Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55795 |
| ensemblid | ENSG00000126226.22 |
| hgncid | 25653 |
| symbol | PCID2 |
| name | PCI domain containing 2 |
| refseq_nuc | NM_001127202.4 |
| refseq_prot | NP_001120674.1 |
| ensembl_nuc | ENST00000337344.9 |
| ensembl_prot | ENSP00000337405.4 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 113177536 |
| end | 113208669 |
| strand | - |
| ver | v1.2 |
| region | chr13:113177536-113208669 |
| region5000 | chr13:113172536-113213669 |
| regionname0 | PCID2_chr13_113177536_113208669 |
| regionname5000 | PCID2_chr13_113172536_113213669 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1197 | 403 | 80 | 80 | 178 | 18 | 45 | PCID2_chr13_113172536_113213669 | PCID2 | ATGGC others(1192): Show |
chr13 | 113172536 | 113213669 | ||
| a0001c0002 | 0/0 | 1197 | 7 | 7 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | ATGGC others(1192): Show |
chr13 | 113172536 | 113213669 | ||
| a0001c0003 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | ATGGC others(1192): Show |
chr13 | 113172536 | 113213669 | ||
| a0001c0004 | 0/0 | 1197 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | ATGGC others(1192): Show |
chr13 | 113172536 | 113213669 | ||
| a0001c0005 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | ATGGC others(1192): Show |
chr13 | 113172536 | 113213669 | ||
| a0001c0006 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | ATGGC others(1192): Show |
chr13 | 113172536 | 113213669 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1897 | 321 | 48 | 73 | 140 | 18 | 41 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0001t0002 | 0/0 | 1897 | 40 | 0 | 2 | 38 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0001t0003 | 1/0 | 1897 | 37 | 31 | 5 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0001t0005 | 0/0 | 1897 | 4 | 0 | 0 | 0 | 0 | 4 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0001t0006 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0002t0004 | 0/0 | 1897 | 7 | 7 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0003t0001 | 0/0 | 1897 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0004t0002 | 0/0 | 1897 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0005t0001 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| a0001c0006t0001 | 0/0 | 1897 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | GTAGG others(1892): Show |
chr13 | 113172536 | 113213669 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 0 | 7 | 12 | 2 | 4 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0003 | 0/0 | 21 | 0 | 2 | 16 | 0 | 3 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0004 | 0/0 | 20 | 1 | 2 | 16 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0005 | 0/0 | 13 | 0 | 6 | 0 | 0 | 7 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0006 | 0/0 | 12 | 1 | 0 | 10 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0007 | 0/0 | 12 | 0 | 5 | 0 | 1 | 6 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0009 | 0/0 | 10 | 4 | 4 | 0 | 2 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 2 | 0 | 3 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0014 | 0/0 | 5 | 3 | 0 | 2 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0019 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0022 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0024 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0035 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0002 | 0/0 | 24 | 0 | 0 | 24 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0033 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0008 | 1/0 | 10 | 8 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0010 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0002t0004g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0002t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0002t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0002t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0004t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| a0001c0006t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | FIN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02155 | hp1 | a0001 | c0004 | t0002 | g0139 | EAS | CDX | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0174 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0148 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0177 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0159 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0054 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03710 | hp2 | a0001 | c0006 | t0001 | g0169 | SAS | PJL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0164 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0170 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0175 | AFR | LWK | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | LWK | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | YRI | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | YRI | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ASW | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0176 | AFR | MSL | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | USA | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | LWK | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0022 | REF | REF | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0008 | REF | REF | PCID2_chr13_113172536_113213669 | PCID2 | chr13 | 113172536 | 113213669 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113178264 | C | T | 1 | a0001c0004 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.1134G>A | p.Ser378Ser | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 14/14 | 1169/1897 | 1134/1200 | 378/399 | chr13 | 113178264 | |||
| chr13:113190934 | C | A | 1 | a0001c0005 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.405G>T | p.Gly135Gly | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/14 | 440/1897 | 405/1200 | 135/399 | chr13 | 113190934 | |||
| chr13:113195116 | A | C | 1 | a0001c0003 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.318T>G | p.Pro106Pro | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/14 | 353/1897 | 318/1200 | 106/399 | chr13 | 113195116 | |||
| chr13:113197234 | A | G | 1 | a0001c0002 | 7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.210T>C | p.Tyr70Tyr | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/14 | 245/1897 | 210/1200 | 70/399 | chr13 | 113197234 | |||
| chr13:113198238 | T | C | 1 | a0001c0006 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.153A>G | p.Gln51Gln | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/14 | 188/1897 | 153/1200 | 51/399 | chr13 | 113198238 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113177592 | T | A | 2 | a0001c0001t0002 a0001c0004t0002 |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*606A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 14/14 | 606 | chr13 | 113177592 | ||||||
| chr13:113177649 | T | C | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(5): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*549A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 14/14 | 549 | chr13 | 113177649 | ||||||
| chr13:113177843 | G | A | 1 | a0001c0002t0004 | 7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*355C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 14/14 | 355 | chr13 | 113177843 | ||||||
| chr13:113177873 | C | T | 1 | a0001c0001t0005 | 4 | HG02602.hp2 HG03017.hp2 HG03927.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*325G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 14/14 | 325 | chr13 | 113177873 | ||||||
| chr13:113177913 | C | T | 1 | a0001c0002t0004 | 7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 14/14 | 285 | chr13 | 113177913 | ||||||
| chr13:113178125 | C | T | 1 | a0001c0001t0006 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*73G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 14/14 | 73 | chr13 | 113178125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113178319 | A | C | 1 | a0001c0001t0003g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1111-32T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178319 | |||||||
| chr13:113178350 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0082 a0001c0001t0001g0089 |
5 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-63C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178350 | |||||||
| chr13:113178411 | G | A | 1 | a0001c0001t0001g0038 | 2 | NA18963.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1111-124C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178411 | |||||||
| chr13:113178484 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1111-197G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178484 | |||||||
| chr13:113178544 | C | T | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1111-257G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178544 | |||||||
| chr13:113178718 | G | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+248C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178718 | |||||||
| chr13:113178758 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1110+208G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178758 | |||||||
| chr13:113178839 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1110+127T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178839 | |||||||
| chr13:113178907 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(40): Show |
92 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1110+59T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 13/13 | chr13 | 113178907 | |||||||
| chr13:113179174 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.987-85C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179174 | |||||||
| chr13:113179185 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.987-96C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179185 | |||||||
| chr13:113179347 | A | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0106 |
2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.987-258T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179347 | |||||||
| chr13:113179413 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.987-324G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179413 | |||||||
| chr13:113179514 | G | GT | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.986+402dupA | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179514 | |||||||
| chr13:113179530 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.986+387G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179530 | |||||||
| chr13:113179618 | T | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.986+299A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179618 | |||||||
| chr13:113179643 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.986+274G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179643 | |||||||
| chr13:113179644 | G | A | 1 | a0001c0001t0001g0026 | 3 | HG00544.hp1 HG00673.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.986+273C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179644 | |||||||
| chr13:113179704 | C | T | 3 | a0001c0002t0004g0175 a0001c0002t0004g0176 a0001c0002t0004g0177 |
3 | HG02886.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.986+213G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179704 | |||||||
| chr13:113179753 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0121 a0001c0001t0001g0122 |
5 | NA18964.hp2 NA18982.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.986+164G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179753 | |||||||
| chr13:113179902 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.986+15G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 12/13 | chr13 | 113179902 | |||||||
| chr13:113180051 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.861-9C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 11/13 | chr13 | 113180051 | |||||||
| chr13:113180478 | G | A | 2 | a0001c0002t0004g0025 a0001c0002t0004g0054 |
4 | HG02280.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-247C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 10/13 | chr13 | 113180478 | |||||||
| chr13:113180849 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.786+281G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 10/13 | chr13 | 113180849 | |||||||
| chr13:113181110 | A | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0030 others(13): Show |
33 | HG00597.hp2 HG01891.hp1 HG02165.hp1 others(30): Show |
intron_variant | MODIFIER | c.786+20T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 10/13 | chr13 | 113181110 | |||||||
| chr13:113181400 | A | G | 1 | a0001c0001t0003g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.686-170T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113181400 | |||||||
| chr13:113181472 | A | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-242T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113181472 | |||||||
| chr13:113181615 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.686-385T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113181615 | |||||||
| chr13:113181653 | G | A | 2 | a0001c0001t0003g0037 a0001c0001t0003g0069 |
3 | HG01243.hp2 HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.686-423C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113181653 | |||||||
| chr13:113181818 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0156 |
4 | NA18947.hp1 NA18965.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-588T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113181818 | |||||||
| chr13:113181863 | C | T | 1 | a0001c0001t0003g0061 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.686-633G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113181863 | |||||||
| chr13:113181864 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.686-634C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113181864 | |||||||
| chr13:113181971 | TG | T | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-742delC | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113181971 | |||||||
| chr13:113182205 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.686-975G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182205 | |||||||
| chr13:113182244 | T | C | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.686-1014A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182244 | |||||||
| chr13:113182517 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.686-1287A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182517 | |||||||
| chr13:113182531 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.686-1301A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182531 | |||||||
| chr13:113182539 | C | T | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-1309G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182539 | |||||||
| chr13:113182574 | A | G | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.686-1344T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182574 | |||||||
| chr13:113182601 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.686-1371C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182601 | |||||||
| chr13:113182681 | T | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-1451A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182681 | |||||||
| chr13:113182684 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.686-1454A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113182684 | |||||||
| chr13:113183026 | G | A | 1 | a0001c0001t0001g0052 | 2 | NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.685+1320C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183026 | |||||||
| chr13:113183132 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.685+1214C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183132 | |||||||
| chr13:113183194 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.685+1152G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183194 | |||||||
| chr13:113183233 | C | T | 2 | a0001c0002t0004g0025 a0001c0002t0004g0054 |
4 | HG02280.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+1113G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183233 | |||||||
| chr13:113183427 | T | G | 1 | a0001c0001t0005g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.685+919A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183427 | |||||||
| chr13:113183557 | C | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.685+789G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183557 | |||||||
| chr13:113183701 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.685+645T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183701 | |||||||
| chr13:113183721 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.685+625T>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183721 | |||||||
| chr13:113183731 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0153 |
5 | HG00597.hp1 HG02083.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.685+615C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183731 | |||||||
| chr13:113183787 | CA | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.685+558delT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183787 | |||||||
| chr13:113183808 | T | C | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.685+538A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183808 | |||||||
| chr13:113183929 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.685+417C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183929 | |||||||
| chr13:113183988 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.685+358C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113183988 | |||||||
| chr13:113184162 | A | G | 6 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(3): Show |
8 | HG02280.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.685+184T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113184162 | |||||||
| chr13:113184222 | T | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.685+124A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113184222 | |||||||
| chr13:113184277 | T | C | 1 | a0001c0001t0006g0135 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.685+69A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113184277 | |||||||
| chr13:113184330 | A | C | 1 | a0001c0001t0003g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.685+16T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 9/13 | chr13 | 113184330 | |||||||
| chr13:113184517 | T | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-30A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113184517 | |||||||
| chr13:113184537 | G | A | 1 | a0001c0006t0001g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.544-50C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113184537 | |||||||
| chr13:113184714 | G | C | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.544-227C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113184714 | |||||||
| chr13:113184814 | C | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0030 others(13): Show |
33 | HG00597.hp2 HG01891.hp1 HG02165.hp1 others(30): Show |
intron_variant | MODIFIER | c.544-327G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113184814 | |||||||
| chr13:113184814 | C | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-327G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113184814 | |||||||
| chr13:113184879 | TCAGGGGG others(48): Show |
T | 1 | a0001c0001t0003g0056 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.544-447_544-393del others(55): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113184879 | |||||||
| chr13:113184894 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.544-407G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113184894 | |||||||
| chr13:113184908 | G | C | 1 | a0001c0001t0001g0030 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.544-421C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113184908 | |||||||
| chr13:113185052 | T | G | 1 | a0001c0001t0003g0064 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.543+433A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113185052 | |||||||
| chr13:113185219 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.543+266A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113185219 | |||||||
| chr13:113185346 | T | A | 1 | a0001c0001t0003g0063 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.543+139A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113185346 | |||||||
| chr13:113185348 | T | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+137A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113185348 | |||||||
| chr13:113185433 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
33 | HG00733.hp2 HG01081.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.543+52G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113185433 | |||||||
| chr13:113185459 | CAGAA | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+22_543+25delTT others(2): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113185459 | |||||||
| chr13:113185474 | CAGA | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
splice_region_variant&intron_variant | LOW | c.543+8_543+10delTCT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 8/13 | chr13 | 113185474 | |||||||
| chr13:113185584 | A | T | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.468-24T>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185584 | |||||||
| chr13:113185606 | T | G | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.468-46A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185606 | |||||||
| chr13:113185614 | A | G | 1 | a0001c0001t0005g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.468-54T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185614 | |||||||
| chr13:113185691 | TATTC | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0048 others(3): Show |
22 | HG00733.hp1 HG00735.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.468-135_468-132del others(4): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185691 | |||||||
| chr13:113185770 | G | A | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.468-210C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185770 | |||||||
| chr13:113185779 | C | A | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.468-219G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185779 | |||||||
| chr13:113185866 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.468-306T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185866 | |||||||
| chr13:113185885 | C | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.468-325G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185885 | |||||||
| chr13:113185975 | C | T | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.468-415G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113185975 | |||||||
| chr13:113186027 | CAAAAACA others(1): Show |
C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.468-475_468-468del others(8): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186027 | |||||||
| chr13:113186196 | TG | T | 3 | a0001c0001t0003g0064 a0001c0001t0003g0134 a0001c0001t0006g0135 |
3 | HG01243.hp1 HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.468-637delC | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186196 | |||||||
| chr13:113186337 | A | C | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.468-777T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186337 | |||||||
| chr13:113186431 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0132 |
4 | HG00438.hp2 NA18949.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.468-871C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186431 | |||||||
| chr13:113186508 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0048 others(3): Show |
22 | HG00733.hp1 HG00735.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.468-948G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186508 | |||||||
| chr13:113186509 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.468-949C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186509 | |||||||
| chr13:113186548 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.468-988C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186548 | |||||||
| chr13:113186587 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(40): Show |
92 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.468-1027C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186587 | |||||||
| chr13:113186764 | C | CG | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.468-1205dupC | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186764 | |||||||
| chr13:113186765 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0075 |
3 | HG00408.hp2 NA18963.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.468-1205C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186765 | |||||||
| chr13:113186860 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.468-1300C>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186860 | |||||||
| chr13:113186953 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.468-1393T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113186953 | |||||||
| chr13:113187068 | A | ATGACCTC others(35): Show |
1 | a0001c0001t0002g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.468-1550_468-1509d others(44): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187068 | |||||||
| chr13:113187199 | C | T | 2 | a0001c0001t0003g0064 a0001c0001t0003g0065 |
2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.468-1639G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187199 | |||||||
| chr13:113187310 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.468-1750C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187310 | |||||||
| chr13:113187384 | C | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.468-1824G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187384 | |||||||
| chr13:113187398 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.468-1838G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187398 | |||||||
| chr13:113187430 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.468-1870A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187430 | |||||||
| chr13:113187438 | C | G | 3 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 |
5 | HG02280.hp1 HG03195.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.468-1878G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187438 | |||||||
| chr13:113187482 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.468-1922C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187482 | |||||||
| chr13:113187513 | G | C | 1 | a0001c0001t0001g0044 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.468-1953C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187513 | |||||||
| chr13:113187685 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG01074.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.468-2125C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187685 | |||||||
| chr13:113187795 | C | T | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.468-2235G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187795 | |||||||
| chr13:113187917 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.468-2357G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187917 | |||||||
| chr13:113187918 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.468-2358C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187918 | |||||||
| chr13:113187932 | T | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.468-2372A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187932 | |||||||
| chr13:113187986 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.468-2426T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187986 | |||||||
| chr13:113187997 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.468-2437C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113187997 | |||||||
| chr13:113188011 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 |
6 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.468-2451C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188011 | |||||||
| chr13:113188044 | C | A | 1 | a0001c0001t0003g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.468-2484G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188044 | |||||||
| chr13:113188168 | C | G | 1 | a0001c0001t0002g0033 | 3 | HG00642.hp1 HG01346.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.468-2608G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188168 | |||||||
| chr13:113188213 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.468-2653C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188213 | |||||||
| chr13:113188248 | G | GA | 12 | a0001c0001t0003g0010 a0001c0001t0003g0036 a0001c0001t0003g0037 others(9): Show |
19 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.467+2623dupT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188248 | |||||||
| chr13:113188365 | T | C | 1 | a0001c0001t0003g0064 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.467+2507A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188365 | |||||||
| chr13:113188473 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.467+2399A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188473 | |||||||
| chr13:113188525 | G | T | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+2347C>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188525 | |||||||
| chr13:113188662 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.467+2210A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188662 | |||||||
| chr13:113188827 | C | A | 1 | a0001c0001t0005g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.467+2045G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188827 | |||||||
| chr13:113188839 | T | C | 1 | a0001c0001t0001g0013 | 5 | HG00642.hp2 HG01099.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.467+2033A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113188839 | |||||||
| chr13:113189093 | C | T | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467+1779G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189093 | |||||||
| chr13:113189113 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(44): Show |
97 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.467+1759C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189113 | |||||||
| chr13:113189231 | C | T | 1 | a0001c0001t0005g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.467+1641G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189231 | |||||||
| chr13:113189318 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.467+1554G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189318 | |||||||
| chr13:113189452 | G | A | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+1420C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189452 | |||||||
| chr13:113189502 | T | G | 1 | a0001c0001t0001g0039 | 2 | NA18966.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.467+1370A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189502 | |||||||
| chr13:113189628 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.467+1244G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189628 | |||||||
| chr13:113189629 | G | A | 1 | a0001c0001t0001g0051 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.467+1243C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189629 | |||||||
| chr13:113189666 | A | C | 2 | a0001c0002t0004g0025 a0001c0002t0004g0054 |
4 | HG02280.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.467+1206T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189666 | |||||||
| chr13:113189719 | G | GA | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.467+1152dupT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189719 | |||||||
| chr13:113189719 | G | GAA | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(46): Show |
102 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.467+1151_467+1152d others(4): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189719 | |||||||
| chr13:113189804 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.467+1068G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189804 | |||||||
| chr13:113189853 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.467+1019A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189853 | |||||||
| chr13:113189866 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.467+1006A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113189866 | |||||||
| chr13:113190016 | CT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.467+855delA | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190016 | |||||||
| chr13:113190023 | C | CA | 4 | a0001c0001t0001g0022 a0001c0001t0001g0079 a0001c0001t0001g0109 others(1): Show |
6 | HG01081.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.467+848dupT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190023 | |||||||
| chr13:113190045 | A | T | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.467+827T>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190045 | |||||||
| chr13:113190140 | C | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0158 a0001c0001t0001g0172 others(1): Show |
5 | HG00741.hp2 HG01346.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.467+732G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190140 | |||||||
| chr13:113190171 | T | C | 1 | a0001c0001t0005g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.467+701A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190171 | |||||||
| chr13:113190197 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.467+675G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190197 | |||||||
| chr13:113190228 | A | AT | 3 | a0001c0001t0001g0016 a0001c0001t0001g0085 a0001c0001t0001g0086 |
7 | HG01081.hp1 HG01109.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.467+643dupA | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190228 | |||||||
| chr13:113190230 | T | TA | 16 | a0001c0001t0001g0146 a0001c0001t0001g0155 a0001c0001t0001g0165 others(13): Show |
45 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.467+641dupT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190230 | |||||||
| chr13:113190230 | TAA | T | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+640_467+641del others(2): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190230 | |||||||
| chr13:113190231 | A | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.467+641T>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190231 | |||||||
| chr13:113190232 | A | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0115 |
2 | HG01070.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.467+640T>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190232 | |||||||
| chr13:113190236 | A | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+636T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190236 | |||||||
| chr13:113190248 | C | A | 1 | a0001c0001t0001g0038 | 2 | NA18963.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.467+624G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190248 | |||||||
| chr13:113190356 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.467+516T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190356 | |||||||
| chr13:113190450 | A | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+422T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190450 | |||||||
| chr13:113190628 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.467+244A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190628 | |||||||
| chr13:113190742 | T | C | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.467+130A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190742 | |||||||
| chr13:113190745 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.467+127A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190745 | |||||||
| chr13:113190855 | C | T | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.467+17G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 7/13 | chr13 | 113190855 | |||||||
| chr13:113191057 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.364-82T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191057 | |||||||
| chr13:113191165 | T | G | 1 | a0001c0001t0005g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.364-190A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191165 | |||||||
| chr13:113191181 | A | T | 6 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(3): Show |
8 | HG02280.hp1 HG02809.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-206T>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191181 | |||||||
| chr13:113191183 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.364-208T>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191183 | |||||||
| chr13:113191204 | C | CT | 17 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(14): Show |
48 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.364-230dupA | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191204 | |||||||
| chr13:113191292 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0089 |
2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-317G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191292 | |||||||
| chr13:113191293 | G | A | 1 | a0001c0001t0001g0029 | 3 | HG02074.hp1 NA19006.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.364-318C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191293 | |||||||
| chr13:113191606 | T | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG01109.hp2 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.364-631A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191606 | |||||||
| chr13:113191906 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.364-931T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113191906 | |||||||
| chr13:113192116 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.364-1141C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113192116 | |||||||
| chr13:113192300 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.364-1325G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113192300 | |||||||
| chr13:113192379 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.364-1404G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113192379 | |||||||
| chr13:113192417 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.364-1442C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113192417 | |||||||
| chr13:113192462 | A | AAACT | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.364-1488_364-1487i others(6): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113192462 | |||||||
| chr13:113192524 | A | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.364-1549T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113192524 | |||||||
| chr13:113192675 | G | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(46): Show |
113 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.364-1700C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113192675 | |||||||
| chr13:113192742 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0101 a0001c0001t0001g0105 others(1): Show |
6 | HG02559.hp2 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1767A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113192742 | |||||||
| chr13:113193017 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.364-2042G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193017 | |||||||
| chr13:113193166 | A | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+1905T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193166 | |||||||
| chr13:113193261 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0102 |
5 | HG02451.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1810A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193261 | |||||||
| chr13:113193277 | TA | T | 7 | a0001c0001t0001g0081 a0001c0001t0001g0157 a0001c0002t0004g0025 others(4): Show |
9 | HG02280.hp1 HG02698.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+1793delT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193277 | |||||||
| chr13:113193285 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.363+1786T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193285 | |||||||
| chr13:113193387 | G | C | 1 | a0001c0001t0003g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.363+1684C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193387 | |||||||
| chr13:113193448 | G | T | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+1623C>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193448 | |||||||
| chr13:113193524 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0073 |
2 | HG03831.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.363+1547T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193524 | |||||||
| chr13:113193663 | G | A | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.363+1408C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193663 | |||||||
| chr13:113193697 | T | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+1374A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193697 | |||||||
| chr13:113193784 | G | A | 1 | a0001c0001t0003g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.363+1287C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193784 | |||||||
| chr13:113193821 | T | C | 10 | a0001c0001t0003g0010 a0001c0001t0003g0036 a0001c0001t0003g0061 others(7): Show |
18 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.363+1250A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193821 | |||||||
| chr13:113193934 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.363+1137C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193934 | |||||||
| chr13:113193979 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.363+1092G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193979 | |||||||
| chr13:113193990 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.363+1081C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113193990 | |||||||
| chr13:113194073 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(41): Show |
93 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.363+998C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194073 | |||||||
| chr13:113194109 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.363+962G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194109 | |||||||
| chr13:113194144 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG01167.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.363+927C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194144 | |||||||
| chr13:113194179 | T | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+892A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194179 | |||||||
| chr13:113194208 | G | C | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.363+863C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194208 | |||||||
| chr13:113194250 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.363+821A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194250 | |||||||
| chr13:113194254 | G | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0121 a0001c0001t0001g0122 |
5 | NA18964.hp2 NA18982.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+817C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194254 | |||||||
| chr13:113194588 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.363+483T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194588 | |||||||
| chr13:113194742 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.363+329G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194742 | |||||||
| chr13:113194799 | T | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+272A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194799 | |||||||
| chr13:113194818 | C | A | 1 | a0001c0002t0004g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363+253G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194818 | |||||||
| chr13:113194863 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0093 a0001c0001t0001g0094 |
6 | HG01070.hp2 HG01071.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+208G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194863 | |||||||
| chr13:113194897 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.363+174G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 6/13 | chr13 | 113194897 | |||||||
| chr13:113195184 | A | G | 1 | a0001c0003t0001g0071 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.309-59T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195184 | |||||||
| chr13:113195204 | C | T | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.309-79G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195204 | |||||||
| chr13:113195579 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.309-454T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195579 | |||||||
| chr13:113195618 | G | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.309-493C>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195618 | |||||||
| chr13:113195624 | G | A | 2 | a0001c0002t0004g0025 a0001c0002t0004g0054 |
4 | HG02280.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.309-499C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195624 | |||||||
| chr13:113195666 | C | CA | 9 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0002g0141 others(6): Show |
11 | HG01884.hp2 HG02056.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.308+514dupT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195666 | |||||||
| chr13:113195683 | A | T | 1 | a0001c0001t0001g0047 | 2 | HG00558.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.308+498T>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195683 | |||||||
| chr13:113195691 | G | A | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.308+490C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195691 | |||||||
| chr13:113195837 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.308+344G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195837 | |||||||
| chr13:113195860 | C | G | 1 | a0001c0002t0004g0176 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.308+321G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 5/13 | chr13 | 113195860 | |||||||
| chr13:113196316 | A | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.267-94T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113196316 | |||||||
| chr13:113196320 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0121 a0001c0001t0001g0122 |
5 | NA18964.hp2 NA18982.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.267-98G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113196320 | |||||||
| chr13:113196324 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.267-102A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113196324 | |||||||
| chr13:113196394 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.267-172G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113196394 | |||||||
| chr13:113196723 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.266+455C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113196723 | |||||||
| chr13:113196788 | A | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+390T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113196788 | |||||||
| chr13:113196885 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.266+293C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113196885 | |||||||
| chr13:113197002 | A | G | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.266+176T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113197002 | |||||||
| chr13:113197105 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.266+73G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 4/13 | chr13 | 113197105 | |||||||
| chr13:113197319 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(40): Show |
92 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.201-76T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113197319 | |||||||
| chr13:113197494 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.201-251A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113197494 | |||||||
| chr13:113197560 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(40): Show |
92 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.201-317A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113197560 | |||||||
| chr13:113197588 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0168 |
2 | NA19056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.201-345C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113197588 | |||||||
| chr13:113197709 | C | A | 1 | a0001c0001t0003g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.201-466G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113197709 | |||||||
| chr13:113197869 | A | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.200+322T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113197869 | |||||||
| chr13:113197947 | A | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.200+244T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113197947 | |||||||
| chr13:113197968 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.200+223T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113197968 | |||||||
| chr13:113198012 | T | TTTTTTTA | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.200+178_200+179ins others(7): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113198012 | |||||||
| chr13:113198111 | C | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.200+80G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 3/13 | chr13 | 113198111 | |||||||
| chr13:113198315 | G | A | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127-51C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198315 | |||||||
| chr13:113198465 | G | A | 1 | a0001c0001t0001g0052 | 2 | NA18945.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.127-201C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198465 | |||||||
| chr13:113198628 | A | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-364T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198628 | |||||||
| chr13:113198645 | T | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-381A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198645 | |||||||
| chr13:113198704 | C | CATAAATA others(5): Show |
2 | a0001c0002t0004g0025 a0001c0002t0004g0054 |
4 | HG02280.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-452_127-441dup others(12): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198704 | |||||||
| chr13:113198704 | C | CATAAATA others(9): Show |
1 | a0001c0002t0004g0175 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-456_127-441dup others(16): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198704 | |||||||
| chr13:113198721 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(17): Show |
63 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.127-457T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198721 | |||||||
| chr13:113198835 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.127-571A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198835 | |||||||
| chr13:113198846 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.127-582C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113198846 | |||||||
| chr13:113199087 | A | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-823T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199087 | |||||||
| chr13:113199093 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.127-829G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199093 | |||||||
| chr13:113199264 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-1000G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199264 | |||||||
| chr13:113199423 | G | A | 1 | a0001c0002t0004g0054 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.126+1004C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199423 | |||||||
| chr13:113199583 | T | C | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+844A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199583 | |||||||
| chr13:113199741 | C | T | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.126+686G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199741 | |||||||
| chr13:113199824 | T | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0054 a0001c0002t0004g0175 others(2): Show |
7 | HG02280.hp1 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+603A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199824 | |||||||
| chr13:113199841 | G | A | 1 | a0001c0001t0003g0059 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.126+586C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199841 | |||||||
| chr13:113199978 | T | C | 12 | a0001c0001t0003g0010 a0001c0001t0003g0036 a0001c0001t0003g0037 others(9): Show |
19 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+449A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113199978 | |||||||
| chr13:113200159 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0021 |
10 | HG00609.hp2 HG00673.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+268G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200159 | |||||||
| chr13:113200246 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(45): Show |
142 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.126+181C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200246 | |||||||
| chr13:113200258 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.126+169T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200258 | |||||||
| chr13:113200286 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.126+141A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200286 | |||||||
| chr13:113200310 | T | G | 1 | a0001c0001t0002g0143 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.126+117A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200310 | |||||||
| chr13:113200316 | A | G | 3 | a0001c0001t0003g0037 a0001c0001t0003g0068 a0001c0001t0003g0069 |
4 | HG01243.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+111T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200316 | |||||||
| chr13:113200328 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+99T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200328 | |||||||
| chr13:113200369 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.126+58C>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200369 | |||||||
| chr13:113200370 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.126+57T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200370 | |||||||
| chr13:113200401 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.126+26G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 2/13 | chr13 | 113200401 | |||||||
| chr13:113200566 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.37-50C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200566 | |||||||
| chr13:113200651 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0115 |
15 | HG00733.hp2 HG01106.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.37-135A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200651 | |||||||
| chr13:113200681 | GGTAAACA others(85): Show |
G | 4 | a0001c0001t0003g0178 a0001c0002t0004g0175 a0001c0002t0004g0176 others(1): Show |
4 | HG01884.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-257_37-166delGA others(90): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200681 | |||||||
| chr13:113200696 | C | CT | 12 | a0001c0001t0001g0012 a0001c0001t0001g0091 a0001c0001t0001g0097 others(9): Show |
12 | HG01175.hp1 HG02145.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.37-181dupA | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200696 | |||||||
| chr13:113200696 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.37-180G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200696 | |||||||
| chr13:113200696 | CT | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0100 others(3): Show |
7 | HG01255.hp1 HG02818.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.37-181delA | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200696 | |||||||
| chr13:113200740 | C | A | 1 | a0001c0001t0001g0014 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.37-224G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200740 | |||||||
| chr13:113200767 | C | G | 12 | a0001c0001t0003g0010 a0001c0001t0003g0036 a0001c0001t0003g0037 others(9): Show |
19 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.37-251G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200767 | |||||||
| chr13:113200858 | C | T | 4 | a0001c0001t0003g0178 a0001c0002t0004g0175 a0001c0002t0004g0176 others(1): Show |
4 | HG01884.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-342G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200858 | |||||||
| chr13:113200961 | C | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(11): Show |
43 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.37-445G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113200961 | |||||||
| chr13:113201048 | T | A | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-532A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201048 | |||||||
| chr13:113201146 | T | TA | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-631dupT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201146 | |||||||
| chr13:113201199 | G | A | 4 | a0001c0001t0003g0178 a0001c0002t0004g0175 a0001c0002t0004g0176 others(1): Show |
4 | HG01884.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.37-683C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201199 | |||||||
| chr13:113201247 | G | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.37-731C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201247 | |||||||
| chr13:113201280 | G | GA | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-765dupT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201280 | |||||||
| chr13:113201345 | T | G | 1 | a0001c0001t0003g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.37-829A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201345 | |||||||
| chr13:113201348 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.37-832C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201348 | |||||||
| chr13:113201357 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.37-841C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201357 | |||||||
| chr13:113201444 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0114 others(2): Show |
17 | HG00733.hp2 HG01106.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.37-928G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201444 | |||||||
| chr13:113201688 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.37-1172G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201688 | |||||||
| chr13:113201700 | T | C | 1 | a0001c0002t0004g0177 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.37-1184A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201700 | |||||||
| chr13:113201815 | C | CA | 17 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0029 others(14): Show |
28 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.37-1300dupT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201815 | |||||||
| chr13:113201815 | C | CAA | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-1301_37-1300dup others(2): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201815 | |||||||
| chr13:113201815 | CA | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
8 | HG01243.hp1 HG01952.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.37-1300delT | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201815 | |||||||
| chr13:113201815 | CAA | C | 13 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(10): Show |
42 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.37-1301_37-1300del others(2): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201815 | |||||||
| chr13:113201839 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.37-1323T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201839 | |||||||
| chr13:113201975 | G | C | 1 | a0001c0001t0003g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.37-1459C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201975 | |||||||
| chr13:113201999 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.37-1483A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113201999 | |||||||
| chr13:113202237 | A | G | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-1721T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202237 | |||||||
| chr13:113202263 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.37-1747A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202263 | |||||||
| chr13:113202355 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG01109.hp2 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.37-1839T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202355 | |||||||
| chr13:113202485 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.37-1969C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202485 | |||||||
| chr13:113202577 | C | G | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-2061G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202577 | |||||||
| chr13:113202645 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0053 others(3): Show |
11 | HG00544.hp2 HG00597.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.37-2129G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202645 | |||||||
| chr13:113202646 | G | C | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-2130C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202646 | |||||||
| chr13:113202664 | G | A | 1 | a0001c0001t0001g0024 | 4 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.37-2148C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202664 | |||||||
| chr13:113202729 | T | C | 1 | a0001c0001t0003g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.37-2213A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202729 | |||||||
| chr13:113202796 | G | A | 1 | a0001c0001t0003g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.37-2280C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202796 | |||||||
| chr13:113202983 | C | T | 1 | a0001c0005t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.37-2467G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202983 | |||||||
| chr13:113202994 | A | C | 5 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(2): Show |
7 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.37-2478T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202994 | |||||||
| chr13:113202995 | C | A | 5 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(2): Show |
7 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.37-2479G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113202995 | |||||||
| chr13:113203319 | C | G | 1 | a0001c0001t0003g0066 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.37-2803G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203319 | |||||||
| chr13:113203373 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0030 others(13): Show |
33 | HG00597.hp2 HG01891.hp1 HG02165.hp1 others(30): Show |
intron_variant | MODIFIER | c.37-2857G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203373 | |||||||
| chr13:113203450 | G | A | 1 | a0001c0001t0001g0030 | 3 | NA18950.hp2 NA18970.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.37-2934C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203450 | |||||||
| chr13:113203525 | A | G | 1 | a0001c0001t0003g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.37-3009T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203525 | |||||||
| chr13:113203566 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.37-3050A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203566 | |||||||
| chr13:113203586 | A | G | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.37-3070T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203586 | |||||||
| chr13:113203678 | C | G | 1 | a0001c0001t0001g0045 | 2 | HG01074.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.37-3162G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203678 | |||||||
| chr13:113203860 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.37-3344C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203860 | |||||||
| chr13:113203913 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.37-3397C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113203913 | |||||||
| chr13:113204007 | G | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.37-3491C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204007 | |||||||
| chr13:113204394 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0151 |
14 | HG01099.hp2 HG01261.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.37-3878T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204394 | |||||||
| chr13:113204403 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.37-3887C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204403 | |||||||
| chr13:113204432 | C | T | 2 | a0001c0001t0003g0064 a0001c0001t0003g0065 |
2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.37-3916G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204432 | |||||||
| chr13:113204475 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(14): Show |
58 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.37-3959G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204475 | |||||||
| chr13:113204554 | T | A | 12 | a0001c0001t0003g0010 a0001c0001t0003g0036 a0001c0001t0003g0037 others(9): Show |
19 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.37-4038A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204554 | |||||||
| chr13:113204596 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.36+4003C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204596 | |||||||
| chr13:113204597 | G | A | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+4002C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204597 | |||||||
| chr13:113204714 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.36+3885T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204714 | |||||||
| chr13:113204882 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.36+3717G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204882 | |||||||
| chr13:113204911 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.36+3688C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113204911 | |||||||
| chr13:113205095 | T | C | 2 | a0001c0001t0003g0134 a0001c0001t0006g0135 |
2 | HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.36+3504A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113205095 | |||||||
| chr13:113205344 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.36+3255A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113205344 | |||||||
| chr13:113205408 | C | A | 3 | a0001c0001t0003g0037 a0001c0001t0003g0068 a0001c0001t0003g0069 |
4 | HG01243.hp2 HG02258.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+3191G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113205408 | |||||||
| chr13:113205569 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.36+3030G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113205569 | |||||||
| chr13:113205802 | C | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.36+2797G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113205802 | |||||||
| chr13:113205807 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(40): Show |
92 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.36+2792C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113205807 | |||||||
| chr13:113205860 | G | C | 2 | a0001c0002t0004g0176 a0001c0002t0004g0177 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.36+2739C>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113205860 | |||||||
| chr13:113205987 | G | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
28 | HG00733.hp2 HG01081.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.36+2612C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113205987 | |||||||
| chr13:113206044 | C | T | 1 | a0001c0001t0001g0021 | 4 | NA18945.hp1 NA18973.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.36+2555G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206044 | |||||||
| chr13:113206098 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.36+2501C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206098 | |||||||
| chr13:113206105 | T | C | 1 | a0001c0001t0003g0036 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.36+2494A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206105 | |||||||
| chr13:113206258 | C | A | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+2341G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206258 | |||||||
| chr13:113206273 | G | T | 5 | a0001c0001t0003g0010 a0001c0001t0003g0036 a0001c0001t0003g0061 others(2): Show |
11 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.36+2326C>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206273 | |||||||
| chr13:113206296 | T | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
4 | HG00099.hp2 HG01074.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+2303A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206296 | |||||||
| chr13:113206329 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.36+2270C>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206329 | |||||||
| chr13:113206426 | G | A | 1 | a0001c0001t0003g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.36+2173C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206426 | |||||||
| chr13:113206586 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0021 others(19): Show |
55 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.36+2013C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206586 | |||||||
| chr13:113206695 | T | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0033 others(9): Show |
41 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.36+1904A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206695 | |||||||
| chr13:113206748 | G | A | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+1851C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206748 | |||||||
| chr13:113206762 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.36+1837G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206762 | |||||||
| chr13:113206835 | A | C | 1 | a0001c0001t0001g0048 | 2 | HG01257.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.36+1764T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206835 | |||||||
| chr13:113206919 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0180 |
3 | HG00544.hp2 NA18942.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.36+1680C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206919 | |||||||
| chr13:113206954 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0145 others(1): Show |
7 | HG00558.hp2 HG01975.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.36+1645G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113206954 | |||||||
| chr13:113207071 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.36+1528G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207071 | |||||||
| chr13:113207088 | T | C | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+1511A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207088 | |||||||
| chr13:113207090 | T | A | 1 | a0001c0001t0003g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.36+1509A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207090 | |||||||
| chr13:113207127 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(93): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.36+1472G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207127 | |||||||
| chr13:113207292 | T | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(42): Show |
94 | HG00280.hp2 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.36+1307A>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207292 | |||||||
| chr13:113207385 | C | A | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+1214G>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207385 | |||||||
| chr13:113207438 | G | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.36+1161C>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207438 | |||||||
| chr13:113207442 | T | C | 1 | a0001c0001t0005g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.36+1157A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207442 | |||||||
| chr13:113207462 | T | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.36+1137A>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207462 | |||||||
| chr13:113207502 | C | T | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+1097G>A | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207502 | |||||||
| chr13:113207750 | A | G | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+849T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207750 | |||||||
| chr13:113207907 | A | C | 1 | a0001c0001t0003g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.36+692T>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207907 | |||||||
| chr13:113207907 | A | G | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+692T>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113207907 | |||||||
| chr13:113208146 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.36+453C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113208146 | |||||||
| chr13:113208233 | ACAGCACC others(16): Show |
A | 6 | a0001c0001t0003g0178 a0001c0002t0004g0025 a0001c0002t0004g0054 others(3): Show |
8 | HG01884.hp2 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.36+343_36+365delAG others(21): Show |
PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113208233 | |||||||
| chr13:113208411 | G | A | 2 | a0001c0002t0004g0025 a0001c0002t0004g0054 |
4 | HG02280.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+188C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113208411 | |||||||
| chr13:113208451 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.36+148C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113208451 | |||||||
| chr13:113208487 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.36+112C>T | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113208487 | |||||||
| chr13:113208588 | C | G | 2 | a0001c0002t0004g0025 a0001c0002t0004g0054 |
4 | HG02280.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.36+11G>C | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113208588 | |||||||
| chr13:113208589 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.36+10A>G | PCID2 | ENSG00000126226.22 | transcript | ENST00000337344.9 | protein_coding | 1/13 | chr13 | 113208589 |