Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1358 |
| ensemblid | ENSG00000158516.12 |
| hgncid | 2297 |
| symbol | CPA2 |
| name | carboxypeptidase A2 |
| refseq_nuc | NM_001869.3 |
| refseq_prot | NP_001860.2 |
| ensembl_nuc | ENST00000222481.9 |
| ensembl_prot | ENSP00000222481.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 130266863 |
| end | 130289798 |
| strand | + |
| ver | v1.2 |
| region | chr7:130266863-130289798 |
| region5000 | chr7:130261863-130294798 |
| regionname0 | CPA2_chr7_130266863_130289798 |
| regionname5000 | CPA2_chr7_130261863_130294798 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 419 | 382 | 77 | 69 | 170 | 16 | 48 | 127 | CPA2_chr7_130261863_130294798 | CPA2 | MAMRL others(414): Show |
chr7 | 130261863 | 130294798 |
| a0002 | 0/0 | 419 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | MAMRL others(414): Show |
chr7 | 130261863 | 130294798 |
| a0003 | 0/0 | 419 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | CPA2_chr7_130261863_130294798 | CPA2 | MAMRL others(414): Show |
chr7 | 130261863 | 130294798 |
| a0004 | 0/0 | 419 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | MAMRL others(414): Show |
chr7 | 130261863 | 130294798 |
| a0005 | 0/0 | 419 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | MAMRL others(414): Show |
chr7 | 130261863 | 130294798 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1257 | 260 | 47 | 47 | 126 | 9 | 30 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 | ||
| a0001c0002 | 1/0 | 1257 | 117 | 30 | 22 | 40 | 7 | 17 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 | ||
| a0001c0006 | 0/0 | 1257 | 4 | 0 | 0 | 3 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 | ||
| a0001c0009 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 | ||
| a0002c0003 | 0/0 | 1257 | 6 | 6 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 | ||
| a0003c0005 | 0/0 | 1257 | 5 | 0 | 0 | 5 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 | ||
| a0003c0008 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 | ||
| a0004c0004 | 0/0 | 1257 | 5 | 5 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 | ||
| a0005c0007 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | ATGGC others(1252): Show |
chr7 | 130261863 | 130294798 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1330 | 259 | 47 | 46 | 126 | 9 | 30 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0001c0001t0002 | 0/0 | 1330 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0001c0002t0001 | 1/0 | 1330 | 117 | 30 | 22 | 40 | 7 | 17 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0001c0006t0001 | 0/0 | 1330 | 4 | 0 | 0 | 3 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0001c0009t0001 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0002c0003t0001 | 0/0 | 1330 | 6 | 6 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0003c0005t0001 | 0/0 | 1330 | 5 | 0 | 0 | 5 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0003c0008t0001 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0004c0004t0001 | 0/0 | 1330 | 5 | 5 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| a0005c0007t0001 | 0/0 | 1330 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | CTGGA others(1325): Show |
chr7 | 130261863 | 130294798 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 50 | 1 | 6 | 36 | 2 | 5 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0002 | 0/0 | 44 | 0 | 6 | 28 | 0 | 10 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0005 | 0/0 | 18 | 1 | 9 | 4 | 3 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0006 | 0/0 | 17 | 3 | 1 | 11 | 0 | 2 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0008 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0009 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0003 | 1/0 | 33 | 7 | 5 | 12 | 4 | 4 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0004 | 0/0 | 18 | 3 | 3 | 9 | 0 | 3 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0007 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0006t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0001c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0002c0003t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0002c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0003c0005t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0003c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0004c0004t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0004c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| a0005c0007t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0062 | EUR | GBR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | FIN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | FIN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00738 | hp1 | a0005 | c0007 | t0001 | g0033 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0018 | EUR | IBS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0018 | EUR | IBS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01891 | hp1 | a0004 | c0004 | t0001 | g0015 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0077 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02683 | hp2 | a0001 | c0006 | t0001 | g0001 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02922 | hp1 | a0004 | c0004 | t0001 | g0015 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0015 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03098 | hp2 | a0004 | c0004 | t0001 | g0135 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03195 | hp2 | a0004 | c0004 | t0001 | g0015 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0133 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0011 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0081 | SAS | STU | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | YRI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18612 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | CHB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | YRI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18950 | hp1 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18953 | hp1 | a0003 | c0008 | t0001 | g0132 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18971 | hp2 | a0001 | c0006 | t0001 | g0010 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18985 | hp1 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18998 | hp1 | a0001 | c0006 | t0001 | g0010 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18999 | hp1 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19011 | hp2 | a0001 | c0009 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | LWK | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19055 | hp2 | a0001 | c0006 | t0001 | g0010 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19091 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | YRI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | GIH | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | USA | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0011 | AFR | USA | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | LWK | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0130 | REF | REF | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0003 | REF | REF | CPA2_chr7_130261863_130294798 | CPA2 | chr7 | 130261863 | 130294798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130269714 | G | A | 1 | a0004 | 5 | HG01891.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
missense_variant | MODERATE | c.199G>A | p.Val67Ile | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 3/11 | 218/1330 | 199/1260 | 67/419 | chr7 | 130269714 | |||
| chr7:130275176 | A | G | 1 | a0002 | 6 | HG02622.hp1 HG02965.hp2 HG03225.hp2 others(3): Show |
missense_variant | MODERATE | c.514A>G | p.Ile172Val | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/11 | 533/1330 | 514/1260 | 172/419 | chr7 | 130275176 | |||
| chr7:130277838 | C | T | 1 | a0003 | 6 | NA18612.hp2 NA18950.hp1 NA18953.hp1 others(3): Show |
missense_variant | MODERATE | c.709C>T | p.Arg237Trp | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/11 | 728/1330 | 709/1260 | 237/419 | chr7 | 130277838 | |||
| chr7:130289628 | C | A | 1 | a0005 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1141C>A | p.Leu381Met | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 11/11 | 1160/1330 | 1141/1260 | 381/419 | chr7 | 130289628 | |||
| chr7:130289746 | A | G | 1 | a0001 | 1 | HG02293.hp2 | stop_lost | HIGH | c.1259A>G | p.Ter420Trpext*? | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 11/11 | 1278/1330 | 1259/1260 | 420/419 | chr7 | 130289746 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130276675 | T | C | 6 | a0001c0001 a0001c0006 a0002c0003 others(3): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
synonymous_variant | LOW | c.633T>C | p.Asp211Asp | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/11 | 652/1330 | 633/1260 | 211/419 | chr7 | 130276675 | |||
| chr7:130279503 | C | T | 1 | a0001c0006 | 4 | HG02683.hp2 NA18971.hp2 NA18998.hp1 others(1): Show |
synonymous_variant | LOW | c.828C>T | p.His276His | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/11 | 847/1330 | 828/1260 | 276/419 | chr7 | 130279503 | |||
| chr7:130289648 | C | T | 1 | a0001c0009 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.1161C>T | p.Tyr387Tyr | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 11/11 | 1180/1330 | 1161/1260 | 387/419 | chr7 | 130289648 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:130267006 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.71+54G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267006 | |||||||
| chr7:130267075 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
24 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.71+123G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267075 | |||||||
| chr7:130267173 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.71+221C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267173 | |||||||
| chr7:130267202 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.71+250C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267202 | |||||||
| chr7:130267301 | C | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0033 others(19): Show |
45 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.71+349C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267301 | |||||||
| chr7:130267343 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71+391C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267343 | |||||||
| chr7:130267487 | A | G | 2 | a0004c0004t0001g0015 a0004c0004t0001g0135 |
5 | HG01891.hp1 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+535A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267487 | |||||||
| chr7:130267562 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.71+610T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267562 | |||||||
| chr7:130267705 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
24 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.71+753A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267705 | |||||||
| chr7:130267715 | T | A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.71+763T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267715 | |||||||
| chr7:130267756 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.71+804T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267756 | |||||||
| chr7:130267759 | TTCTTTCT others(7): Show |
T | 2 | a0001c0001t0001g0134 a0002c0003t0001g0133 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.71+823_71+836delCT others(12): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267759 | ||||||
| chr7:130267763 | TTCTTTCT others(3): Show |
T | 1 | a0002c0003t0001g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.71+823_71+832delCT others(8): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267763 | ||||||
| chr7:130267767 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.71+815T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267767 | |||||||
| chr7:130267767 | TTCTTTC | T | 2 | a0002c0003t0001g0011 a0002c0003t0001g0047 |
3 | HG02622.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.71+823_71+828delCT others(4): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267767 | ||||||
| chr7:130267769 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.71+817C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267769 | |||||||
| chr7:130267771 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0030 |
2 | HG01109.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.71+819T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267771 | |||||||
| chr7:130267771 | T | TCTCTCTC others(10): Show |
1 | a0001c0001t0001g0037 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.71+819_71+820insCT others(15): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267771 | |||||||
| chr7:130267771 | T | TCTCTTCT others(3): Show |
1 | a0001c0001t0001g0100 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.71+819_71+820insCT others(8): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267771 | |||||||
| chr7:130267771 | T | TCTCTTCT others(11): Show |
1 | a0001c0001t0001g0043 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.71+819_71+820insCT others(16): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267771 | |||||||
| chr7:130267771 | T | TCTCTTTC others(4): Show |
1 | a0001c0001t0001g0026 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.71+819_71+820insCT others(9): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267771 | |||||||
| chr7:130267771 | T | TTCTC | 1 | a0001c0001t0001g0005 | 4 | HG00323.hp2 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+821_71+824dupCT others(2): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267771 | ||||||
| chr7:130267771 | T | TTTTCTTT others(9): Show |
1 | a0001c0002t0001g0066 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.71+820_71+821insTT others(14): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267771 | ||||||
| chr7:130267773 | C | CTCTCTCT others(13): Show |
1 | a0001c0001t0001g0005 | 2 | NA18952.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.71+824_71+825insCT others(18): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0005 | 2 | NA18953.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.71+824_71+825insCT others(22): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTCTCT others(35): Show |
1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.71+824_71+825insCT others(40): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0005 a0001c0002t0001g0023 |
5 | HG00140.hp1 HG01257.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+824_71+825insCT others(10): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTCTCT others(9): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0038 |
3 | HG00642.hp1 HG01255.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.71+824_71+825insCT others(14): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.71+824_71+825insCT others(26): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTCTCT others(29): Show |
1 | a0001c0001t0001g0025 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.71+824_71+825insCT others(34): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTCTCT others(37): Show |
1 | a0001c0001t0001g0025 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.71+824_71+825insCT others(42): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(36): Show |
70 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.71+880_71+883dupTT others(2): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTCTC others(10): Show |
1 | a0001c0001t0001g0002 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.71+825_71+826insCT others(15): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTTCT others(1): Show |
37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(34): Show |
69 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.71+876_71+883dupTT others(6): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTTCT others(5): Show |
40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(37): Show |
73 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.71+872_71+883dupTT others(10): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTTCT others(9): Show |
25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(22): Show |
47 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.71+868_71+883dupTT others(14): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTTCT others(13): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(12): Show |
21 | HG00621.hp2 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.71+864_71+883dupTT others(18): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTTCT others(17): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0028 others(5): Show |
11 | HG00438.hp2 HG02132.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+860_71+883dupTT others(22): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTTCT others(21): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(5): Show |
10 | HG00544.hp2 HG00673.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.71+856_71+883dupTT others(26): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTTCT others(25): Show |
1 | a0001c0002t0001g0003 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.71+852_71+883dupTT others(30): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTCTTTCT others(29): Show |
1 | a0001c0001t0001g0002 | 2 | NA18946.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.71+848_71+883dupTT others(34): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTTCTTTC others(6): Show |
1 | a0001c0002t0001g0021 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.71+822_71+823insTC others(11): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTTTCTCT others(17): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0101 |
2 | HG02155.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.71+822_71+823insTT others(22): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | CTTTCTTT others(15): Show |
1 | a0001c0001t0001g0001 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.71+822_71+823insTT others(20): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0037 others(3): Show |
6 | HG01256.hp1 HG02056.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+821C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267773 | |||||||
| chr7:130267773 | CTCTT | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0045 others(3): Show |
8 | HG02486.hp1 HG02647.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.71+880_71+883delTT others(2): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | CTCTTTCT others(1): Show |
C | 3 | a0001c0002t0001g0065 a0001c0002t0001g0067 a0001c0002t0001g0082 |
3 | HG02886.hp1 HG03704.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.71+876_71+883delTT others(6): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | CTCTTTCT others(5): Show |
C | 1 | a0001c0002t0001g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.71+872_71+883delTT others(10): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267773 | CTCTTTCT others(9): Show |
C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0006 |
2 | HG02129.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.71+868_71+883delTT others(14): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267773 | ||||||
| chr7:130267777 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+825T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267777 | |||||||
| chr7:130267779 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.71+827C>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267779 | |||||||
| chr7:130267832 | T | TTTCTTTC others(4): Show |
3 | a0001c0001t0001g0035 a0001c0001t0001g0151 a0001c0002t0001g0131 |
3 | HG01243.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.71+883_71+884insTT others(9): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267832 | ||||||
| chr7:130267832 | T | TTTCTTTC others(12): Show |
1 | a0003c0008t0001g0132 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.71+883_71+884insTT others(17): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130267832 | ||||||
| chr7:130267870 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG02145.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71+918C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267870 | |||||||
| chr7:130267996 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.72-933A>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130267996 | |||||||
| chr7:130268058 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.72-871G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268058 | |||||||
| chr7:130268181 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.72-748C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268181 | |||||||
| chr7:130268232 | A | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.72-697A>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268232 | |||||||
| chr7:130268292 | AGG | A | 10 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0122 others(7): Show |
14 | HG00735.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.72-633_72-632delGG | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130268292 | ||||||
| chr7:130268294 | GGGGT | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(10): Show |
24 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(21): Show |
intron_variant | MODIFIER | c.72-633_72-630delGG others(2): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130268294 | ||||||
| chr7:130268294 | GGGGTGT | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(30): Show |
84 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.72-633_72-628delGG others(4): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130268294 | ||||||
| chr7:130268294 | GGGGTGTG others(1): Show |
G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(22): Show |
60 | HG00323.hp2 HG00597.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.72-633_72-626delGG others(6): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130268294 | ||||||
| chr7:130268294 | GGGGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0149 |
2 | HG02615.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.72-633_72-624delGG others(8): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130268294 | ||||||
| chr7:130268296 | G | GGT | 7 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0042 others(4): Show |
11 | HG01884.hp1 HG03486.hp2 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.72-594_72-593dupGT | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130268296 | ||||||
| chr7:130268296 | G | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0127 |
2 | HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.72-633G>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268296 | |||||||
| chr7:130268296 | GGT | G | 18 | a0001c0001t0001g0049 a0001c0001t0001g0153 a0001c0002t0001g0003 others(15): Show |
36 | HG00280.hp2 HG00639.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-594_72-593delGT | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130268296 | ||||||
| chr7:130268296 | GGTGTGT | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(29): Show |
83 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.72-598_72-593delGT others(4): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 130268296 | ||||||
| chr7:130268606 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.72-323A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268606 | |||||||
| chr7:130268652 | G | A | 1 | a0001c0002t0001g0042 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.72-277G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268652 | |||||||
| chr7:130268767 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0137 |
2 | HG02809.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.72-162G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268767 | |||||||
| chr7:130268783 | A | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0033 others(19): Show |
45 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.72-146A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268783 | |||||||
| chr7:130268790 | A | G | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(25): Show |
69 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.72-139A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268790 | |||||||
| chr7:130268858 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.72-71G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 1/10 | chr7 | 130268858 | |||||||
| chr7:130269540 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.154-129T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 2/10 | chr7 | 130269540 | |||||||
| chr7:130270465 | G | A | 1 | a0004c0004t0001g0015 | 4 | HG01891.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-228G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 3/10 | chr7 | 130270465 | |||||||
| chr7:130270483 | A | T | 1 | a0001c0002t0001g0121 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.289-210A>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 3/10 | chr7 | 130270483 | |||||||
| chr7:130270616 | T | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0134 |
3 | HG01496.hp1 HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.289-77T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 3/10 | chr7 | 130270616 | |||||||
| chr7:130270623 | C | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(63): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.289-70C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 3/10 | chr7 | 130270623 | |||||||
| chr7:130270978 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.384+190G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130270978 | |||||||
| chr7:130271112 | C | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0033 others(16): Show |
42 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.384+324C>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271112 | |||||||
| chr7:130271181 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.384+393C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271181 | |||||||
| chr7:130271238 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.384+450A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271238 | |||||||
| chr7:130271256 | T | A | 1 | a0001c0001t0001g0013 | 4 | HG02135.hp1 NA18972.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+468T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271256 | |||||||
| chr7:130271398 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(107): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.384+610A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271398 | |||||||
| chr7:130271631 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.384+843T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271631 | |||||||
| chr7:130271660 | G | A | 32 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(29): Show |
73 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.384+872G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271660 | |||||||
| chr7:130271792 | C | A | 1 | a0001c0001t0001g0024 | 2 | NA18941.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.384+1004C>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271792 | |||||||
| chr7:130271864 | T | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(33): Show |
80 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.384+1076T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271864 | |||||||
| chr7:130271904 | A | G | 1 | a0001c0002t0001g0066 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.384+1116A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130271904 | |||||||
| chr7:130272001 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.385-1075T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272001 | |||||||
| chr7:130272026 | G | A | 1 | a0002c0003t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385-1050G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272026 | |||||||
| chr7:130272305 | A | AATAC | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(33): Show |
80 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.385-768_385-767ins others(4): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 130272305 | ||||||
| chr7:130272324 | T | A | 1 | a0001c0002t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.385-752T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272324 | |||||||
| chr7:130272328 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(33): Show |
80 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.385-748C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272328 | |||||||
| chr7:130272509 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-567C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272509 | |||||||
| chr7:130272597 | C | T | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(22): Show |
50 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.385-479C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272597 | |||||||
| chr7:130272762 | A | G | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(36): Show |
85 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.385-314A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272762 | |||||||
| chr7:130272908 | C | T | 2 | a0001c0002t0001g0081 a0001c0002t0001g0082 |
2 | HG03704.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.385-168C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272908 | |||||||
| chr7:130272943 | C | T | 3 | a0002c0003t0001g0011 a0002c0003t0001g0047 a0002c0003t0001g0133 |
6 | HG02622.hp1 HG02965.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-133C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 4/10 | chr7 | 130272943 | |||||||
| chr7:130273285 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.486+108T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273285 | |||||||
| chr7:130273358 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
22 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.486+181T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273358 | |||||||
| chr7:130273367 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG02145.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.486+190C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273367 | |||||||
| chr7:130273457 | C | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(22): Show |
50 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.486+280C>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273457 | |||||||
| chr7:130273497 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.486+320G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273497 | |||||||
| chr7:130273527 | C | T | 1 | a0001c0002t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.486+350C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273527 | |||||||
| chr7:130273578 | A | AAC | 32 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0048 others(29): Show |
61 | HG00438.hp1 HG00639.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.486+421_486+422dup others(2): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 130273578 | ||||||
| chr7:130273578 | A | AACAC | 19 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0034 others(16): Show |
42 | HG00423.hp1 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.486+419_486+422dup others(4): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 130273578 | ||||||
| chr7:130273578 | A | AACACAC | 4 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0001t0001g0122 others(1): Show |
4 | HG00738.hp1 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+417_486+422dup others(6): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 130273578 | ||||||
| chr7:130273578 | AAC | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0064 |
3 | HG00609.hp2 NA19030.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.486+421_486+422del others(2): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 130273578 | ||||||
| chr7:130273590 | C | CACACACA others(5): Show |
1 | a0001c0001t0001g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.486+422_486+423ins others(12): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 130273590 | ||||||
| chr7:130273676 | CT | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(13): Show |
44 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.486+517delT | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 130273676 | ||||||
| chr7:130273680 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(81): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.486+503T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273680 | |||||||
| chr7:130273681 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0086 a0001c0002t0001g0114 |
3 | HG00544.hp2 HG01975.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.486+504T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273681 | |||||||
| chr7:130273682 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.486+505T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273682 | |||||||
| chr7:130273695 | G | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG02145.hp2 HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.486+518G>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273695 | |||||||
| chr7:130273729 | G | A | 1 | a0004c0004t0001g0015 | 4 | HG01891.hp1 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+552G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273729 | |||||||
| chr7:130273795 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0134 |
3 | HG01496.hp1 HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.486+618G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130273795 | |||||||
| chr7:130273936 | GA | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(21): Show |
49 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.486+768delA | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 130273936 | ||||||
| chr7:130274154 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.486+977C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130274154 | |||||||
| chr7:130274479 | G | A | 1 | a0001c0002t0001g0055 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.487-670G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130274479 | |||||||
| chr7:130274487 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.487-662T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130274487 | |||||||
| chr7:130274527 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.487-622A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130274527 | |||||||
| chr7:130274674 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.487-475C>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130274674 | |||||||
| chr7:130274895 | A | G | 1 | a0001c0002t0001g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.487-254A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130274895 | |||||||
| chr7:130274956 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.487-193C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130274956 | |||||||
| chr7:130275130 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.487-19G>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 5/10 | chr7 | 130275130 | |||||||
| chr7:130275544 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.585+297C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130275544 | |||||||
| chr7:130275698 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.585+451C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130275698 | |||||||
| chr7:130276091 | A | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0029 others(4): Show |
16 | HG01099.hp1 HG01884.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.586-537A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130276091 | |||||||
| chr7:130276119 | A | G | 1 | a0001c0002t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.586-509A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130276119 | |||||||
| chr7:130276168 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.586-460C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130276168 | |||||||
| chr7:130276190 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(55): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.586-438A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130276190 | |||||||
| chr7:130276228 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0134 others(1): Show |
4 | HG01496.hp1 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-400A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130276228 | |||||||
| chr7:130276485 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.586-143C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130276485 | |||||||
| chr7:130276486 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.586-142G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130276486 | |||||||
| chr7:130276550 | A | AAC | 58 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(55): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.586-75_586-74dupAC | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 130276550 | ||||||
| chr7:130276605 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0134 others(1): Show |
4 | HG01496.hp1 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.586-23A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 6/10 | chr7 | 130276605 | |||||||
| chr7:130276869 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.696+131C>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130276869 | |||||||
| chr7:130276898 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.696+160T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130276898 | |||||||
| chr7:130276952 | C | G | 3 | a0002c0003t0001g0011 a0002c0003t0001g0047 a0002c0003t0001g0133 |
6 | HG02622.hp1 HG02965.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.696+214C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130276952 | |||||||
| chr7:130276996 | A | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0002t0001g0075 |
3 | HG02615.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.696+258A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130276996 | |||||||
| chr7:130277120 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.696+382A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130277120 | |||||||
| chr7:130277290 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(99): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.697-536A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130277290 | |||||||
| chr7:130277296 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.697-530T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130277296 | |||||||
| chr7:130277302 | C | T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(21): Show |
49 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.697-524C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130277302 | |||||||
| chr7:130277355 | A | C | 1 | a0001c0001t0001g0043 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.697-471A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130277355 | |||||||
| chr7:130277399 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.697-427C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130277399 | |||||||
| chr7:130277417 | G | A | 1 | a0001c0002t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.697-409G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130277417 | |||||||
| chr7:130277590 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.697-236G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 7/10 | chr7 | 130277590 | |||||||
| chr7:130277923 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0127 |
2 | HG02145.hp2 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.787+7G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130277923 | |||||||
| chr7:130277956 | G | T | 1 | a0001c0001t0001g0031 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.787+40G>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130277956 | |||||||
| chr7:130278182 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.787+266G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130278182 | |||||||
| chr7:130278462 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.787+546C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130278462 | |||||||
| chr7:130278985 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.788-478G>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130278985 | |||||||
| chr7:130279107 | C | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.788-356C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130279107 | |||||||
| chr7:130279161 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.788-302A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130279161 | |||||||
| chr7:130279265 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.788-198T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130279265 | |||||||
| chr7:130279316 | A | G | 1 | a0003c0008t0001g0132 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.788-147A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 8/10 | chr7 | 130279316 | |||||||
| chr7:130279677 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0096 a0001c0001t0001g0120 |
5 | HG02523.hp2 NA18943.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+15C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130279677 | |||||||
| chr7:130279775 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.987+113A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130279775 | |||||||
| chr7:130280148 | C | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(29): Show |
90 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.987+486C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280148 | |||||||
| chr7:130280234 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.987+572T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280234 | |||||||
| chr7:130280250 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(29): Show |
90 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.987+588C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280250 | |||||||
| chr7:130280285 | G | A | 1 | a0001c0002t0001g0023 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.987+623G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280285 | |||||||
| chr7:130280303 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.987+641A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280303 | |||||||
| chr7:130280379 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.987+717C>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280379 | |||||||
| chr7:130280399 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.987+737T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280399 | |||||||
| chr7:130280450 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0127 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.987+788C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280450 | |||||||
| chr7:130280798 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.987+1136C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280798 | |||||||
| chr7:130280836 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(32): Show |
98 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.987+1174A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280836 | |||||||
| chr7:130280884 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.988-1220T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280884 | |||||||
| chr7:130280979 | T | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(20): Show |
48 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.988-1125T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130280979 | |||||||
| chr7:130281052 | T | G | 1 | a0001c0002t0001g0051 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.988-1052T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281052 | |||||||
| chr7:130281056 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.988-1048A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281056 | |||||||
| chr7:130281095 | AAGAG | A | 1 | a0001c0002t0001g0018 | 3 | HG01516.hp2 HG01517.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.988-1002_988-999de others(5): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr7 | 130281095 | ||||||
| chr7:130281392 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0108 a0001c0001t0001g0109 |
4 | NA18983.hp1 NA18985.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-712A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281392 | |||||||
| chr7:130281396 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0134 others(2): Show |
5 | HG01496.hp1 HG02258.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-708C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281396 | |||||||
| chr7:130281442 | A | G | 3 | a0002c0003t0001g0011 a0002c0003t0001g0047 a0002c0003t0001g0133 |
6 | HG02622.hp1 HG02965.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-662A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281442 | |||||||
| chr7:130281520 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.988-584A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281520 | |||||||
| chr7:130281526 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.988-578C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281526 | |||||||
| chr7:130281682 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG00741.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.988-422G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281682 | |||||||
| chr7:130281722 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.988-382A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281722 | |||||||
| chr7:130281790 | A | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(35): Show |
101 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.988-314A>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130281790 | |||||||
| chr7:130282018 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.988-86G>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130282018 | |||||||
| chr7:130282084 | C | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0134 others(1): Show |
4 | HG01496.hp1 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-20C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 9/10 | chr7 | 130282084 | |||||||
| chr7:130282425 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1072+237G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130282425 | |||||||
| chr7:130282462 | T | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0078 others(2): Show |
9 | HG02155.hp1 NA18941.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.1072+274T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130282462 | |||||||
| chr7:130282562 | A | G | 1 | a0001c0002t0001g0063 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1072+374A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130282562 | |||||||
| chr7:130282658 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(91): Show |
240 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.1072+470T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130282658 | |||||||
| chr7:130282858 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1072+670T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130282858 | |||||||
| chr7:130283206 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1072+1018C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283206 | |||||||
| chr7:130283254 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1072+1066A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283254 | |||||||
| chr7:130283324 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1072+1136T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283324 | |||||||
| chr7:130283441 | C | CTTAT | 38 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(35): Show |
101 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1072+1272_1072+127 others(8): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 130283441 | ||||||
| chr7:130283441 | C | CTTATTTA others(1): Show |
28 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(25): Show |
53 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1072+1268_1072+127 others(12): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 130283441 | ||||||
| chr7:130283453 | T | A | 1 | a0001c0002t0001g0056 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1072+1265T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283453 | |||||||
| chr7:130283485 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(25): Show |
86 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1072+1297T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283485 | |||||||
| chr7:130283560 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1072+1372G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283560 | |||||||
| chr7:130283572 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1072+1384G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283572 | |||||||
| chr7:130283676 | G | T | 1 | a0001c0002t0001g0065 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1072+1488G>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283676 | |||||||
| chr7:130283782 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1072+1594G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283782 | |||||||
| chr7:130283821 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1072+1633G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283821 | |||||||
| chr7:130283925 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(36): Show |
102 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1072+1737C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130283925 | |||||||
| chr7:130284017 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1072+1829G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284017 | |||||||
| chr7:130284061 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1072+1873C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284061 | |||||||
| chr7:130284125 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(32): Show |
98 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1072+1937G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284125 | |||||||
| chr7:130284130 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(32): Show |
98 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1072+1942G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284130 | |||||||
| chr7:130284219 | T | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1072+2031T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284219 | |||||||
| chr7:130284381 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1072+2193G>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284381 | |||||||
| chr7:130284611 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0029 others(4): Show |
16 | HG01099.hp1 HG01884.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1072+2423G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284611 | |||||||
| chr7:130284661 | G | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(28): Show |
92 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1072+2473G>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284661 | |||||||
| chr7:130284803 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(36): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1072+2615G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284803 | |||||||
| chr7:130284874 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1072+2686G>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284874 | |||||||
| chr7:130284898 | T | C | 1 | a0001c0002t0001g0140 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1072+2710T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284898 | |||||||
| chr7:130284936 | C | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0085 a0001c0001t0001g0115 |
5 | HG01884.hp2 HG02622.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072+2748C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284936 | |||||||
| chr7:130284938 | G | A | 1 | a0001c0002t0001g0071 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1072+2750G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130284938 | |||||||
| chr7:130284942 | C | CA | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(32): Show |
95 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1072+2766dupA | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 130284942 | ||||||
| chr7:130285174 | G | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(28): Show |
92 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1072+2986G>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285174 | |||||||
| chr7:130285271 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1072+3083G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285271 | |||||||
| chr7:130285301 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1072+3113G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285301 | |||||||
| chr7:130285551 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1072+3363G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285551 | |||||||
| chr7:130285575 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1072+3387G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285575 | |||||||
| chr7:130285704 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0101 |
2 | HG02155.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1072+3516C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285704 | |||||||
| chr7:130285782 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(104): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1072+3594T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285782 | |||||||
| chr7:130285847 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1072+3659G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285847 | |||||||
| chr7:130285849 | T | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1072+3661T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285849 | |||||||
| chr7:130285858 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1072+3670C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285858 | |||||||
| chr7:130285902 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(36): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1073-3658C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285902 | |||||||
| chr7:130285910 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1073-3650C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285910 | |||||||
| chr7:130285968 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1073-3592G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285968 | |||||||
| chr7:130285971 | C | T | 2 | a0001c0001t0001g0109 a0001c0002t0001g0061 |
2 | HG02280.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1073-3589C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285971 | |||||||
| chr7:130285990 | CTCAAAAA | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0153 |
3 | HG02135.hp2 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1073-3569_1073-356 others(11): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285990 | |||||||
| chr7:130285990 | CTCAAAAA others(1): Show |
C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(27): Show |
89 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1073-3569_1073-356 others(12): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285990 | |||||||
| chr7:130285992 | C | CA | 11 | a0001c0001t0001g0025 a0001c0002t0001g0003 a0001c0002t0001g0004 others(8): Show |
28 | HG00609.hp2 HG00733.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1073-3544dupA | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 130285992 | ||||||
| chr7:130285992 | C | CAA | 6 | a0001c0002t0001g0003 a0001c0002t0001g0007 a0001c0002t0001g0040 others(3): Show |
7 | HG00438.hp2 HG00741.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073-3545_1073-354 others(6): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 130285992 | ||||||
| chr7:130285992 | CAAAAAA | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(29): Show |
59 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1073-3549_1073-354 others(10): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 130285992 | ||||||
| chr7:130285992 | CAAAAAAA | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(39): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.1073-3550_1073-354 others(11): Show |
CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 130285992 | ||||||
| chr7:130285999 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0153 |
3 | HG02135.hp2 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1073-3561A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130285999 | |||||||
| chr7:130286000 | A | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(27): Show |
89 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1073-3560A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130286000 | |||||||
| chr7:130286134 | G | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1073-3426G>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130286134 | |||||||
| chr7:130286372 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(102): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1073-3188T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130286372 | |||||||
| chr7:130286454 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1073-3106G>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130286454 | |||||||
| chr7:130286557 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0001g0107 a0004c0004t0001g0015 |
6 | HG01891.hp1 HG02922.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1073-3003A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130286557 | |||||||
| chr7:130286782 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(103): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1073-2778T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130286782 | |||||||
| chr7:130286800 | C | T | 4 | a0001c0002t0001g0012 a0001c0002t0001g0056 a0001c0002t0001g0064 others(1): Show |
7 | HG00609.hp2 NA18956.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073-2760C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130286800 | |||||||
| chr7:130287065 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1073-2495C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287065 | |||||||
| chr7:130287184 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
26 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.1073-2376T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287184 | |||||||
| chr7:130287272 | A | C | 1 | a0001c0002t0001g0056 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1073-2288A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287272 | |||||||
| chr7:130287307 | T | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0127 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1073-2253T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287307 | |||||||
| chr7:130287307 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1073-2253T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287307 | |||||||
| chr7:130287316 | A | AT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0030 others(18): Show |
40 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1073-2231dupT | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr7 | 130287316 | ||||||
| chr7:130287317 | T | A | 1 | a0001c0002t0001g0051 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1073-2243T>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287317 | |||||||
| chr7:130287361 | A | C | 1 | a0001c0002t0001g0056 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1073-2199A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287361 | |||||||
| chr7:130287402 | C | A | 1 | a0001c0002t0001g0052 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1073-2158C>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287402 | |||||||
| chr7:130287443 | C | T | 7 | a0001c0002t0001g0021 a0001c0002t0001g0073 a0001c0002t0001g0075 others(4): Show |
9 | HG00735.hp1 HG01106.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073-2117C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287443 | |||||||
| chr7:130287447 | A | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(24): Show |
52 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1073-2113A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287447 | |||||||
| chr7:130287520 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0151 |
4 | HG01243.hp2 HG02129.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073-2040G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287520 | |||||||
| chr7:130287547 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1073-2013G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287547 | |||||||
| chr7:130287557 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(29): Show |
92 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1073-2003C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287557 | |||||||
| chr7:130287558 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(99): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1073-2002A>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287558 | |||||||
| chr7:130287578 | T | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0134 others(1): Show |
4 | HG01496.hp1 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-1982T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287578 | |||||||
| chr7:130287852 | T | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0024 others(24): Show |
52 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1073-1708T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287852 | |||||||
| chr7:130287938 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0019 others(29): Show |
86 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1073-1622G>A | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130287938 | |||||||
| chr7:130288002 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1073-1558A>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130288002 | |||||||
| chr7:130288146 | A | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0084 a0001c0001t0001g0107 others(1): Show |
10 | HG01943.hp1 HG01993.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1073-1414A>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130288146 | |||||||
| chr7:130288334 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0019 others(23): Show |
78 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1073-1226C>T | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130288334 | |||||||
| chr7:130288352 | T | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(103): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1073-1208T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130288352 | |||||||
| chr7:130288669 | T | G | 1 | a0001c0002t0001g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1073-891T>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130288669 | |||||||
| chr7:130289112 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1073-448A>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130289112 | |||||||
| chr7:130289250 | C | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(36): Show |
100 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1073-310C>G | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130289250 | |||||||
| chr7:130289402 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1073-158T>C | CPA2 | ENSG00000158516.12 | transcript | ENST00000222481.9 | protein_coding | 10/10 | chr7 | 130289402 |