Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MRGNL others(266): Show |
chr2 | 3590112 | 3649644 |
| a0002 | 0/0 | 271 | 86 | 70 | 7 | 4 | 1 | 4 | 3 | COLEC11_chr2_3590112_3649644 | COLEC11 | MRGNL others(266): Show |
chr2 | 3590112 | 3649644 |
| a0003 | 0/0 | 271 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | MRGNL others(266): Show |
chr2 | 3590112 | 3649644 |
| a0004 | 0/0 | 271 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | MRGNL others(266): Show |
chr2 | 3590112 | 3649644 |
| a0005 | 0/0 | 271 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | MRGNL others(266): Show |
chr2 | 3590112 | 3649644 |
| a0006 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | MRGNL others(266): Show |
chr2 | 3590112 | 3649644 |
| a0007 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | MRGNL others(266): Show |
chr2 | 3590112 | 3649644 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 813 | 280 | 21 | 67 | 144 | 15 | 31 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0001c0007 | 0/0 | 813 | 3 | 1 | 0 | 0 | 0 | 2 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0001c0014 | 0/0 | 813 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0002c0002 | 0/0 | 813 | 50 | 46 | 3 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0002c0003 | 0/0 | 813 | 13 | 2 | 3 | 4 | 1 | 3 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0002c0004 | 0/0 | 813 | 9 | 9 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0002c0005 | 0/0 | 813 | 8 | 8 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0002c0006 | 0/0 | 813 | 6 | 5 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0003c0009 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0003c0010 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0003c0012 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0004c0008 | 0/0 | 813 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0005c0011 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0006c0013 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
chr2 | 3590112 | 3649644 | ||
| a0007c0015 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | ATGAG others(808): Show |
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 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0001c0001t0003 | 0/0 | 1425 | 3 | 0 | 0 | 3 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0001c0001t0004 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0001c0001t0005 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0001c0007t0001 | 0/0 | 1425 | 3 | 1 | 0 | 0 | 0 | 2 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0001c0014t0001 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0002c0002t0001 | 0/0 | 1425 | 50 | 46 | 3 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0002c0003t0001 | 0/0 | 1425 | 13 | 2 | 3 | 4 | 1 | 3 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0002c0004t0001 | 0/0 | 1425 | 9 | 9 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0002c0005t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0002c0005t0002 | 0/0 | 1425 | 7 | 7 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0002c0006t0001 | 0/0 | 1425 | 6 | 5 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0003c0009t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0003c0010t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0003c0012t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0004c0008t0001 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0005c0011t0001 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0006c0013t0001 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| a0007c0015t0001 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | AGTGT others(1420): Show |
chr2 | 3590112 | 3649644 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0040 | 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 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0065 | 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 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0156 | 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 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0194 | 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 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0001t0005g0130 | 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 |
| a0001c0007t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0007t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0001c0014t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0001 | 0/0 | 3 | 3 | 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 |
| a0002c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0019 | 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 |
| a0002c0002t0001g0034 | 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 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0188 | 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 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0204 | 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 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 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 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0306 | 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 |
| a0002c0002t0001g0312 | 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 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0005 | 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 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0003t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0004t0001g0318 | 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 |
| a0002c0005t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0180 | 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 |
| a0002c0005t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0005t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0002c0006t0001g0324 | 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 |
| a0003c0009t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0003c0010t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0003c0012t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0004c0008t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0004c0008t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0005c0011t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0006c0013t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| a0007c0015t0001g0147 | 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 | g0182 | EUR | GBR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | FIN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0349 | EUR | FIN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0157 | 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 | g0172 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0330 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0246 | 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 | g0023 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01099 | hp2 | a0002 | c0006 | t0001 | g0197 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0217 | 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 | g0340 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0109 | 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 | g0006 | EUR | IBS | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01884 | hp1 | a0005 | c0011 | t0001 | g0031 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01884 | hp2 | a0003 | c0010 | t0001 | g0353 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0219 | 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 | g0341 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0221 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02015 | hp2 | a0006 | c0013 | t0001 | g0258 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0052 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02055 | hp1 | a0002 | c0005 | t0002 | g0181 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0206 | 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 | g0271 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0049 | 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 | g0199 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02145 | hp2 | a0002 | c0004 | t0001 | g0285 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02451 | hp1 | a0002 | c0004 | t0001 | g0229 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0304 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02572 | hp2 | a0003 | c0012 | t0001 | g0354 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02622 | hp1 | a0002 | c0005 | t0002 | g0179 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02622 | hp2 | a0002 | c0006 | t0001 | g0329 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0343 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0189 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02647 | hp2 | a0002 | c0004 | t0001 | g0318 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0061 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02683 | hp2 | a0001 | c0007 | t0001 | g0257 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0227 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02717 | hp2 | a0004 | c0008 | t0001 | g0042 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0323 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0215 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0320 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02895 | hp2 | a0002 | c0004 | t0001 | g0244 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02896 | hp1 | a0002 | c0005 | t0002 | g0210 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02897 | hp1 | a0002 | c0005 | t0002 | g0209 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0192 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0306 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0322 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02970 | hp1 | a0002 | c0005 | t0002 | g0344 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02970 | hp2 | a0002 | c0006 | t0001 | g0198 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02976 | hp2 | a0002 | c0005 | t0002 | g0020 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0355 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0130 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | GWD | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03098 | hp2 | a0002 | c0006 | t0001 | g0324 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0298 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03195 | hp1 | a0003 | c0009 | t0001 | g0352 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03195 | hp2 | a0004 | c0008 | t0001 | g0223 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0305 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03209 | hp2 | a0002 | c0004 | t0001 | g0213 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03225 | hp1 | a0002 | c0006 | t0001 | g0311 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0193 | 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 | g0121 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0282 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0274 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0039 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0313 | 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 | g0310 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0184 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0214 | 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 | g0174 | 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 | g0107 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04115 | hp2 | a0001 | c0014 | t0001 | g0150 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0169 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | CHB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0277 | 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 | g0225 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0195 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18977 | hp1 | a0007 | c0015 | t0001 | g0147 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0278 | 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 | g0347 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0176 | 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 | g0050 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0359 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0337 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0076 | 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 | g0248 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0357 | 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 | g0011 | AFR | YRI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ASW | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ASW | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0231 | 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 | g0068 | SAS | GIH | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | CLM | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0312 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02486 | hp2 | a0002 | c0006 | t0001 | g0030 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0261 | AFR | ACB | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0314 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG03471 | hp2 | a0002 | c0005 | t0002 | g0180 | AFR | MSL | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | USA | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0309 | AFR | USA | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | 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 | g0249 | AFR | USA | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA21309 | hp1 | a0002 | c0005 | t0001 | g0358 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| NA21309 | hp2 | a0001 | c0007 | t0001 | g0222 | AFR | LWK | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0272 | REF | REF | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0137 | REF | REF | COLEC11_chr2_3590112_3649644 | COLEC11 | chr2 | 3590112 | 3649644 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:3595166 | 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 | a0003 a0005 |
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 | a0002 a0003 |
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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:3637573 | T | C | 2 | a0001c0007 a0002c0003 |
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 | a0002c0005 a0002c0006 a0003c0009 others(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 | a0002c0006 a0003c0010 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:3595125 | 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:3595303 | A | G | 1 | a0001c0001t0001g0361 | 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 | a0001c0001t0001g0360 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
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 | a0002c0002t0001g0018 | 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 | 15 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): 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 | a0002c0002t0001g0359 | 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 | a0002c0005t0001g0358 | 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 | a0001c0001t0001g0357 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
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 | a0002c0002t0001g0034 a0002c0002t0001g0035 a0002c0002t0001g0036 others(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 | a0001c0001t0001g0356 | 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 | 185 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(182): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): 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 | a0001c0001t0001g0355 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0002c0002t0001g0043 others(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 | a0003c0012t0001g0354 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0199 a0002c0002t0001g0043 a0002c0005t0001g0358 others(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 | a0001c0001t0001g0201 | 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | 11 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(8): 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 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0351 | 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 | 21 | a0001c0001t0001g0012 a0001c0001t0001g0201 a0001c0001t0001g0262 others(18): Show |
22 | HG00738.hp2 HG01099.hp1 HG01192.hp1 others(19): 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 | a0002c0004t0001g0282 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0346 a0001c0001t0001g0347 others(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 | a0002c0002t0001g0064 a0002c0002t0001g0298 a0002c0002t0001g0359 |
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 | 104 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(101): Show |
108 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(105): 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 | a0001c0001t0001g0203 | 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | a0001c0001t0001g0199 a0002c0002t0001g0043 a0002c0006t0001g0198 |
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 | a0001c0001t0001g0182 a0001c0001t0001g0345 |
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 | a0001c0001t0001g0297 | 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0006t0001g0030 others(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 | a0002c0004t0001g0261 | 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 | a0003c0010t0001g0353 | 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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | 105 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(102): Show |
109 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.-27+3387C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3598555 | |||||||
| chr2:3598555 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(23): 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 | a0002c0005t0002g0344 | 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 | 102 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(99): Show |
106 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(103): 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 | a0002c0005t0001g0358 | 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 | a0002c0002t0001g0064 a0002c0002t0001g0298 a0002c0002t0001g0359 |
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 | a0001c0001t0001g0065 | 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 | a0002c0002t0001g0309 a0002c0002t0001g0310 a0002c0002t0001g0312 others(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 | a0002c0002t0001g0309 a0002c0002t0001g0310 a0002c0002t0001g0312 others(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 | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(226): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): 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 | a0002c0002t0001g0189 | 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | a0002c0005t0001g0358 | 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 | 21 | a0001c0001t0001g0012 a0001c0001t0001g0201 a0001c0001t0001g0262 others(18): Show |
22 | HG00738.hp2 HG01099.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-27+4222G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3599390 | |||||||
| chr2:3599527 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(27): 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 | a0001c0001t0001g0342 a0002c0002t0001g0187 a0002c0002t0001g0188 others(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 | a0002c0002t0001g0064 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0176 | 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 | a0002c0002t0001g0204 | 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 | a0002c0006t0001g0197 | 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 | a0001c0001t0001g0067 | 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 | 30 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(27): 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 | a0001c0001t0001g0068 | 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 | 59 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(56): 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 | 26 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(23): 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 | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(226): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): 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 | a0001c0001t0001g0067 | 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 | a0002c0003t0001g0052 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0002c0003t0001g0050 |
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 | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(226): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): 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 | a0001c0001t0001g0248 | 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 | a0002c0004t0001g0313 | 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 | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(177): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0001c0001t0001g0067 a0002c0002t0001g0018 a0002c0002t0001g0177 others(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 | a0001c0001t0001g0315 a0002c0002t0001g0314 |
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 | a0002c0002t0001g0034 | 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 | a0001c0001t0001g0175 | 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 | 92 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0073 others(89): Show |
95 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(92): 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | 14 | a0001c0001t0001g0012 a0001c0001t0001g0268 a0001c0001t0001g0269 others(11): Show |
15 | HG00738.hp2 HG01099.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-26-2664C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 1/6 | chr2 | 3601651 | |||||||
| chr2:3601729 | G | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
97 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(94): 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 | a0001c0001t0001g0174 | 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 | 25 | a0001c0001t0001g0012 a0001c0001t0001g0069 a0001c0001t0001g0075 others(22): Show |
27 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(24): 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 | a0001c0001t0001g0199 a0002c0002t0001g0043 a0002c0006t0001g0198 |
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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0315 | 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 | a0002c0002t0001g0061 | 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 | a0002c0002t0001g0178 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0280 a0001c0001t0004g0172 |
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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0319 others(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 | a0002c0002t0001g0343 a0002c0004t0001g0282 |
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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0315 a0002c0002t0001g0178 a0002c0004t0001g0229 others(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 | a0001c0001t0001g0252 | 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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(148): 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 | a0001c0001t0001g0060 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0253 | 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 | a0002c0005t0001g0358 | 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 | a0002c0006t0001g0197 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | a0002c0002t0001g0043 a0002c0002t0001g0178 a0002c0004t0001g0229 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0107 | 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | 10 | a0001c0001t0001g0060 a0002c0002t0001g0001 a0002c0002t0001g0018 others(7): 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 | a0005c0011t0001g0031 | 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 | a0001c0001t0001g0060 a0002c0003t0001g0169 a0006c0013t0001g0258 |
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 | a0001c0001t0001g0026 a0002c0002t0001g0309 |
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 | a0001c0001t0001g0236 | 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 | a0005c0011t0001g0031 | 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 | 20 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(17): 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 | a0002c0005t0002g0209 a0002c0005t0002g0210 |
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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | a0005c0011t0001g0031 | 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 | 18 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(15): 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | a0001c0001t0001g0171 | 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 a0003c0012t0001g0354 others(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 | a0002c0006t0001g0197 | 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 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0140 | 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 | a0002c0002t0001g0187 | 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 | a0002c0006t0001g0329 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0108 | 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 | 277 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(274): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): 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 | a0001c0001t0001g0076 | 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | 206 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): 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 | a0002c0002t0001g0312 | 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 | 279 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): 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 | a0002c0003t0001g0052 | 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 | a0001c0001t0001g0230 a0001c0001t0001g0315 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0001g0301 a0002c0002t0001g0028 a0002c0002t0001g0029 others(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 | a0002c0003t0001g0169 a0006c0013t0001g0258 |
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 | a0002c0004t0001g0282 | 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 | a0002c0006t0001g0197 a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | a0001c0001t0001g0237 | 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0005c0011t0001g0031 |
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 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0002c0002t0001g0027 others(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 | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): 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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0043 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0002c0002t0001g0027 others(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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 |
221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(218): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): 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 | a0002c0002t0001g0027 a0002c0002t0001g0191 a0002c0002t0001g0298 others(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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0134 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0190 a0001c0001t0001g0325 others(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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0076 a0001c0001t0001g0190 a0001c0001t0001g0325 others(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 | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(218): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): 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 | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.130+937A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605407 | |||||||
| chr2:3605409 | T | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(219): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0289 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0002c0002t0001g0027 others(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 |
223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(220): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): 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 | a0003c0012t0001g0354 | 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0325 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0325 a0001c0001t0001g0342 others(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 | a0001c0001t0001g0076 | 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 | 224 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(221): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): 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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0325 a0001c0001t0001g0342 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(231): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(126): 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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 |
151 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(148): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): 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 | 284 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(281): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.130+1073T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3605543 | |||||||
| chr2:3605543 | T | TGAG | 16 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(13): 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 | a0001c0001t0001g0190 a0001c0001t0001g0342 a0002c0003t0001g0274 others(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 | 320 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(317): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): 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 | a0002c0002t0001g0027 a0002c0002t0001g0191 a0002c0002t0001g0298 others(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 | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(231): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): 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 | a0002c0002t0001g0310 | 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 | a0002c0002t0001g0298 a0002c0002t0001g0359 |
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 | 250 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(247): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): 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 | a0005c0011t0001g0031 | 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0003c0012t0001g0354 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0134 a0001c0001t0001g0193 others(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 | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(278): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0026 a0002c0002t0001g0309 |
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 | a0001c0001t0001g0325 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0160 a0001c0001t0001g0171 others(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 | a0002c0002t0001g0220 | 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 | 239 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(236): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): 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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0319 |
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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | a0003c0012t0001g0354 | 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 | a0002c0005t0002g0344 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0066 a0001c0001t0001g0134 others(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 | a0002c0004t0001g0282 | 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 | a0001c0001t0001g0301 | 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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(84): 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 | a0001c0001t0001g0214 a0001c0001t0001g0236 |
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 | 262 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(259): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0001c0001t0001g0048 a0001c0001t0001g0063 a0001c0001t0001g0113 others(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 | 183 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(180): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): 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 | a0001c0001t0001g0017 a0001c0001t0001g0088 a0001c0001t0001g0106 others(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 | a0001c0001t0001g0060 a0002c0002t0001g0298 a0002c0002t0001g0312 others(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 | a0002c0003t0001g0330 a0005c0011t0001g0031 |
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 | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(29): 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0134 a0001c0001t0001g0182 others(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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | 274 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(271): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): 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 | a0002c0002t0001g0312 | 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 | 274 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(271): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.130+3292T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3607762 | |||||||
| chr2:3607763 | T | A | 274 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(271): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): 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 | a0001c0001t0001g0059 a0001c0001t0001g0134 a0001c0001t0001g0182 others(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 | a0002c0002t0001g0034 a0002c0002t0001g0061 a0002c0006t0001g0311 |
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 | 274 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(271): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): 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 | a0001c0001t0001g0327 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0141 a0001c0001t0001g0262 others(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 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(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 | 225 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(222): Show |
231 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(228): 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 | a0001c0001t0001g0325 | 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 | 285 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(282): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.130+3745C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608215 | |||||||
| chr2:3608232 | G | A | 274 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(271): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.130+3762G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3608232 | |||||||
| chr2:3608265 | T | A | 274 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(271): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): 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 | a0002c0002t0001g0310 | 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0060 a0002c0003t0001g0169 a0002c0003t0001g0221 others(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 | a0001c0001t0001g0251 | 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 | a0001c0001t0001g0347 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0134 a0001c0001t0001g0182 others(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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0323 |
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 | a0001c0001t0001g0190 a0002c0003t0001g0274 a0002c0004t0001g0285 |
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 | a0002c0002t0001g0312 | 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 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(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 | a0002c0002t0001g0191 | 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 | a0003c0012t0001g0354 | 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 | a0001c0001t0001g0009 | 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 | a0002c0002t0001g0034 a0002c0002t0001g0061 a0002c0006t0001g0311 |
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 | a0002c0002t0001g0027 a0002c0002t0001g0034 a0002c0002t0001g0061 others(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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(22): 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 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(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 | 78 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0046 others(75): Show |
80 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(77): 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 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0060 a0002c0002t0001g0298 a0002c0002t0001g0359 others(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 | 6 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0099 others(3): 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 | a0001c0001t0001g0060 a0002c0002t0001g0298 a0002c0002t0001g0359 others(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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(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 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(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 | a0002c0002t0001g0037 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0074 others(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 | 78 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0046 others(75): Show |
80 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(77): 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 | a0002c0003t0001g0330 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0060 a0002c0002t0001g0298 a0002c0002t0001g0359 others(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 | a0001c0001t0001g0060 a0002c0002t0001g0298 a0002c0002t0001g0359 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0134 others(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 | a0002c0002t0001g0312 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0021 a0001c0001t0001g0190 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0074 others(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 | 78 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0046 others(75): Show |
80 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.131-3952T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3609359 | |||||||
| chr2:3609360 | T | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0046 others(75): Show |
80 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(77): 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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0190 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0190 a0001c0001t0001g0211 |
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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0166 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | 209 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(206): Show |
215 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(212): 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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0063 others(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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0240 a0001c0001t0001g0338 |
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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0002c0002t0001g0178 | 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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0003c0009t0001g0352 a0003c0010t0001g0353 |
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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-3277G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610034 | |||||||
| chr2:3610065 | G | C | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-3246G>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610065 | |||||||
| chr2:3610117 | G | A | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-3194G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610117 | |||||||
| chr2:3610139 | T | C | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-3172T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610139 | |||||||
| chr2:3610141 | T | C | 256 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(253): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0201 | 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 | a0002c0006t0001g0197 | 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0002c0002t0001g0312 | 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 | 2 | a0002c0002t0001g0001 a0002c0002t0001g0018 |
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 | 256 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(253): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.131-2996A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610315 | |||||||
| chr2:3610377 | C | T | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-2934C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610377 | |||||||
| chr2:3610404 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0230 a0001c0001t0001g0237 |
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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-2870T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610441 | |||||||
| chr2:3610442 | T | C | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0001c0001t0001g0260 | 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 | 254 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.131-2769A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610542 | |||||||
| chr2:3610577 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(22): 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 | a0001c0001t0001g0325 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0134 a0001c0001t0001g0182 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0044 a0001c0001t0001g0047 |
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 | a0002c0002t0001g0043 | 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 | a0002c0002t0001g0027 a0002c0002t0001g0034 a0002c0002t0001g0061 others(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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-2380C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3610931 | |||||||
| chr2:3610973 | T | C | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 254 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0065 | 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 | a0001c0001t0001g0325 | 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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0084 a0001c0001t0001g0148 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0190 others(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 | 254 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | 19 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(16): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0060 | 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 | a0005c0011t0001g0031 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0002c0003t0001g0184 |
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 | 255 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(252): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): 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 | a0001c0001t0005g0130 | 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 | a0002c0004t0001g0244 | 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 | a0001c0001t0001g0246 | 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 | 251 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): 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 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0054 | 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 | a0002c0002t0001g0310 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0067 a0002c0002t0001g0019 a0002c0002t0001g0028 others(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 | a0001c0001t0001g0240 a0001c0001t0001g0338 |
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 | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(21): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0034 a0002c0002t0001g0061 a0002c0006t0001g0311 |
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 | 252 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(249): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0002c0002t0001g0034 a0002c0002t0001g0061 a0002c0006t0001g0311 |
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 | 247 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(244): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.131-1075C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 2/6 | chr2 | 3612236 | |||||||
| chr2:3612248 | G | C | 222 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(219): Show |
228 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(225): 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 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0295 | 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 | a0002c0005t0002g0181 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0095 | 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 | 18 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(15): 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 | 258 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(255): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0174 others(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 | 255 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(252): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): 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 | a0005c0011t0001g0031 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0100 a0001c0001t0001g0253 |
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 | a0001c0001t0001g0077 a0001c0001t0001g0286 |
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 | 261 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 211 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(208): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): 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 | a0001c0001t0001g0321 a0002c0002t0001g0011 a0002c0002t0001g0013 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0060 others(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 | 24 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0193 others(21): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 24 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0193 others(21): 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 | a0001c0001t0001g0190 a0002c0003t0001g0274 a0002c0004t0001g0285 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 2 | a0002c0002t0001g0001 a0002c0002t0001g0018 |
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 | 263 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0001c0001t0001g0173 a0001c0001t0004g0172 |
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 | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(21): 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 | a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 251 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(248): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 260 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(257): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0027 a0002c0002t0001g0034 a0002c0002t0001g0061 others(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 | a0001c0001t0001g0203 a0002c0002t0001g0027 a0002c0002t0001g0034 others(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 | 252 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(249): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0006c0013t0001g0258 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0078 | 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 | 261 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(258): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 211 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(208): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): 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 | a0001c0001t0001g0054 a0001c0001t0001g0062 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0269 a0001c0001t0001g0275 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0264 a0002c0002t0001g0298 a0002c0002t0001g0359 others(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 | a0002c0002t0001g0298 a0002c0002t0001g0359 a0005c0011t0001g0031 |
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 | a0001c0001t0001g0207 | 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0003c0012t0001g0354 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 207 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(204): Show |
213 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(210): 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | 43 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0190 others(40): 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 | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(212): Show |
221 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(218): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0005c0011t0001g0031 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0204 a0002c0002t0001g0219 a0002c0002t0001g0314 |
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 | a0002c0002t0001g0204 | 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 | 256 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(253): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0072 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0361 |
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 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0292 |
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 | a0001c0001t0001g0217 | 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 | a0002c0003t0001g0169 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0204 a0002c0002t0001g0219 a0002c0002t0001g0314 |
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 | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.202+2402T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615784 | |||||||
| chr2:3615790 | G | A | 26 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0193 others(23): 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 | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): 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 | a0001c0001t0001g0076 | 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 | a0001c0001t0001g0336 | 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 | a0001c0001t0001g0239 a0001c0001t0001g0315 a0001c0001t0001g0319 others(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 |
G | 1 | a0001c0001t0001g0336 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.202+2466_202+2511d others(48): Show |
COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3615848 | |||||||
| chr2:3615850 | G | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 24 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(21): 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 | a0001c0001t0001g0239 | 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 | 24 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0193 others(21): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0204 a0002c0002t0001g0219 a0002c0002t0001g0314 |
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 | a0002c0006t0001g0197 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 32 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0190 others(29): 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 | 215 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(212): Show |
221 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(218): 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 | a0002c0004t0001g0282 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0003c0009t0001g0352 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0114 a0001c0001t0001g0118 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0360 | 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 | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.202+2731A>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3616113 | |||||||
| chr2:3616117 | C | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0259 | 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 | a0005c0011t0001g0031 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0312 | 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 | 2 | a0002c0002t0001g0001 a0002c0002t0001g0018 |
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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 256 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(253): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0101 a0001c0001t0001g0138 others(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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0005t0002g0181 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0062 a0001c0001t0001g0101 a0001c0001t0001g0138 others(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 | a0002c0006t0001g0030 | 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 | a0001c0001t0001g0332 | 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0003g0117 | 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 | a0001c0001t0003g0117 | 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 | a0001c0001t0001g0190 a0002c0003t0001g0274 a0002c0004t0001g0285 others(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 | a0002c0002t0001g0323 | 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 | a0001c0001t0001g0146 | 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 | a0002c0006t0001g0198 a0003c0010t0001g0353 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0003t0001g0221 | 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 | a0002c0004t0001g0244 | 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 | 32 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0190 others(29): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 others(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 | a0001c0001t0001g0327 a0001c0001t0001g0355 |
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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0001c0001t0001g0321 a0002c0002t0001g0011 a0002c0002t0001g0013 others(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 | a0002c0004t0001g0313 | 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 | 264 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(261): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0237 a0002c0002t0001g0323 |
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 | a0002c0002t0001g0204 a0002c0002t0001g0219 a0002c0002t0001g0314 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0175 | 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 | 211 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(208): Show |
217 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(214): 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 | a0001c0001t0001g0142 | 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0026 others(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 | a0002c0002t0001g0304 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0004t0001g0282 | 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 | a0001c0001t0001g0334 | 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 | a0002c0002t0001g0312 | 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0001c0001t0001g0289 | 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 | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.202+4166C>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3617548 | |||||||
| chr2:3617556 | T | C | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | a0004c0008t0001g0223 | 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 | 271 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(268): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): 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 | a0002c0002t0001g0298 a0002c0002t0001g0359 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0142 others(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 | 255 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(252): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0003c0012t0001g0354 | 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | a0002c0004t0001g0282 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 212 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(209): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0067 a0002c0002t0001g0019 a0002c0002t0001g0028 others(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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | 62 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0033 others(59): Show |
65 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(62): 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 40 | a0001c0001t0001g0134 a0001c0001t0001g0182 a0001c0001t0001g0190 others(37): 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 | a0002c0002t0001g0061 | 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 | a0001c0001t0001g0140 a0001c0001t0001g0265 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0325 | 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 | a0002c0004t0001g0282 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0079 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0317 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0001c0001t0001g0067 a0002c0002t0001g0019 a0002c0002t0001g0028 others(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 | a0001c0001t0003g0081 | 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 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(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 | 259 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(256): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.202+6899T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3620281 | |||||||
| chr2:3620406 | A | G | 257 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(254): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): 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 | a0002c0002t0001g0027 a0002c0002t0001g0034 a0002c0002t0001g0061 others(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 | 256 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(253): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0201 | 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 | a0002c0002t0001g0178 | 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 | a0001c0001t0001g0321 a0002c0002t0001g0011 a0002c0002t0001g0013 others(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 | a0002c0002t0001g0310 | 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 | a0002c0002t0001g0298 a0002c0002t0001g0359 a0005c0011t0001g0031 |
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 | 193 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(190): Show |
199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): 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 | a0001c0001t0003g0159 | 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 | a0003c0012t0001g0354 | 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 | a0001c0001t0001g0067 a0002c0002t0001g0019 a0002c0002t0001g0028 others(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 | 212 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(209): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): 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 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
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 | a0006c0013t0001g0258 | 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0002c0004t0001g0282 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0216 | 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 | a0002c0002t0001g0027 a0002c0002t0001g0034 a0002c0002t0001g0061 others(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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | 263 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(260): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0001g0055 a0001c0001t0001g0097 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0107 | 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 | a0002c0002t0001g0298 a0002c0002t0001g0359 |
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 | a0002c0006t0001g0198 a0003c0010t0001g0353 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0129 a0001c0001t0001g0289 |
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 | a0001c0001t0001g0292 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0166 a0001c0001t0001g0230 others(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 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0071 | 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 | a0002c0005t0002g0181 | 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 | a0002c0002t0001g0191 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0001c0001t0001g0093 | 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 | a0002c0002t0001g0204 a0002c0002t0001g0219 a0002c0002t0001g0314 |
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 | a0001c0001t0001g0361 | 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0001c0001t0001g0033 | 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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0323 |
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 | 133 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(130): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.202+10276A>T | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3623658 | |||||||
| chr2:3623659 | A | T | 11 | a0001c0001t0001g0058 a0001c0001t0001g0094 a0001c0001t0001g0109 others(8): Show |
11 | HG00280.hp1 HG00735.hp2 HG01074.hp2 others(8): 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 | a0001c0001t0001g0190 a0002c0003t0001g0274 a0002c0004t0001g0285 |
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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | 4 | a0001c0001t0001g0094 a0001c0001t0001g0109 a0001c0001t0001g0112 others(1): Show |
4 | HG00735.hp2 HG01516.hp2 HG01517.hp1 others(1): 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0315 a0001c0001t0001g0319 a0002c0002t0001g0189 |
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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0001c0001t0001g0292 | 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 | 17 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0134 others(14): 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 | 17 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0134 others(14): 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 | a0007c0015t0001g0147 | 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 | a0001c0001t0001g0082 a0001c0001t0001g0269 a0001c0001t0001g0275 |
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 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0002c0002t0001g0312 | 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 | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(89): 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 | 22 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(19): 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 | a0001c0001t0001g0067 a0002c0002t0001g0312 a0002c0006t0001g0198 others(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 | a0002c0002t0001g0027 a0002c0002t0001g0038 a0002c0006t0001g0198 |
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 | a0001c0001t0001g0067 a0001c0001t0001g0193 a0001c0001t0001g0196 others(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 | a0002c0002t0001g0019 a0002c0002t0001g0027 |
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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0016 others(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 | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(46): 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 | a0001c0001t0001g0333 | 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 | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0002c0004t0001g0213 others(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 | a0001c0001t0001g0190 | 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 | a0002c0002t0001g0305 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0325 | 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 | a0001c0001t0001g0083 a0001c0001t0001g0252 |
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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0002c0002t0001g0309 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0090 a0002c0002t0001g0019 others(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 | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(42): 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 | a0001c0001t0001g0032 a0001c0001t0001g0101 a0001c0001t0001g0146 others(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 | 139 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(136): Show |
144 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(141): 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 |
53 | a0001c0001t0001g0026 a0001c0001t0001g0078 a0001c0001t0001g0107 others(50): 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 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0134 others(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 | a0002c0003t0001g0052 a0002c0005t0002g0181 |
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 | a0002c0006t0001g0311 | 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 | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): 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 | a0002c0005t0001g0358 | 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 | a0002c0002t0001g0177 a0002c0002t0001g0178 a0002c0002t0001g0304 others(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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0177 others(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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0242 | 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 | a0002c0006t0001g0324 a0002c0006t0001g0329 |
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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(52): 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 | a0001c0001t0001g0190 a0002c0002t0001g0312 a0002c0006t0001g0030 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0120 a0001c0001t0001g0149 others(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 | 40 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(37): 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 | a0001c0001t0001g0287 | 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 | a0002c0003t0001g0330 | 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 | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(58): 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 | a0002c0006t0001g0198 a0003c0010t0001g0353 |
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 | a0001c0001t0001g0308 | 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 | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.203-10662G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3626871 | |||||||
| chr2:3626899 | G | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): 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 | a0001c0001t0001g0355 | 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 | a0001c0001t0001g0066 | 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 | 305 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): 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 | a0001c0001t0001g0331 | 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 | 171 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(168): Show |
177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): 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 | 60 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0134 others(57): 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 | a0002c0002t0001g0019 a0002c0002t0001g0043 a0002c0002t0001g0192 |
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 | 304 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(301): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0001c0001t0001g0295 | 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 | 166 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(163): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): 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 | a0002c0002t0001g0029 | 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 | a0002c0003t0001g0274 | 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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0317 |
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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0317 |
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 | a0002c0002t0001g0312 a0002c0006t0001g0030 a0002c0006t0001g0197 others(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 | a0001c0001t0001g0303 a0002c0003t0001g0169 a0002c0003t0001g0221 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0317 |
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 | 165 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(162): Show |
171 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(168): 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 | 41 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(38): 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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0189 others(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 | a0001c0001t0001g0316 | 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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): 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 | a0002c0002t0001g0035 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | a0001c0001t0001g0303 | 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 | 100 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0014 others(97): Show |
103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.203-8905C>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3628628 | |||||||
| chr2:3628682 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(115): 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 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0134 others(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 | a0002c0005t0001g0358 | 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 | a0001c0001t0001g0190 | 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 | a0002c0002t0001g0043 a0002c0002t0001g0192 |
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 | a0002c0003t0001g0039 | 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 | a0002c0002t0001g0343 | 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 | a0001c0001t0001g0067 | 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 | a0002c0002t0001g0027 a0002c0002t0001g0036 a0002c0006t0001g0311 |
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 | a0002c0004t0001g0244 | 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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): 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 | a0001c0001t0001g0316 | 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 | 39 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(36): 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 | 39 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(36): 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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | a0001c0001t0001g0350 | 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 | a0002c0006t0001g0197 a0002c0006t0001g0324 a0002c0006t0001g0329 |
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 | a0002c0002t0001g0177 a0002c0002t0001g0178 a0002c0002t0001g0304 others(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 | a0001c0001t0001g0051 | 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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): 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 | 41 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(38): 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 | a0001c0001t0001g0339 | 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 | a0002c0002t0001g0178 | 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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | 3 | a0001c0001t0001g0003 a0001c0001t0001g0230 a0001c0001t0001g0237 |
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 | 3 | a0001c0001t0001g0003 a0001c0001t0001g0230 a0001c0001t0001g0237 |
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 | 234 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(231): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): 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 | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): 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 | 35 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(32): 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 | a0001c0001t0001g0333 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.203-7269T>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3630264 | |||||||
| chr2:3630361 | A | G | 4 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0002c0002t0001g0036 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0317 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0317 |
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 | a0003c0010t0001g0353 | 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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0236 | 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 | a0002c0002t0001g0036 | 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0001c0001t0001g0334 | 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 | a0001c0001t0001g0321 a0002c0002t0001g0215 a0002c0002t0001g0228 others(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 | a0002c0002t0001g0027 a0002c0002t0001g0036 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0297 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0233 | 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 | a0002c0002t0001g0035 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | 59 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0134 others(56): 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 | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.203-6155G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631378 | |||||||
| chr2:3631491 | T | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.203-6042T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3631491 | |||||||
| chr2:3631533 | C | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0002c0002t0001g0027 a0002c0002t0001g0036 |
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 | 21 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(18): 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 | a0001c0001t0001g0346 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0190 a0002c0005t0001g0358 |
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 | a0002c0002t0001g0035 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | a0002c0006t0001g0324 | 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 | a0002c0002t0001g0036 | 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 | a0002c0002t0001g0206 | 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 | a0002c0002t0001g0027 a0002c0002t0001g0035 a0002c0002t0001g0036 others(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 | 45 | a0001c0001t0001g0190 a0001c0001t0001g0316 a0002c0002t0001g0001 others(42): 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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | 187 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(184): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): 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 | a0001c0001t0001g0098 | 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): 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 | a0001c0001t0001g0199 | 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): 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 | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): 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 | a0001c0001t0001g0058 | 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 | a0002c0006t0001g0198 a0003c0010t0001g0353 |
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 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0002c0002t0001g0191 others(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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(59): 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): 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 | a0002c0003t0001g0184 | 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 | a0001c0001t0003g0117 a0001c0001t0003g0159 |
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 | a0001c0001t0001g0077 | 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 | a0002c0005t0001g0358 | 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 | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): 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 | 39 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(36): 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0196 others(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 | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0002c0002t0001g0177 a0002c0002t0001g0178 a0002c0002t0001g0304 others(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 | a0002c0005t0001g0358 | 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 | 34 | a0001c0001t0001g0321 a0002c0002t0001g0001 a0002c0002t0001g0011 others(31): 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 | a0002c0002t0001g0177 a0002c0002t0001g0178 a0002c0002t0001g0304 others(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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0190 | 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 | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0073 a0001c0001t0001g0141 a0001c0001t0001g0262 others(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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0040 | 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 | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0190 a0002c0002t0001g0191 a0002c0002t0001g0312 others(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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0067 a0002c0002t0001g0191 a0002c0006t0001g0197 others(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 | a0001c0001t0001g0155 | 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 | 173 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(170): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.203-2652C>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3634881 | |||||||
| chr2:3634914 | G | GC | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(110): 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 | a0002c0002t0001g0343 | 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 | a0001c0001t0001g0224 | 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0001c0001t0001g0233 | 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 |
65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(62): 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 | a0001c0001t0001g0245 | 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 | 181 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(178): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): 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 | a0001c0001t0001g0088 | 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 | 63 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(60): 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0263 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0083 | 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 | a0002c0003t0001g0005 a0002c0003t0001g0050 |
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 | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(103): 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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0357 |
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 | a0001c0001t0001g0146 | 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 | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(68): 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0002c0003t0001g0231 | 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 | a0002c0002t0001g0343 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.203-1675G>A | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635858 | |||||||
| chr2:3635967 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.203-1566A>G | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3635967 | |||||||
| chr2:3636025 | G | A | 306 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | 67 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): 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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | 304 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(301): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0002c0006t0001g0198 a0003c0010t0001g0353 |
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 | a0002c0003t0001g0169 | 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 | a0001c0001t0001g0128 | 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 | a0002c0002t0001g0019 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0168 | 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 | 303 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0001g0060 | 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 | 304 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(301): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0002c0002t0001g0011 a0002c0002t0001g0206 a0002c0002t0001g0220 others(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 | a0001c0001t0001g0347 | 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 | a0001c0001t0001g0190 a0002c0003t0001g0169 a0002c0003t0001g0221 others(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 | a0002c0006t0001g0311 | 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 | a0001c0001t0001g0190 a0002c0002t0001g0191 a0002c0006t0001g0197 others(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 | a0002c0005t0001g0358 | 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 | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): 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 | a0002c0003t0001g0274 | 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 | a0002c0002t0001g0019 a0002c0002t0001g0043 a0002c0002t0001g0192 |
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 | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): 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 | a0002c0005t0002g0179 a0002c0005t0002g0180 |
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 | 303 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.203-77T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 3/6 | chr2 | 3637456 | |||||||
| chr2:3637459 | G | T | 38 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(35): 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 | 38 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(35): 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 | a0002c0002t0001g0215 | 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 | a0002c0006t0001g0198 a0003c0010t0001g0353 |
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 | 303 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): 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 | a0001c0001t0001g0014 a0001c0001t0001g0114 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0079 a0001c0001t0001g0087 others(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 | a0002c0005t0001g0358 | 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 | a0001c0001t0001g0190 a0002c0003t0001g0169 a0002c0003t0001g0221 others(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 | a0002c0006t0001g0198 a0003c0010t0001g0353 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0317 |
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 | a0002c0003t0001g0169 | 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 | a0002c0002t0001g0013 a0002c0002t0001g0177 a0002c0002t0001g0304 others(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 | a0005c0011t0001g0031 | 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 | 27 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(24): 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0002c0002t0001g0343 others(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 | a0001c0001t0001g0190 a0002c0006t0001g0030 a0002c0006t0001g0197 others(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 | a0001c0001t0001g0076 | 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 | a0002c0003t0001g0005 a0002c0003t0001g0024 a0002c0003t0001g0039 others(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 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0002c0002t0001g0343 others(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 | a0002c0005t0001g0358 | 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 | a0001c0001t0001g0190 a0002c0006t0001g0030 a0002c0006t0001g0197 others(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 | a0002c0002t0001g0187 a0002c0002t0001g0188 a0002c0002t0001g0343 others(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 | a0002c0002t0001g0013 a0002c0002t0001g0027 a0002c0002t0001g0036 others(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 | a0002c0002t0001g0178 | 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 | 69 | a0001c0001t0001g0190 a0002c0002t0001g0001 a0002c0002t0001g0011 others(66): 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 | a0002c0002t0001g0013 a0002c0002t0001g0177 a0002c0002t0001g0178 others(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 | a0002c0004t0001g0213 a0002c0004t0001g0229 a0002c0004t0001g0244 others(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 | a0002c0006t0001g0311 | 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 | 29 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(26): 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 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0182 |
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 | a0001c0001t0001g0162 | 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 | 69 | a0001c0001t0001g0190 a0002c0002t0001g0001 a0002c0002t0001g0011 others(66): 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 | a0001c0001t0001g0286 | 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 | a0006c0013t0001g0258 | 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 | a0002c0002t0001g0013 a0002c0002t0001g0027 a0002c0002t0001g0036 others(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 | 76 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0013 others(73): 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 | 76 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0013 others(73): 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 | a0001c0001t0001g0055 a0001c0001t0001g0273 a0002c0002t0001g0312 others(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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0001c0001t0001g0108 | 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 | a0002c0002t0001g0312 a0003c0012t0001g0354 |
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 | a0001c0001t0001g0319 | 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 | a0002c0006t0001g0030 a0002c0006t0001g0197 a0002c0006t0001g0198 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0182 |
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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | a0002c0002t0001g0061 | 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 | a0002c0002t0001g0187 a0002c0002t0001g0188 |
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 | a0002c0005t0002g0180 | 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0002c0003t0001g0169 | 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 | a0002c0002t0001g0013 a0002c0002t0001g0027 a0002c0002t0001g0036 others(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 | 83 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0013 others(80): 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 | a0002c0006t0001g0197 a0002c0006t0001g0324 a0002c0006t0001g0329 |
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 | 72 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0013 others(69): 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 | a0002c0003t0001g0169 | 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 | a0002c0002t0001g0013 a0002c0002t0001g0177 a0002c0002t0001g0178 others(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 | a0002c0003t0001g0169 | 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 | a0002c0003t0001g0221 a0002c0003t0001g0231 a0002c0003t0001g0330 others(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 | a0001c0001t0001g0340 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0001c0001t0001g0317 | 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 | a0002c0002t0001g0312 a0003c0012t0001g0354 |
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 | a0002c0002t0001g0029 | 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 | a0002c0005t0001g0358 | 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 | a0002c0002t0001g0028 a0002c0002t0001g0035 a0002c0002t0001g0037 others(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 | a0001c0001t0001g0125 a0002c0003t0001g0024 |
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 | a0001c0001t0001g0094 a0001c0001t0001g0108 a0001c0001t0001g0170 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(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 | a0001c0001t0001g0186 | 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 |
4 | a0001c0001t0001g0046 a0001c0001t0001g0109 a0001c0001t0001g0112 others(1): Show |
4 | HG00735.hp2 HG01346.hp1 HG01516.hp2 others(1): 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 | a0001c0001t0001g0012 a0001c0001t0001g0083 a0001c0001t0001g0252 others(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 | a0002c0003t0001g0169 | 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 | a0002c0003t0001g0169 | 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 | a0002c0003t0001g0169 | 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 | a0002c0003t0001g0221 a0002c0003t0001g0231 a0002c0003t0001g0330 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0216 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0233 |
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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | a0001c0001t0001g0119 | 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 | a0002c0002t0001g0036 | 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 | a0002c0002t0001g0206 a0002c0003t0001g0169 |
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 | a0002c0002t0001g0019 a0002c0002t0001g0043 a0002c0002t0001g0187 others(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 | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0193 a0001c0001t0001g0207 others(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 |
204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): 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 | a0001c0001t0001g0026 a0001c0001t0001g0317 a0001c0001t0001g0348 |
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 | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): 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 | 28 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(25): 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 | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): 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 | a0001c0001t0001g0125 a0002c0006t0001g0197 |
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 | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): 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 | a0001c0001t0001g0125 a0002c0006t0001g0197 |
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 | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): 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 | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): 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 | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): 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 | a0001c0001t0001g0340 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0101 others(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 | a0002c0003t0001g0005 a0002c0003t0001g0024 a0002c0003t0001g0039 others(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 | a0001c0001t0001g0207 a0002c0006t0001g0197 |
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 | a0001c0001t0001g0207 a0002c0006t0001g0197 |
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 | 28 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(25): 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 | 30 | a0001c0001t0001g0207 a0002c0002t0001g0001 a0002c0002t0001g0011 others(27): 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 | 30 | a0001c0001t0001g0207 a0002c0002t0001g0001 a0002c0002t0001g0011 others(27): 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 | a0001c0001t0001g0207 a0002c0005t0002g0020 a0002c0005t0002g0179 others(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 | a0002c0002t0001g0204 | 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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0035 others(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 | 35 | a0001c0001t0001g0023 a0001c0001t0001g0216 a0002c0002t0001g0001 others(32): 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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0035 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0288 |
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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | a0001c0001t0001g0232 a0001c0001t0001g0328 a0002c0002t0001g0019 others(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 | a0002c0002t0001g0036 | 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 | a0002c0006t0001g0030 a0002c0006t0001g0197 a0002c0006t0001g0198 others(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 | a0001c0007t0001g0135 a0001c0007t0001g0222 a0001c0007t0001g0257 |
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 | a0001c0001t0001g0041 | 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 | a0002c0002t0001g0013 a0002c0002t0001g0027 a0002c0002t0001g0036 others(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 | a0001c0001t0001g0082 | 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 | a0002c0005t0001g0358 | 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 | 66 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(63): 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 | a0001c0001t0001g0207 | 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 | a0002c0005t0002g0179 a0002c0005t0002g0180 |
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 | a0002c0002t0001g0013 a0002c0002t0001g0027 a0002c0002t0001g0036 others(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 | a0002c0006t0001g0030 a0002c0006t0001g0197 a0002c0006t0001g0198 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0268 |
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 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0035 others(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 | 343 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(340): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): 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 | a0002c0002t0001g0035 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | a0002c0002t0001g0027 a0002c0002t0001g0036 |
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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0338 |
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 | 76 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0013 others(73): 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 | a0001c0001t0001g0057 | 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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0132 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0128 | 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 | a0002c0003t0001g0330 | 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 | 22 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(19): 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0056 |
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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0125 | 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 | 76 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0013 others(73): 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 | a0001c0001t0001g0250 | 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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | a0002c0005t0002g0020 a0002c0005t0002g0179 a0002c0005t0002g0180 others(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 | 84 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0013 others(81): 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 | a0002c0005t0001g0358 | 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 | a0002c0002t0001g0227 | 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 | a0002c0005t0001g0358 | 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 | a0002c0003t0001g0169 a0002c0003t0001g0221 a0002c0003t0001g0231 others(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 | 29 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(26): 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 | a0002c0002t0001g0035 a0002c0002t0001g0037 a0002c0002t0001g0038 others(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 | 29 | a0002c0002t0001g0001 a0002c0002t0001g0011 a0002c0002t0001g0018 others(26): 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 | a0002c0006t0001g0030 a0002c0006t0001g0197 a0002c0006t0001g0198 others(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 | a0002c0005t0001g0358 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0296 | 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 | a0002c0006t0001g0197 | 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 | a0001c0001t0001g0361 | 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 | a0001c0001t0001g0239 | 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 | a0002c0002t0001g0036 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0108 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.425-60T>C | COLEC11 | ENSG00000118004.18 | transcript | ENST00000349077.9 | protein_coding | 6/6 | chr2 | 3643667 |