Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 147495 |
| ensemblid | ENSG00000154856.13 |
| hgncid | 15718 |
| symbol | APCDD1 |
| name | APC down-regulated 1 |
| refseq_nuc | NM_153000.5 |
| refseq_prot | NP_694545.1 |
| ensembl_nuc | ENST00000355285.10 |
| ensembl_prot | ENSP00000347433.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 10454635 |
| end | 10489949 |
| strand | + |
| ver | v1.2 |
| region | chr18:10454635-10489949 |
| region5000 | chr18:10449635-10494949 |
| regionname0 | APCDD1_chr18_10454635_10489949 |
| regionname5000 | APCDD1_chr18_10449635_10494949 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 514 | 365 | 94 | 61 | 161 | 16 | 31 | 125 | APCDD1_chr18_10449635_10494949 | APCDD1 | MSWPR others(509): Show |
chr18 | 10449635 | 10494949 |
| a0002 | 0/0 | 514 | 50 | 0 | 9 | 26 | 2 | 13 | 20 | APCDD1_chr18_10449635_10494949 | APCDD1 | MSWPR others(509): Show |
chr18 | 10449635 | 10494949 |
| a0003 | 0/0 | 514 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | MSWPR others(509): Show |
chr18 | 10449635 | 10494949 |
| a0004 | 0/0 | 514 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | MSWPR others(509): Show |
chr18 | 10449635 | 10494949 |
| a0005 | 0/0 | 514 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | MSWPR others(509): Show |
chr18 | 10449635 | 10494949 |
| a0006 | 0/0 | 514 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | MSWPR others(509): Show |
chr18 | 10449635 | 10494949 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1542 | 171 | 46 | 25 | 70 | 11 | 17 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0002 | 0/0 | 1542 | 159 | 18 | 33 | 90 | 5 | 13 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0004 | 0/0 | 1542 | 24 | 23 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0007 | 0/0 | 1542 | 3 | 0 | 2 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0008 | 0/0 | 1542 | 2 | 2 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0011 | 0/0 | 1542 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0012 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0013 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0014 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0015 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0001c0016 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0002c0003 | 0/0 | 1542 | 43 | 0 | 7 | 25 | 2 | 9 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0002c0005 | 0/0 | 1542 | 7 | 0 | 2 | 1 | 0 | 4 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0003c0006 | 0/0 | 1542 | 4 | 3 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0004c0010 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0005c0017 | 0/0 | 1542 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 | ||
| a0006c0009 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | ATGTC others(1537): Show |
chr18 | 10449635 | 10494949 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 3803 | 67 | 9 | 13 | 32 | 6 | 7 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0004 | 1/0 | 3803 | 48 | 1 | 6 | 28 | 3 | 9 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0007 | 0/0 | 3804 | 12 | 11 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3799): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0008 | 0/0 | 3805 | 8 | 6 | 2 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0009 | 0/0 | 3803 | 5 | 5 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0010 | 0/0 | 3802 | 6 | 1 | 0 | 5 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3797): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0012 | 0/0 | 3806 | 2 | 1 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3801): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0013 | 0/0 | 3806 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3801): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0016 | 0/0 | 3803 | 3 | 0 | 1 | 0 | 2 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0018 | 0/0 | 3805 | 2 | 2 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0019 | 0/0 | 3802 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3797): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0020 | 0/0 | 3803 | 2 | 2 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0021 | 0/0 | 3805 | 2 | 2 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0023 | 0/0 | 3806 | 2 | 1 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3801): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0025 | 0/0 | 3803 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0026 | 0/0 | 3803 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0027 | 0/0 | 3803 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0028 | 0/0 | 3803 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0029 | 0/0 | 3806 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3801): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0031 | 0/0 | 3805 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0035 | 0/0 | 3806 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3801): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0037 | 0/1 | 3803 | 1 | 0 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0001t0038 | 0/0 | 3803 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0001 | 0/0 | 3803 | 89 | 7 | 19 | 52 | 4 | 7 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0003 | 0/0 | 3805 | 18 | 1 | 2 | 13 | 0 | 2 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0005 | 0/0 | 3803 | 29 | 5 | 4 | 16 | 0 | 4 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0011 | 0/0 | 3803 | 6 | 1 | 4 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0013 | 0/0 | 3806 | 3 | 3 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3801): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0014 | 0/0 | 3803 | 4 | 0 | 0 | 4 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0015 | 0/0 | 3803 | 4 | 0 | 4 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0022 | 0/0 | 3803 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0033 | 0/0 | 3803 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0034 | 0/0 | 3803 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0036 | 0/0 | 3806 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3801): Show |
chr18 | 10449635 | 10494949 |
| a0001c0002t0041 | 0/0 | 3805 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0001c0004t0006 | 0/0 | 3800 | 17 | 17 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3795): Show |
chr18 | 10449635 | 10494949 |
| a0001c0004t0017 | 0/0 | 3805 | 3 | 3 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0001c0004t0024 | 0/0 | 3800 | 2 | 1 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3795): Show |
chr18 | 10449635 | 10494949 |
| a0001c0004t0030 | 0/0 | 3800 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3795): Show |
chr18 | 10449635 | 10494949 |
| a0001c0004t0040 | 0/0 | 3800 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3795): Show |
chr18 | 10449635 | 10494949 |
| a0001c0007t0002 | 0/0 | 3803 | 2 | 0 | 2 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0007t0042 | 0/0 | 3803 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0008t0009 | 0/0 | 3803 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0008t0039 | 0/0 | 3803 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0011t0002 | 0/0 | 3803 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0012t0007 | 0/0 | 3804 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3799): Show |
chr18 | 10449635 | 10494949 |
| a0001c0013t0006 | 0/0 | 3800 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3795): Show |
chr18 | 10449635 | 10494949 |
| a0001c0014t0009 | 0/0 | 3803 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0015t0001 | 0/0 | 3803 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0001c0016t0032 | 0/0 | 3802 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3797): Show |
chr18 | 10449635 | 10494949 |
| a0002c0003t0001 | 0/0 | 3803 | 6 | 0 | 1 | 2 | 0 | 3 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0002c0003t0003 | 0/0 | 3805 | 36 | 0 | 6 | 23 | 2 | 5 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0002c0003t0005 | 0/0 | 3803 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0002c0005t0002 | 0/0 | 3803 | 3 | 0 | 1 | 1 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0002c0005t0004 | 0/0 | 3803 | 4 | 0 | 1 | 0 | 0 | 3 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0003c0006t0012 | 0/0 | 3806 | 4 | 3 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3801): Show |
chr18 | 10449635 | 10494949 |
| a0004c0010t0004 | 0/0 | 3803 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3798): Show |
chr18 | 10449635 | 10494949 |
| a0005c0017t0003 | 0/0 | 3805 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3800): Show |
chr18 | 10449635 | 10494949 |
| a0006c0009t0006 | 0/0 | 3800 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | GAAGA others(3795): Show |
chr18 | 10449635 | 10494949 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0001 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0004 | 1/0 | 6 | 1 | 2 | 0 | 1 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0007g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0008g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0008g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0010g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0012g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0012g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0013g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0016g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0018g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0018g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0019g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0019g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0020g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0020g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0021g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0021g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0023g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0023g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0025g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0026g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0027g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0028g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0029g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0031g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0035g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0037g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0001t0038g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0011g0010 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0011g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0011g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0013g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0014g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0014g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0015g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0015g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0015g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0022g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0022g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0033g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0034g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0036g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0002t0041g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0006g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0017g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0017g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0017g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0024g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0024g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0030g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0004t0040g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0007t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0007t0042g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0008t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0008t0039g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0011t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0012t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0013t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0014t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0015t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0001c0016t0032g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0003t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0005t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0005t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0005t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0005t0004g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0002c0005t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0003c0006t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0003c0006t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0003c0006t0012g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0003c0006t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0004c0010t0004g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0005c0017t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| a0006c0009t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0003 | g0224 | EUR | GBR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0033 | EUR | GBR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0323 | EUR | GBR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00140 | hp2 | a0002 | c0003 | t0003 | g0278 | EUR | GBR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0170 | EUR | FIN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | FIN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0072 | EUR | FIN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00323 | hp2 | a0001 | c0002 | t0011 | g0010 | EUR | FIN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00408 | hp1 | a0001 | c0001 | t0010 | g0255 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00544 | hp1 | a0001 | c0002 | t0005 | g0289 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00558 | hp2 | a0001 | c0002 | t0005 | g0100 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00621 | hp1 | a0002 | c0003 | t0003 | g0062 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00621 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00639 | hp1 | a0001 | c0001 | t0023 | g0198 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00673 | hp1 | a0002 | c0003 | t0003 | g0312 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00673 | hp2 | a0001 | c0002 | t0003 | g0144 | EAS | CHS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0324 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0013 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00735 | hp2 | a0001 | c0007 | t0002 | g0035 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00741 | hp1 | a0002 | c0005 | t0002 | g0275 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG00741 | hp2 | a0002 | c0003 | t0003 | g0158 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01070 | hp1 | a0001 | c0002 | t0011 | g0010 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01071 | hp2 | a0001 | c0002 | t0011 | g0010 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0090 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01081 | hp2 | a0001 | c0002 | t0011 | g0337 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0203 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0159 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01106 | hp1 | a0001 | c0002 | t0011 | g0010 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01106 | hp2 | a0001 | c0004 | t0024 | g0173 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0305 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01109 | hp2 | a0002 | c0003 | t0003 | g0045 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01168 | hp2 | a0001 | c0002 | t0015 | g0021 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01169 | hp1 | a0001 | c0002 | t0015 | g0021 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0028 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01243 | hp1 | a0003 | c0006 | t0012 | g0253 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0330 | AMR | PUR | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01255 | hp1 | a0001 | c0001 | t0016 | g0011 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01257 | hp2 | a0002 | c0003 | t0003 | g0034 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0292 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01358 | hp2 | a0002 | c0005 | t0004 | g0283 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01361 | hp1 | a0001 | c0002 | t0005 | g0104 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0313 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0085 | EUR | IBS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01515 | hp2 | a0001 | c0001 | t0016 | g0011 | EUR | IBS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0287 | EUR | IBS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | IBS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0286 | EUR | IBS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01517 | hp2 | a0001 | c0001 | t0016 | g0011 | EUR | IBS | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0222 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01891 | hp1 | a0003 | c0006 | t0012 | g0162 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01928 | hp1 | a0001 | c0002 | t0005 | g0107 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01943 | hp2 | a0001 | c0007 | t0002 | g0035 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0328 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01952 | hp2 | a0002 | c0003 | t0003 | g0277 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01978 | hp1 | a0001 | c0002 | t0015 | g0049 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01978 | hp2 | a0001 | c0002 | t0005 | g0080 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02040 | hp1 | a0001 | c0002 | t0005 | g0126 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02055 | hp2 | a0001 | c0001 | t0029 | g0336 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0228 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02083 | hp1 | a0001 | c0002 | t0022 | g0194 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02129 | hp2 | a0001 | c0001 | t0027 | g0246 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02145 | hp1 | a0001 | c0004 | t0006 | g0251 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0182 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02148 | hp1 | a0002 | c0003 | t0003 | g0013 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02148 | hp2 | a0001 | c0002 | t0015 | g0309 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02155 | hp1 | a0002 | c0005 | t0002 | g0190 | EAS | CDX | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0109 | EAS | CDX | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | CDX | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | CDX | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02258 | hp2 | a0001 | c0001 | t0021 | g0167 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02273 | hp2 | a0004 | c0010 | t0004 | g0015 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0327 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0282 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02293 | hp2 | a0001 | c0002 | t0005 | g0023 | AMR | PEL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02451 | hp1 | a0001 | c0004 | t0006 | g0230 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02451 | hp2 | a0001 | c0004 | t0006 | g0248 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0189 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02523 | hp2 | a0001 | c0002 | t0022 | g0106 | EAS | KHV | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0208 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02572 | hp2 | a0001 | c0012 | t0007 | g0335 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0092 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02615 | hp1 | a0001 | c0004 | t0006 | g0008 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0181 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0221 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02622 | hp2 | a0001 | c0004 | t0006 | g0334 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0249 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02630 | hp2 | a0001 | c0002 | t0005 | g0032 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0241 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0027 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02698 | hp1 | a0002 | c0005 | t0002 | g0243 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02698 | hp2 | a0001 | c0002 | t0005 | g0077 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02717 | hp1 | a0001 | c0001 | t0013 | g0329 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02717 | hp2 | a0001 | c0004 | t0006 | g0160 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02723 | hp1 | a0001 | c0008 | t0039 | g0239 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02723 | hp2 | a0001 | c0004 | t0006 | g0214 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0027 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02735 | hp2 | a0001 | c0002 | t0005 | g0302 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02738 | hp1 | a0002 | c0003 | t0003 | g0034 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02738 | hp2 | a0001 | c0007 | t0042 | g0069 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02809 | hp1 | a0001 | c0004 | t0006 | g0256 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02809 | hp2 | a0001 | c0002 | t0013 | g0220 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0084 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0219 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0038 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02895 | hp2 | a0001 | c0004 | t0006 | g0008 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02896 | hp1 | a0001 | c0002 | t0005 | g0257 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0038 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02922 | hp1 | a0001 | c0004 | t0006 | g0259 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02922 | hp2 | a0001 | c0001 | t0023 | g0178 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02965 | hp1 | a0001 | c0002 | t0013 | g0172 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02965 | hp2 | a0001 | c0004 | t0006 | g0298 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02976 | hp1 | a0001 | c0004 | t0006 | g0165 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0217 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0169 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0032 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0215 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03098 | hp1 | a0001 | c0002 | t0041 | g0238 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03098 | hp2 | a0001 | c0001 | t0020 | g0237 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03130 | hp1 | a0001 | c0004 | t0024 | g0175 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03130 | hp2 | a0001 | c0001 | t0035 | g0055 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03195 | hp1 | a0001 | c0004 | t0017 | g0204 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03195 | hp2 | a0001 | c0004 | t0006 | g0319 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03209 | hp1 | a0001 | c0004 | t0006 | g0295 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0151 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03225 | hp1 | a0001 | c0004 | t0017 | g0054 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03239 | hp1 | a0002 | c0003 | t0005 | g0284 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0316 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03453 | hp1 | a0001 | c0004 | t0017 | g0053 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0161 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03486 | hp1 | a0001 | c0008 | t0009 | g0206 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0070 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0149 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0300 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0268 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0150 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03516 | hp1 | a0001 | c0004 | t0006 | g0008 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03516 | hp2 | a0001 | c0001 | t0021 | g0202 | AFR | ESN | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0218 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | GWD | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0195 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0293 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03688 | hp1 | a0002 | c0005 | t0004 | g0014 | SAS | STU | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | STU | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03704 | hp2 | a0002 | c0003 | t0003 | g0281 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03710 | hp1 | a0002 | c0003 | t0003 | g0279 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0089 | SAS | PJL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03831 | hp1 | a0002 | c0003 | t0001 | g0046 | SAS | BEB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | BEB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03834 | hp1 | a0001 | c0002 | t0005 | g0125 | SAS | BEB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0042 | SAS | BEB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0307 | SAS | BEB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0304 | SAS | BEB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG04115 | hp1 | a0002 | c0003 | t0003 | g0013 | SAS | STU | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG04115 | hp2 | a0001 | c0001 | t0028 | g0048 | SAS | STU | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG04184 | hp2 | a0002 | c0005 | t0004 | g0014 | SAS | BEB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | STU | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | STU | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | STU | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | STU | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18522 | hp1 | a0001 | c0004 | t0030 | g0200 | AFR | YRI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18522 | hp2 | a0001 | c0004 | t0006 | g0008 | AFR | YRI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18612 | hp1 | a0001 | c0002 | t0005 | g0291 | EAS | CHB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18612 | hp2 | a0002 | c0003 | t0003 | g0235 | EAS | CHB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | CHB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | CHB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18906 | hp1 | a0001 | c0001 | t0018 | g0242 | AFR | YRI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18906 | hp2 | a0001 | c0001 | t0020 | g0056 | AFR | YRI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18942 | hp2 | a0001 | c0002 | t0033 | g0233 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18943 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18943 | hp2 | a0001 | c0001 | t0025 | g0113 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18944 | hp2 | a0001 | c0002 | t0005 | g0331 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18947 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18952 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18953 | hp1 | a0002 | c0003 | t0003 | g0058 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18954 | hp2 | a0001 | c0002 | t0005 | g0163 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18956 | hp1 | a0001 | c0002 | t0005 | g0288 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18957 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18960 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18960 | hp2 | a0001 | c0002 | t0014 | g0006 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18962 | hp2 | a0001 | c0001 | t0026 | g0001 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18963 | hp2 | a0001 | c0002 | t0036 | g0183 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0258 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18964 | hp2 | a0001 | c0001 | t0019 | g0112 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18965 | hp2 | a0002 | c0003 | t0003 | g0285 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18972 | hp2 | a0002 | c0003 | t0003 | g0068 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18977 | hp1 | a0001 | c0002 | t0014 | g0006 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18980 | hp1 | a0001 | c0011 | t0002 | g0093 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18980 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18982 | hp1 | a0001 | c0001 | t0010 | g0267 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18982 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18983 | hp2 | a0002 | c0003 | t0003 | g0266 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0110 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18985 | hp1 | a0005 | c0017 | t0003 | g0252 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18990 | hp2 | a0001 | c0002 | t0005 | g0147 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18995 | hp2 | a0002 | c0003 | t0003 | g0273 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18998 | hp2 | a0001 | c0002 | t0014 | g0322 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18999 | hp1 | a0001 | c0002 | t0005 | g0310 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA18999 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0118 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19003 | hp1 | a0001 | c0002 | t0005 | g0306 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0232 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19011 | hp1 | a0002 | c0003 | t0003 | g0059 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19011 | hp2 | a0001 | c0002 | t0005 | g0023 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19012 | hp1 | a0002 | c0003 | t0003 | g0299 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19030 | hp1 | a0001 | c0016 | t0032 | g0211 | AFR | LWK | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19030 | hp2 | a0006 | c0009 | t0006 | g0261 | AFR | LWK | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19043 | hp1 | a0003 | c0006 | t0012 | g0240 | AFR | LWK | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0332 | AFR | LWK | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19054 | hp2 | a0001 | c0002 | t0034 | g0264 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19055 | hp1 | a0002 | c0003 | t0003 | g0060 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19055 | hp2 | a0001 | c0002 | t0005 | g0127 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19056 | hp1 | a0001 | c0001 | t0010 | g0105 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19062 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19063 | hp1 | a0001 | c0001 | t0019 | g0148 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19074 | hp2 | a0001 | c0002 | t0005 | g0003 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19076 | hp2 | a0001 | c0002 | t0014 | g0006 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0120 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19079 | hp2 | a0001 | c0002 | t0005 | g0271 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19084 | hp1 | a0001 | c0001 | t0010 | g0108 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19086 | hp2 | a0002 | c0003 | t0003 | g0057 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19088 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19240 | hp1 | a0001 | c0001 | t0038 | g0201 | AFR | YRI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA19240 | hp2 | a0001 | c0002 | t0013 | g0205 | AFR | YRI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ASW | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ASW | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0325 | EUR | TSI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0269 | EUR | TSI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | TSI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | TSI | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20905 | hp1 | a0002 | c0005 | t0004 | g0014 | SAS | GIH | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20905 | hp2 | a0002 | c0003 | t0003 | g0071 | SAS | GIH | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02109 | hp2 | a0001 | c0013 | t0006 | g0174 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02486 | hp1 | a0001 | c0002 | t0011 | g0297 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02559 | hp1 | a0001 | c0001 | t0031 | g0210 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG02559 | hp2 | a0001 | c0015 | t0001 | g0276 | AFR | ACB | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03471 | hp1 | a0003 | c0006 | t0012 | g0262 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG03471 | hp2 | a0001 | c0004 | t0040 | g0236 | AFR | MSL | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | USA | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| HG06807 | hp2 | a0001 | c0014 | t0009 | g0209 | AFR | USA | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20300 | hp1 | a0001 | c0004 | t0006 | g0180 | AFR | USA | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | USA | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0164 | AFR | LWK | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | LWK | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0037 | g0043 | REF | REF | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0004 | REF | REF | APCDD1_chr18_10449635_10494949 | APCDD1 | chr18 | 10449635 | 10494949 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:10454998 | G | T | 1 | a0005 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.17G>T | p.Arg6Leu | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/5 | 364/3803 | 17/1545 | 6/514 | chr18 | 10454998 | |||
| chr18:10471735 | G | A | 2 | a0002 a0005 |
51 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(48): Show |
missense_variant | MODERATE | c.448G>A | p.Val150Ile | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/5 | 795/3803 | 448/1545 | 150/514 | chr18 | 10471735 | |||
| chr18:10471768 | G | A | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.481G>A | p.Glu161Lys | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/5 | 828/3803 | 481/1545 | 161/514 | chr18 | 10471768 | |||
| chr18:10471793 | G | A | 1 | a0004 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.506G>A | p.Arg169His | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/5 | 853/3803 | 506/1545 | 169/514 | chr18 | 10471793 | |||
| chr18:10485738 | G | A | 1 | a0003 | 4 | HG01243.hp1 HG01891.hp1 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.1051G>A | p.Val351Ile | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/5 | 1398/3803 | 1051/1545 | 351/514 | chr18 | 10485738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:10468599 | A | C | 1 | a0001c0008 | 2 | HG02723.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.189A>C | p.Ala63Ala | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/5 | 536/3803 | 189/1545 | 63/514 | chr18 | 10468599 | |||
| chr18:10468638 | C | T | 1 | a0001c0016 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.228C>T | p.His76His | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/5 | 575/3803 | 228/1545 | 76/514 | chr18 | 10468638 | |||
| chr18:10471767 | C | T | 5 | a0001c0014 a0001c0015 a0002c0003 others(2): Show |
53 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(50): Show |
synonymous_variant | LOW | c.480C>T | p.Ala160Ala | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/5 | 827/3803 | 480/1545 | 160/514 | chr18 | 10471767 | |||
| chr18:10471776 | C | G | 5 | a0001c0014 a0001c0015 a0002c0003 others(2): Show |
53 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(50): Show |
synonymous_variant | LOW | c.489C>G | p.Leu163Leu | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/5 | 836/3803 | 489/1545 | 163/514 | chr18 | 10471776 | |||
| chr18:10485506 | A | G | 1 | a0001c0013 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.819A>G | p.Ser273Ser | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/5 | 1166/3803 | 819/1545 | 273/514 | chr18 | 10485506 | |||
| chr18:10485683 | G | A | 1 | a0001c0011 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.996G>A | p.Pro332Pro | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/5 | 1343/3803 | 996/1545 | 332/514 | chr18 | 10485683 | |||
| chr18:10485713 | C | T | 1 | a0001c0012 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1026C>T | p.Tyr342Tyr | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/5 | 1373/3803 | 1026/1545 | 342/514 | chr18 | 10485713 | |||
| chr18:10487787 | C | A | 1 | a0001c0007 | 3 | HG00735.hp2 HG01943.hp2 HG02738.hp2 |
synonymous_variant | LOW | c.1294C>A | p.Arg432Arg | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1641/3803 | 1294/1545 | 432/514 | chr18 | 10487787 | |||
| chr18:10487921 | C | T | 4 | a0001c0002 a0001c0015 a0002c0003 others(1): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
synonymous_variant | LOW | c.1428C>T | p.Leu476Leu | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1775/3803 | 1428/1545 | 476/514 | chr18 | 10487921 | |||
| chr18:10488002 | C | T | 3 | a0001c0004 a0001c0013 a0006c0009 |
26 | HG01106.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
synonymous_variant | LOW | c.1509C>T | p.Cys503Cys | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1856/3803 | 1509/1545 | 503/514 | chr18 | 10488002 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:10454726 | G | A | 1 | a0001c0001t0018 | 2 | HG02647.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-256G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/5 | 256 | chr18 | 10454726 | ||||||
| chr18:10454727 | A | T | 1 | a0001c0007t0042 | 1 | HG02738.hp2 | 5_prime_UTR_variant | MODIFIER | c.-255A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/5 | 255 | chr18 | 10454727 | ||||||
| chr18:10454772 | G | C | 1 | a0001c0001t0025 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/5 | 210 | chr18 | 10454772 | ||||||
| chr18:10454873 | G | T | 1 | a0001c0004t0024 | 2 | HG01106.hp2 HG03130.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/5 | chr18 | 10454873 | |||||||
| chr18:10454908 | G | T | 4 | a0001c0001t0038 a0001c0002t0041 a0001c0004t0040 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-74G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/5 | 74 | chr18 | 10454908 | ||||||
| chr18:10488067 | C | T | 4 | a0001c0002t0003 a0001c0002t0036 a0002c0003t0003 others(1): Show |
56 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*29C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 29 | chr18 | 10488067 | ||||||
| chr18:10488094 | G | T | 31 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0023 others(28): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*56G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 56 | chr18 | 10488094 | ||||||
| chr18:10488167 | C | T | 2 | a0001c0001t0023 a0001c0001t0035 |
3 | HG00639.hp1 HG02922.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*129C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 129 | chr18 | 10488167 | ||||||
| chr18:10488180 | A | G | 4 | a0001c0001t0009 a0001c0008t0009 a0001c0008t0039 others(1): Show |
8 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*142A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 142 | chr18 | 10488180 | ||||||
| chr18:10488192 | A | C | 1 | a0001c0001t0029 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*154A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 154 | chr18 | 10488192 | ||||||
| chr18:10488233 | G | A | 1 | a0001c0001t0016 | 3 | HG01255.hp1 HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*195G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 195 | chr18 | 10488233 | ||||||
| chr18:10488303 | A | G | 5 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0018 others(2): Show |
19 | HG00408.hp1 HG01167.hp2 HG01169.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*265A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 265 | chr18 | 10488303 | ||||||
| chr18:10488334 | AGGGCC | A | 6 | a0001c0004t0006 a0001c0004t0024 a0001c0004t0030 others(3): Show |
23 | HG01106.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*297_*301delGGGCC | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 297 | chr18 | 10488334 | ||||||
| chr18:10488340 | T | C | 6 | a0001c0004t0006 a0001c0004t0024 a0001c0004t0030 others(3): Show |
23 | HG01106.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*302T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 302 | chr18 | 10488340 | ||||||
| chr18:10488342 | T | A | 6 | a0001c0004t0006 a0001c0004t0024 a0001c0004t0030 others(3): Show |
23 | HG01106.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*304T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 304 | chr18 | 10488342 | ||||||
| chr18:10488343 | T | A | 6 | a0001c0004t0006 a0001c0004t0024 a0001c0004t0030 others(3): Show |
23 | HG01106.hp2 HG02109.hp2 HG02145.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 305 | chr18 | 10488343 | ||||||
| chr18:10488428 | C | T | 1 | a0001c0002t0022 | 2 | HG02083.hp1 HG02523.hp2 |
3_prime_UTR_variant | MODIFIER | c.*390C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 390 | chr18 | 10488428 | ||||||
| chr18:10488437 | C | T | 1 | a0001c0001t0020 | 2 | HG03098.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*399C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 399 | chr18 | 10488437 | ||||||
| chr18:10488453 | G | A | 4 | a0001c0002t0003 a0001c0002t0036 a0002c0003t0003 others(1): Show |
56 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*415G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 415 | chr18 | 10488453 | ||||||
| chr18:10488565 | A | G | 1 | a0001c0001t0029 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 527 | chr18 | 10488565 | ||||||
| chr18:10488618 | A | G | 4 | a0001c0002t0003 a0001c0002t0036 a0002c0003t0003 others(1): Show |
56 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*580A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 580 | chr18 | 10488618 | ||||||
| chr18:10488618 | A | T | 5 | a0001c0001t0012 a0001c0001t0023 a0001c0001t0029 others(2): Show |
10 | HG00639.hp1 HG01099.hp1 HG01243.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*580A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 580 | chr18 | 10488618 | ||||||
| chr18:10488658 | G | A | 7 | a0001c0004t0006 a0001c0004t0017 a0001c0004t0024 others(4): Show |
26 | HG01106.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*620G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 620 | chr18 | 10488658 | ||||||
| chr18:10488713 | T | C | 1 | a0001c0001t0026 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 675 | chr18 | 10488713 | ||||||
| chr18:10488735 | G | A | 1 | a0001c0001t0027 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 697 | chr18 | 10488735 | ||||||
| chr18:10488742 | G | C | 36 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0012 others(33): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*704G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 704 | chr18 | 10488742 | ||||||
| chr18:10488784 | T | TA | 36 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0012 others(33): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*746_*747insA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 747 | chr18 | 10488784 | ||||||
| chr18:10488852 | C | CAG | 26 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0012 others(23): Show |
119 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*814_*815insAG | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 815 | chr18 | 10488852 | ||||||
| chr18:10488942 | A | T | 1 | a0001c0001t0029 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*904A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 904 | chr18 | 10488942 | ||||||
| chr18:10488970 | A | G | 1 | a0001c0002t0014 | 4 | NA18960.hp2 NA18977.hp1 NA18998.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*932A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 932 | chr18 | 10488970 | ||||||
| chr18:10489016 | A | G | 36 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0012 others(33): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*978A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 978 | chr18 | 10489016 | ||||||
| chr18:10489170 | C | A | 1 | a0001c0004t0030 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1132C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1132 | chr18 | 10489170 | ||||||
| chr18:10489244 | G | A | 1 | a0001c0001t0021 | 2 | HG02258.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1206G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1206 | chr18 | 10489244 | ||||||
| chr18:10489249 | T | C | 1 | a0001c0002t0033 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1211T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1211 | chr18 | 10489249 | ||||||
| chr18:10489287 | C | T | 1 | a0001c0001t0028 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1249C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1249 | chr18 | 10489287 | ||||||
| chr18:10489382 | C | T | 1 | a0001c0001t0023 | 2 | HG00639.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1344C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1344 | chr18 | 10489382 | ||||||
| chr18:10489383 | G | A | 17 | a0001c0001t0013 a0001c0002t0001 a0001c0002t0003 others(14): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1345G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1345 | chr18 | 10489383 | ||||||
| chr18:10489438 | C | A | 1 | a0001c0002t0011 | 6 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1400C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1400 | chr18 | 10489438 | ||||||
| chr18:10489454 | C | T | 1 | a0001c0002t0034 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1416C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1416 | chr18 | 10489454 | ||||||
| chr18:10489648 | G | A | 6 | a0001c0002t0001 a0001c0002t0011 a0001c0002t0014 others(3): Show |
107 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1610G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1610 | chr18 | 10489648 | ||||||
| chr18:10489664 | G | A | 1 | a0001c0002t0041 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1626G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1626 | chr18 | 10489664 | ||||||
| chr18:10489698 | C | CA | 2 | a0001c0001t0007 a0001c0012t0007 |
13 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1674dupA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1675 | INFO_REALIGN_3_PRIME | chr18 | 10489698 | |||||
| chr18:10489698 | CA | C | 28 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0018 others(25): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1674delA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1674 | INFO_REALIGN_3_PRIME | chr18 | 10489698 | |||||
| chr18:10489755 | TACA | T | 3 | a0001c0001t0010 a0001c0001t0019 a0001c0016t0032 |
9 | HG00408.hp1 HG02155.hp2 NA18964.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1720_*1722delAAC | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1720 | INFO_REALIGN_3_PRIME | chr18 | 10489755 | |||||
| chr18:10489789 | G | A | 51 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(48): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
3_prime_UTR_variant | MODIFIER | c.*1751G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 5/5 | 1751 | chr18 | 10489789 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:10455080 | A | G | 198 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(195): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.58+41A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455080 | |||||||
| chr18:10455084 | A | G | 2 | a0001c0002t0011g0010 a0001c0002t0011g0337 |
5 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+45A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455084 | |||||||
| chr18:10455136 | C | T | 198 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(195): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.58+97C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455136 | |||||||
| chr18:10455144 | G | A | 1 | a0003c0006t0012g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58+105G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455144 | |||||||
| chr18:10455153 | G | A | 1 | a0001c0001t0004g0039 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.58+114G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455153 | |||||||
| chr18:10455221 | T | G | 1 | a0001c0002t0001g0040 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.58+182T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455221 | |||||||
| chr18:10455310 | A | C | 3 | a0001c0001t0009g0161 a0001c0004t0006g0008 a0001c0004t0006g0160 |
6 | HG02615.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+271A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455310 | |||||||
| chr18:10455433 | C | T | 330 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(327): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.58+394C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455433 | |||||||
| chr18:10455683 | T | G | 197 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(194): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.58+644T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455683 | |||||||
| chr18:10455685 | T | A | 1 | a0001c0002t0005g0163 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.58+646T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455685 | |||||||
| chr18:10455811 | A | G | 3 | a0001c0004t0006g0334 a0001c0012t0007g0335 a0003c0006t0012g0162 |
3 | HG01891.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.58+772A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10455811 | |||||||
| chr18:10456016 | G | C | 1 | a0001c0001t0004g0039 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.58+977G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456016 | |||||||
| chr18:10456017 | C | T | 1 | a0001c0001t0004g0039 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.58+978C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456017 | |||||||
| chr18:10456019 | C | G | 99 | a0001c0001t0002g0260 a0001c0001t0002g0270 a0001c0001t0002g0286 others(96): Show |
120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.58+980C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456019 | |||||||
| chr18:10456302 | A | G | 1 | a0001c0002t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.58+1263A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456302 | |||||||
| chr18:10456371 | A | G | 1 | a0001c0002t0001g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58+1332A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456371 | |||||||
| chr18:10456397 | G | C | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG00609.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.58+1358G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456397 | |||||||
| chr18:10456447 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.58+1408C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456447 | |||||||
| chr18:10456484 | A | G | 4 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(1): Show |
4 | HG00642.hp1 HG01346.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+1445A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456484 | |||||||
| chr18:10456537 | A | G | 1 | a0001c0001t0008g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.58+1498A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456537 | |||||||
| chr18:10456784 | G | A | 15 | a0001c0001t0002g0260 a0001c0001t0010g0164 a0001c0001t0010g0255 others(12): Show |
16 | HG00408.hp1 HG01243.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.58+1745G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456784 | |||||||
| chr18:10456957 | A | G | 1 | a0001c0001t0008g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.58+1918A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456957 | |||||||
| chr18:10456963 | T | G | 98 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(95): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.58+1924T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10456963 | |||||||
| chr18:10457004 | A | T | 3 | a0001c0004t0006g0334 a0001c0012t0007g0335 a0003c0006t0012g0162 |
3 | HG01891.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.58+1965A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457004 | |||||||
| chr18:10457005 | T | TA | 49 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(46): Show |
59 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+1971dupA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10457005 | ||||||
| chr18:10457086 | A | G | 96 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(93): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.58+2047A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457086 | |||||||
| chr18:10457126 | T | C | 2 | a0001c0001t0002g0199 a0001c0001t0023g0198 |
2 | HG00639.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.58+2087T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457126 | |||||||
| chr18:10457173 | G | A | 94 | a0001c0001t0002g0260 a0001c0001t0002g0286 a0001c0001t0002g0287 others(91): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.58+2134G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457173 | |||||||
| chr18:10457212 | A | T | 4 | a0001c0002t0001g0031 a0001c0002t0041g0238 a0001c0008t0039g0239 others(1): Show |
5 | HG02723.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+2173A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457212 | |||||||
| chr18:10457216 | G | C | 93 | a0001c0001t0002g0260 a0001c0001t0002g0286 a0001c0001t0002g0287 others(90): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.58+2177G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457216 | |||||||
| chr18:10457218 | T | C | 1 | a0001c0004t0030g0200 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58+2179T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457218 | |||||||
| chr18:10457261 | G | A | 22 | a0001c0001t0004g0280 a0001c0002t0001g0272 a0001c0002t0001g0274 others(19): Show |
27 | HG00140.hp2 HG00735.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.58+2222G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457261 | |||||||
| chr18:10457265 | T | C | 1 | a0001c0004t0006g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.58+2226T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457265 | |||||||
| chr18:10457283 | T | C | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.58+2244T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457283 | |||||||
| chr18:10457367 | A | G | 23 | a0001c0001t0004g0029 a0001c0001t0004g0223 a0001c0001t0004g0333 others(20): Show |
25 | HG00099.hp1 HG00408.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.58+2328A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457367 | |||||||
| chr18:10457511 | A | G | 8 | a0001c0001t0002g0216 a0001c0001t0007g0222 a0001c0001t0009g0218 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+2472A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457511 | |||||||
| chr18:10457519 | G | A | 96 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(93): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.58+2480G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457519 | |||||||
| chr18:10457657 | T | C | 3 | a0001c0004t0006g0334 a0001c0012t0007g0335 a0003c0006t0012g0162 |
3 | HG01891.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.58+2618T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457657 | |||||||
| chr18:10457736 | T | A | 1 | a0002c0003t0003g0062 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.58+2697T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457736 | |||||||
| chr18:10457827 | T | C | 1 | a0001c0001t0038g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.58+2788T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457827 | |||||||
| chr18:10457850 | C | T | 94 | a0001c0001t0002g0260 a0001c0001t0002g0286 a0001c0001t0002g0287 others(91): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.58+2811C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457850 | |||||||
| chr18:10457921 | T | G | 2 | a0001c0001t0004g0041 a0001c0001t0004g0042 |
2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.58+2882T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10457921 | |||||||
| chr18:10458083 | A | G | 1 | a0001c0001t0029g0336 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58+3044A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458083 | |||||||
| chr18:10458093 | C | T | 49 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(46): Show |
59 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+3054C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458093 | |||||||
| chr18:10458205 | G | C | 5 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0066 others(2): Show |
7 | HG00733.hp2 HG01255.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+3166G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458205 | |||||||
| chr18:10458259 | C | A | 49 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(46): Show |
59 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+3220C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458259 | |||||||
| chr18:10458366 | C | T | 2 | a0001c0001t0004g0149 a0001c0001t0004g0150 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.58+3327C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458366 | |||||||
| chr18:10458393 | A | G | 2 | a0001c0002t0001g0031 a0003c0006t0012g0240 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.58+3354A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458393 | |||||||
| chr18:10458412 | T | C | 6 | a0001c0002t0001g0272 a0002c0003t0003g0057 a0002c0003t0003g0058 others(3): Show |
6 | NA18953.hp1 NA18973.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+3373T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458412 | |||||||
| chr18:10458630 | C | G | 1 | a0001c0001t0004g0325 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.58+3591C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458630 | |||||||
| chr18:10458656 | C | T | 2 | a0001c0001t0002g0323 a0001c0001t0004g0324 |
2 | HG00140.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.58+3617C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458656 | |||||||
| chr18:10458806 | A | C | 2 | a0001c0001t0008g0038 a0001c0002t0003g0332 |
3 | HG02895.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.58+3767A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458806 | |||||||
| chr18:10458859 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.58+3820G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10458859 | |||||||
| chr18:10459026 | G | A | 1 | a0002c0003t0003g0068 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.58+3987G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10459026 | |||||||
| chr18:10459092 | A | G | 49 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(46): Show |
59 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.58+4053A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10459092 | |||||||
| chr18:10459314 | G | T | 6 | a0001c0001t0007g0212 a0001c0001t0007g0213 a0001c0001t0007g0215 others(3): Show |
6 | HG01891.hp2 HG02723.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+4275G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10459314 | |||||||
| chr18:10459316 | G | GCA | 113 | a0001c0001t0002g0018 a0001c0001t0002g0026 a0001c0001t0002g0073 others(110): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.58+4300_58+4301dup others(2): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10459316 | ||||||
| chr18:10459316 | G | GCACA | 82 | a0001c0001t0002g0207 a0001c0001t0002g0286 a0001c0001t0002g0287 others(79): Show |
96 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.58+4298_58+4301dup others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10459316 | ||||||
| chr18:10459316 | G | GCACACA | 10 | a0001c0001t0004g0325 a0001c0001t0012g0203 a0001c0001t0021g0202 others(7): Show |
11 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+4296_58+4301dup others(6): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10459316 | ||||||
| chr18:10459316 | G | GCACACAC others(1): Show |
4 | a0001c0002t0001g0290 a0001c0002t0005g0288 a0001c0002t0005g0289 others(1): Show |
4 | HG00544.hp1 NA18612.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+4294_58+4301dup others(8): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10459316 | ||||||
| chr18:10459316 | G | GCACACAC others(3): Show |
12 | a0001c0001t0002g0260 a0001c0001t0010g0255 a0001c0001t0020g0237 others(9): Show |
13 | HG00408.hp1 HG01243.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+4292_58+4301dup others(10): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10459316 | ||||||
| chr18:10459316 | G | GCACACAC others(5): Show |
3 | a0001c0001t0010g0164 a0001c0004t0006g0165 a0001c0004t0006g0251 |
3 | HG02145.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.58+4290_58+4301dup others(12): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10459316 | ||||||
| chr18:10459316 | GCACA | G | 3 | a0001c0004t0006g0334 a0001c0012t0007g0335 a0003c0006t0012g0162 |
3 | HG01891.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.58+4298_58+4301del others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10459316 | ||||||
| chr18:10459634 | G | A | 1 | a0001c0002t0001g0272 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.58+4595G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10459634 | |||||||
| chr18:10459704 | T | C | 1 | a0002c0003t0003g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.58+4665T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10459704 | |||||||
| chr18:10459859 | C | CTT | 197 | a0001c0001t0002g0026 a0001c0001t0002g0091 a0001c0001t0002g0176 others(194): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.58+4820_58+4821ins others(2): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10459859 | |||||||
| chr18:10459961 | A | C | 98 | a0001c0001t0002g0196 a0001c0001t0002g0260 a0001c0001t0002g0286 others(95): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.58+4922A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10459961 | |||||||
| chr18:10460071 | C | T | 2 | a0001c0001t0002g0199 a0001c0001t0023g0198 |
2 | HG00639.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.58+5032C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460071 | |||||||
| chr18:10460244 | G | A | 1 | a0001c0004t0006g0248 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.58+5205G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460244 | |||||||
| chr18:10460308 | C | T | 2 | a0001c0001t0019g0148 a0001c0002t0005g0147 |
2 | NA18990.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.58+5269C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460308 | |||||||
| chr18:10460311 | C | G | 175 | a0001c0001t0002g0026 a0001c0001t0002g0091 a0001c0001t0002g0176 others(172): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.58+5272C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460311 | |||||||
| chr18:10460346 | C | T | 3 | a0001c0004t0006g0334 a0001c0012t0007g0335 a0003c0006t0012g0162 |
3 | HG01891.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.58+5307C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460346 | |||||||
| chr18:10460406 | G | T | 1 | a0001c0001t0002g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.58+5367G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460406 | |||||||
| chr18:10460426 | G | A | 1 | a0001c0001t0008g0028 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.58+5387G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460426 | |||||||
| chr18:10460464 | C | T | 2 | a0001c0001t0008g0028 a0001c0004t0006g0248 |
3 | HG01167.hp2 HG01169.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.58+5425C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460464 | |||||||
| chr18:10460532 | C | CA | 41 | a0001c0001t0002g0152 a0001c0001t0002g0196 a0001c0001t0004g0096 others(38): Show |
43 | HG00408.hp1 HG00544.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.58+5506dupA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10460532 | ||||||
| chr18:10460532 | C | CAA | 10 | a0001c0001t0002g0197 a0001c0001t0020g0237 a0001c0001t0021g0202 others(7): Show |
11 | HG01891.hp1 HG02723.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+5505_58+5506dup others(2): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10460532 | ||||||
| chr18:10460545 | AC | A | 3 | a0001c0002t0001g0292 a0001c0002t0011g0337 a0002c0003t0003g0057 |
3 | HG01081.hp2 HG01358.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.58+5507delC | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460545 | |||||||
| chr18:10460546 | C | A | 91 | a0001c0001t0002g0196 a0001c0001t0002g0260 a0001c0001t0002g0286 others(88): Show |
109 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.58+5507C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460546 | |||||||
| chr18:10460552 | A | G | 1 | a0001c0004t0040g0236 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.58+5513A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460552 | |||||||
| chr18:10460553 | C | A | 1 | a0001c0002t0001g0294 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.58+5514C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460553 | |||||||
| chr18:10460796 | T | C | 2 | a0001c0001t0038g0201 a0001c0002t0005g0208 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58+5757T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460796 | |||||||
| chr18:10460805 | A | C | 1 | a0001c0001t0002g0146 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.58+5766A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460805 | |||||||
| chr18:10460881 | C | T | 1 | a0001c0001t0007g0222 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58+5842C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460881 | |||||||
| chr18:10460913 | C | G | 8 | a0001c0001t0002g0216 a0001c0001t0007g0222 a0001c0001t0009g0218 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+5874C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10460913 | |||||||
| chr18:10461090 | GT | G | 99 | a0001c0001t0002g0196 a0001c0001t0002g0260 a0001c0001t0002g0286 others(96): Show |
118 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.58+6054delT | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10461090 | ||||||
| chr18:10461160 | A | G | 190 | a0001c0001t0002g0026 a0001c0001t0002g0091 a0001c0001t0002g0176 others(187): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.58+6121A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461160 | |||||||
| chr18:10461170 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.58+6131C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461170 | |||||||
| chr18:10461197 | G | A | 66 | a0001c0001t0002g0196 a0001c0001t0002g0286 a0001c0001t0002g0287 others(63): Show |
82 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.58+6158G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461197 | |||||||
| chr18:10461221 | C | T | 1 | a0001c0001t0007g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.58+6182C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461221 | |||||||
| chr18:10461386 | A | G | 83 | a0001c0001t0002g0026 a0001c0001t0002g0091 a0001c0001t0002g0176 others(80): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.58+6347A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461386 | |||||||
| chr18:10461439 | C | T | 4 | a0001c0002t0001g0031 a0001c0002t0041g0238 a0001c0008t0039g0239 others(1): Show |
5 | HG02723.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+6400C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461439 | |||||||
| chr18:10461476 | G | T | 1 | a0001c0002t0001g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58+6437G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461476 | |||||||
| chr18:10461531 | G | T | 46 | a0001c0001t0002g0026 a0001c0001t0002g0176 a0001c0001t0002g0191 others(43): Show |
56 | HG00099.hp2 HG00280.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.58+6492G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461531 | |||||||
| chr18:10461797 | A | T | 183 | a0001c0001t0002g0026 a0001c0001t0002g0091 a0001c0001t0002g0176 others(180): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.59-6672A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461797 | |||||||
| chr18:10461900 | T | G | 1 | a0001c0001t0004g0072 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.59-6569T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461900 | |||||||
| chr18:10461902 | C | T | 1 | a0001c0007t0042g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.59-6567C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461902 | |||||||
| chr18:10461967 | G | A | 1 | a0001c0014t0009g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59-6502G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461967 | |||||||
| chr18:10461968 | T | C | 2 | a0001c0001t0008g0028 a0001c0004t0006g0248 |
3 | HG01167.hp2 HG01169.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.59-6501T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10461968 | |||||||
| chr18:10462194 | A | G | 2 | a0001c0001t0007g0213 a0001c0004t0006g0214 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.59-6275A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462194 | |||||||
| chr18:10462201 | T | A | 3 | a0001c0002t0001g0033 a0001c0002t0001g0268 a0001c0002t0001g0269 |
4 | HG00099.hp2 HG00639.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-6268T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462201 | |||||||
| chr18:10462294 | T | G | 1 | a0001c0014t0009g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59-6175T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462294 | |||||||
| chr18:10462407 | TTTCCTTC others(232): Show |
T | 1 | a0001c0001t0007g0195 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.59-6043_59-5805del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462407 | ||||||
| chr18:10462407 | TTTCCTTC others(236): Show |
T | 2 | a0001c0001t0002g0216 a0001c0001t0012g0217 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.59-6043_59-5801del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462407 | ||||||
| chr18:10462407 | TTTCCTTC others(240): Show |
T | 77 | a0001c0001t0002g0091 a0001c0001t0002g0176 a0001c0001t0002g0191 others(74): Show |
88 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.59-6043_59-5797del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462407 | ||||||
| chr18:10462407 | TTTCCTTC others(244): Show |
T | 4 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0002t0001g0171 others(1): Show |
4 | HG00280.hp1 HG00642.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-6043_59-5793del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462407 | ||||||
| chr18:10462407 | TTTCCTTC others(252): Show |
T | 1 | a0001c0002t0041g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.59-6043_59-5785del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462407 | ||||||
| chr18:10462408 | TTCCTTCC others(228): Show |
T | 19 | a0001c0001t0002g0260 a0001c0001t0004g0280 a0001c0001t0007g0222 others(16): Show |
20 | HG01069.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.59-6043_59-5809del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462408 | ||||||
| chr18:10462412 | TTCCTTCC others(224): Show |
T | 27 | a0001c0001t0002g0315 a0001c0001t0002g0317 a0001c0001t0004g0316 others(24): Show |
35 | HG00735.hp1 HG01167.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.59-6043_59-5813del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462412 | ||||||
| chr18:10462416 | TTCCTTCC others(220): Show |
T | 54 | a0001c0001t0002g0012 a0001c0001t0002g0196 a0001c0001t0002g0286 others(51): Show |
63 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.59-6043_59-5817del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462416 | ||||||
| chr18:10462420 | TTCCTTTC others(216): Show |
T | 12 | a0001c0001t0004g0308 a0001c0001t0012g0203 a0001c0002t0001g0097 others(9): Show |
12 | HG01099.hp1 HG01943.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-6043_59-5821del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462420 | ||||||
| chr18:10462424 | TTTCCCCC others(208): Show |
T | 1 | a0001c0001t0021g0202 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.59-6043_59-5829del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462424 | ||||||
| chr18:10462424 | TTTCCCCC others(212): Show |
T | 2 | a0001c0004t0006g0248 a0002c0003t0005g0284 |
2 | HG02451.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.59-6043_59-5825del | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462424 | ||||||
| chr18:10462465 | C | T | 1 | a0001c0001t0004g0001 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.59-6004C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462465 | |||||||
| chr18:10462492 | C | CCCTT | 3 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0004t0006g0008 |
3 | HG02895.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.59-5949_59-5946dup others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462492 | ||||||
| chr18:10462492 | C | CCCTTCCT others(105): Show |
1 | a0001c0001t0026g0001 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.59-5970_59-5969ins others(112): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462492 | ||||||
| chr18:10462492 | C | CCCTTCCT others(1): Show |
4 | a0001c0001t0023g0198 a0001c0001t0038g0201 a0001c0002t0005g0208 others(1): Show |
4 | HG00639.hp1 HG02572.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-5953_59-5946dup others(8): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462492 | ||||||
| chr18:10462492 | C | CCCTTCCT others(137): Show |
1 | a0001c0002t0001g0131 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.59-5950_59-5949ins others(144): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462492 | ||||||
| chr18:10462492 | C | CCCTTCCT others(141): Show |
4 | a0001c0001t0002g0135 a0001c0002t0001g0129 a0001c0002t0005g0104 others(1): Show |
4 | HG01361.hp1 NA18980.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-5950_59-5949ins others(148): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462492 | ||||||
| chr18:10462492 | C | CCCTTCCT others(141): Show |
1 | a0001c0001t0002g0199 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.59-5946_59-5945ins others(148): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462492 | ||||||
| chr18:10462536 | T | C | 1 | a0001c0002t0003g0110 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.59-5933T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462536 | |||||||
| chr18:10462540 | C | CCCTTCCT others(114): Show |
1 | a0001c0001t0002g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.59-5878_59-5877ins others(121): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(117): Show |
1 | a0001c0001t0002g0012 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.59-5867_59-5866ins others(124): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(101): Show |
1 | a0001c0001t0023g0198 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.59-5859_59-5858ins others(108): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(145): Show |
1 | a0001c0001t0004g0037 | 2 | NA18944.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.59-5855_59-5854ins others(152): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(113): Show |
1 | a0001c0002t0005g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(120): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(141): Show |
5 | a0001c0001t0002g0064 a0001c0001t0008g0151 a0001c0001t0013g0329 others(2): Show |
5 | HG02129.hp2 HG02717.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(148): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(173): Show |
1 | a0001c0001t0004g0166 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(180): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(141): Show |
11 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(8): Show |
12 | HG00673.hp2 HG01346.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(148): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(145): Show |
60 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(57): Show |
87 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(152): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(265): Show |
1 | a0004c0010t0004g0015 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(272): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(145): Show |
1 | a0001c0001t0010g0108 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(152): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(149): Show |
6 | a0001c0001t0002g0005 a0001c0001t0004g0004 a0001c0002t0001g0130 others(3): Show |
7 | HG00558.hp1 HG01261.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(156): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(441): Show |
1 | a0001c0002t0003g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(448): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(149): Show |
1 | a0001c0001t0002g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.59-5847_59-5846ins others(156): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCCTTCCT others(225): Show |
1 | a0001c0001t0004g0001 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.59-5914_59-5913ins others(232): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | CCTTCCTT others(212): Show |
1 | a0001c0002t0003g0110 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.59-5928_59-5927ins others(219): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462540 | ||||||
| chr18:10462540 | C | T | 5 | a0001c0001t0002g0199 a0001c0001t0026g0001 a0001c0002t0001g0129 others(2): Show |
5 | HG01361.hp1 HG03139.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-5929C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462540 | |||||||
| chr18:10462568 | T | TCCTTCCT others(20): Show |
1 | a0001c0001t0002g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.59-5883_59-5882ins others(27): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462568 | ||||||
| chr18:10462587 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.59-5882C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462587 | |||||||
| chr18:10462591 | C | CTCCTTCC others(333): Show |
1 | a0002c0003t0003g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(340): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462591 | ||||||
| chr18:10462591 | C | CTCCTTCC others(149): Show |
1 | a0001c0001t0002g0114 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(156): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462591 | ||||||
| chr18:10462595 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.59-5874T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462595 | |||||||
| chr18:10462595 | T | TTCCTTCC others(133): Show |
1 | a0001c0002t0001g0328 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(140): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462595 | ||||||
| chr18:10462595 | T | TTCCTTCC others(137): Show |
4 | a0001c0001t0004g0001 a0001c0001t0004g0096 a0001c0001t0007g0327 others(1): Show |
4 | HG01243.hp2 HG02280.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(144): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462595 | ||||||
| chr18:10462595 | T | TTCCTTCC others(137): Show |
1 | a0001c0001t0002g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(144): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462595 | ||||||
| chr18:10462595 | T | TTCCTTCC others(141): Show |
16 | a0001c0001t0002g0005 a0001c0001t0002g0026 a0001c0001t0002g0081 others(13): Show |
17 | HG00609.hp1 HG01496.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(148): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462595 | ||||||
| chr18:10462595 | T | TTCCTTCC others(145): Show |
2 | a0001c0002t0001g0016 a0001c0002t0003g0244 |
3 | HG00621.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(152): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462595 | ||||||
| chr18:10462599 | T | TTCCTTCC others(129): Show |
1 | a0001c0001t0008g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(136): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462599 | ||||||
| chr18:10462599 | T | TTCCTTCC others(133): Show |
2 | a0001c0001t0009g0161 a0001c0004t0006g0008 |
5 | HG02615.hp1 HG02895.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(140): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462599 | ||||||
| chr18:10462599 | T | TTCCTTCC others(137): Show |
14 | a0001c0001t0002g0073 a0001c0001t0002g0076 a0001c0001t0002g0086 others(11): Show |
15 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(144): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462599 | ||||||
| chr18:10462603 | T | TTCCCTCC others(129): Show |
1 | a0001c0014t0009g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59-5863_59-5862ins others(136): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462603 | ||||||
| chr18:10462603 | T | TTCCTTCC others(101): Show |
1 | a0001c0001t0004g0072 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.59-5851_59-5850ins others(108): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462603 | ||||||
| chr18:10462607 | T | C | 1 | a0001c0014t0009g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59-5862T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462607 | |||||||
| chr18:10462607 | T | TTCCTTCC others(129): Show |
3 | a0001c0001t0002g0146 a0001c0001t0038g0201 a0001c0002t0005g0208 |
3 | HG02572.hp1 NA19060.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(136): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462607 | ||||||
| chr18:10462611 | T | TTCCTTCC others(117): Show |
2 | a0001c0002t0003g0090 a0001c0002t0003g0159 |
2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(124): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462611 | ||||||
| chr18:10462611 | T | TTCCTTCC others(121): Show |
4 | a0001c0001t0002g0075 a0001c0002t0001g0074 a0001c0002t0003g0089 others(1): Show |
4 | HG01943.hp1 HG02717.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-5851_59-5850ins others(128): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462611 | ||||||
| chr18:10462627 | C | T | 40 | a0001c0001t0002g0073 a0001c0001t0002g0075 a0001c0001t0002g0076 others(37): Show |
44 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.59-5842C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462627 | |||||||
| chr18:10462631 | T | C | 30 | a0001c0001t0002g0073 a0001c0001t0002g0076 a0001c0001t0002g0086 others(27): Show |
34 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.59-5838T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462631 | |||||||
| chr18:10462639 | C | T | 40 | a0001c0001t0002g0073 a0001c0001t0002g0075 a0001c0001t0002g0076 others(37): Show |
44 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.59-5830C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462639 | |||||||
| chr18:10462643 | C | CTCCT | 11 | a0001c0001t0002g0018 a0001c0001t0004g0001 a0001c0001t0004g0119 others(8): Show |
14 | HG00673.hp2 HG01346.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.59-5786_59-5783dup others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462643 | ||||||
| chr18:10462643 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0021g0202 |
2 | HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.59-5826C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462643 | |||||||
| chr18:10462647 | T | C | 30 | a0001c0001t0002g0073 a0001c0001t0002g0076 a0001c0001t0002g0086 others(27): Show |
34 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.59-5822T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462647 | |||||||
| chr18:10462651 | T | TTCCCTCC others(1): Show |
7 | a0001c0001t0002g0075 a0001c0001t0002g0146 a0001c0002t0001g0074 others(4): Show |
7 | HG01074.hp1 HG01099.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-5815_59-5814ins others(8): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462651 | ||||||
| chr18:10462655 | T | C | 3 | a0001c0001t0038g0201 a0001c0002t0005g0208 a0001c0014t0009g0209 |
3 | HG02572.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.59-5814T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462655 | |||||||
| chr18:10462659 | T | C | 3 | a0001c0001t0038g0201 a0001c0002t0005g0208 a0001c0014t0009g0209 |
3 | HG02572.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.59-5810T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462659 | |||||||
| chr18:10462691 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.59-5778T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462691 | |||||||
| chr18:10462693 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.59-5776C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462693 | |||||||
| chr18:10462891 | C | A | 1 | a0001c0001t0004g0223 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.59-5578C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10462891 | |||||||
| chr18:10462917 | CA | C | 126 | a0001c0001t0002g0091 a0001c0001t0002g0176 a0001c0001t0002g0191 others(123): Show |
139 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.59-5545delA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10462917 | ||||||
| chr18:10463115 | G | A | 43 | a0001c0001t0002g0091 a0001c0001t0002g0176 a0001c0001t0002g0216 others(40): Show |
47 | HG00408.hp1 HG00544.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.59-5354G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463115 | |||||||
| chr18:10463293 | C | T | 1 | a0001c0001t0007g0195 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.59-5176C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463293 | |||||||
| chr18:10463305 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.59-5164C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463305 | |||||||
| chr18:10463404 | G | A | 2 | a0001c0002t0005g0100 a0003c0006t0012g0162 |
2 | HG00558.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.59-5065G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463404 | |||||||
| chr18:10463464 | G | T | 4 | a0001c0001t0009g0218 a0001c0001t0009g0219 a0001c0001t0009g0221 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-5005G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463464 | |||||||
| chr18:10463471 | G | A | 10 | a0001c0001t0008g0028 a0001c0001t0009g0218 a0001c0001t0009g0219 others(7): Show |
11 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-4998G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463471 | |||||||
| chr18:10463534 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.59-4935C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463534 | |||||||
| chr18:10463543 | T | A | 1 | a0001c0001t0004g0223 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.59-4926T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463543 | |||||||
| chr18:10463604 | C | T | 7 | a0001c0001t0002g0260 a0001c0001t0038g0201 a0001c0002t0005g0032 others(4): Show |
8 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-4865C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463604 | |||||||
| chr18:10463605 | C | G | 2 | a0001c0001t0023g0198 a0001c0002t0005g0070 |
2 | HG00639.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.59-4864C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463605 | |||||||
| chr18:10463829 | A | C | 1 | a0001c0001t0004g0039 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.59-4640A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463829 | |||||||
| chr18:10463835 | T | A | 1 | a0001c0001t0004g0223 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.59-4634T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463835 | |||||||
| chr18:10463933 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.59-4536G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463933 | |||||||
| chr18:10463933 | G | T | 2 | a0001c0001t0002g0140 a0001c0001t0002g0145 |
2 | NA18950.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.59-4536G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463933 | |||||||
| chr18:10463978 | C | T | 1 | a0001c0014t0009g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.59-4491C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10463978 | |||||||
| chr18:10464005 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.59-4464C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464005 | |||||||
| chr18:10464010 | G | A | 4 | a0001c0001t0035g0055 a0001c0002t0001g0052 a0001c0004t0017g0053 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-4459G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464010 | |||||||
| chr18:10464130 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.59-4339G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464130 | |||||||
| chr18:10464311 | A | AAC | 57 | a0001c0001t0004g0044 a0001c0001t0004g0119 a0001c0001t0004g0149 others(54): Show |
67 | HG00099.hp1 HG00408.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.59-4126_59-4125dup others(2): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464311 | ||||||
| chr18:10464311 | A | AACAC | 28 | a0001c0001t0002g0076 a0001c0001t0002g0101 a0001c0001t0008g0151 others(25): Show |
29 | HG00544.hp1 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-4128_59-4125dup others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464311 | ||||||
| chr18:10464311 | A | AACACAC | 15 | a0001c0001t0002g0114 a0001c0001t0002g0154 a0001c0001t0002g0260 others(12): Show |
15 | HG00140.hp2 HG00544.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.59-4130_59-4125dup others(6): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464311 | ||||||
| chr18:10464311 | A | AACACACA others(1): Show |
46 | a0001c0001t0002g0012 a0001c0001t0002g0024 a0001c0001t0002g0075 others(43): Show |
60 | HG00280.hp1 HG00558.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.59-4132_59-4125dup others(8): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464311 | ||||||
| chr18:10464311 | A | AACACACA others(3): Show |
59 | a0001c0001t0002g0005 a0001c0001t0002g0140 a0001c0001t0002g0141 others(56): Show |
76 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.59-4134_59-4125dup others(10): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464311 | ||||||
| chr18:10464311 | A | AACACACA others(5): Show |
22 | a0001c0001t0002g0007 a0001c0001t0002g0026 a0001c0001t0002g0067 others(19): Show |
28 | HG01361.hp1 HG02071.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.59-4136_59-4125dup others(12): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464311 | ||||||
| chr18:10464311 | A | AACACACA others(7): Show |
5 | a0001c0001t0002g0019 a0001c0001t0002g0139 a0001c0001t0007g0215 others(2): Show |
6 | HG02080.hp2 HG03041.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-4138_59-4125dup others(14): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464311 | ||||||
| chr18:10464311 | A | ACACACAC others(6): Show |
1 | a0001c0001t0002g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.59-4158_59-4157ins others(13): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464311 | |||||||
| chr18:10464311 | AAC | A | 5 | a0001c0002t0001g0138 a0001c0002t0003g0089 a0001c0002t0003g0090 others(2): Show |
5 | HG00741.hp1 HG01074.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-4126_59-4125del others(2): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464311 | ||||||
| chr18:10464317 | C | CACACACA others(4): Show |
1 | a0001c0001t0004g0223 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.59-4151_59-4141dup others(11): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464317 | ||||||
| chr18:10464339 | C | G | 3 | a0001c0001t0002g0091 a0001c0001t0002g0207 a0001c0002t0013g0205 |
3 | HG02257.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.59-4130C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464339 | |||||||
| chr18:10464343 | C | CACACACA others(5): Show |
1 | a0001c0002t0001g0272 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.59-4125_59-4124ins others(12): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464343 | ||||||
| chr18:10464343 | C | G | 15 | a0001c0001t0002g0176 a0001c0001t0002g0270 a0001c0001t0007g0025 others(12): Show |
16 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-4126C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464343 | |||||||
| chr18:10464343 | CAG | C | 4 | a0001c0001t0007g0327 a0001c0001t0018g0241 a0001c0001t0018g0242 others(1): Show |
4 | HG01952.hp1 HG02280.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-4124_59-4123del others(2): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464343 | ||||||
| chr18:10464344 | AGACAC | A | 3 | a0001c0001t0002g0091 a0001c0001t0002g0207 a0001c0002t0013g0205 |
3 | HG02257.hp1 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.59-4124_59-4120del others(5): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464344 | |||||||
| chr18:10464345 | G | C | 21 | a0001c0001t0002g0176 a0001c0001t0002g0270 a0001c0001t0007g0025 others(18): Show |
22 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-4124G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464345 | |||||||
| chr18:10464348 | AC | A | 15 | a0001c0001t0002g0176 a0001c0001t0002g0270 a0001c0001t0007g0025 others(12): Show |
16 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-4120delC | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464348 | |||||||
| chr18:10464355 | C | T | 4 | a0001c0001t0035g0055 a0001c0002t0001g0052 a0001c0004t0017g0053 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-4114C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464355 | |||||||
| chr18:10464359 | A | C | 4 | a0001c0001t0009g0218 a0001c0001t0009g0219 a0001c0001t0009g0221 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4110A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464359 | |||||||
| chr18:10464395 | A | G | 3 | a0001c0001t0018g0241 a0001c0001t0018g0242 a0001c0001t0029g0336 |
3 | HG02055.hp2 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.59-4074A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464395 | |||||||
| chr18:10464413 | G | A | 1 | a0001c0002t0001g0268 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.59-4056G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464413 | |||||||
| chr18:10464416 | T | A | 1 | a0001c0001t0004g0223 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.59-4053T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464416 | |||||||
| chr18:10464699 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.59-3770G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464699 | |||||||
| chr18:10464713 | G | GC | 8 | a0001c0001t0009g0218 a0001c0001t0009g0219 a0001c0001t0009g0221 others(5): Show |
8 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3753dupC | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr18 | 10464713 | ||||||
| chr18:10464787 | C | T | 3 | a0001c0001t0002g0136 a0001c0001t0004g0096 a0001c0001t0004g0137 |
3 | HG00609.hp1 NA18956.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.59-3682C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464787 | |||||||
| chr18:10464944 | G | T | 1 | a0001c0001t0004g0039 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.59-3525G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10464944 | |||||||
| chr18:10465008 | C | T | 3 | a0001c0002t0011g0010 a0001c0002t0011g0297 a0001c0002t0011g0337 |
6 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-3461C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465008 | |||||||
| chr18:10465057 | A | C | 165 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(162): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.59-3412A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465057 | |||||||
| chr18:10465213 | C | T | 2 | a0001c0001t0004g0313 a0001c0001t0004g0325 |
2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.59-3256C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465213 | |||||||
| chr18:10465296 | C | T | 1 | a0001c0001t0007g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.59-3173C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465296 | |||||||
| chr18:10465316 | T | C | 125 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(122): Show |
155 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.59-3153T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465316 | |||||||
| chr18:10465352 | A | G | 125 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(122): Show |
155 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.59-3117A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465352 | |||||||
| chr18:10465404 | T | C | 132 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(129): Show |
163 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.59-3065T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465404 | |||||||
| chr18:10465707 | T | C | 1 | a0001c0002t0041g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.59-2762T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465707 | |||||||
| chr18:10465758 | A | G | 2 | a0001c0002t0001g0031 a0003c0006t0012g0240 |
3 | HG02896.hp2 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.59-2711A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465758 | |||||||
| chr18:10465810 | T | A | 8 | a0001c0001t0007g0212 a0001c0001t0008g0249 a0001c0001t0012g0203 others(5): Show |
8 | HG01099.hp1 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-2659T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465810 | |||||||
| chr18:10465989 | G | A | 1 | a0001c0002t0003g0228 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.59-2480G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10465989 | |||||||
| chr18:10466004 | A | T | 19 | a0001c0001t0002g0075 a0001c0001t0002g0199 a0001c0001t0004g0029 others(16): Show |
21 | HG00408.hp2 HG02027.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-2465A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466004 | |||||||
| chr18:10466005 | A | G | 2 | a0001c0015t0001g0276 a0003c0006t0012g0253 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.59-2464A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466005 | |||||||
| chr18:10466021 | T | C | 221 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(218): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.59-2448T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466021 | |||||||
| chr18:10466160 | C | T | 4 | a0001c0001t0009g0218 a0001c0001t0009g0219 a0001c0001t0009g0221 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-2309C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466160 | |||||||
| chr18:10466322 | G | A | 227 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(224): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.59-2147G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466322 | |||||||
| chr18:10466361 | G | A | 2 | a0001c0015t0001g0276 a0003c0006t0012g0253 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.59-2108G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466361 | |||||||
| chr18:10466614 | A | G | 226 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(223): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.59-1855A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466614 | |||||||
| chr18:10466643 | G | T | 207 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(204): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.59-1826G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466643 | |||||||
| chr18:10466645 | G | C | 1 | a0001c0001t0004g0041 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.59-1824G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466645 | |||||||
| chr18:10466671 | C | G | 8 | a0001c0001t0007g0212 a0001c0001t0008g0249 a0001c0001t0012g0203 others(5): Show |
8 | HG01099.hp1 HG01891.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1798C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466671 | |||||||
| chr18:10466692 | A | G | 259 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(256): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.59-1777A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466692 | |||||||
| chr18:10466945 | A | G | 16 | a0001c0001t0007g0215 a0001c0001t0010g0105 a0001c0001t0010g0255 others(13): Show |
17 | HG00408.hp1 HG01106.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-1524A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10466945 | |||||||
| chr18:10467129 | T | G | 36 | a0001c0001t0004g0280 a0001c0002t0001g0099 a0001c0002t0001g0274 others(33): Show |
51 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.59-1340T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10467129 | |||||||
| chr18:10467389 | A | G | 16 | a0001c0001t0007g0215 a0001c0001t0010g0105 a0001c0001t0010g0255 others(13): Show |
17 | HG00408.hp1 HG01106.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-1080A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10467389 | |||||||
| chr18:10467559 | A | T | 1 | a0001c0001t0010g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.59-910A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10467559 | |||||||
| chr18:10467641 | A | G | 1 | a0002c0003t0003g0285 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.59-828A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10467641 | |||||||
| chr18:10467699 | A | G | 2 | a0001c0001t0021g0202 a0001c0004t0017g0204 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.59-770A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10467699 | |||||||
| chr18:10467704 | T | A | 157 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(154): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.59-765T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10467704 | |||||||
| chr18:10467745 | G | GT | 16 | a0001c0001t0007g0215 a0001c0001t0010g0105 a0001c0001t0010g0255 others(13): Show |
17 | HG00408.hp1 HG01106.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-724_59-723insT | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10467745 | |||||||
| chr18:10467749 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.59-720G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10467749 | |||||||
| chr18:10468025 | C | T | 16 | a0001c0001t0007g0215 a0001c0001t0010g0105 a0001c0001t0010g0255 others(13): Show |
17 | HG00408.hp1 HG01106.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.59-444C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468025 | |||||||
| chr18:10468029 | T | C | 2 | a0001c0001t0018g0241 a0001c0001t0018g0242 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.59-440T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468029 | |||||||
| chr18:10468132 | T | C | 261 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(258): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.59-337T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468132 | |||||||
| chr18:10468318 | A | G | 69 | a0001c0001t0002g0260 a0001c0001t0004g0280 a0001c0001t0007g0215 others(66): Show |
86 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.59-151A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468318 | |||||||
| chr18:10468323 | C | T | 2 | a0001c0001t0008g0151 a0001c0001t0013g0329 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.59-146C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468323 | |||||||
| chr18:10468329 | C | T | 15 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 others(12): Show |
16 | HG00408.hp1 HG01106.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-140C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468329 | |||||||
| chr18:10468330 | A | G | 68 | a0001c0001t0002g0260 a0001c0001t0004g0280 a0001c0001t0007g0222 others(65): Show |
85 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.59-139A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468330 | |||||||
| chr18:10468361 | A | G | 3 | a0001c0001t0021g0202 a0001c0001t0023g0198 a0001c0004t0017g0204 |
3 | HG00639.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.59-108A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468361 | |||||||
| chr18:10468456 | C | T | 166 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(163): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.59-13C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 1/4 | chr18 | 10468456 | |||||||
| chr18:10468682 | C | T | 6 | a0001c0001t0038g0201 a0001c0002t0005g0032 a0001c0002t0005g0070 others(3): Show |
7 | HG01106.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+30C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10468682 | |||||||
| chr18:10468699 | A | G | 2 | a0001c0001t0002g0135 a0001c0011t0002g0093 |
2 | NA18980.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.242+47A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10468699 | |||||||
| chr18:10468720 | T | A | 9 | a0001c0001t0007g0212 a0001c0001t0008g0249 a0001c0001t0012g0203 others(6): Show |
9 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+68T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10468720 | |||||||
| chr18:10468750 | C | T | 4 | a0001c0002t0001g0031 a0001c0004t0006g0214 a0003c0006t0012g0240 others(1): Show |
5 | HG02723.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.242+98C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10468750 | |||||||
| chr18:10468871 | A | T | 9 | a0001c0001t0007g0212 a0001c0001t0008g0249 a0001c0001t0012g0203 others(6): Show |
9 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+219A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10468871 | |||||||
| chr18:10468956 | G | A | 2 | a0001c0001t0010g0105 a0001c0001t0010g0267 |
2 | NA18982.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.242+304G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10468956 | |||||||
| chr18:10469012 | C | T | 9 | a0001c0001t0007g0212 a0001c0001t0008g0249 a0001c0001t0012g0203 others(6): Show |
9 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.242+360C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469012 | |||||||
| chr18:10469104 | G | A | 18 | a0001c0001t0002g0091 a0001c0001t0002g0176 a0001c0001t0002g0207 others(15): Show |
19 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.242+452G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469104 | |||||||
| chr18:10469144 | A | G | 1 | a0001c0001t0008g0028 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.242+492A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469144 | |||||||
| chr18:10469280 | C | T | 3 | a0001c0001t0021g0202 a0001c0001t0023g0198 a0001c0004t0017g0204 |
3 | HG00639.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.242+628C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469280 | |||||||
| chr18:10469289 | C | A | 1 | a0001c0001t0029g0336 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.242+637C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469289 | |||||||
| chr18:10469509 | T | C | 1 | a0001c0002t0033g0233 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.242+857T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469509 | |||||||
| chr18:10469692 | AG | A | 6 | a0001c0001t0038g0201 a0001c0002t0005g0032 a0001c0002t0005g0070 others(3): Show |
7 | HG01106.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+1043delG | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 10469692 | ||||||
| chr18:10469794 | T | G | 221 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(218): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.242+1142T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469794 | |||||||
| chr18:10469845 | C | T | 10 | a0001c0001t0018g0241 a0001c0001t0018g0242 a0001c0001t0038g0201 others(7): Show |
11 | HG01106.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.242+1193C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469845 | |||||||
| chr18:10469855 | A | G | 45 | a0001c0001t0004g0280 a0001c0001t0018g0241 a0001c0001t0018g0242 others(42): Show |
61 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.242+1203A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469855 | |||||||
| chr18:10469860 | G | T | 1 | a0001c0002t0003g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.242+1208G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469860 | |||||||
| chr18:10469919 | G | A | 3 | a0001c0001t0009g0161 a0001c0004t0006g0008 a0001c0004t0006g0160 |
6 | HG02615.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.242+1267G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469919 | |||||||
| chr18:10469967 | C | T | 1 | a0001c0002t0001g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.242+1315C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10469967 | |||||||
| chr18:10470065 | A | G | 2 | a0001c0004t0006g0214 a0006c0009t0006g0261 |
2 | HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.242+1413A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470065 | |||||||
| chr18:10470099 | C | T | 1 | a0001c0002t0001g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.243-1431C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470099 | |||||||
| chr18:10470206 | T | C | 19 | a0001c0001t0002g0091 a0001c0001t0002g0260 a0001c0001t0007g0222 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.243-1324T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470206 | |||||||
| chr18:10470289 | T | C | 2 | a0001c0001t0002g0101 a0001c0002t0005g0288 |
2 | HG02132.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.243-1241T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470289 | |||||||
| chr18:10470611 | A | G | 4 | a0001c0001t0007g0222 a0001c0001t0007g0327 a0001c0001t0007g0330 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.243-919A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470611 | |||||||
| chr18:10470621 | T | C | 5 | a0001c0001t0009g0218 a0001c0001t0009g0219 a0001c0001t0009g0221 others(2): Show |
5 | HG02451.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.243-909T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470621 | |||||||
| chr18:10470721 | T | C | 127 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(124): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.243-809T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470721 | |||||||
| chr18:10470982 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.243-548A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470982 | |||||||
| chr18:10470984 | A | G | 234 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(231): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.243-546A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10470984 | |||||||
| chr18:10471030 | C | A | 10 | a0001c0001t0007g0212 a0001c0001t0008g0249 a0001c0001t0012g0203 others(7): Show |
10 | HG01099.hp1 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.243-500C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10471030 | |||||||
| chr18:10471056 | G | A | 3 | a0001c0004t0006g0295 a0001c0004t0006g0298 a0001c0004t0040g0236 |
3 | HG02965.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.243-474G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10471056 | |||||||
| chr18:10471287 | A | C | 74 | a0001c0001t0002g0091 a0001c0001t0002g0176 a0001c0001t0002g0207 others(71): Show |
91 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.243-243A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10471287 | |||||||
| chr18:10471375 | G | C | 1 | a0001c0001t0002g0304 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.243-155G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10471375 | |||||||
| chr18:10471524 | G | A | 7 | a0001c0001t0002g0101 a0001c0002t0001g0156 a0001c0002t0005g0077 others(4): Show |
7 | HG00544.hp1 HG01433.hp1 HG01978.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.243-6G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 2/4 | chr18 | 10471524 | |||||||
| chr18:10472077 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.774+16G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472077 | |||||||
| chr18:10472136 | T | C | 2 | a0001c0002t0001g0168 a0001c0002t0001g0186 |
2 | NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.774+75T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472136 | |||||||
| chr18:10472511 | G | A | 1 | a0002c0005t0002g0275 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.774+450G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472511 | |||||||
| chr18:10472593 | C | T | 1 | a0001c0001t0008g0028 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.774+532C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472593 | |||||||
| chr18:10472610 | G | A | 1 | a0001c0014t0009g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.774+549G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472610 | |||||||
| chr18:10472620 | C | T | 1 | a0001c0001t0004g0247 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.774+559C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472620 | |||||||
| chr18:10472627 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.774+566A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472627 | |||||||
| chr18:10472636 | G | A | 1 | a0002c0003t0003g0281 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.774+575G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472636 | |||||||
| chr18:10472859 | G | A | 1 | a0001c0004t0006g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.774+798G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472859 | |||||||
| chr18:10472894 | C | A | 33 | a0001c0001t0004g0047 a0002c0003t0001g0027 a0002c0003t0001g0189 others(30): Show |
46 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.774+833C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10472894 | |||||||
| chr18:10473054 | G | A | 6 | a0001c0001t0009g0218 a0001c0001t0009g0219 a0001c0001t0009g0221 others(3): Show |
6 | HG02451.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+993G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473054 | |||||||
| chr18:10473093 | T | G | 1 | a0001c0001t0007g0195 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.774+1032T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473093 | |||||||
| chr18:10473156 | A | G | 1 | a0001c0004t0024g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.774+1095A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473156 | |||||||
| chr18:10473196 | G | A | 3 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 |
3 | HG00408.hp1 NA18982.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.774+1135G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473196 | |||||||
| chr18:10473286 | C | A | 36 | a0001c0002t0003g0089 a0001c0002t0003g0090 a0001c0002t0003g0159 others(33): Show |
50 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.774+1225C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473286 | |||||||
| chr18:10473338 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.774+1277G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473338 | |||||||
| chr18:10473452 | C | G | 144 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(141): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.774+1391C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473452 | |||||||
| chr18:10473476 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.774+1415T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473476 | |||||||
| chr18:10473485 | C | T | 2 | a0001c0001t0008g0151 a0001c0001t0013g0329 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.774+1424C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473485 | |||||||
| chr18:10473493 | A | G | 52 | a0001c0001t0002g0075 a0001c0001t0002g0091 a0001c0001t0002g0176 others(49): Show |
57 | HG00408.hp2 HG00558.hp1 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.774+1432A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473493 | |||||||
| chr18:10473508 | G | A | 198 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(195): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.774+1447G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473508 | |||||||
| chr18:10473564 | T | C | 5 | a0001c0001t0009g0218 a0001c0001t0009g0219 a0001c0002t0013g0220 others(2): Show |
5 | HG02451.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+1503T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473564 | |||||||
| chr18:10473720 | T | C | 1 | a0001c0001t0004g0245 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.774+1659T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473720 | |||||||
| chr18:10473722 | G | C | 1 | a0001c0015t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.774+1661G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473722 | |||||||
| chr18:10473729 | A | G | 145 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(142): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.774+1668A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473729 | |||||||
| chr18:10473894 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.774+1833G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10473894 | |||||||
| chr18:10473925 | A | AT | 22 | a0001c0001t0002g0114 a0001c0001t0002g0136 a0001c0001t0002g0153 others(19): Show |
23 | HG00544.hp2 HG00741.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.774+1883dupT | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10473925 | ||||||
| chr18:10473925 | A | ATT | 17 | a0001c0001t0008g0249 a0001c0001t0009g0218 a0001c0001t0009g0219 others(14): Show |
18 | HG01106.hp2 HG02055.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.774+1882_774+1883d others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10473925 | ||||||
| chr18:10473925 | A | ATTT | 45 | a0001c0001t0002g0075 a0001c0001t0002g0176 a0001c0001t0002g0207 others(42): Show |
49 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.774+1881_774+1883d others(5): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10473925 | ||||||
| chr18:10473925 | A | ATTTT | 12 | a0001c0001t0002g0091 a0001c0001t0002g0260 a0001c0001t0007g0182 others(9): Show |
13 | HG02145.hp2 HG02486.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.774+1880_774+1883d others(6): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10473925 | ||||||
| chr18:10474038 | C | T | 13 | a0001c0001t0008g0249 a0001c0001t0009g0218 a0001c0001t0009g0219 others(10): Show |
13 | HG01106.hp2 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.774+1977C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474038 | |||||||
| chr18:10474042 | A | C | 8 | a0001c0001t0007g0215 a0001c0001t0010g0105 a0001c0001t0010g0255 others(5): Show |
9 | HG00408.hp1 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.774+1981A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474042 | |||||||
| chr18:10474089 | A | G | 212 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(209): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.774+2028A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474089 | |||||||
| chr18:10474133 | A | G | 206 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(203): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.774+2072A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474133 | |||||||
| chr18:10474190 | C | A | 3 | a0001c0001t0021g0202 a0001c0001t0023g0198 a0001c0004t0017g0204 |
3 | HG00639.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.774+2129C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474190 | |||||||
| chr18:10474218 | G | T | 191 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(188): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.774+2157G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474218 | |||||||
| chr18:10474225 | CG | C | 11 | a0001c0001t0007g0212 a0001c0001t0007g0215 a0001c0001t0010g0105 others(8): Show |
11 | HG00408.hp1 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.774+2165delG | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474225 | |||||||
| chr18:10474368 | G | A | 6 | a0001c0001t0007g0212 a0001c0001t0012g0217 a0001c0016t0032g0211 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.774+2307G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474368 | |||||||
| chr18:10474431 | AG | A | 3 | a0001c0001t0021g0202 a0001c0001t0023g0198 a0001c0004t0017g0204 |
3 | HG00639.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.774+2371delG | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474431 | |||||||
| chr18:10474601 | C | G | 47 | a0001c0001t0008g0249 a0001c0001t0009g0218 a0001c0001t0009g0219 others(44): Show |
61 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.774+2540C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474601 | |||||||
| chr18:10474818 | G | A | 1 | a0001c0015t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.774+2757G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474818 | |||||||
| chr18:10474985 | G | C | 1 | a0001c0002t0003g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.774+2924G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474985 | |||||||
| chr18:10474988 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.774+2927G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10474988 | |||||||
| chr18:10475125 | C | G | 1 | a0001c0001t0004g0042 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.774+3064C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475125 | |||||||
| chr18:10475436 | G | A | 1 | a0001c0001t0010g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.774+3375G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475436 | |||||||
| chr18:10475557 | T | C | 223 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(220): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.774+3496T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475557 | |||||||
| chr18:10475662 | TA | T | 174 | a0001c0001t0002g0075 a0001c0001t0002g0091 a0001c0001t0002g0101 others(171): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.774+3615delA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10475662 | ||||||
| chr18:10475677 | G | C | 35 | a0001c0001t0007g0215 a0001c0002t0003g0089 a0001c0002t0003g0090 others(32): Show |
48 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+3616G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475677 | |||||||
| chr18:10475792 | GA | G | 7 | a0001c0001t0007g0212 a0001c0001t0009g0221 a0001c0001t0012g0217 others(4): Show |
7 | HG01243.hp1 HG02622.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.774+3732delA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475792 | |||||||
| chr18:10475793 | A | AG | 89 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0012 others(86): Show |
100 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.774+3744dupG | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10475793 | ||||||
| chr18:10475793 | A | AGG | 20 | a0001c0001t0002g0091 a0001c0001t0002g0176 a0001c0001t0002g0199 others(17): Show |
21 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.774+3743_774+3744d others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10475793 | ||||||
| chr18:10475793 | AG | A | 39 | a0001c0001t0004g0001 a0001c0001t0004g0039 a0001c0001t0004g0128 others(36): Show |
49 | HG00099.hp1 HG00140.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.774+3744delG | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10475793 | ||||||
| chr18:10475793 | AGG | A | 25 | a0001c0001t0002g0018 a0001c0001t0002g0101 a0001c0001t0002g0124 others(22): Show |
26 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+3743_774+3744d others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10475793 | ||||||
| chr18:10475795 | G | A | 1 | a0001c0002t0003g0122 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.774+3734G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475795 | |||||||
| chr18:10475795 | G | T | 1 | a0001c0002t0001g0307 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.774+3734G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475795 | |||||||
| chr18:10475796 | G | A | 2 | a0001c0001t0002g0286 a0001c0001t0002g0287 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.774+3735G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475796 | |||||||
| chr18:10475796 | G | C | 2 | a0001c0001t0002g0315 a0001c0002t0003g0232 |
2 | NA19006.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.774+3735G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475796 | |||||||
| chr18:10475797 | G | C | 8 | a0001c0001t0007g0212 a0001c0001t0009g0221 a0001c0001t0012g0217 others(5): Show |
9 | HG01243.hp1 HG02622.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.774+3736G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475797 | |||||||
| chr18:10475797 | G | T | 1 | a0001c0002t0001g0082 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.774+3736G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475797 | |||||||
| chr18:10475798 | G | C | 1 | a0001c0016t0032g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.774+3737G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475798 | |||||||
| chr18:10475798 | G | T | 16 | a0001c0001t0002g0018 a0001c0001t0002g0101 a0001c0001t0002g0124 others(13): Show |
17 | HG00544.hp1 HG01346.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.774+3737G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475798 | |||||||
| chr18:10475799 | G | T | 3 | a0001c0002t0001g0263 a0001c0002t0001g0265 a0001c0002t0034g0264 |
3 | HG00597.hp2 HG02027.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.774+3738G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475799 | |||||||
| chr18:10475803 | G | C | 1 | a0001c0004t0017g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.774+3742G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475803 | |||||||
| chr18:10475803 | G | T | 3 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 |
3 | HG00408.hp1 NA18982.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.774+3742G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10475803 | |||||||
| chr18:10476063 | G | A | 1 | a0001c0002t0001g0307 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.774+4002G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476063 | |||||||
| chr18:10476152 | A | C | 92 | a0001c0001t0002g0086 a0001c0001t0002g0091 a0001c0001t0002g0199 others(89): Show |
108 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.774+4091A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476152 | |||||||
| chr18:10476172 | A | G | 2 | a0001c0002t0005g0077 a0001c0002t0005g0080 |
2 | HG01978.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.774+4111A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476172 | |||||||
| chr18:10476343 | C | T | 3 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 |
3 | HG00408.hp1 NA18982.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.774+4282C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476343 | |||||||
| chr18:10476425 | G | A | 2 | a0001c0001t0002g0086 a0001c0002t0001g0085 |
2 | HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.774+4364G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476425 | |||||||
| chr18:10476470 | C | T | 7 | a0001c0001t0002g0176 a0001c0001t0038g0201 a0001c0002t0001g0052 others(4): Show |
8 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.774+4409C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476470 | |||||||
| chr18:10476664 | A | G | 2 | a0001c0008t0009g0206 a0001c0008t0039g0239 |
2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.774+4603A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476664 | |||||||
| chr18:10476800 | G | A | 7 | a0001c0001t0009g0133 a0001c0001t0009g0161 a0001c0001t0009g0218 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+4739G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476800 | |||||||
| chr18:10476824 | G | T | 97 | a0001c0001t0002g0018 a0001c0001t0002g0091 a0001c0001t0002g0124 others(94): Show |
113 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.774+4763G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10476824 | |||||||
| chr18:10477022 | C | A | 1 | a0001c0001t0010g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.774+4961C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477022 | |||||||
| chr18:10477098 | G | T | 1 | a0001c0002t0005g0127 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.774+5037G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477098 | |||||||
| chr18:10477099 | G | T | 29 | a0001c0001t0002g0091 a0001c0001t0002g0199 a0001c0001t0002g0207 others(26): Show |
31 | HG01099.hp1 HG01106.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.774+5038G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477099 | |||||||
| chr18:10477289 | C | T | 1 | a0001c0001t0002g0024 | 2 | NA18957.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.774+5228C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477289 | |||||||
| chr18:10477567 | C | T | 3 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 |
3 | HG00408.hp1 NA18982.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.774+5506C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477567 | |||||||
| chr18:10477607 | T | C | 224 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(221): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.774+5546T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477607 | |||||||
| chr18:10477653 | C | G | 88 | a0001c0001t0002g0091 a0001c0001t0002g0199 a0001c0001t0002g0207 others(85): Show |
103 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.774+5592C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477653 | |||||||
| chr18:10477676 | C | G | 4 | a0001c0001t0007g0222 a0001c0001t0007g0327 a0001c0001t0007g0330 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+5615C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477676 | |||||||
| chr18:10477789 | A | G | 1 | a0001c0002t0001g0169 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.774+5728A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477789 | |||||||
| chr18:10477843 | A | G | 1 | a0001c0001t0007g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.774+5782A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477843 | |||||||
| chr18:10477884 | C | T | 1 | a0001c0002t0001g0103 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.774+5823C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477884 | |||||||
| chr18:10477954 | T | A | 1 | a0001c0015t0001g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.774+5893T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477954 | |||||||
| chr18:10477954 | T | C | 212 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(209): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.774+5893T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477954 | |||||||
| chr18:10477954 | T | G | 4 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 others(1): Show |
4 | HG00408.hp1 HG02559.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+5893T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477954 | |||||||
| chr18:10477958 | C | A | 4 | a0001c0001t0004g0029 a0001c0001t0004g0192 a0001c0001t0004g0223 others(1): Show |
5 | HG00408.hp2 NA18945.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+5897C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477958 | |||||||
| chr18:10477976 | G | A | 1 | a0001c0001t0028g0048 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.774+5915G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10477976 | |||||||
| chr18:10478130 | C | A | 3 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 |
3 | HG00408.hp1 NA18982.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.774+6069C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478130 | |||||||
| chr18:10478301 | A | C | 7 | a0001c0001t0002g0207 a0001c0001t0007g0195 a0001c0001t0012g0203 others(4): Show |
7 | HG01099.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.774+6240A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478301 | |||||||
| chr18:10478318 | G | A | 2 | a0001c0001t0021g0167 a0001c0004t0017g0204 |
2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.774+6257G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478318 | |||||||
| chr18:10478558 | C | T | 1 | a0002c0003t0003g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.774+6497C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478558 | |||||||
| chr18:10478585 | A | G | 8 | a0001c0001t0007g0212 a0001c0001t0012g0217 a0001c0002t0013g0172 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+6524A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478585 | |||||||
| chr18:10478634 | T | C | 224 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(221): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.774+6573T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478634 | |||||||
| chr18:10478673 | C | T | 1 | a0001c0001t0002g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.774+6612C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478673 | |||||||
| chr18:10478762 | T | C | 176 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(173): Show |
205 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.775-6700T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478762 | |||||||
| chr18:10478815 | G | A | 120 | a0001c0001t0002g0075 a0001c0001t0002g0081 a0001c0001t0002g0101 others(117): Show |
146 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.775-6647G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478815 | |||||||
| chr18:10478857 | T | C | 41 | a0001c0001t0007g0212 a0001c0001t0012g0217 a0001c0002t0003g0089 others(38): Show |
54 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.775-6605T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478857 | |||||||
| chr18:10478878 | G | A | 29 | a0001c0001t0002g0091 a0001c0001t0002g0199 a0001c0001t0002g0207 others(26): Show |
31 | HG01099.hp1 HG01106.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.775-6584G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10478878 | |||||||
| chr18:10479059 | G | C | 210 | a0001c0001t0002g0075 a0001c0001t0002g0081 a0001c0001t0002g0091 others(207): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.775-6403G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479059 | |||||||
| chr18:10479135 | C | G | 210 | a0001c0001t0002g0075 a0001c0001t0002g0081 a0001c0001t0002g0091 others(207): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.775-6327C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479135 | |||||||
| chr18:10479260 | T | C | 2 | a0001c0001t0008g0151 a0001c0001t0013g0329 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.775-6202T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479260 | |||||||
| chr18:10479342 | A | G | 1 | a0001c0001t0018g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.775-6120A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479342 | |||||||
| chr18:10479399 | A | G | 10 | a0001c0001t0002g0018 a0001c0001t0002g0124 a0001c0001t0010g0164 others(7): Show |
11 | HG00639.hp1 HG01346.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.775-6063A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479399 | |||||||
| chr18:10479438 | A | G | 202 | a0001c0001t0002g0075 a0001c0001t0002g0081 a0001c0001t0002g0091 others(199): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.775-6024A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479438 | |||||||
| chr18:10479483 | C | T | 223 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(220): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.775-5979C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479483 | |||||||
| chr18:10479559 | T | A | 1 | a0002c0003t0001g0027 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.775-5903T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479559 | |||||||
| chr18:10479566 | T | C | 1 | a0002c0003t0003g0299 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.775-5896T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479566 | |||||||
| chr18:10479574 | C | A | 6 | a0001c0002t0001g0050 a0001c0002t0001g0117 a0001c0002t0001g0290 others(3): Show |
6 | HG02165.hp2 NA18954.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-5888C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479574 | |||||||
| chr18:10479634 | G | A | 1 | a0001c0001t0008g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.775-5828G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479634 | |||||||
| chr18:10479831 | T | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0124 a0001c0002t0001g0157 |
4 | HG01346.hp2 HG01496.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-5631T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479831 | |||||||
| chr18:10479879 | T | C | 2 | a0001c0001t0008g0151 a0001c0001t0013g0329 |
2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.775-5583T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10479879 | |||||||
| chr18:10480061 | A | C | 1 | a0001c0001t0008g0028 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.775-5401A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480061 | |||||||
| chr18:10480081 | A | G | 8 | a0001c0001t0007g0212 a0001c0001t0012g0217 a0001c0002t0013g0172 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-5381A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480081 | |||||||
| chr18:10480134 | C | T | 7 | a0001c0001t0007g0212 a0001c0001t0012g0217 a0001c0002t0013g0172 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-5328C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480134 | |||||||
| chr18:10480356 | T | C | 1 | a0002c0003t0003g0299 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.775-5106T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480356 | |||||||
| chr18:10480375 | A | T | 8 | a0001c0001t0007g0212 a0001c0001t0012g0217 a0001c0002t0013g0172 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-5087A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480375 | |||||||
| chr18:10480552 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0124 a0001c0002t0001g0157 |
4 | HG01346.hp2 HG01496.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-4910A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480552 | |||||||
| chr18:10480589 | A | T | 1 | a0001c0002t0001g0156 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.775-4873A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480589 | |||||||
| chr18:10480624 | G | A | 13 | a0001c0001t0002g0091 a0001c0001t0002g0199 a0001c0001t0002g0260 others(10): Show |
14 | HG01106.hp2 HG02486.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.775-4838G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480624 | |||||||
| chr18:10480707 | C | CA | 190 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(187): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.775-4745dupA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10480707 | ||||||
| chr18:10480790 | C | G | 2 | a0003c0006t0012g0162 a0003c0006t0012g0240 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.775-4672C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480790 | |||||||
| chr18:10480946 | T | TA | 126 | a0001c0001t0002g0075 a0001c0001t0002g0081 a0001c0001t0002g0101 others(123): Show |
153 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.775-4508dupA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10480946 | ||||||
| chr18:10480958 | G | A | 7 | a0001c0001t0002g0176 a0001c0001t0038g0201 a0001c0002t0001g0052 others(4): Show |
8 | HG02055.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.775-4504G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480958 | |||||||
| chr18:10480976 | T | G | 126 | a0001c0001t0002g0075 a0001c0001t0002g0081 a0001c0001t0002g0101 others(123): Show |
153 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.775-4486T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10480976 | |||||||
| chr18:10481017 | A | G | 1 | a0002c0005t0002g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.775-4445A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481017 | |||||||
| chr18:10481033 | C | T | 1 | a0001c0001t0004g0313 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.775-4429C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481033 | |||||||
| chr18:10481046 | A | C | 10 | a0001c0001t0002g0018 a0001c0001t0002g0124 a0001c0001t0010g0164 others(7): Show |
11 | HG00639.hp1 HG01346.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.775-4416A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481046 | |||||||
| chr18:10481130 | G | T | 7 | a0001c0001t0009g0133 a0001c0001t0009g0161 a0001c0001t0009g0218 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-4332G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481130 | |||||||
| chr18:10481145 | G | T | 1 | a0001c0002t0001g0087 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.775-4317G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481145 | |||||||
| chr18:10481425 | C | T | 1 | a0001c0002t0001g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.775-4037C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481425 | |||||||
| chr18:10481529 | A | G | 226 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(223): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.775-3933A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481529 | |||||||
| chr18:10481546 | G | A | 1 | a0001c0016t0032g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.775-3916G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481546 | |||||||
| chr18:10481611 | AAC | A | 15 | a0001c0001t0002g0207 a0001c0001t0002g0270 a0001c0001t0007g0025 others(12): Show |
16 | HG01099.hp1 HG01167.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.775-3849_775-3848d others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10481611 | ||||||
| chr18:10481652 | C | G | 3 | a0001c0001t0021g0202 a0001c0001t0023g0198 a0001c0004t0024g0175 |
3 | HG00639.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.775-3810C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481652 | |||||||
| chr18:10481682 | T | TA | 23 | a0001c0001t0004g0029 a0001c0001t0004g0192 a0001c0001t0004g0223 others(20): Show |
24 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.775-3768dupA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10481682 | ||||||
| chr18:10481682 | T | TAA | 104 | a0001c0001t0002g0081 a0001c0001t0002g0101 a0001c0001t0002g0176 others(101): Show |
130 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.775-3769_775-3768d others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10481682 | ||||||
| chr18:10481682 | T | TAAA | 43 | a0001c0001t0002g0075 a0001c0001t0007g0212 a0001c0001t0008g0249 others(40): Show |
56 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.775-3770_775-3768d others(5): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10481682 | ||||||
| chr18:10481806 | G | A | 1 | a0001c0001t0002g0315 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.775-3656G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481806 | |||||||
| chr18:10481825 | C | CA | 7 | a0001c0001t0009g0133 a0001c0001t0009g0161 a0001c0001t0009g0218 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-3629dupA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10481825 | ||||||
| chr18:10481825 | CA | C | 169 | a0001c0001t0002g0075 a0001c0001t0002g0081 a0001c0001t0002g0101 others(166): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.775-3629delA | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10481825 | ||||||
| chr18:10481853 | C | T | 4 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 others(1): Show |
4 | HG00408.hp1 HG02559.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-3609C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481853 | |||||||
| chr18:10481944 | G | A | 223 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(220): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.775-3518G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481944 | |||||||
| chr18:10481963 | C | T | 1 | a0001c0001t0008g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.775-3499C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10481963 | |||||||
| chr18:10482046 | C | A | 10 | a0001c0001t0002g0018 a0001c0001t0002g0124 a0001c0001t0010g0164 others(7): Show |
11 | HG00639.hp1 HG01346.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.775-3416C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482046 | |||||||
| chr18:10482051 | A | C | 1 | a0001c0002t0005g0107 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.775-3411A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482051 | |||||||
| chr18:10482096 | A | G | 223 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0081 others(220): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.775-3366A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482096 | |||||||
| chr18:10482265 | G | A | 1 | a0001c0001t0009g0218 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.775-3197G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482265 | |||||||
| chr18:10482361 | G | A | 7 | a0001c0001t0009g0133 a0001c0001t0009g0161 a0001c0001t0009g0218 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-3101G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482361 | |||||||
| chr18:10482425 | C | G | 1 | a0001c0001t0029g0336 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.775-3037C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482425 | |||||||
| chr18:10482444 | G | A | 6 | a0001c0001t0002g0091 a0001c0002t0001g0031 a0001c0004t0006g0214 others(3): Show |
7 | HG02486.hp2 HG02723.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-3018G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482444 | |||||||
| chr18:10482463 | G | A | 1 | a0001c0002t0001g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.775-2999G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482463 | |||||||
| chr18:10482481 | G | T | 7 | a0001c0001t0009g0133 a0001c0001t0009g0161 a0001c0001t0009g0218 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-2981G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482481 | |||||||
| chr18:10482504 | G | A | 4 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 others(1): Show |
4 | HG00408.hp1 HG02559.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-2958G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482504 | |||||||
| chr18:10482520 | C | T | 1 | a0001c0001t0007g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.775-2942C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482520 | |||||||
| chr18:10482552 | G | A | 1 | a0001c0002t0005g0125 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.775-2910G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482552 | |||||||
| chr18:10482599 | A | G | 1 | a0001c0001t0004g0185 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.775-2863A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482599 | |||||||
| chr18:10482779 | A | G | 1 | a0006c0009t0006g0261 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.775-2683A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482779 | |||||||
| chr18:10482793 | T | C | 222 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0091 others(219): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.775-2669T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482793 | |||||||
| chr18:10482852 | T | G | 15 | a0001c0001t0002g0091 a0001c0001t0002g0199 a0001c0001t0002g0260 others(12): Show |
16 | HG01106.hp2 HG02486.hp2 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.775-2610T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10482852 | |||||||
| chr18:10483153 | C | T | 3 | a0001c0001t0008g0249 a0001c0001t0018g0241 a0001c0001t0018g0242 |
3 | HG02630.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.775-2309C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483153 | |||||||
| chr18:10483311 | G | A | 3 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 |
3 | HG00408.hp1 NA18982.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.775-2151G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483311 | |||||||
| chr18:10483373 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.775-2089G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483373 | |||||||
| chr18:10483466 | C | G | 4 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 others(1): Show |
4 | HG00408.hp1 HG02559.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-1996C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483466 | |||||||
| chr18:10483583 | C | T | 3 | a0001c0001t0002g0114 a0001c0001t0002g0123 a0001c0001t0002g0141 |
3 | HG00544.hp2 HG00597.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.775-1879C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483583 | |||||||
| chr18:10483692 | G | C | 4 | a0001c0001t0010g0105 a0001c0001t0010g0255 a0001c0001t0010g0267 others(1): Show |
4 | HG00408.hp1 HG02559.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-1770G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483692 | |||||||
| chr18:10483749 | A | G | 13 | a0001c0001t0008g0151 a0001c0001t0009g0133 a0001c0001t0009g0161 others(10): Show |
13 | HG00408.hp1 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.775-1713A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483749 | |||||||
| chr18:10483761 | T | C | 2 | a0001c0004t0017g0053 a0001c0004t0017g0054 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.775-1701T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483761 | |||||||
| chr18:10483898 | C | T | 1 | a0001c0002t0001g0169 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.775-1564C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10483898 | |||||||
| chr18:10484092 | C | T | 133 | a0001c0001t0002g0075 a0001c0001t0002g0101 a0001c0001t0002g0176 others(130): Show |
159 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.775-1370C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484092 | |||||||
| chr18:10484125 | C | CTTCTGGA others(1): Show |
7 | a0001c0001t0009g0133 a0001c0001t0009g0161 a0001c0001t0009g0218 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-1336_775-1329d others(10): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10484125 | ||||||
| chr18:10484132 | A | C | 1 | a0001c0002t0005g0126 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.775-1330A>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484132 | |||||||
| chr18:10484224 | C | T | 1 | a0001c0014t0009g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.775-1238C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484224 | |||||||
| chr18:10484262 | G | T | 2 | a0001c0001t0035g0055 a0001c0004t0024g0175 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.775-1200G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484262 | |||||||
| chr18:10484271 | A | T | 1 | a0001c0002t0001g0117 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-1191A>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484271 | |||||||
| chr18:10484365 | G | T | 2 | a0001c0001t0007g0215 a0001c0001t0008g0028 |
3 | HG01167.hp2 HG01169.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.775-1097G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484365 | |||||||
| chr18:10484454 | T | C | 15 | a0001c0001t0007g0212 a0001c0001t0010g0105 a0001c0001t0010g0255 others(12): Show |
15 | HG00408.hp1 HG01099.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.775-1008T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484454 | |||||||
| chr18:10484496 | G | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0044 a0004c0010t0004g0015 |
3 | HG01081.hp1 HG01257.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.775-966G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484496 | |||||||
| chr18:10484499 | T | C | 167 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0091 others(164): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.775-963T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484499 | |||||||
| chr18:10484512 | A | G | 193 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0091 others(190): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.775-950A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484512 | |||||||
| chr18:10484588 | C | A | 36 | a0001c0002t0003g0089 a0001c0002t0003g0090 a0001c0002t0003g0110 others(33): Show |
49 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.775-874C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484588 | |||||||
| chr18:10484588 | C | G | 2 | a0001c0001t0002g0304 a0001c0001t0035g0055 |
2 | HG03130.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.775-874C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484588 | |||||||
| chr18:10484589 | C | G | 6 | a0001c0001t0002g0091 a0001c0001t0007g0222 a0001c0001t0007g0327 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-873C>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484589 | |||||||
| chr18:10484651 | C | T | 124 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0101 others(121): Show |
150 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.775-811C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484651 | |||||||
| chr18:10484815 | CATCT | C | 13 | a0001c0001t0008g0177 a0001c0001t0008g0249 a0001c0001t0018g0241 others(10): Show |
14 | HG01106.hp2 HG02109.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.775-646_775-643del others(4): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10484815 | |||||||
| chr18:10484980 | TTTTTG | T | 5 | a0001c0001t0002g0091 a0001c0001t0002g0176 a0001c0001t0002g0199 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.775-462_775-458del others(5): Show |
APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 10484980 | ||||||
| chr18:10485030 | A | G | 44 | a0001c0002t0003g0020 a0001c0002t0003g0089 a0001c0002t0003g0090 others(41): Show |
58 | HG00099.hp1 HG00140.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.775-432A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485030 | |||||||
| chr18:10485047 | G | C | 230 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0091 others(227): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.775-415G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485047 | |||||||
| chr18:10485253 | A | G | 247 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0091 others(244): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.775-209A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485253 | |||||||
| chr18:10485261 | G | C | 1 | a0001c0016t0032g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.775-201G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485261 | |||||||
| chr18:10485302 | C | A | 1 | a0001c0004t0017g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.775-160C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485302 | |||||||
| chr18:10485333 | G | A | 1 | a0001c0001t0035g0055 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.775-129G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485333 | |||||||
| chr18:10485360 | T | C | 221 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(218): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.775-102T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485360 | |||||||
| chr18:10485366 | T | C | 212 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(209): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.775-96T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485366 | |||||||
| chr18:10485372 | G | A | 212 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(209): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.775-90G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 3/4 | chr18 | 10485372 | |||||||
| chr18:10485859 | G | A | 11 | a0001c0001t0002g0091 a0001c0001t0002g0176 a0001c0001t0002g0199 others(8): Show |
12 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1096+76G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10485859 | |||||||
| chr18:10485934 | G | A | 9 | a0001c0001t0002g0270 a0001c0001t0008g0028 a0001c0001t0008g0151 others(6): Show |
10 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096+151G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10485934 | |||||||
| chr18:10486066 | C | A | 2 | a0001c0004t0017g0053 a0001c0004t0017g0054 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1096+283C>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486066 | |||||||
| chr18:10486079 | C | T | 1 | a0001c0001t0007g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1096+296C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486079 | |||||||
| chr18:10486080 | G | A | 1 | a0002c0003t0001g0189 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1096+297G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486080 | |||||||
| chr18:10486094 | G | A | 8 | a0001c0001t0002g0270 a0001c0001t0008g0028 a0001c0001t0008g0151 others(5): Show |
9 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096+311G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486094 | |||||||
| chr18:10486162 | G | T | 1 | a0001c0001t0008g0028 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1096+379G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486162 | |||||||
| chr18:10486205 | T | A | 1 | a0001c0001t0008g0249 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1096+422T>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486205 | |||||||
| chr18:10486309 | A | G | 209 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(206): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1096+526A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486309 | |||||||
| chr18:10486370 | A | G | 206 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(203): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1096+587A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486370 | |||||||
| chr18:10486426 | G | A | 1 | a0001c0001t0035g0055 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1096+643G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486426 | |||||||
| chr18:10486462 | A | G | 1 | a0001c0004t0006g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1096+679A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486462 | |||||||
| chr18:10486633 | G | A | 1 | a0001c0001t0021g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1096+850G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486633 | |||||||
| chr18:10486676 | G | T | 2 | a0001c0002t0001g0051 a0001c0002t0001g0098 |
2 | HG00609.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1096+893G>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486676 | |||||||
| chr18:10486697 | CT | C | 214 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(211): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1097-884delT | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 10486697 | ||||||
| chr18:10486775 | C | T | 1 | a0001c0002t0013g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1097-815C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486775 | |||||||
| chr18:10486790 | C | T | 1 | a0002c0003t0005g0284 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1097-800C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486790 | |||||||
| chr18:10486948 | C | T | 1 | a0001c0002t0041g0238 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1097-642C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486948 | |||||||
| chr18:10486971 | C | T | 1 | a0001c0001t0021g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1097-619C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486971 | |||||||
| chr18:10486972 | G | A | 115 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(112): Show |
143 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1097-618G>A | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10486972 | |||||||
| chr18:10487046 | A | G | 210 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(207): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1097-544A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487046 | |||||||
| chr18:10487059 | C | T | 1 | a0002c0003t0003g0281 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1097-531C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487059 | |||||||
| chr18:10487103 | A | G | 1 | a0002c0003t0003g0279 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1097-487A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487103 | |||||||
| chr18:10487262 | A | G | 5 | a0001c0001t0013g0329 a0001c0002t0013g0172 a0001c0002t0013g0205 others(2): Show |
5 | HG02717.hp1 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1097-328A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487262 | |||||||
| chr18:10487356 | A | G | 214 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(211): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1097-234A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487356 | |||||||
| chr18:10487362 | A | G | 2 | a0001c0002t0003g0090 a0001c0002t0003g0159 |
2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1097-228A>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487362 | |||||||
| chr18:10487446 | T | C | 215 | a0001c0001t0002g0018 a0001c0001t0002g0075 a0001c0001t0002g0124 others(212): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.1097-144T>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487446 | |||||||
| chr18:10487508 | G | C | 1 | a0001c0001t0007g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1097-82G>C | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487508 | |||||||
| chr18:10487529 | T | G | 2 | a0001c0001t0019g0112 a0001c0001t0019g0148 |
2 | NA18964.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1097-61T>G | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487529 | |||||||
| chr18:10487548 | C | T | 1 | a0001c0001t0004g0128 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1097-42C>T | APCDD1 | ENSG00000154856.13 | transcript | ENST00000355285.10 | protein_coding | 4/4 | chr18 | 10487548 |