | 17 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-3926_131-3925d others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609352 | |||||
| chr2:3609352
|
ATTTTT | A | 14 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(11): Show | 17 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-3929_131-3925d others(7): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609352 | |||||
| chr2:3609352
|
ATTTTTTT others(7): Show |
A | 1 | a0002c0002t0001g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-3938_131-3925d others(16): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609352 | |||||
| chr2:3609353
|
T | C | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.131-3958T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609353 | ||||||
| chr2:3609354
|
T | C | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0075others(6): Show | 10 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-3957T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609354 | ||||||
| chr2:3609355
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0047others(76): Show | 81 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.131-3956T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609355 | ||||||
| chr2:3609356
|
T | A | 1 | a0002c0003t0001g0334 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.131-3955T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609356 | ||||||
| chr2:3609356
|
T | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.131-3955T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609356 | ||||||
| chr2:3609356
|
T | G | 7 | a0001c0001t0001g0061a0002c0002t0001g0302a0002c0002t0001g0363others(4): Show | 7 | HG00639.hp1 HG02004.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-3955T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609356 | ||||||
| chr2:3609357
|
T | A | 7 | a0001c0001t0001g0061a0002c0002t0001g0302a0002c0002t0001g0363others(4): Show | 7 | HG00639.hp1 HG02004.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-3954T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609357 | ||||||
| chr2:3609357
|
T | C | 31 | a0001c0001t0001g0020a0001c0001t0001g0060a0001c0001t0001g0137others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.131-3954T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609357 | ||||||
| chr2:3609357
|
T | G | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.131-3954T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609357 | ||||||
| chr2:3609358
|
T | A | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.131-3953T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609358 | ||||||
| chr2:3609358
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0213 | 3 | HG02257.hp2 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-3953T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609358 | ||||||
| chr2:3609358
|
T | G | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0075others(6): Show | 10 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-3953T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609358 | ||||||
| chr2:3609359
|
T | A | 9 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0075others(6): Show | 10 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-3952T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609359 | ||||||
| chr2:3609359
|
T | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0047others(76): Show | 81 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.131-3952T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609359 | ||||||
| chr2:3609360
|
T | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0047others(76): Show | 81 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.131-3951T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609360 | ||||||
| chr2:3609360
|
T | G | 126 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.131-3951T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609360 | ||||||
| chr2:3609361
|
T | A | 126 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.131-3950T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609361 | ||||||
| chr2:3609361
|
T | G | 31 | a0001c0001t0001g0020a0001c0001t0001g0060a0001c0001t0001g0137others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.131-3950T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609361 | ||||||
| chr2:3609362
|
T | A | 31 | a0001c0001t0001g0020a0001c0001t0001g0060a0001c0001t0001g0137others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.131-3949T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609362 | ||||||
| chr2:3609362
|
T | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0213 | 3 | HG02257.hp2 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-3949T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609362 | ||||||
| chr2:3609363
|
T | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0213 | 3 | HG02257.hp2 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-3948T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609363 | ||||||
| chr2:3609388
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.131-3923G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609388 | ||||||
| chr2:3609427
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.131-3884T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609427 | ||||||
| chr2:3609492
|
C | T | 5 | a0001c0001t0001g0105a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG00735.hp1 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-3819C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609492 | ||||||
| chr2:3609535
|
A | ATT | 48 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0061others(45): Show | 48 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.131-3766_131-3765d others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609535 | |||||
| chr2:3609535
|
A | ATTT | 210 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(207): Show | 216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.131-3767_131-3765d others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3609535 | |||||
| chr2:3609678
|
C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3633C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609678 | ||||||
| chr2:3609777
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-3534G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609777 | ||||||
| chr2:3609784
|
G | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3527G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609784 | ||||||
| chr2:3609791
|
A | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0064others(8): Show | 12 | HG00423.hp2 NA18947.hp2 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-3520A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609791 | ||||||
| chr2:3609793
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3518A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609793 | ||||||
| chr2:3609850
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0342 | 2 | NA18955.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.131-3461G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609850 | ||||||
| chr2:3609864
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3447G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609864 | ||||||
| chr2:3609974
|
T | C | 1 | a0002c0002t0001g0180 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.131-3337T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609974 | ||||||
| chr2:3610000
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3311T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610000 | ||||||
| chr2:3610024
|
A | G | 2 | a0003c0009t0001g0356a0003c0010t0001g0357 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.131-3287A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610024 | ||||||
| chr2:3610034
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3277G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610034 | ||||||
| chr2:3610065
|
G | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3246G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610065 | ||||||
| chr2:3610117
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3194G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610117 | ||||||
| chr2:3610139
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-3172T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610139 | ||||||
| chr2:3610141
|
T | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(254): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-3170T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610141 | ||||||
| chr2:3610153
|
A | T | 1 | a0001c0001t0001g0042 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.131-3158A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610153 | ||||||
| chr2:3610157
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.131-3154G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610157 | ||||||
| chr2:3610158
|
C | T | 1 | a0002c0006t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.131-3153C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610158 | ||||||
| chr2:3610182
|
C | T | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.131-3129C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610182 | ||||||
| chr2:3610236
|
C | T | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.131-3075C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610236 | ||||||
| chr2:3610285
|
C | T | 3 | a0002c0002t0001g0001a0002c0002t0001g0016a0002c0002t0001g0028 | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-3026C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610285 | ||||||
| chr2:3610315
|
A | G | 257 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(254): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-2996A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610315 | ||||||
| chr2:3610377
|
C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-2934C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610377 | ||||||
| chr2:3610404
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0232others(1): Show | 4 | HG00140.hp2 HG00733.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-2907C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610404 | ||||||
| chr2:3610441
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-2870T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610441 | ||||||
| chr2:3610442
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-2869T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610442 | ||||||
| chr2:3610453
|
G | A | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.131-2858G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610453 | ||||||
| chr2:3610476
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.131-2835A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610476 | ||||||
| chr2:3610542
|
A | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.131-2769A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610542 | ||||||
| chr2:3610577
|
C | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(24): Show | 29 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.131-2734C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610577 | ||||||
| chr2:3610609
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.131-2702T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610609 | ||||||
| chr2:3610688
|
C | T | 29 | a0001c0001t0001g0060a0001c0001t0001g0137a0001c0001t0001g0184others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.131-2623C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610688 | ||||||
| chr2:3610722
|
C | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-2589C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610722 | ||||||
| chr2:3610776
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0048 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.131-2535C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610776 | ||||||
| chr2:3610843
|
T | G | 1 | a0002c0002t0001g0044 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.131-2468T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610843 | ||||||
| chr2:3610849
|
C | T | 7 | a0002c0002t0001g0027a0002c0002t0001g0035a0002c0002t0001g0062others(4): Show | 7 | HG02683.hp1 HG03225.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-2462C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610849 | ||||||
| chr2:3610931
|
C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-2380C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610931 | ||||||
| chr2:3610973
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-2338T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610973 | ||||||
| chr2:3610975
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-2336A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610975 | ||||||
| chr2:3610977
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.131-2334G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610977 | ||||||
| chr2:3610979
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-2332T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610979 | ||||||
| chr2:3611019
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.131-2292G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611019 | ||||||
| chr2:3611031
|
G | C | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.131-2280G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611031 | ||||||
| chr2:3611084
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-2227A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611084 | ||||||
| chr2:3611107
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0154 | 2 | NA18995.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.131-2204G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611107 | ||||||
| chr2:3611134
|
T | C | 33 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0192others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.131-2177T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611134 | ||||||
| chr2:3611196
|
AAAAC | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.131-2103_131-2100d others(6): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3611196 | |||||
| chr2:3611210
|
A | G | 20 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(17): Show | 23 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-2101A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611210 | ||||||
| chr2:3611217
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-2094C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611217 | ||||||
| chr2:3611261
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-2050C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611261 | ||||||
| chr2:3611292
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-2019T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611292 | ||||||
| chr2:3611328
|
C | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-1983C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611328 | ||||||
| chr2:3611347
|
T | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-1964T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611347 | ||||||
| chr2:3611421
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.131-1890A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611421 | ||||||
| chr2:3611430
|
G | A | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.131-1881G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611430 | ||||||
| chr2:3611450
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.131-1861C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611450 | ||||||
| chr2:3611535
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.131-1776A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611535 | ||||||
| chr2:3611604
|
C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01192.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.131-1707C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611604 | ||||||
| chr2:3611644
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-1667C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611644 | ||||||
| chr2:3611705
|
C | G | 3 | a0001c0001t0001g0137a0001c0001t0001g0184a0002c0003t0001g0186 | 3 | HG00099.hp1 HG00140.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.131-1606C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611705 | ||||||
| chr2:3611710
|
G | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(253): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.131-1601G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611710 | ||||||
| chr2:3611785
|
C | T | 1 | a0001c0001t0005g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.131-1526C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611785 | ||||||
| chr2:3611926
|
C | T | 1 | a0002c0004t0001g0246 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.131-1385C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611926 | ||||||
| chr2:3611933
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.131-1378G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611933 | ||||||
| chr2:3611974
|
C | A | 252 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(249): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.131-1337C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611974 | ||||||
| chr2:3611989
|
A | C | 23 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0195others(20): Show | 23 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.131-1322A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3611989 | ||||||
| chr2:3612006
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-1305G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612006 | ||||||
| chr2:3612041
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.131-1270G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612041 | ||||||
| chr2:3612049
|
G | A | 1 | a0002c0002t0001g0314 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.131-1262G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612049 | ||||||
| chr2:3612063
|
ATGGC | A | 22 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0195others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-1241_131-1238d others(6): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3612063 | |||||
| chr2:3612064
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-1247T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612064 | ||||||
| chr2:3612123
|
C | T | 10 | a0001c0001t0001g0068a0002c0002t0001g0017a0002c0002t0001g0029others(7): Show | 10 | HG01884.hp2 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-1188C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612123 | ||||||
| chr2:3612194
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0001g0342 | 2 | NA18955.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.131-1117G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612194 | ||||||
| chr2:3612218
|
ACACG | A | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(23): Show | 28 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.131-1089_131-1086d others(6): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3612218 | |||||
| chr2:3612218
|
ACACGCAC others(11): Show |
A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-1085_131-1068d others(20): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3612218 | |||||
| chr2:3612224
|
A | ACCCACAT others(1): Show |
3 | a0002c0002t0001g0035a0002c0002t0001g0062a0002c0006t0001g0315 | 3 | HG02683.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.131-1086_131-1085i others(10): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3612224 | |||||
| chr2:3612226
|
A | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.131-1085A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612226 | ||||||
| chr2:3612231
|
T | C | 3 | a0002c0002t0001g0035a0002c0002t0001g0062a0002c0006t0001g0315 | 3 | HG02683.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.131-1080T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612231 | ||||||
| chr2:3612236
|
C | A | 248 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(245): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.131-1075C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612236 | ||||||
| chr2:3612248
|
G | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(220): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.131-1063G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612248 | ||||||
| chr2:3612290
|
T | C | 28 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0192others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.131-1021T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612290 | ||||||
| chr2:3612320
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.131-991C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612320 | ||||||
| chr2:3612328
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.131-983A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612328 | ||||||
| chr2:3612388
|
G | A | 1 | a0002c0005t0002g0183 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.131-923G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612388 | ||||||
| chr2:3612400
|
C | G | 22 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0195others(19): Show | 22 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-911C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612400 | ||||||
| chr2:3612400
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.131-911C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612400 | ||||||
| chr2:3612407
|
G | A | 19 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(16): Show | 22 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.131-904G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612407 | ||||||
| chr2:3612414
|
G | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(256): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.131-897G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612414 | ||||||
| chr2:3612495
|
AC | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-814delC | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3612495 | |||||
| chr2:3612504
|
C | T | 14 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(11): Show | 14 | HG01884.hp2 HG02257.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-807C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612504 | ||||||
| chr2:3612544
|
C | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0176others(12): Show | 17 | HG00642.hp1 HG01069.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-767C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612544 | ||||||
| chr2:3612618
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(253): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.131-693A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612618 | ||||||
| chr2:3612623
|
G | C | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.131-688G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612623 | ||||||
| chr2:3612735
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.131-576C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612735 | ||||||
| chr2:3612749
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-562C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612749 | ||||||
| chr2:3612762
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-549T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612762 | ||||||
| chr2:3612805
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-506G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612805 | ||||||
| chr2:3612826
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0255 | 3 | HG02129.hp2 HG02165.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.131-485C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612826 | ||||||
| chr2:3612861
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0290 | 2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.131-450G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612861 | ||||||
| chr2:3612867
|
T | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(259): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.131-444T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612867 | ||||||
| chr2:3612901
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-410C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612901 | ||||||
| chr2:3612916
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-395T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612916 | ||||||
| chr2:3612950
|
GC | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-360delC | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612950 | ||||||
| chr2:3613016
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-295G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3613016 | ||||||
| chr2:3613041
|
G | GGAGCCCG others(42): Show |
3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-254_131-253ins others(49): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 3613041 | |||||
| chr2:3613139
|
G | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-172G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3613139 | ||||||
| chr2:3613148
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-163A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3613148 | ||||||
| chr2:3613153
|
C | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.131-158C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3613153 | ||||||
| chr2:3613162
|
T | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(209): Show | 218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.131-149T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3613162 | ||||||
| chr2:3613204
|
C | T | 16 | a0001c0001t0001g0325a0002c0002t0001g0010a0002c0002t0001g0011others(13): Show | 18 | HG01106.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.131-107C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3613204 | ||||||
| chr2:3613266
|
G | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0061others(14): Show | 17 | HG00639.hp1 HG00642.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.131-45G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3613266 | ||||||
| chr2:3613279
|
G | A | 25 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0195others(22): Show | 26 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.131-32G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3613279 | ||||||
| chr2:3613401
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+19C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613401 | ||||||
| chr2:3613412
|
G | A | 25 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0195others(22): Show | 26 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.202+30G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613412 | ||||||
| chr2:3613431
|
C | T | 3 | a0001c0001t0001g0192a0002c0003t0001g0277a0002c0004t0001g0289 | 3 | HG02145.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.202+49C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613431 | ||||||
| chr2:3613446
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+64C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613446 | ||||||
| chr2:3613474
|
A | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+92A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613474 | ||||||
| chr2:3613475
|
G | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+93G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613475 | ||||||
| chr2:3613476
|
A | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+94A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613476 | ||||||
| chr2:3613554
|
G | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+172G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613554 | ||||||
| chr2:3613568
|
C | T | 3 | a0002c0002t0001g0001a0002c0002t0001g0016a0002c0002t0001g0028 | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+186C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613568 | ||||||
| chr2:3613591
|
T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(262): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.202+209T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613591 | ||||||
| chr2:3613749
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.202+367C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613749 | ||||||
| chr2:3613760
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+378G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613760 | ||||||
| chr2:3613784
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.202+402G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613784 | ||||||
| chr2:3613802
|
C | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+420C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613802 | ||||||
| chr2:3613891
|
G | C | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+509G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613891 | ||||||
| chr2:3613957
|
T | G | 2 | a0001c0001t0001g0175a0001c0001t0004g0174 | 2 | HG00438.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.202+575T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613957 | ||||||
| chr2:3613964
|
TTTTC | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(23): Show | 28 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.202+598_202+601del others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3613964 | |||||
| chr2:3613976
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0323a0002c0002t0001g0191 | 2 | HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+597_202+598ins others(10): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3613976 | |||||
| chr2:3613980
|
C | CT | 253 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(250): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.202+612dupT | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3613980 | |||||
| chr2:3613980
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+598C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3613980 | ||||||
| chr2:3614002
|
A | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+620A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614002 | ||||||
| chr2:3614006
|
T | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+624T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614006 | ||||||
| chr2:3614033
|
G | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(259): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.202+651G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614033 | ||||||
| chr2:3614124
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+742C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614124 | ||||||
| chr2:3614142
|
T | TG | 10 | a0002c0002t0001g0027a0002c0002t0001g0035a0002c0002t0001g0062others(7): Show | 10 | HG01884.hp2 HG02683.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.202+760_202+761ins others(1): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614142 | ||||||
| chr2:3614143
|
T | G | 11 | a0001c0001t0001g0205a0002c0002t0001g0027a0002c0002t0001g0035others(8): Show | 11 | HG01884.hp2 HG02683.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.202+761T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614143 | ||||||
| chr2:3614143
|
T | TG | 254 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(251): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.202+767dupG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3614143 | |||||
| chr2:3614237
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+855A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614237 | ||||||
| chr2:3614283
|
A | G | 1 | a0006c0013t0001g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.202+901A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614283 | ||||||
| chr2:3614338
|
A | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+956A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614338 | ||||||
| chr2:3614369
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.202+987T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614369 | ||||||
| chr2:3614412
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(260): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.202+1030G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614412 | ||||||
| chr2:3614443
|
T | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1061T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614443 | ||||||
| chr2:3614470
|
C | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(209): Show | 218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.202+1088C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614470 | ||||||
| chr2:3614472
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0001g0063 | 2 | HG01109.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.202+1090T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614472 | ||||||
| chr2:3614494
|
C | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1112C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614494 | ||||||
| chr2:3614498
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1116G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614498 | ||||||
| chr2:3614511
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1129A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614511 | ||||||
| chr2:3614558
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.202+1176C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614558 | ||||||
| chr2:3614567
|
A | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1185A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614567 | ||||||
| chr2:3614642
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0276 | 2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.202+1260A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614642 | ||||||
| chr2:3614656
|
G | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1274G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614656 | ||||||
| chr2:3614744
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.202+1362T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614744 | ||||||
| chr2:3614782
|
C | T | 9 | a0001c0001t0001g0266a0002c0002t0001g0302a0002c0002t0001g0363others(6): Show | 9 | HG00741.hp1 HG01884.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+1400C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614782 | ||||||
| chr2:3614796
|
A | G | 3 | a0002c0002t0001g0302a0002c0002t0001g0363a0005c0011t0001g0032 | 3 | HG01884.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.202+1414A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614796 | ||||||
| chr2:3614834
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.202+1452G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3614834 | ||||||
| chr2:3615001
|
A | G | 3 | a0002c0002t0001g0189a0002c0002t0001g0190a0003c0012t0001g0358 | 3 | HG02572.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+1619A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615001 | ||||||
| chr2:3615092
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1710G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615092 | ||||||
| chr2:3615108
|
C | CT | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(205): Show | 214 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.202+1736dupT | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615108 | |||||
| chr2:3615126
|
T | TTTTA | 5 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(2): Show | 5 | HG00741.hp1 HG02004.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+1764_202+1767d others(6): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615126 | |||||
| chr2:3615130
|
A | AT | 44 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0192others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.202+1751dupT | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615130 | |||||
| chr2:3615131
|
TTTA | T | 216 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(213): Show | 222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.202+1752_202+1754d others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615131 | |||||
| chr2:3615176
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1794A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615176 | ||||||
| chr2:3615183
|
G | A | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.202+1801G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615183 | ||||||
| chr2:3615251
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1869A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615251 | ||||||
| chr2:3615293
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.202+1911G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615293 | ||||||
| chr2:3615304
|
G | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1922G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615304 | ||||||
| chr2:3615346
|
C | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+1964C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615346 | ||||||
| chr2:3615381
|
C | G | 3 | a0002c0002t0001g0206a0002c0002t0001g0221a0002c0002t0001g0318 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202+1999C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615381 | ||||||
| chr2:3615393
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.202+2011C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615393 | ||||||
| chr2:3615448
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.202+2066G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615448 | ||||||
| chr2:3615465
|
A | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2083A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615465 | ||||||
| chr2:3615530
|
T | A | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.202+2148T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615530 | ||||||
| chr2:3615604
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2222T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615604 | ||||||
| chr2:3615613
|
C | T | 8 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0103others(5): Show | 8 | HG02027.hp2 HG02129.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.202+2231C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615613 | ||||||
| chr2:3615614
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.202+2232G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615614 | ||||||
| chr2:3615633
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2251A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615633 | ||||||
| chr2:3615666
|
C | CG | 13 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0001g0100others(10): Show | 14 | HG00597.hp2 HG02004.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.202+2288dupG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615666 | |||||
| chr2:3615696
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.202+2314A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615696 | ||||||
| chr2:3615749
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0365 | 2 | NA19057.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.202+2367C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615749 | ||||||
| chr2:3615755
|
C | G | 3 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0296 | 3 | HG00639.hp2 HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.202+2373C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615755 | ||||||
| chr2:3615756
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.202+2374C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615756 | ||||||
| chr2:3615757
|
G | A | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.202+2375G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615757 | ||||||
| chr2:3615773
|
C | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2391C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615773 | ||||||
| chr2:3615778
|
C | A | 3 | a0002c0002t0001g0206a0002c0002t0001g0221a0002c0002t0001g0318 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202+2396C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615778 | ||||||
| chr2:3615784
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.202+2402T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615784 | ||||||
| chr2:3615790
|
G | A | 27 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0195others(24): Show | 28 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.202+2408G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615790 | ||||||
| chr2:3615798
|
AGGCAGGG others(39): Show |
A | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(256): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.202+2466_202+2511d others(48): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615798 | |||||
| chr2:3615814
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.202+2432C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615814 | ||||||
| chr2:3615847
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.202+2465C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615847 | ||||||
| chr2:3615848
|
A | G | 4 | a0001c0001t0001g0244a0001c0001t0001g0319a0001c0001t0001g0323others(1): Show | 4 | HG01169.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+2466A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615848 | ||||||
| chr2:3615848
|
AGGGGCTG others(39): Show |
A | 1 | a0001c0001t0001g0339 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.202+2496_202+2541d others(48): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615848 | |||||
| chr2:3615850
|
G | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2468G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615850 | ||||||
| chr2:3615866
|
C | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(23): Show | 28 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.202+2484C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615866 | ||||||
| chr2:3615873
|
GGACGCGG others(79): Show |
G | 1 | a0001c0001t0001g0244 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.202+2496_202+2581d others(88): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615873 | |||||
| chr2:3615878
|
C | T | 25 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0195others(22): Show | 26 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.202+2496C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615878 | ||||||
| chr2:3615927
|
G | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2545G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615927 | ||||||
| chr2:3615928
|
G | T | 3 | a0002c0002t0001g0206a0002c0002t0001g0221a0002c0002t0001g0318 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202+2546G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615928 | ||||||
| chr2:3615937
|
G | T | 1 | a0002c0006t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.202+2555G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615937 | ||||||
| chr2:3615938
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2556T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615938 | ||||||
| chr2:3615945
|
G | A | 33 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0192others(30): Show | 34 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.202+2563G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615945 | ||||||
| chr2:3615945
|
GCTC | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(213): Show | 222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.202+2567_202+2569d others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615945 | |||||
| chr2:3615959
|
A | T | 1 | a0002c0004t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.202+2577A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615959 | ||||||
| chr2:3615967
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.202+2585C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615967 | ||||||
| chr2:3615968
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2586G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615968 | ||||||
| chr2:3615974
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2592T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615974 | ||||||
| chr2:3615978
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2596T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615978 | ||||||
| chr2:3615978
|
TGGAGGGG others(33): Show |
T | 1 | a0003c0009t0001g0356 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.202+2612_202+2651d others(42): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3615978 | |||||
| chr2:3615986
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.202+2604C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615986 | ||||||
| chr2:3615988
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.202+2606C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615988 | ||||||
| chr2:3615997
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.202+2615T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615997 | ||||||
| chr2:3616019
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0131 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.202+2637G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616019 | ||||||
| chr2:3616041
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2659G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616041 | ||||||
| chr2:3616045
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.202+2663G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616045 | ||||||
| chr2:3616093
|
G | A | 1 | a0001c0001t0001g0364 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.202+2711G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616093 | ||||||
| chr2:3616113
|
A | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.202+2731A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616113 | ||||||
| chr2:3616117
|
C | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.202+2735C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616117 | ||||||
| chr2:3616131
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2749T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616131 | ||||||
| chr2:3616141
|
C | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2759C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616141 | ||||||
| chr2:3616141
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.202+2759C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616141 | ||||||
| chr2:3616142
|
G | T | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.202+2760G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616142 | ||||||
| chr2:3616160
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2778A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616160 | ||||||
| chr2:3616164
|
C | T | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.202+2782C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616164 | ||||||
| chr2:3616165
|
G | A | 3 | a0002c0002t0001g0001a0002c0002t0001g0016a0002c0002t0001g0028 | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+2783G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616165 | ||||||
| chr2:3616167
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.202+2785C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616167 | ||||||
| chr2:3616196
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2814C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616196 | ||||||
| chr2:3616203
|
C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.202+2821C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616203 | ||||||
| chr2:3616217
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2835C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616217 | ||||||
| chr2:3616236
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2854A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616236 | ||||||
| chr2:3616239
|
A | G | 4 | a0001c0001t0001g0005a0001c0001t0001g0102a0001c0001t0001g0139others(1): Show | 5 | NA18939.hp1 NA18942.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.202+2857A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616239 | ||||||
| chr2:3616285
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2903G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616285 | ||||||
| chr2:3616307
|
C | T | 1 | a0002c0005t0002g0183 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.202+2925C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616307 | ||||||
| chr2:3616308
|
G | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2926G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616308 | ||||||
| chr2:3616313
|
T | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2931T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616313 | ||||||
| chr2:3616334
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+2952A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616334 | ||||||
| chr2:3616351
|
C | CG | 8 | a0001c0001t0001g0063a0001c0001t0001g0102a0001c0001t0001g0139others(5): Show | 8 | HG00597.hp2 HG01978.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.202+2973dupG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3616351 | |||||
| chr2:3616351
|
C | T | 1 | a0002c0006t0001g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.202+2969C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616351 | ||||||
| chr2:3616360
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.202+2978G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616360 | ||||||
| chr2:3616363
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.202+2981C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616363 | ||||||
| chr2:3616431
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3049A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616431 | ||||||
| chr2:3616434
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.202+3052C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616434 | ||||||
| chr2:3616435
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.202+3053C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616435 | ||||||
| chr2:3616451
|
C | T | 4 | a0001c0001t0001g0192a0002c0003t0001g0277a0002c0004t0001g0289others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+3069C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616451 | ||||||
| chr2:3616469
|
A | C | 1 | a0002c0002t0001g0327 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.202+3087A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616469 | ||||||
| chr2:3616469
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.202+3087A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616469 | ||||||
| chr2:3616476
|
A | G | 2 | a0002c0006t0001g0200a0003c0010t0001g0357 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.202+3094A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616476 | ||||||
| chr2:3616481
|
G | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3099G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616481 | ||||||
| chr2:3616485
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3103A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616485 | ||||||
| chr2:3616494
|
C | T | 1 | a0002c0003t0001g0223 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.202+3112C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616494 | ||||||
| chr2:3616505
|
C | T | 1 | a0002c0004t0001g0246 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.202+3123C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616505 | ||||||
| chr2:3616543
|
G | A | 33 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0192others(30): Show | 34 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.202+3161G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616543 | ||||||
| chr2:3616566
|
G | A | 4 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191others(1): Show | 4 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.202+3184G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616566 | ||||||
| chr2:3616574
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.202+3192C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616574 | ||||||
| chr2:3616577
|
C | T | 2 | a0001c0001t0001g0331a0001c0001t0001g0359 | 2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.202+3195C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616577 | ||||||
| chr2:3616578
|
G | A | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+3196G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616578 | ||||||
| chr2:3616627
|
C | T | 15 | a0001c0001t0001g0325a0002c0002t0001g0010a0002c0002t0001g0011others(12): Show | 17 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.202+3245C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616627 | ||||||
| chr2:3616671
|
A | G | 1 | a0002c0004t0001g0317 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.202+3289A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616671 | ||||||
| chr2:3616729
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(263): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.202+3347A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616729 | ||||||
| chr2:3616745
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3363T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616745 | ||||||
| chr2:3616746
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3364C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616746 | ||||||
| chr2:3616753
|
A | AGAGAGGG others(16): Show |
2 | a0001c0001t0001g0239a0002c0002t0001g0327 | 2 | HG02818.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.202+3412_202+3434d others(25): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3616753 | |||||
| chr2:3616753
|
AGAGAGGG others(16): Show |
A | 3 | a0002c0002t0001g0206a0002c0002t0001g0221a0002c0002t0001g0318 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202+3412_202+3434d others(25): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3616753 | |||||
| chr2:3616760
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3378G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616760 | ||||||
| chr2:3616789
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3407G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616789 | ||||||
| chr2:3616794
|
CGTGGGGA others(16): Show |
C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3430_202+3452d others(25): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3616794 | |||||
| chr2:3616850
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.202+3468T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616850 | ||||||
| chr2:3616879
|
A | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(209): Show | 218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.202+3497A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616879 | ||||||
| chr2:3616898
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.202+3516G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616898 | ||||||
| chr2:3616981
|
C | T | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+3599C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616981 | ||||||
| chr2:3616994
|
T | A | 5 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(2): Show | 5 | HG00741.hp1 HG02004.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+3612T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616994 | ||||||
| chr2:3616994
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.202+3612T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616994 | ||||||
| chr2:3617005
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3623T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617005 | ||||||
| chr2:3617044
|
A | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0026others(58): Show | 64 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.202+3662A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617044 | ||||||
| chr2:3617072
|
T | G | 1 | a0002c0002t0001g0308 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.202+3690T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617072 | ||||||
| chr2:3617098
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3716T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617098 | ||||||
| chr2:3617242
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3860A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617242 | ||||||
| chr2:3617255
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+3873G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617255 | ||||||
| chr2:3617363
|
C | A | 1 | a0002c0004t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.202+3981C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617363 | ||||||
| chr2:3617435
|
A | T | 1 | a0001c0001t0001g0337 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.202+4053A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617435 | ||||||
| chr2:3617442
|
C | T | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.202+4060C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617442 | ||||||
| chr2:3617541
|
C | T | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+4159C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617541 | ||||||
| chr2:3617542
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.202+4160G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617542 | ||||||
| chr2:3617548
|
C | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.202+4166C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617548 | ||||||
| chr2:3617556
|
T | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.202+4174T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617556 | ||||||
| chr2:3617579
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.202+4197G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617579 | ||||||
| chr2:3617580
|
T | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+4198T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617580 | ||||||
| chr2:3617627
|
T | C | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+4245T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617627 | ||||||
| chr2:3617638
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+4256C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617638 | ||||||
| chr2:3617704
|
C | T | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.202+4322C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617704 | ||||||
| chr2:3617720
|
G | A | 1 | a0004c0008t0001g0225 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.202+4338G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617720 | ||||||
| chr2:3617752
|
T | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(270): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.202+4370T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617752 | ||||||
| chr2:3617811
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+4429A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617811 | ||||||
| chr2:3617848
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+4466A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617848 | ||||||
| chr2:3617855
|
A | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.202+4473A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617855 | ||||||
| chr2:3617966
|
A | G | 2 | a0002c0002t0001g0302a0002c0002t0001g0363 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.202+4584A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617966 | ||||||
| chr2:3618068
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+4686A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618068 | ||||||
| chr2:3618084
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.202+4702G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618084 | ||||||
| chr2:3618124
|
G | GTCT | 7 | a0001c0001t0001g0013a0001c0001t0001g0073a0001c0001t0001g0143others(4): Show | 8 | HG00438.hp1 HG02015.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.202+4745_202+4747d others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3618124 | |||||
| chr2:3618162
|
G | T | 257 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(254): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.202+4780G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618162 | ||||||
| chr2:3618276
|
A | G | 1 | a0003c0012t0001g0358 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.202+4894A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618276 | ||||||
| chr2:3618291
|
T | C | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.202+4909T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618291 | ||||||
| chr2:3618293
|
C | G | 1 | a0002c0004t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.202+4911C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618293 | ||||||
| chr2:3618353
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+4971T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618353 | ||||||
| chr2:3618391
|
G | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(210): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.202+5009G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618391 | ||||||
| chr2:3618491
|
TTATTTCT others(18): Show |
T | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.202+5114_202+5138d others(27): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3618491 | |||||
| chr2:3618605
|
C | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+5223C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618605 | ||||||
| chr2:3618703
|
T | C | 6 | a0001c0001t0001g0068a0002c0002t0001g0017a0002c0002t0001g0029others(3): Show | 6 | HG02258.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+5321T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618703 | ||||||
| chr2:3618747
|
A | T | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.202+5365A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618747 | ||||||
| chr2:3618749
|
T | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0034others(60): Show | 66 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.202+5367T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618749 | ||||||
| chr2:3618790
|
TATTA | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+5412_202+5415d others(6): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3618790 | |||||
| chr2:3618831
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+5449A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618831 | ||||||
| chr2:3618872
|
C | T | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.202+5490C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618872 | ||||||
| chr2:3618904
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.202+5522A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3618904 | ||||||
| chr2:3619147
|
A | ATCCCTCC others(1): Show |
3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+5769_202+5776d others(10): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3619147 | |||||
| chr2:3619162
|
T | C | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+5780T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619162 | ||||||
| chr2:3619197
|
C | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+5815C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619197 | ||||||
| chr2:3619210
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+5828C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619210 | ||||||
| chr2:3619231
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.202+5849C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619231 | ||||||
| chr2:3619257
|
T | C | 41 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0001g0192others(38): Show | 42 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.202+5875T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619257 | ||||||
| chr2:3619335
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.202+5953C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619335 | ||||||
| chr2:3619368
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0267 | 2 | NA18967.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.202+5986T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619368 | ||||||
| chr2:3619418
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+6036G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619418 | ||||||
| chr2:3619510
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.202+6128A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619510 | ||||||
| chr2:3619716
|
C | T | 1 | a0002c0004t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.202+6334C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619716 | ||||||
| chr2:3619746
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+6364C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619746 | ||||||
| chr2:3619903
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+6521A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619903 | ||||||
| chr2:3619916
|
G | C | 8 | a0001c0001t0001g0041a0001c0001t0001g0080a0001c0001t0001g0087others(5): Show | 8 | HG02135.hp2 NA18747.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.202+6534G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619916 | ||||||
| chr2:3619920
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.202+6538C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619920 | ||||||
| chr2:3619922
|
G | A | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+6540G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619922 | ||||||
| chr2:3619979
|
A | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+6597A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3619979 | ||||||
| chr2:3620015
|
T | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+6633T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620015 | ||||||
| chr2:3620088
|
C | G | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+6706C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620088 | ||||||
| chr2:3620106
|
T | C | 6 | a0001c0001t0001g0068a0002c0002t0001g0017a0002c0002t0001g0029others(3): Show | 6 | HG02258.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+6724T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620106 | ||||||
| chr2:3620163
|
T | C | 1 | a0001c0001t0003g0082 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.202+6781T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620163 | ||||||
| chr2:3620242
|
G | C | 4 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0038others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+6860G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620242 | ||||||
| chr2:3620281
|
T | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(258): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.202+6899T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620281 | ||||||
| chr2:3620406
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(256): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.202+7024A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620406 | ||||||
| chr2:3620522
|
C | G | 8 | a0002c0002t0001g0027a0002c0002t0001g0035a0002c0002t0001g0062others(5): Show | 8 | HG01884.hp2 HG02683.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.202+7140C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620522 | ||||||
| chr2:3620536
|
C | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(255): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.202+7154C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620536 | ||||||
| chr2:3620649
|
A | T | 1 | a0001c0001t0001g0203 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.202+7267A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620649 | ||||||
| chr2:3620651
|
T | A | 1 | a0001c0001t0001g0203 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.202+7269T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620651 | ||||||
| chr2:3620723
|
A | G | 1 | a0002c0002t0001g0180 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.202+7341A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620723 | ||||||
| chr2:3620811
|
GTTGT | G | 14 | a0001c0001t0001g0325a0002c0002t0001g0010a0002c0002t0001g0011others(11): Show | 16 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+7432_202+7435d others(6): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3620811 | |||||
| chr2:3620856
|
T | G | 1 | a0002c0002t0001g0314 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.202+7474T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620856 | ||||||
| chr2:3620951
|
G | A | 3 | a0002c0002t0001g0302a0002c0002t0001g0363a0005c0011t0001g0032 | 3 | HG01884.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.202+7569G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620951 | ||||||
| chr2:3621067
|
A | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(191): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.202+7685A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621067 | ||||||
| chr2:3621247
|
T | A | 1 | a0001c0001t0003g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.202+7865T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621247 | ||||||
| chr2:3621256
|
C | T | 1 | a0003c0012t0001g0358 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.202+7874C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621256 | ||||||
| chr2:3621285
|
A | C | 6 | a0001c0001t0001g0068a0002c0002t0001g0017a0002c0002t0001g0029others(3): Show | 6 | HG02258.hp2 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.202+7903A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621285 | ||||||
| chr2:3621498
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(210): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.202+8116C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621498 | ||||||
| chr2:3621533
|
T | C | 2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.202+8151T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621533 | ||||||
| chr2:3621543
|
T | A | 1 | a0006c0013t0001g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.202+8161T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621543 | ||||||
| chr2:3621648
|
T | C | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+8266T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621648 | ||||||
| chr2:3621740
|
A | G | 1 | a0002c0004t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.202+8358A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621740 | ||||||
| chr2:3621752
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.202+8370A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621752 | ||||||
| chr2:3621758
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.202+8376A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621758 | ||||||
| chr2:3621799
|
A | T | 8 | a0002c0002t0001g0027a0002c0002t0001g0035a0002c0002t0001g0062others(5): Show | 8 | HG01884.hp2 HG02683.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.202+8417A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621799 | ||||||
| chr2:3621851
|
T | C | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.202+8469T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621851 | ||||||
| chr2:3621892
|
C | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(262): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.202+8510C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621892 | ||||||
| chr2:3621964
|
G | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0099a0001c0001t0001g0275others(1): Show | 4 | HG01358.hp2 HG01433.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+8582G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621964 | ||||||
| chr2:3621974
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.202+8592C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621974 | ||||||
| chr2:3621987
|
G | A | 2 | a0002c0002t0001g0302a0002c0002t0001g0363 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.202+8605G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3621987 | ||||||
| chr2:3622033
|
C | T | 2 | a0002c0006t0001g0200a0003c0010t0001g0357 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.202+8651C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622033 | ||||||
| chr2:3622147
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0126a0001c0001t0001g0293 | 3 | HG00280.hp2 HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.202+8765C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622147 | ||||||
| chr2:3622163
|
C | A | 1 | a0001c0001t0001g0296 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.202+8781C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622163 | ||||||
| chr2:3622168
|
C | CA | 8 | a0001c0001t0001g0108a0001c0001t0001g0168a0001c0001t0001g0232others(5): Show | 8 | HG01243.hp2 HG01981.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.202+8803dupA | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3622168 | |||||
| chr2:3622168
|
CA | C | 15 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0104others(12): Show | 15 | HG01884.hp1 HG02004.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.202+8803delA | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3622168 | |||||
| chr2:3622336
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.202+8954A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622336 | ||||||
| chr2:3622338
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.202+8956C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622338 | ||||||
| chr2:3622396
|
C | T | 1 | a0002c0005t0002g0183 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.202+9014C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622396 | ||||||
| chr2:3622425
|
C | T | 1 | a0002c0002t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.202+9043C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622425 | ||||||
| chr2:3622515
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.202+9133C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622515 | ||||||
| chr2:3622545
|
C | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+9163C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622545 | ||||||
| chr2:3622886
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.202+9504G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622886 | ||||||
| chr2:3622889
|
A | G | 3 | a0002c0002t0001g0206a0002c0002t0001g0221a0002c0002t0001g0318 | 3 | HG01891.hp1 HG02258.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.202+9507A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622889 | ||||||
| chr2:3622963
|
A | G | 1 | a0001c0001t0001g0365 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.202+9581A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3622963 | ||||||
| chr2:3623224
|
C | T | 5 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(2): Show | 5 | HG00741.hp1 HG02004.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+9842C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623224 | ||||||
| chr2:3623345
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.202+9963A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623345 | ||||||
| chr2:3623501
|
C | A | 3 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0327 | 3 | HG02818.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.202+10119C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623501 | ||||||
| chr2:3623658
|
A | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(131): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.202+10276A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623658 | ||||||
| chr2:3623659
|
A | T | 12 | a0001c0001t0001g0056a0001c0001t0001g0098a0001c0001t0001g0112others(9): Show | 12 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.202+10277A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623659 | ||||||
| chr2:3623793
|
G | C | 3 | a0001c0001t0001g0192a0002c0003t0001g0277a0002c0004t0001g0289 | 3 | HG02145.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.202+10411G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623793 | ||||||
| chr2:3623809
|
C | G | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+10427C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623809 | ||||||
| chr2:3623822
|
A | C | 5 | a0001c0001t0001g0098a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG00735.hp2 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.202+10440A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623822 | ||||||
| chr2:3624143
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.202+10761C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624143 | ||||||
| chr2:3624212
|
A | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0323a0002c0002t0001g0191 | 3 | HG02647.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.202+10830A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624212 | ||||||
| chr2:3624250
|
G | A | 5 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(2): Show | 5 | HG00741.hp1 HG02004.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+10868G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624250 | ||||||
| chr2:3624261
|
G | C | 1 | a0001c0001t0001g0296 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.202+10879G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624261 | ||||||
| chr2:3624329
|
A | C | 18 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0137others(15): Show | 19 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.202+10947A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624329 | ||||||
| chr2:3624330
|
C | A | 18 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0137others(15): Show | 19 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.202+10948C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624330 | ||||||
| chr2:3624333
|
G | T | 1 | a0007c0015t0001g0159 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.202+10951G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624333 | ||||||
| chr2:3624339
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0001g0271a0001c0001t0001g0276 | 3 | HG00738.hp2 HG01358.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.202+10957C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624339 | ||||||
| chr2:3624345
|
C | CATCA | 4 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0038others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+10964_202+1096 others(8): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3624345 | |||||
| chr2:3624360
|
G | T | 5 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(2): Show | 5 | HG00741.hp1 HG02004.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+10978G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624360 | ||||||
| chr2:3624482
|
A | C | 1 | a0002c0002t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.202+11100A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624482 | ||||||
| chr2:3624569
|
A | T | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(92): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.202+11187A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624569 | ||||||
| chr2:3624570
|
C | T | 24 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(21): Show | 26 | HG00140.hp2 HG00423.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.202+11188C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624570 | ||||||
| chr2:3624663
|
G | A | 4 | a0001c0001t0001g0068a0002c0002t0001g0316a0002c0006t0001g0200others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+11281G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624663 | ||||||
| chr2:3624821
|
A | G | 3 | a0002c0002t0001g0027a0002c0002t0001g0039a0002c0006t0001g0200 | 3 | HG02970.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.202+11439A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624821 | ||||||
| chr2:3624830
|
T | C | 24 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0001t0001g0198others(21): Show | 25 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.202+11448T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624830 | ||||||
| chr2:3624841
|
T | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0027 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.202+11459T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624841 | ||||||
| chr2:3624970
|
A | G | 78 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0014others(75): Show | 81 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.202+11588A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3624970 | ||||||
| chr2:3625080
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 56 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.202+11698A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625080 | ||||||
| chr2:3625233
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.202+11851G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625233 | ||||||
| chr2:3625275
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(301): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.202+11893A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625275 | ||||||
| chr2:3625336
|
G | A | 9 | a0002c0002t0001g0189a0002c0002t0001g0190a0002c0004t0001g0214others(6): Show | 9 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+11954G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625336 | ||||||
| chr2:3625354
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202+11972C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625354 | ||||||
| chr2:3625370
|
G | A | 1 | a0002c0002t0001g0309 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+11988G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625370 | ||||||
| chr2:3625440
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.202+12058G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625440 | ||||||
| chr2:3625513
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.203-12020C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625513 | ||||||
| chr2:3625550
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0254 | 2 | HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.203-11983G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625550 | ||||||
| chr2:3625560
|
C | T | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-11973C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625560 | ||||||
| chr2:3625591
|
C | T | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-11942C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625591 | ||||||
| chr2:3625609
|
C | A | 1 | a0002c0002t0001g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.203-11924C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625609 | ||||||
| chr2:3625625
|
C | CTTTT | 11 | a0001c0001t0001g0046a0001c0001t0001g0091a0002c0002t0001g0017others(8): Show | 11 | HG02258.hp2 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-11892_203-1188 others(8): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3625625 | |||||
| chr2:3625625
|
C | CTTTTT | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 52 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.203-11893_203-1188 others(9): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3625625 | |||||
| chr2:3625625
|
C | CTTTTTT | 20 | a0001c0001t0001g0033a0001c0001t0001g0102a0001c0001t0001g0147others(17): Show | 20 | HG01256.hp2 HG01884.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.203-11894_203-1188 others(10): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3625625 | |||||
| chr2:3625625
|
C | CTTTTTTT | 140 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(137): Show | 145 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.203-11895_203-1188 others(11): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3625625 | |||||
| chr2:3625625
|
C | CTTTTTTT others(1): Show |
54 | a0001c0001t0001g0026a0001c0001t0001g0079a0001c0001t0001g0108others(51): Show | 56 | HG00099.hp1 HG00423.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.203-11896_203-1188 others(12): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3625625 | |||||
| chr2:3625625
|
C | CTTTTTTT others(2): Show |
22 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0137others(19): Show | 23 | HG00140.hp1 HG01243.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.203-11897_203-1188 others(13): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3625625 | |||||
| chr2:3625625
|
C | CTTTTTTT others(3): Show |
2 | a0002c0003t0001g0053a0002c0005t0002g0183 | 2 | HG02040.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.203-11898_203-1188 others(14): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3625625 | |||||
| chr2:3625625
|
C | CTTTTTTT others(5): Show |
1 | a0002c0006t0001g0315 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.203-11900_203-1188 others(16): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3625625 | |||||
| chr2:3625673
|
T | C | 301 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(298): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.203-11860T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625673 | ||||||
| chr2:3625725
|
C | T | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-11808C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625725 | ||||||
| chr2:3625732
|
A | G | 5 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0308others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-11801A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625732 | ||||||
| chr2:3625789
|
C | G | 19 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0179others(16): Show | 19 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-11744C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625789 | ||||||
| chr2:3625874
|
C | G | 1 | a0001c0001t0001g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-11659C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625874 | ||||||
| chr2:3625900
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.203-11633C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625900 | ||||||
| chr2:3625920
|
G | A | 2 | a0002c0006t0001g0329a0002c0006t0001g0333 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.203-11613G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3625920 | ||||||
| chr2:3626019
|
A | G | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-11514A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626019 | ||||||
| chr2:3626058
|
G | A | 58 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(55): Show | 61 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.203-11475G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626058 | ||||||
| chr2:3626090
|
A | G | 5 | a0001c0001t0001g0192a0002c0002t0001g0316a0002c0006t0001g0031others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-11443A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626090 | ||||||
| chr2:3626260
|
C | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0117a0001c0001t0001g0155others(3): Show | 6 | HG00438.hp1 HG00597.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-11273C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626260 | ||||||
| chr2:3626261
|
G | A | 41 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(38): Show | 43 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.203-11272G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626261 | ||||||
| chr2:3626264
|
C | A | 1 | a0001c0001t0001g0292 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.203-11269C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626264 | ||||||
| chr2:3626408
|
C | T | 1 | a0002c0003t0001g0334 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.203-11125C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626408 | ||||||
| chr2:3626487
|
C | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(61): Show | 67 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.203-11046C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626487 | ||||||
| chr2:3626636
|
A | G | 2 | a0002c0006t0001g0200a0003c0010t0001g0357 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.203-10897A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626636 | ||||||
| chr2:3626856
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.203-10677G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626856 | ||||||
| chr2:3626871
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(242): Show | 254 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.203-10662G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626871 | ||||||
| chr2:3626899
|
G | T | 314 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(311): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.203-10634G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626899 | ||||||
| chr2:3626921
|
C | T | 1 | a0001c0001t0001g0359 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.203-10612C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626921 | ||||||
| chr2:3627166
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.203-10367C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627166 | ||||||
| chr2:3627257
|
T | C | 310 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(307): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.203-10276T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627257 | ||||||
| chr2:3627317
|
TGACGGGG others(8): Show |
T | 1 | a0001c0001t0001g0340 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.203-10213_203-1019 others(19): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3627317 | |||||
| chr2:3627332
|
C | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(169): Show | 178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.203-10201C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627332 | ||||||
| chr2:3627347
|
GGGCATGA others(19): Show |
G | 61 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0137others(58): Show | 64 | HG00099.hp1 HG00140.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-10179_203-1015 others(30): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3627347 | |||||
| chr2:3627469
|
A | G | 3 | a0002c0002t0001g0017a0002c0002t0001g0044a0002c0002t0001g0194 | 3 | HG02258.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.203-10064A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627469 | ||||||
| chr2:3627515
|
A | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(306): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.203-10018A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627515 | ||||||
| chr2:3627517
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.203-10016C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627517 | ||||||
| chr2:3627565
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(164): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.203-9968C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627565 | ||||||
| chr2:3627693
|
C | T | 1 | a0002c0002t0001g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.203-9840C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627693 | ||||||
| chr2:3627720
|
T | A | 1 | a0002c0003t0001g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.203-9813T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627720 | ||||||
| chr2:3627828
|
C | T | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-9705C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627828 | ||||||
| chr2:3627858
|
C | G | 1 | a0001c0001t0001g0299 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.203-9675C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627858 | ||||||
| chr2:3627887
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203-9646G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3627887 | ||||||
| chr2:3628006
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.203-9527T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628006 | ||||||
| chr2:3628029
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203-9504C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628029 | ||||||
| chr2:3628114
|
C | T | 5 | a0002c0002t0001g0316a0002c0006t0001g0031a0002c0006t0001g0199others(2): Show | 5 | HG01099.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-9419C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628114 | ||||||
| chr2:3628115
|
G | A | 5 | a0001c0001t0001g0307a0002c0003t0001g0171a0002c0003t0001g0223others(2): Show | 5 | HG00741.hp1 HG02004.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-9418G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628115 | ||||||
| chr2:3628171
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203-9362A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628171 | ||||||
| chr2:3628239
|
TC | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(163): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.203-9290delC | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3628239 | |||||
| chr2:3628252
|
C | T | 42 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(39): Show | 44 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.203-9281C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628252 | ||||||
| chr2:3628305
|
A | C | 4 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0191others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-9228A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628305 | ||||||
| chr2:3628330
|
G | C | 1 | a0001c0001t0001g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-9203G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628330 | ||||||
| chr2:3628377
|
T | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 73 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.203-9156T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628377 | ||||||
| chr2:3628420
|
C | G | 4 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0039others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-9113C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628420 | ||||||
| chr2:3628544
|
G | C | 1 | a0001c0001t0001g0307 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.203-8989G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628544 | ||||||
| chr2:3628628
|
C | G | 101 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0012others(98): Show | 104 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.203-8905C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628628 | ||||||
| chr2:3628682
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.203-8851A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628682 | ||||||
| chr2:3628762
|
A | C | 13 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0137others(10): Show | 14 | HG00099.hp1 HG00140.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.203-8771A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628762 | ||||||
| chr2:3628802
|
C | G | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-8731C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628802 | ||||||
| chr2:3628917
|
G | C | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.203-8616G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628917 | ||||||
| chr2:3629008
|
C | T | 2 | a0002c0002t0001g0044a0002c0002t0001g0194 | 2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.203-8525C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629008 | ||||||
| chr2:3629014
|
G | T | 1 | a0002c0003t0001g0040 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.203-8519G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629014 | ||||||
| chr2:3629037
|
C | G | 1 | a0002c0002t0001g0347 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-8496C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629037 | ||||||
| chr2:3629067
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.203-8466G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629067 | ||||||
| chr2:3629161
|
C | G | 3 | a0002c0002t0001g0027a0002c0002t0001g0038a0002c0006t0001g0315 | 3 | HG02451.hp2 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.203-8372C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629161 | ||||||
| chr2:3629339
|
A | G | 1 | a0002c0004t0001g0246 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.203-8194A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629339 | ||||||
| chr2:3629432
|
T | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 73 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.203-8101T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629432 | ||||||
| chr2:3629482
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-8051A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629482 | ||||||
| chr2:3629501
|
C | T | 40 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(37): Show | 42 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.203-8032C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629501 | ||||||
| chr2:3629533
|
T | C | 40 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(37): Show | 42 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.203-8000T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629533 | ||||||
| chr2:3629620
|
G | T | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-7913G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629620 | ||||||
| chr2:3629661
|
T | C | 1 | a0001c0001t0001g0354 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.203-7872T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629661 | ||||||
| chr2:3629707
|
C | A | 3 | a0002c0006t0001g0199a0002c0006t0001g0329a0002c0006t0001g0333 | 3 | HG01099.hp2 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.203-7826C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629707 | ||||||
| chr2:3629715
|
T | C | 4 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0308others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-7818T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629715 | ||||||
| chr2:3629762
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.203-7771C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629762 | ||||||
| chr2:3629765
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 73 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.203-7768G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629765 | ||||||
| chr2:3629872
|
C | G | 42 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(39): Show | 44 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.203-7661C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629872 | ||||||
| chr2:3629935
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.203-7598C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3629935 | ||||||
| chr2:3630053
|
C | T | 1 | a0002c0002t0001g0180 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.203-7480C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630053 | ||||||
| chr2:3630054
|
G | A | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-7479G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630054 | ||||||
| chr2:3630071
|
A | ATC | 302 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.203-7460_203-7459d others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3630071 | |||||
| chr2:3630074
|
T | TCTG | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0232others(1): Show | 4 | HG00140.hp2 HG00733.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-7459_203-7458i others(5): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630074 | ||||||
| chr2:3630075
|
G | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0232others(1): Show | 4 | HG00140.hp2 HG00733.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-7458G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630075 | ||||||
| chr2:3630131
|
C | CTG | 236 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(233): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.203-7401_203-7400i others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3630131 | |||||
| chr2:3630131
|
CTATG | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 72 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.203-7400_203-7397d others(6): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3630131 | |||||
| chr2:3630187
|
A | G | 36 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(33): Show | 38 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.203-7346A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630187 | ||||||
| chr2:3630264
|
T | G | 1 | a0001c0001t0001g0336 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.203-7269T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630264 | ||||||
| chr2:3630283
|
T | C | 1 | a0001c0001t0001g0274 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.203-7250T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630283 | ||||||
| chr2:3630361
|
A | G | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-7172A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630361 | ||||||
| chr2:3630390
|
C | G | 1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.203-7143C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630390 | ||||||
| chr2:3630392
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203-7141A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630392 | ||||||
| chr2:3630393
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.203-7140T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630393 | ||||||
| chr2:3630528
|
T | C | 1 | a0003c0010t0001g0357 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.203-7005T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630528 | ||||||
| chr2:3630548
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.203-6985A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630548 | ||||||
| chr2:3630629
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.203-6904T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630629 | ||||||
| chr2:3630687
|
G | T | 1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.203-6846G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630687 | ||||||
| chr2:3630779
|
C | T | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-6754C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630779 | ||||||
| chr2:3630813
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.203-6720G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630813 | ||||||
| chr2:3630939
|
C | T | 4 | a0001c0001t0001g0325a0002c0002t0001g0217a0002c0002t0001g0229others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-6594C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630939 | ||||||
| chr2:3630967
|
C | T | 2 | a0002c0002t0001g0027a0002c0002t0001g0038 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.203-6566C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630967 | ||||||
| chr2:3631007
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0301 | 2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.203-6526C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631007 | ||||||
| chr2:3631089
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.203-6444G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631089 | ||||||
| chr2:3631183
|
ATTGCACT others(7): Show |
A | 1 | a0001c0001t0001g0235 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.203-6348_203-6335d others(16): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3631183 | |||||
| chr2:3631213
|
A | C | 4 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0039others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-6320A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631213 | ||||||
| chr2:3631260
|
A | G | 60 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0137others(57): Show | 63 | HG00099.hp1 HG00140.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.203-6273A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631260 | ||||||
| chr2:3631378
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.203-6155G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631378 | ||||||
| chr2:3631491
|
T | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(311): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.203-6042T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631491 | ||||||
| chr2:3631533
|
C | T | 302 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.203-6000C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631533 | ||||||
| chr2:3631554
|
C | A | 2 | a0002c0002t0001g0027a0002c0002t0001g0038 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.203-5979C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631554 | ||||||
| chr2:3631611
|
C | T | 22 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(19): Show | 24 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-5922C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631611 | ||||||
| chr2:3631667
|
C | T | 1 | a0001c0001t0001g0350 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.203-5866C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631667 | ||||||
| chr2:3631680
|
A | AGGGGCCC others(26): Show |
1 | a0002c0002t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.203-5843_203-5811d others(35): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3631680 | |||||
| chr2:3631698
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.203-5835G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631698 | ||||||
| chr2:3631710
|
G | A | 2 | a0001c0001t0001g0192a0002c0005t0001g0362 | 2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.203-5823G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631710 | ||||||
| chr2:3631720
|
C | T | 4 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0039others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-5813C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631720 | ||||||
| chr2:3631723
|
A | ACTCGGAG others(9): Show |
1 | a0002c0006t0001g0329 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.203-5799_203-5784d others(18): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3631723 | |||||
| chr2:3631723
|
A | G | 1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.203-5810A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631723 | ||||||
| chr2:3631727
|
G | A | 1 | a0002c0002t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.203-5806G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631727 | ||||||
| chr2:3631751
|
C | G | 1 | a0002c0002t0001g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.203-5782C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631751 | ||||||
| chr2:3631818
|
T | C | 7 | a0002c0002t0001g0027a0002c0002t0001g0036a0002c0002t0001g0037others(4): Show | 7 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.203-5715T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631818 | ||||||
| chr2:3631834
|
G | A | 46 | a0001c0001t0001g0192a0001c0001t0001g0320a0002c0002t0001g0001others(43): Show | 49 | HG01099.hp2 HG01106.hp2 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.203-5699G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631834 | ||||||
| chr2:3631868
|
C | T | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-5665C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631868 | ||||||
| chr2:3631966
|
A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(186): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.203-5567A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631966 | ||||||
| chr2:3632062
|
C | T | 1 | a0002c0002t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.203-5471C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632062 | ||||||
| chr2:3632068
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.203-5465C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632068 | ||||||
| chr2:3632136
|
G | A | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-5397G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632136 | ||||||
| chr2:3632194
|
A | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 137 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.203-5339A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632194 | ||||||
| chr2:3632243
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.203-5290G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632243 | ||||||
| chr2:3632246
|
G | C | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-5287G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632246 | ||||||
| chr2:3632273
|
A | G | 139 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 145 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.203-5260A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632273 | ||||||
| chr2:3632435
|
G | T | 137 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(134): Show | 143 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.203-5098G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632435 | ||||||
| chr2:3632466
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.203-5067C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632466 | ||||||
| chr2:3632489
|
C | T | 2 | a0002c0006t0001g0200a0003c0010t0001g0357 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.203-5044C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632489 | ||||||
| chr2:3632492
|
G | A | 19 | a0002c0002t0001g0189a0002c0002t0001g0190a0002c0002t0001g0193others(16): Show | 19 | HG01099.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-5041G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632492 | ||||||
| chr2:3632632
|
C | T | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-4901C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632632 | ||||||
| chr2:3632633
|
G | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(62): Show | 68 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.203-4900G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632633 | ||||||
| chr2:3632712
|
G | A | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-4821G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632712 | ||||||
| chr2:3632742
|
A | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 72 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.203-4791A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632742 | ||||||
| chr2:3632768
|
G | A | 1 | a0002c0003t0001g0186 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.203-4765G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632768 | ||||||
| chr2:3632780
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0003g0152 | 2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.203-4753A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632780 | ||||||
| chr2:3632795
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.203-4738G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632795 | ||||||
| chr2:3632842
|
G | A | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-4691G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632842 | ||||||
| chr2:3632906
|
C | CAG | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.203-4627_203-4626i others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632906 | ||||||
| chr2:3632932
|
C | T | 40 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(37): Show | 42 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.203-4601C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3632932 | ||||||
| chr2:3633057
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.203-4476A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633057 | ||||||
| chr2:3633265
|
C | T | 8 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(5): Show | 9 | HG02257.hp2 HG02559.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.203-4268C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633265 | ||||||
| chr2:3633276
|
G | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 71 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.203-4257G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633276 | ||||||
| chr2:3633455
|
C | T | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-4078C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633455 | ||||||
| chr2:3633456
|
G | A | 4 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0308others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-4077G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633456 | ||||||
| chr2:3633466
|
C | T | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-4067C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633466 | ||||||
| chr2:3633778
|
C | T | 35 | a0001c0001t0001g0325a0002c0002t0001g0001a0002c0002t0001g0010others(32): Show | 37 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.203-3755C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633778 | ||||||
| chr2:3633818
|
G | A | 4 | a0002c0002t0001g0179a0002c0002t0001g0180a0002c0002t0001g0308others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-3715G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633818 | ||||||
| chr2:3633836
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.203-3697G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633836 | ||||||
| chr2:3633841
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.203-3692G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633841 | ||||||
| chr2:3633863
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.203-3670G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633863 | ||||||
| chr2:3633884
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.203-3649C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633884 | ||||||
| chr2:3633888
|
C | G | 68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 71 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.203-3645C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633888 | ||||||
| chr2:3633889
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.203-3644G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633889 | ||||||
| chr2:3633889
|
G | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0142a0001c0001t0001g0264others(1): Show | 4 | NA18960.hp1 NA18967.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-3644G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633889 | ||||||
| chr2:3633894
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.203-3639C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633894 | ||||||
| chr2:3633966
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.203-3567C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3633966 | ||||||
| chr2:3634060
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0058 | 2 | HG00408.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.203-3473C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634060 | ||||||
| chr2:3634488
|
A | C | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.203-3045A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634488 | ||||||
| chr2:3634522
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.203-3011C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634522 | ||||||
| chr2:3634529
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.203-3004C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634529 | ||||||
| chr2:3634605
|
G | C | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.203-2928G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634605 | ||||||
| chr2:3634647
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.203-2886A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634647 | ||||||
| chr2:3634657
|
A | G | 9 | a0001c0001t0001g0192a0002c0002t0001g0193a0002c0002t0001g0316others(6): Show | 9 | HG01099.hp2 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.203-2876A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634657 | ||||||
| chr2:3634695
|
AG | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 74 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.203-2837delG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634695 | ||||||
| chr2:3634720
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.203-2813G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634720 | ||||||
| chr2:3634738
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.203-2795C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634738 | ||||||
| chr2:3634792
|
G | A | 7 | a0001c0001t0001g0068a0002c0002t0001g0193a0002c0006t0001g0199others(4): Show | 7 | HG01099.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.203-2741G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634792 | ||||||
| chr2:3634863
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.203-2670G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634863 | ||||||
| chr2:3634881
|
C | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(171): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.203-2652C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634881 | ||||||
| chr2:3634914
|
G | GC | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 123 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.203-2614dupC | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3634914 | |||||
| chr2:3634964
|
G | A | 1 | a0002c0002t0001g0347 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-2569G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634964 | ||||||
| chr2:3635001
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.203-2532C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635001 | ||||||
| chr2:3635072
|
T | TCCCTCTC others(12): Show |
4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-2438_203-2420d others(21): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3635072 | |||||
| chr2:3635077
|
C | CTCCCCTG others(31): Show |
1 | a0001c0001t0001g0235 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.203-2439_203-2438i others(40): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3635077 | |||||
| chr2:3635077
|
C | CTCCCCTG others(30): Show |
68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 72 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.203-2432_203-2396d others(39): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3635077 | |||||
| chr2:3635077
|
C | CTCCCCTG others(67): Show |
1 | a0001c0001t0001g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.203-2396_203-2395i others(76): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3635077 | |||||
| chr2:3635077
|
CTCCCCTG others(30): Show |
C | 182 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(179): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.203-2432_203-2396d others(39): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 3635077 | |||||
| chr2:3635130
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.203-2403C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635130 | ||||||
| chr2:3635230
|
C | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(62): Show | 69 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.203-2303C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635230 | ||||||
| chr2:3635231
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.203-2302G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635231 | ||||||
| chr2:3635242
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.203-2291A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635242 | ||||||
| chr2:3635297
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.203-2236A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635297 | ||||||
| chr2:3635391
|
G | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0047others(52): Show | 56 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.203-2142G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635391 | ||||||
| chr2:3635444
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.203-2089G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635444 | ||||||
| chr2:3635480
|
G | A | 2 | a0002c0003t0001g0003a0002c0003t0001g0051 | 3 | NA19004.hp1 NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.203-2053G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635480 | ||||||
| chr2:3635501
|
C | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 116 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.203-2032C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635501 | ||||||
| chr2:3635546
|
C | T | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-1987C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635546 | ||||||
| chr2:3635569
|
C | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0361 | 2 | NA19082.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.203-1964C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635569 | ||||||
| chr2:3635574
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.203-1959G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635574 | ||||||
| chr2:3635632
|
T | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 78 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.203-1901T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635632 | ||||||
| chr2:3635680
|
T | G | 11 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(8): Show | 11 | HG00741.hp1 HG02004.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.203-1853T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635680 | ||||||
| chr2:3635683
|
G | A | 1 | a0002c0003t0001g0233 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.203-1850G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635683 | ||||||
| chr2:3635858
|
G | A | 1 | a0002c0002t0001g0347 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-1675G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635858 | ||||||
| chr2:3635871
|
A | G | 364 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(361): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.203-1662A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635871 | ||||||
| chr2:3635967
|
A | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.203-1566A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635967 | ||||||
| chr2:3636025
|
G | A | 311 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(308): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.203-1508G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636025 | ||||||
| chr2:3636037
|
T | C | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-1496T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636037 | ||||||
| chr2:3636061
|
G | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(67): Show | 74 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.203-1472G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636061 | ||||||
| chr2:3636093
|
G | A | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-1440G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636093 | ||||||
| chr2:3636128
|
A | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(306): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.203-1405A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636128 | ||||||
| chr2:3636170
|
C | T | 2 | a0002c0006t0001g0200a0003c0010t0001g0357 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.203-1363C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636170 | ||||||
| chr2:3636184
|
G | A | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.203-1349G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636184 | ||||||
| chr2:3636199
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.203-1334G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636199 | ||||||
| chr2:3636318
|
G | C | 1 | a0002c0002t0001g0017 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.203-1215G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636318 | ||||||
| chr2:3636334
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.203-1199A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636334 | ||||||
| chr2:3636486
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.203-1047T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636486 | ||||||
| chr2:3636752
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(305): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.203-781T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636752 | ||||||
| chr2:3636822
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.203-711G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636822 | ||||||
| chr2:3636831
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.203-702T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636831 | ||||||
| chr2:3636922
|
T | C | 309 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(306): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.203-611T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636922 | ||||||
| chr2:3636991
|
T | C | 4 | a0002c0002t0001g0010a0002c0002t0001g0208a0002c0002t0001g0222others(1): Show | 5 | HG01106.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-542T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3636991 | ||||||
| chr2:3637050
|
C | T | 1 | a0001c0001t0001g0351 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.203-483C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637050 | ||||||
| chr2:3637131
|
A | G | 13 | a0001c0001t0001g0192a0002c0003t0001g0171a0002c0003t0001g0223others(10): Show | 13 | HG00741.hp1 HG02004.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.203-402A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637131 | ||||||
| chr2:3637134
|
G | A | 1 | a0002c0006t0001g0315 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.203-399G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637134 | ||||||
| chr2:3637144
|
C | T | 7 | a0001c0001t0001g0192a0002c0002t0001g0193a0002c0006t0001g0199others(4): Show | 7 | HG01099.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.203-389C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637144 | ||||||
| chr2:3637245
|
C | T | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-288C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637245 | ||||||
| chr2:3637269
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(239): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.203-264G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637269 | ||||||
| chr2:3637289
|
A | G | 1 | a0002c0003t0001g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.203-244A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637289 | ||||||
| chr2:3637299
|
G | A | 3 | a0002c0002t0001g0017a0002c0002t0001g0044a0002c0002t0001g0194 | 3 | HG02258.hp2 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.203-234G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637299 | ||||||
| chr2:3637322
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.203-211C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637322 | ||||||
| chr2:3637373
|
T | C | 2 | a0002c0005t0002g0181a0002c0005t0002g0182 | 2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.203-160T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637373 | ||||||
| chr2:3637456
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(305): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.203-77T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637456 | ||||||
| chr2:3637459
|
G | T | 39 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(36): Show | 41 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.203-74G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637459 | ||||||
| chr2:3637464
|
C | T | 39 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(36): Show | 41 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.203-69C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637464 | ||||||
| chr2:3637468
|
T | C | 1 | a0002c0002t0001g0217 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.203-65T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637468 | ||||||
| chr2:3637483
|
C | T | 2 | a0002c0006t0001g0200a0003c0010t0001g0357 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.203-50C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637483 | ||||||
| chr2:3637484
|
A | G | 308 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(305): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.203-49A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637484 | ||||||
| chr2:3637485
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0115a0001c0001t0001g0122others(3): Show | 7 | HG01169.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.203-48C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637485 | ||||||
| chr2:3637486
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0080a0001c0001t0001g0087others(6): Show | 9 | HG00621.hp1 HG02135.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.203-47G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637486 | ||||||
| chr2:3637503
|
G | A | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203-30G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637503 | ||||||
| chr2:3637738
|
A | G | 13 | a0001c0001t0001g0192a0002c0003t0001g0171a0002c0003t0001g0223others(10): Show | 13 | HG00741.hp1 HG02004.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.274+134A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3637738 | ||||||
| chr2:3637802
|
T | C | 2 | a0002c0006t0001g0200a0003c0010t0001g0357 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.274+198T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3637802 | ||||||
| chr2:3637901
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0321 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.274+297A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3637901 | ||||||
| chr2:3637958
|
C | A | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.274+354C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3637958 | ||||||
| chr2:3637973
|
C | T | 5 | a0002c0002t0001g0011a0002c0002t0001g0179a0002c0002t0001g0308others(2): Show | 6 | HG02572.hp1 HG02630.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+369C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3637973 | ||||||
| chr2:3637981
|
G | C | 1 | a0005c0011t0001g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.274+377G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3637981 | ||||||
| chr2:3638030
|
G | C | 28 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(25): Show | 30 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.274+426G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638030 | ||||||
| chr2:3638039
|
A | G | 12 | a0002c0002t0001g0189a0002c0002t0001g0190a0002c0002t0001g0347others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.274+435A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638039 | ||||||
| chr2:3638059
|
C | T | 6 | a0001c0001t0001g0192a0002c0006t0001g0031a0002c0006t0001g0199others(3): Show | 6 | HG01099.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.274+455C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638059 | ||||||
| chr2:3638060
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.274+456G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638060 | ||||||
| chr2:3638077
|
A | G | 8 | a0002c0003t0001g0003a0002c0003t0001g0024a0002c0003t0001g0040others(5): Show | 9 | HG01361.hp2 HG02040.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.274+473A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638077 | ||||||
| chr2:3638126
|
C | T | 12 | a0002c0002t0001g0189a0002c0002t0001g0190a0002c0002t0001g0347others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.274+522C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638126 | ||||||
| chr2:3638243
|
C | T | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.274+639C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638243 | ||||||
| chr2:3638263
|
C | CCAT | 8 | a0001c0001t0001g0192a0002c0006t0001g0031a0002c0006t0001g0199others(5): Show | 8 | HG01099.hp2 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+661_274+663dup others(3): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 3638263 | |||||
| chr2:3638279
|
C | G | 12 | a0002c0002t0001g0189a0002c0002t0001g0190a0002c0002t0001g0347others(9): Show | 12 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.274+675C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638279 | ||||||
| chr2:3638330
|
G | A | 10 | a0002c0002t0001g0011a0002c0002t0001g0027a0002c0002t0001g0038others(7): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.274+726G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638330 | ||||||
| chr2:3638368
|
C | G | 1 | a0002c0002t0001g0180 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.274+764C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638368 | ||||||
| chr2:3638411
|
A | G | 70 | a0001c0001t0001g0192a0002c0002t0001g0001a0002c0002t0001g0010others(67): Show | 73 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(70): Show |
intron_variant | MODIFIER | c.274+807A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638411 | ||||||
| chr2:3638641
|
G | C | 6 | a0002c0002t0001g0011a0002c0002t0001g0179a0002c0002t0001g0180others(3): Show | 7 | HG02572.hp1 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+1037G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638641 | ||||||
| chr2:3638751
|
G | A | 9 | a0002c0004t0001g0214a0002c0004t0001g0231a0002c0004t0001g0246others(6): Show | 9 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.274+1147G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638751 | ||||||
| chr2:3638763
|
A | G | 1 | a0002c0006t0001g0315 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.274+1159A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638763 | ||||||
| chr2:3638846
|
T | C | 30 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(27): Show | 32 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.274+1242T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638846 | ||||||
| chr2:3638884
|
G | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0184 | 3 | HG00099.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.274+1280G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638884 | ||||||
| chr2:3638987
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.275-1291C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3638987 | ||||||
| chr2:3639004
|
A | G | 70 | a0001c0001t0001g0192a0002c0002t0001g0001a0002c0002t0001g0010others(67): Show | 73 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(70): Show |
intron_variant | MODIFIER | c.275-1274A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3639004 | ||||||
| chr2:3639027
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.275-1251A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3639027 | ||||||
| chr2:3639127
|
G | A | 1 | a0006c0013t0001g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.275-1151G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3639127 | ||||||
| chr2:3639382
|
A | C | 11 | a0002c0002t0001g0011a0002c0002t0001g0027a0002c0002t0001g0038others(8): Show | 12 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.275-896A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3639382 | ||||||
| chr2:3639764
|
A | AG | 77 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(74): Show | 80 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(77): Show |
intron_variant | MODIFIER | c.275-512dupG | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 3639764 | |||||
| chr2:3639804
|
A | G | 77 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(74): Show | 80 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(77): Show |
intron_variant | MODIFIER | c.275-474A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3639804 | ||||||
| chr2:3639853
|
G | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0275a0002c0002t0001g0316others(1): Show | 4 | HG02109.hp1 HG02572.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-425G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3639853 | ||||||
| chr2:3639883
|
G | GCGTGGCG others(14): Show |
4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-391_275-371dup others(21): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 3639883 | |||||
| chr2:3639905
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.275-373C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3639905 | ||||||
| chr2:3639925
|
C | T | 2 | a0002c0002t0001g0316a0003c0012t0001g0358 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.275-353C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3639925 | ||||||
| chr2:3640067
|
C | G | 1 | a0001c0001t0001g0323 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.275-211C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3640067 | ||||||
| chr2:3640184
|
C | T | 7 | a0002c0006t0001g0031a0002c0006t0001g0199a0002c0006t0001g0200others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.275-94C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3640184 | ||||||
| chr2:3640186
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0184 | 3 | HG00099.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.275-92C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3640186 | ||||||
| chr2:3640223
|
A | G | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-55A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 4/6 | chr2 | 3640223 | ||||||
| chr2:3640367
|
T | C | 1 | a0002c0002t0001g0062 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.328+36T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640367 | ||||||
| chr2:3640415
|
GATCCCAC others(51): Show |
G | 2 | a0002c0002t0001g0189a0002c0002t0001g0190 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.328+108_328+165del others(58): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640415 | |||||
| chr2:3640452
|
AGTGGACA others(51): Show |
A | 1 | a0002c0005t0002g0182 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.328+150_328+207del others(58): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640452 | |||||
| chr2:3640599
|
A | G | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+268A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640599 | ||||||
| chr2:3640601
|
TGGACACC others(22): Show |
T | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.328+288_328+316del others(29): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640601 | |||||
| chr2:3640616
|
G | T | 10 | a0002c0002t0001g0011a0002c0002t0001g0027a0002c0002t0001g0038others(7): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.328+285G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640616 | ||||||
| chr2:3640619
|
G | A | 84 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(81): Show | 88 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(85): Show |
intron_variant | MODIFIER | c.328+288G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640619 | ||||||
| chr2:3640659
|
C | G | 3 | a0002c0006t0001g0199a0002c0006t0001g0329a0002c0006t0001g0333 | 3 | HG01099.hp2 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.328+328C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640659 | ||||||
| chr2:3640659
|
C | T | 73 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(70): Show | 76 | HG00741.hp1 HG01106.hp2 HG01123.hp2 others(73): Show |
intron_variant | MODIFIER | c.328+328C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640659 | ||||||
| chr2:3640686
|
G | A | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.328+355G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640686 | ||||||
| chr2:3640714
|
C | T | 6 | a0002c0002t0001g0011a0002c0002t0001g0179a0002c0002t0001g0180others(3): Show | 7 | HG02572.hp1 HG02630.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+383C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640714 | ||||||
| chr2:3640746
|
TGGACACC others(53): Show |
T | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.328+428_328+487del others(60): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640746 | |||||
| chr2:3640775
|
A | G | 10 | a0002c0003t0001g0223a0002c0003t0001g0233a0002c0003t0001g0334others(7): Show | 10 | HG00741.hp1 HG02004.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+444A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640775 | ||||||
| chr2:3640777
|
T | C | 4 | a0001c0001t0001g0344a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+446T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640777 | ||||||
| chr2:3640777
|
T | TGGACACC others(22): Show |
1 | a0001c0001t0001g0321 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.328+473_328+501dup others(29): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640777 | |||||
| chr2:3640777
|
T | TGGACACC others(51): Show |
2 | a0002c0002t0001g0316a0003c0012t0001g0358 | 2 | HG02109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.328+472_328+473ins others(58): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640777 | |||||
| chr2:3640777
|
T | TGGACACC others(80): Show |
1 | a0002c0002t0001g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.328+472_328+473ins others(87): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640777 | |||||
| chr2:3640777
|
T | TGGACACC others(109): Show |
1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.328+472_328+473ins others(116): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640777 | |||||
| chr2:3640777
|
T | TGGACACC others(138): Show |
17 | a0002c0002t0001g0029a0002c0002t0001g0036a0002c0002t0001g0037others(14): Show | 17 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.328+472_328+473ins others(145): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640777 | |||||
| chr2:3640804
|
A | AGCGGACA others(51): Show |
2 | a0001c0001t0001g0122a0002c0003t0001g0024 | 2 | HG01361.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.328+562_328+619dup others(58): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640804 | |||||
| chr2:3640804
|
A | AGCGGACA others(80): Show |
10 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0172others(7): Show | 11 | HG02040.hp2 HG02738.hp1 HG03486.hp1 others(8): Show |
intron_variant | MODIFIER | c.328+533_328+619dup others(87): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640804 | |||||
| chr2:3640804
|
A | AGCGGACA others(109): Show |
54 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0020others(51): Show | 55 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.328+504_328+619dup others(116): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640804 | |||||
| chr2:3640804
|
A | AGCGGACA others(138): Show |
1 | a0001c0001t0001g0187 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.328+475_328+619dup others(145): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640804 | |||||
| chr2:3640804
|
A | AGCGGACA others(51): Show |
5 | a0001c0001t0001g0047a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG00735.hp2 HG01346.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.328+529_328+530ins others(58): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640804 | |||||
| chr2:3640804
|
A | G | 42 | a0001c0001t0001g0088a0001c0001t0001g0254a0001c0001t0001g0282others(39): Show | 43 | HG00741.hp1 HG02004.hp2 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.328+473A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640804 | ||||||
| chr2:3640850
|
G | A | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.328+519G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640850 | ||||||
| chr2:3640852
|
C | T | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.328+521C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640852 | ||||||
| chr2:3640854
|
C | G | 1 | a0002c0003t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.328+523C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640854 | ||||||
| chr2:3640856
|
TCCCACGG others(142): Show |
T | 3 | a0002c0003t0001g0223a0002c0003t0001g0233a0002c0003t0001g0334 | 3 | HG00741.hp1 HG02004.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.328+533_328+681del | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640856 | |||||
| chr2:3640885
|
TCCCACGG others(82): Show |
T | 2 | a0001c0001t0001g0021a0001c0001t0001g0218 | 2 | HG01081.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.328+562_328+650del others(89): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640885 | |||||
| chr2:3640893
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0235 | 2 | HG02027.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.328+562C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640893 | ||||||
| chr2:3640893
|
CGGACACC others(82): Show |
C | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+575_328+663del others(89): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640893 | |||||
| chr2:3640894
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.328+563G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640894 | ||||||
| chr2:3640943
|
T | TCCCACGG others(53): Show |
1 | a0002c0002t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.328+619_328+620ins others(60): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640943 | |||||
| chr2:3640943
|
T | TCCCACGG others(53): Show |
1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.328+619_328+620ins others(60): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640943 | |||||
| chr2:3640943
|
TCCCACGG others(55): Show |
T | 2 | a0002c0002t0001g0208a0002c0003t0001g0171 | 2 | HG02055.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.328+748_328+809del others(62): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640943 | |||||
| chr2:3640948
|
C | T | 5 | a0002c0002t0001g0017a0002c0002t0001g0044a0002c0002t0001g0189others(2): Show | 5 | HG02258.hp2 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+617C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640948 | ||||||
| chr2:3640951
|
T | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.328+620T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640951 | ||||||
| chr2:3640962
|
C | CCCCGTCA others(49): Show |
1 | a0001c0001t0001g0292 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.328+632_328+633ins others(56): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 3640962 | |||||
| chr2:3640963
|
C | CCCGTCAC others(19): Show |
15 | a0001c0001t0001g0195a0001c0001t0001g0209a0001c0001t0001g0282others(12): Show | 16 | HG00738.hp1 HG01884.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.328+632_328+633ins others(26): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640963 | ||||||
| chr2:3640963
|
C | CCCGTCAC others(48): Show |
206 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(203): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.328+632_328+633ins others(55): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640963 | ||||||
| chr2:3640963
|
C | CCCGTCAC others(77): Show |
3 | a0001c0001t0001g0026a0001c0001t0001g0321a0001c0001t0001g0353 | 3 | HG02257.hp1 HG03540.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.328+632_328+633ins others(84): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640963 | ||||||
| chr2:3640964
|
A | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.328+633A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640964 | ||||||
| chr2:3640965
|
CCATGTAG others(27): Show |
C | 29 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(26): Show | 31 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.328+635_328+668del others(34): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640965 | ||||||
| chr2:3640967
|
A | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.328+636A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640967 | ||||||
| chr2:3640967
|
A | G | 2 | a0001c0001t0001g0122a0002c0006t0001g0199 | 2 | HG01099.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.328+636A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640967 | ||||||
| chr2:3640968
|
T | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.328+637T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640968 | ||||||
| chr2:3640970
|
T | C | 2 | a0001c0001t0001g0122a0002c0006t0001g0199 | 2 | HG01099.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.328+639T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640970 | ||||||
| chr2:3640970
|
T | TC | 225 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.328+639_328+640ins others(1): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640970 | ||||||
| chr2:3640972
|
G | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(224): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.328+641G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640972 | ||||||
| chr2:3640974
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(224): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.328+643C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640974 | ||||||
| chr2:3640980
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.328+649G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640980 | ||||||
| chr2:3640982
|
T | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0102others(27): Show | 33 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.328+651T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640982 | ||||||
| chr2:3640992
|
C | T | 8 | a0002c0003t0001g0003a0002c0003t0001g0024a0002c0003t0001g0040others(5): Show | 9 | HG01361.hp2 HG02040.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+661C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640992 | ||||||
| chr2:3640998
|
A | G | 2 | a0001c0001t0001g0209a0002c0006t0001g0199 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.328+667A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3640998 | ||||||
| chr2:3641001
|
T | C | 2 | a0001c0001t0001g0209a0002c0006t0001g0199 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.328+670T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641001 | ||||||
| chr2:3641001
|
T | TC | 29 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(26): Show | 31 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.328+670_328+671ins others(1): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641001 | ||||||
| chr2:3641003
|
G | C | 31 | a0001c0001t0001g0209a0002c0002t0001g0001a0002c0002t0001g0010others(28): Show | 33 | HG00738.hp1 HG01099.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.328+672G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641003 | ||||||
| chr2:3641005
|
C | T | 31 | a0001c0001t0001g0209a0002c0002t0001g0001a0002c0002t0001g0010others(28): Show | 33 | HG00738.hp1 HG01099.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.328+674C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641005 | ||||||
| chr2:3641013
|
T | C | 9 | a0001c0001t0001g0209a0002c0005t0002g0018a0002c0005t0002g0181others(6): Show | 9 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+682T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641013 | ||||||
| chr2:3641092
|
T | G | 1 | a0002c0002t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328+761T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641092 | ||||||
| chr2:3641148
|
C | T | 18 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0036others(15): Show | 18 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.328+817C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641148 | ||||||
| chr2:3641149
|
G | A | 36 | a0001c0001t0001g0021a0001c0001t0001g0218a0002c0002t0001g0001others(33): Show | 38 | HG00741.hp1 HG01081.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.328+818G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641149 | ||||||
| chr2:3641247
|
G | A | 18 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0036others(15): Show | 18 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.328+916G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641247 | ||||||
| chr2:3641253
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0291 | 2 | NA18941.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.328+922G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641253 | ||||||
| chr2:3641271
|
G | A | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+940G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641271 | ||||||
| chr2:3641320
|
C | T | 7 | a0001c0001t0001g0234a0001c0001t0001g0332a0002c0002t0001g0017others(4): Show | 7 | HG00099.hp2 HG01257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.328+989C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641320 | ||||||
| chr2:3641411
|
T | A | 1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.328+1080T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641411 | ||||||
| chr2:3641411
|
T | C | 7 | a0002c0006t0001g0031a0002c0006t0001g0199a0002c0006t0001g0200others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.328+1080T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641411 | ||||||
| chr2:3641462
|
C | T | 3 | a0001c0007t0001g0135a0001c0007t0001g0224a0001c0007t0001g0259 | 3 | HG02683.hp2 HG03834.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.328+1131C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641462 | ||||||
| chr2:3641467
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.328+1136C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641467 | ||||||
| chr2:3641494
|
G | C | 10 | a0002c0002t0001g0011a0002c0002t0001g0027a0002c0002t0001g0038others(7): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.328+1163G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641494 | ||||||
| chr2:3641525
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.328+1194T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641525 | ||||||
| chr2:3641528
|
G | A | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.328+1197G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641528 | ||||||
| chr2:3641622
|
C | A | 67 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(64): Show | 69 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(66): Show |
intron_variant | MODIFIER | c.328+1291C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641622 | ||||||
| chr2:3641624
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.328+1293A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641624 | ||||||
| chr2:3641717
|
G | T | 2 | a0002c0005t0002g0181a0002c0005t0002g0182 | 2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.328+1386G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641717 | ||||||
| chr2:3641743
|
C | T | 10 | a0002c0002t0001g0011a0002c0002t0001g0027a0002c0002t0001g0038others(7): Show | 11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.328+1412C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641743 | ||||||
| chr2:3641878
|
C | G | 7 | a0002c0006t0001g0031a0002c0006t0001g0199a0002c0006t0001g0200others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.328+1547C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641878 | ||||||
| chr2:3641879
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0107a0001c0001t0001g0270 | 3 | HG02735.hp1 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.328+1548C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641879 | ||||||
| chr2:3641880
|
G | A | 18 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0036others(15): Show | 18 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.328+1549G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641880 | ||||||
| chr2:3641884
|
A | G | 348 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(345): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.328+1553A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641884 | ||||||
| chr2:3641896
|
G | T | 4 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0039others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-1548G>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3641896 | ||||||
| chr2:3642027
|
G | A | 2 | a0002c0002t0001g0027a0002c0002t0001g0038 | 2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.329-1417G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642027 | ||||||
| chr2:3642032
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.329-1412G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642032 | ||||||
| chr2:3642070
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0342 | 2 | NA18955.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.329-1374C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642070 | ||||||
| chr2:3642115
|
G | C | 77 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(74): Show | 80 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(77): Show |
intron_variant | MODIFIER | c.329-1329G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642115 | ||||||
| chr2:3642152
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-1292G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642152 | ||||||
| chr2:3642157
|
G | A | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.329-1287G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642157 | ||||||
| chr2:3642193
|
CAG | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0129a0001c0001t0001g0157others(3): Show | 6 | NA18612.hp2 NA18944.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-1250_329-1249d others(4): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642193 | ||||||
| chr2:3642218
|
AGCCCAGA others(4): Show |
A | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.329-1225_329-1215d others(13): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642218 | ||||||
| chr2:3642246
|
C | T | 1 | a0002c0003t0001g0334 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.329-1198C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642246 | ||||||
| chr2:3642265
|
G | A | 23 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(20): Show | 25 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.329-1179G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642265 | ||||||
| chr2:3642316
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.329-1128T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642316 | ||||||
| chr2:3642327
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.329-1117G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642327 | ||||||
| chr2:3642337
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0058 | 2 | HG00408.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.329-1107G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642337 | ||||||
| chr2:3642401
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.329-1043C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642401 | ||||||
| chr2:3642516
|
T | A | 1 | a0001c0001t0001g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.329-928T>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642516 | ||||||
| chr2:3642593
|
G | C | 77 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(74): Show | 80 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(77): Show |
intron_variant | MODIFIER | c.329-851G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642593 | ||||||
| chr2:3642654
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.329-790C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642654 | ||||||
| chr2:3642739
|
C | T | 14 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(11): Show | 14 | HG01099.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.329-705C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642739 | ||||||
| chr2:3642765
|
C | G | 7 | a0002c0005t0002g0018a0002c0005t0002g0181a0002c0005t0002g0182others(4): Show | 7 | HG02055.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.329-679C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642765 | ||||||
| chr2:3642846
|
T | C | 85 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0011others(82): Show | 89 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(86): Show |
intron_variant | MODIFIER | c.329-598T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642846 | ||||||
| chr2:3642854
|
C | T | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.329-590C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642854 | ||||||
| chr2:3642858
|
C | T | 1 | a0002c0002t0001g0228 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.329-586C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642858 | ||||||
| chr2:3642866
|
C | T | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.329-578C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642866 | ||||||
| chr2:3642927
|
C | A | 4 | a0002c0003t0001g0171a0002c0003t0001g0223a0002c0003t0001g0233others(1): Show | 4 | HG00741.hp1 HG02004.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-517C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642927 | ||||||
| chr2:3642927
|
C | G | 30 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(27): Show | 32 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.329-517C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3642927 | ||||||
| chr2:3643132
|
C | A | 4 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0039others(1): Show | 4 | HG02615.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-312C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3643132 | ||||||
| chr2:3643132
|
C | T | 30 | a0002c0002t0001g0001a0002c0002t0001g0010a0002c0002t0001g0016others(27): Show | 32 | HG01106.hp2 HG01123.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.329-312C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3643132 | ||||||
| chr2:3643133
|
C | A | 7 | a0002c0006t0001g0031a0002c0006t0001g0199a0002c0006t0001g0200others(4): Show | 7 | HG01099.hp2 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.329-311C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3643133 | ||||||
| chr2:3643283
|
C | G | 1 | a0002c0005t0001g0362 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.329-161C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3643283 | ||||||
| chr2:3643338
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.329-106G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3643338 | ||||||
| chr2:3643398
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.329-46C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3643398 | ||||||
| chr2:3643423
|
G | A | 1 | a0002c0006t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.329-21G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 5/6 | chr2 | 3643423 | ||||||
| chr2:3643562
|
C | G | 1 | a0001c0001t0001g0365 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.424+23C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/6 | chr2 | 3643562 | ||||||
| chr2:3643610
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.424+71C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/6 | chr2 | 3643610 | ||||||
| chr2:3643624
|
C | T | 1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.424+85C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/6 | chr2 | 3643624 | ||||||
| chr2:3643639
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.425-88C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/6 | chr2 | 3643639 | ||||||
| chr2:3643667
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.425-60T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/6 | chr2 | 3643667 |