Item | Value |
---|---|
geneid | 5858 |
ensemblid | ENSG00000126838.10 |
hgncid | 9750 |
symbol | PZP |
name | PZP alpha-2-macroglobulin like |
refseq_nuc | NM_002864.3 |
refseq_prot | NP_002855.2 |
ensembl_nuc | ENST00000261336.7 |
ensembl_prot | ENSP00000261336.2 |
mane_status | MANE Select |
chr | chr12 |
start | 9148840 |
end | 9208395 |
strand | - |
ver | v1.2 |
region | chr12:9148840-9208395 |
region5000 | chr12:9143840-9213395 |
regionname0 | PZP_chr12_9148840_9208395 |
regionname5000 | PZP_chr12_9143840_9213395 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1482 | 87 | 21 | 17 | 42 | 3 | 4 | 34 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0002 | 0/0 | 1482 | 43 | 6 | 10 | 24 | 2 | 1 | 14 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0003 | 0/0 | 1482 | 27 | 13 | 4 | 8 | 0 | 2 | 8 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0004 | 0/0 | 1482 | 17 | 2 | 10 | 0 | 2 | 3 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0005 | 0/0 | 597 | 17 | 0 | 0 | 15 | 0 | 2 | 11 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(592): Show |
chr12 | 9143840 | 9213395 |
a0006 | 0/0 | 1482 | 16 | 2 | 1 | 9 | 0 | 4 | 7 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0007 | 0/1 | 1482 | 16 | 3 | 0 | 8 | 2 | 2 | 5 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0008 | 0/0 | 1482 | 15 | 6 | 3 | 3 | 0 | 3 | 1 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0009 | 0/0 | 1482 | 14 | 0 | 1 | 6 | 3 | 4 | 4 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0010 | 0/0 | 1482 | 11 | 3 | 7 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0011 | 0/0 | 1482 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0012 | 1/0 | 1482 | 7 | 6 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0013 | 0/0 | 1482 | 6 | 0 | 2 | 1 | 0 | 3 | 1 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0014 | 0/0 | 1482 | 5 | 1 | 2 | 1 | 1 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0015 | 0/0 | 1482 | 5 | 0 | 2 | 1 | 0 | 2 | 1 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0016 | 0/0 | 1482 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0017 | 0/0 | 1482 | 5 | 0 | 0 | 2 | 0 | 3 | 2 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0018 | 0/0 | 1482 | 4 | 2 | 1 | 1 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0019 | 0/0 | 1482 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0020 | 0/0 | 1482 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0021 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1162): Show |
chr12 | 9143840 | 9213395 |
a0022 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0023 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0024 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0025 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0026 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0027 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0028 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0029 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0030 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0031 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0032 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0033 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0034 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0035 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0036 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
a0037 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1162): Show |
chr12 | 9143840 | 9213395 |
a0038 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | MRKDR others(1477): Show |
chr12 | 9143840 | 9213395 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4446 | 70 | 7 | 16 | 41 | 2 | 4 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0013 | 0/0 | 4446 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0021 | 0/0 | 4446 | 3 | 2 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0026 | 0/0 | 4446 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0031 | 0/0 | 4446 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0038 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0046 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0055 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0058 | 0/0 | 4446 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0001c0059 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0002c0002 | 0/0 | 4446 | 42 | 6 | 10 | 23 | 2 | 1 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0002c0065 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0003c0003 | 0/0 | 4446 | 23 | 12 | 2 | 8 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0003c0022 | 0/0 | 4446 | 3 | 1 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0003c0041 | 0/0 | 4446 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0004c0004 | 0/0 | 4446 | 17 | 2 | 10 | 0 | 2 | 3 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0005c0008 | 0/0 | 4446 | 13 | 0 | 0 | 12 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0005c0019 | 0/0 | 4446 | 4 | 0 | 0 | 3 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0006c0007 | 0/0 | 4446 | 13 | 1 | 1 | 8 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0006c0029 | 0/0 | 4446 | 2 | 1 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0006c0035 | 0/0 | 4446 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0007c0005 | 0/1 | 4446 | 15 | 2 | 0 | 8 | 2 | 2 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0007c0056 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0008c0012 | 0/0 | 4446 | 5 | 0 | 2 | 0 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0008c0020 | 0/0 | 4446 | 3 | 3 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0008c0023 | 0/0 | 4446 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0008c0025 | 0/0 | 4446 | 2 | 0 | 1 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0008c0039 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0008c0043 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0008c0057 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0009c0006 | 0/0 | 4446 | 14 | 0 | 1 | 6 | 3 | 4 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0010c0009 | 0/0 | 4446 | 10 | 3 | 7 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0010c0054 | 0/0 | 4446 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0011c0010 | 0/0 | 4446 | 7 | 7 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0011c0066 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0012c0014 | 1/0 | 4446 | 5 | 4 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0012c0024 | 0/0 | 4446 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0013c0011 | 0/0 | 4446 | 6 | 0 | 2 | 1 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0014c0016 | 0/0 | 4446 | 5 | 1 | 2 | 1 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0015c0018 | 0/0 | 4446 | 5 | 0 | 2 | 1 | 0 | 2 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0016c0017 | 0/0 | 4446 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0017c0015 | 0/0 | 4446 | 5 | 0 | 0 | 2 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0018c0030 | 0/0 | 4446 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0018c0037 | 0/0 | 4446 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0018c0045 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0019c0032 | 0/0 | 4446 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0019c0033 | 0/0 | 4446 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0020c0034 | 0/0 | 4446 | 2 | 0 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0021c0027 | 0/0 | 4446 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0022c0028 | 0/0 | 4446 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0023c0053 | 0/0 | 4446 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0024c0040 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0025c0063 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0026c0064 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0027c0051 | 0/0 | 4446 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0028c0048 | 0/0 | 4446 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0029c0049 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0030c0061 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0031c0060 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0032c0050 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0033c0036 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0034c0062 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0035c0052 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0036c0047 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0037c0044 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 | ||
a0038c0042 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | ATGCG others(4441): Show |
chr12 | 9143840 | 9213395 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4635 | 70 | 7 | 16 | 41 | 2 | 4 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0013t0001 | 0/0 | 4635 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0021t0001 | 0/0 | 4635 | 3 | 2 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0026t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0031t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0038t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0046t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0055t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0058t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0001c0059t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0002c0002t0001 | 0/0 | 4635 | 42 | 6 | 10 | 23 | 2 | 1 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0002c0065t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0003c0003t0001 | 0/0 | 4635 | 23 | 12 | 2 | 8 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0003c0022t0001 | 0/0 | 4635 | 3 | 1 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0003c0041t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0004c0004t0001 | 0/0 | 4635 | 17 | 2 | 10 | 0 | 2 | 3 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0005c0008t0001 | 0/0 | 4635 | 13 | 0 | 0 | 12 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0005c0019t0001 | 0/0 | 4635 | 4 | 0 | 0 | 3 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0006c0007t0001 | 0/0 | 4635 | 13 | 1 | 1 | 8 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0006c0029t0001 | 0/0 | 4635 | 2 | 1 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0006c0035t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0007c0005t0001 | 0/1 | 4635 | 15 | 2 | 0 | 8 | 2 | 2 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0007c0056t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0008c0012t0001 | 0/0 | 4635 | 5 | 0 | 2 | 0 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0008c0020t0001 | 0/0 | 4635 | 3 | 3 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0008c0023t0001 | 0/0 | 4635 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0008c0025t0001 | 0/0 | 4635 | 2 | 0 | 1 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0008c0039t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0008c0043t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0008c0057t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0009c0006t0001 | 0/0 | 4635 | 14 | 0 | 1 | 6 | 3 | 4 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0010c0009t0001 | 0/0 | 4635 | 10 | 3 | 7 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0010c0054t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0011c0010t0001 | 0/0 | 4635 | 7 | 7 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0011c0066t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0012c0014t0001 | 1/0 | 4635 | 5 | 4 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0012c0024t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0013c0011t0001 | 0/0 | 4635 | 6 | 0 | 2 | 1 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0014c0016t0001 | 0/0 | 4635 | 5 | 1 | 2 | 1 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0015c0018t0001 | 0/0 | 4635 | 5 | 0 | 2 | 1 | 0 | 2 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0016c0017t0001 | 0/0 | 4635 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0017c0015t0001 | 0/0 | 4635 | 5 | 0 | 0 | 2 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0018c0030t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0018c0037t0001 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0018c0045t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0019c0032t0001 | 0/0 | 4635 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0019c0033t0001 | 0/0 | 4635 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0020c0034t0001 | 0/0 | 4635 | 2 | 0 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0021c0027t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0022c0028t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0023c0053t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0024c0040t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0025c0063t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0026c0064t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0027c0051t0001 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0028c0048t0001 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0029c0049t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0030c0061t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0031c0060t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0032c0050t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0033c0036t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0034c0062t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0035c0052t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0036c0047t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0037c0044t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
a0038c0042t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | AGGGC others(4630): Show |
chr12 | 9143840 | 9213395 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 2 | 5 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0007 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0008 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0013t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0013t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0013t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0013t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0013t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0021t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0021t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0021t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0026t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0026t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0031t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0038t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0046t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0055t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0058t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0001c0059t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0002c0065t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0022t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0022t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0022t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0003c0041t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0004 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0004c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0019t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0019t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0019t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0005c0019t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0007t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0029t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0029t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0006c0035t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0007c0056t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0012t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0012t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0012t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0012t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0012t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0020t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0020t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0023t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0025t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0025t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0039t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0043t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0008c0057t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0005 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0009c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0009t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0009t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0009t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0009t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0009t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0009t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0009t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0010c0054t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0011c0010t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0011c0010t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0011c0010t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0011c0010t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0011c0010t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0011c0010t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0011c0066t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0012c0014t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0012c0014t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0012c0014t0001g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0012c0024t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0012c0024t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0013c0011t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0013c0011t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0013c0011t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0013c0011t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0013c0011t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0013c0011t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0014c0016t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0014c0016t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0014c0016t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0014c0016t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0014c0016t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0015c0018t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0015c0018t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0015c0018t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0015c0018t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0015c0018t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0016c0017t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0016c0017t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0016c0017t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0017c0015t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0017c0015t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0017c0015t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0017c0015t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0017c0015t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0018c0030t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0018c0037t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0018c0045t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0019c0032t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0019c0032t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0019c0033t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0019c0033t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0020c0034t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0020c0034t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0021c0027t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0022c0028t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0022c0028t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0023c0053t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0024c0040t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0025c0063t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0026c0064t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0027c0051t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0028c0048t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0029c0049t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0030c0061t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0031c0060t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0032c0050t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0033c0036t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0034c0062t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0035c0052t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0036c0047t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0037c0044t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
a0038c0042t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00099 | hp2 | a0014 | c0016 | t0001 | g0156 | EUR | GBR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00140 | hp1 | a0004 | c0004 | t0001 | g0273 | EUR | GBR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00280 | hp1 | a0004 | c0004 | t0001 | g0004 | EUR | FIN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00280 | hp2 | a0023 | c0053 | t0001 | g0195 | EUR | FIN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00408 | hp2 | a0009 | c0006 | t0001 | g0066 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00423 | hp1 | a0005 | c0019 | t0001 | g0180 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00438 | hp2 | a0024 | c0040 | t0001 | g0077 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00609 | hp2 | a0025 | c0063 | t0001 | g0148 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00621 | hp2 | a0026 | c0064 | t0001 | g0171 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00639 | hp2 | a0003 | c0022 | t0001 | g0233 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00642 | hp2 | a0004 | c0004 | t0001 | g0230 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00673 | hp1 | a0002 | c0065 | t0001 | g0138 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00735 | hp2 | a0013 | c0011 | t0001 | g0086 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00738 | hp1 | a0018 | c0037 | t0001 | g0254 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG00738 | hp2 | a0015 | c0018 | t0001 | g0166 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01070 | hp1 | a0008 | c0012 | t0001 | g0259 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01070 | hp2 | a0014 | c0016 | t0001 | g0155 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01071 | hp1 | a0008 | c0012 | t0001 | g0261 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01071 | hp2 | a0009 | c0006 | t0001 | g0014 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01074 | hp1 | a0008 | c0025 | t0001 | g0232 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01106 | hp1 | a0004 | c0004 | t0001 | g0222 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01106 | hp2 | a0010 | c0009 | t0001 | g0221 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01109 | hp1 | a0010 | c0009 | t0001 | g0012 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0200 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01168 | hp1 | a0004 | c0004 | t0001 | g0030 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01175 | hp1 | a0027 | c0051 | t0001 | g0207 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01243 | hp1 | a0003 | c0022 | t0001 | g0236 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01257 | hp2 | a0006 | c0007 | t0001 | g0118 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01346 | hp1 | a0004 | c0004 | t0001 | g0258 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01346 | hp2 | a0020 | c0034 | t0001 | g0150 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0199 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01361 | hp1 | a0004 | c0004 | t0001 | g0004 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01361 | hp2 | a0028 | c0048 | t0001 | g0265 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01433 | hp1 | a0010 | c0009 | t0001 | g0242 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01496 | hp1 | a0004 | c0004 | t0001 | g0272 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01516 | hp1 | a0009 | c0006 | t0001 | g0005 | EUR | IBS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01516 | hp2 | a0007 | c0005 | t0001 | g0018 | EUR | IBS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01517 | hp1 | a0009 | c0006 | t0001 | g0005 | EUR | IBS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01517 | hp2 | a0001 | c0058 | t0001 | g0201 | EUR | IBS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01884 | hp1 | a0011 | c0010 | t0001 | g0109 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01884 | hp2 | a0016 | c0017 | t0001 | g0026 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01891 | hp1 | a0003 | c0003 | t0001 | g0203 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01928 | hp1 | a0010 | c0009 | t0001 | g0012 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01928 | hp2 | a0013 | c0011 | t0001 | g0061 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01934 | hp1 | a0014 | c0016 | t0001 | g0140 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01943 | hp2 | a0010 | c0009 | t0001 | g0251 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01952 | hp1 | a0015 | c0018 | t0001 | g0127 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01952 | hp2 | a0010 | c0009 | t0001 | g0241 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01978 | hp1 | a0004 | c0004 | t0001 | g0263 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01978 | hp2 | a0010 | c0009 | t0001 | g0237 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01993 | hp1 | a0001 | c0021 | t0001 | g0123 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG01993 | hp2 | a0004 | c0004 | t0001 | g0231 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02015 | hp2 | a0029 | c0049 | t0001 | g0099 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02040 | hp2 | a0030 | c0061 | t0001 | g0142 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02055 | hp1 | a0001 | c0021 | t0001 | g0193 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02055 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02056 | hp1 | a0019 | c0032 | t0001 | g0161 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02071 | hp2 | a0007 | c0005 | t0001 | g0271 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02074 | hp1 | a0005 | c0019 | t0001 | g0174 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02074 | hp2 | a0006 | c0007 | t0001 | g0228 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02080 | hp1 | a0008 | c0023 | t0001 | g0016 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02083 | hp1 | a0007 | c0005 | t0001 | g0034 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02083 | hp2 | a0005 | c0008 | t0001 | g0177 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02129 | hp2 | a0031 | c0060 | t0001 | g0178 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02135 | hp2 | a0009 | c0006 | t0001 | g0068 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02145 | hp1 | a0003 | c0022 | t0001 | g0121 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02145 | hp2 | a0032 | c0050 | t0001 | g0168 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02155 | hp1 | a0007 | c0005 | t0001 | g0045 | EAS | CDX | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02155 | hp2 | a0006 | c0007 | t0001 | g0244 | EAS | CDX | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02257 | hp1 | a0001 | c0013 | t0001 | g0111 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02257 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02258 | hp1 | a0001 | c0031 | t0001 | g0025 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02258 | hp2 | a0033 | c0036 | t0001 | g0227 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02273 | hp1 | a0004 | c0004 | t0001 | g0243 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02280 | hp1 | a0001 | c0026 | t0001 | g0035 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02280 | hp2 | a0011 | c0010 | t0001 | g0107 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02293 | hp1 | a0020 | c0034 | t0001 | g0134 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02293 | hp2 | a0004 | c0004 | t0001 | g0223 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02451 | hp1 | a0012 | c0014 | t0001 | g0011 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0103 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02572 | hp1 | a0014 | c0016 | t0001 | g0149 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02572 | hp2 | a0001 | c0013 | t0001 | g0275 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02622 | hp1 | a0021 | c0027 | t0001 | g0028 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02622 | hp2 | a0012 | c0014 | t0001 | g0011 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02630 | hp1 | a0010 | c0009 | t0001 | g0038 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02630 | hp2 | a0001 | c0055 | t0001 | g0212 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02647 | hp1 | a0008 | c0020 | t0001 | g0268 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02683 | hp1 | a0009 | c0006 | t0001 | g0079 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02683 | hp2 | a0015 | c0018 | t0001 | g0169 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02698 | hp1 | a0008 | c0012 | t0001 | g0262 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02698 | hp2 | a0007 | c0005 | t0001 | g0069 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02717 | hp2 | a0012 | c0024 | t0001 | g0249 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02723 | hp1 | a0021 | c0027 | t0001 | g0028 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02735 | hp1 | a0013 | c0011 | t0001 | g0279 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02735 | hp2 | a0017 | c0015 | t0001 | g0133 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02738 | hp1 | a0006 | c0007 | t0001 | g0229 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02738 | hp2 | a0008 | c0012 | t0001 | g0260 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02809 | hp1 | a0011 | c0066 | t0001 | g0209 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02809 | hp2 | a0018 | c0030 | t0001 | g0024 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02818 | hp1 | a0011 | c0010 | t0001 | g0036 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02818 | hp2 | a0016 | c0017 | t0001 | g0027 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02886 | hp2 | a0011 | c0010 | t0001 | g0108 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02895 | hp2 | a0004 | c0004 | t0001 | g0030 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02922 | hp1 | a0001 | c0059 | t0001 | g0197 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02922 | hp2 | a0034 | c0062 | t0001 | g0216 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02965 | hp1 | a0003 | c0003 | t0001 | g0105 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02965 | hp2 | a0006 | c0029 | t0001 | g0098 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02976 | hp2 | a0022 | c0028 | t0001 | g0204 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03017 | hp1 | a0004 | c0004 | t0001 | g0004 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03017 | hp2 | a0015 | c0018 | t0001 | g0170 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0102 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03130 | hp1 | a0018 | c0030 | t0001 | g0024 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03130 | hp2 | a0008 | c0039 | t0001 | g0067 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03139 | hp1 | a0007 | c0056 | t0001 | g0208 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03139 | hp2 | a0006 | c0007 | t0001 | g0253 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03195 | hp1 | a0010 | c0009 | t0001 | g0101 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03209 | hp2 | a0001 | c0021 | t0001 | g0255 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03225 | hp1 | a0007 | c0005 | t0001 | g0124 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0205 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03239 | hp1 | a0009 | c0006 | t0001 | g0014 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03239 | hp2 | a0006 | c0035 | t0001 | g0042 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03486 | hp1 | a0022 | c0028 | t0001 | g0194 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03486 | hp2 | a0011 | c0010 | t0001 | g0021 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03490 | hp1 | a0004 | c0004 | t0001 | g0031 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03492 | hp1 | a0004 | c0004 | t0001 | g0031 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03492 | hp2 | a0003 | c0041 | t0001 | g0088 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03516 | hp1 | a0011 | c0010 | t0001 | g0110 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03516 | hp2 | a0035 | c0052 | t0001 | g0106 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03540 | hp1 | a0008 | c0020 | t0001 | g0033 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03540 | hp2 | a0016 | c0017 | t0001 | g0217 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03654 | hp1 | a0007 | c0005 | t0001 | g0240 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03654 | hp2 | a0005 | c0008 | t0001 | g0182 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03669 | hp1 | a0017 | c0015 | t0001 | g0128 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03669 | hp2 | a0009 | c0006 | t0001 | g0015 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03831 | hp1 | a0010 | c0054 | t0001 | g0219 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03831 | hp2 | a0006 | c0007 | t0001 | g0081 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03834 | hp2 | a0005 | c0019 | t0001 | g0048 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03927 | hp1 | a0013 | c0011 | t0001 | g0278 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03927 | hp2 | a0003 | c0003 | t0001 | g0202 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03942 | hp2 | a0008 | c0012 | t0001 | g0257 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG04115 | hp1 | a0006 | c0007 | t0001 | g0250 | SAS | STU | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG04115 | hp2 | a0009 | c0006 | t0001 | g0218 | SAS | STU | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG04184 | hp2 | a0017 | c0015 | t0001 | g0129 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG04204 | hp1 | a0013 | c0011 | t0001 | g0053 | SAS | STU | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18522 | hp1 | a0001 | c0026 | t0001 | g0126 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18522 | hp2 | a0011 | c0010 | t0001 | g0021 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18612 | hp1 | a0008 | c0023 | t0001 | g0016 | EAS | CHB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18612 | hp2 | a0005 | c0008 | t0001 | g0022 | EAS | CHB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18906 | hp1 | a0003 | c0003 | t0001 | g0097 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18906 | hp2 | a0008 | c0043 | t0001 | g0270 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18940 | hp2 | a0006 | c0007 | t0001 | g0238 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18947 | hp1 | a0006 | c0007 | t0001 | g0256 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18947 | hp2 | a0015 | c0018 | t0001 | g0120 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18953 | hp1 | a0003 | c0003 | t0001 | g0056 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18953 | hp2 | a0007 | c0005 | t0001 | g0100 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18959 | hp1 | a0009 | c0006 | t0001 | g0015 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18959 | hp2 | a0007 | c0005 | t0001 | g0034 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18960 | hp1 | a0001 | c0046 | t0001 | g0051 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18961 | hp2 | a0006 | c0007 | t0001 | g0037 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18962 | hp1 | a0005 | c0008 | t0001 | g0022 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18964 | hp1 | a0005 | c0008 | t0001 | g0191 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18967 | hp2 | a0036 | c0047 | t0001 | g0063 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18968 | hp1 | a0007 | c0005 | t0001 | g0269 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18968 | hp2 | a0005 | c0008 | t0001 | g0181 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18969 | hp1 | a0008 | c0025 | t0001 | g0247 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18969 | hp2 | a0014 | c0016 | t0001 | g0153 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0043 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18972 | hp1 | a0005 | c0008 | t0001 | g0190 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18974 | hp1 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18974 | hp2 | a0018 | c0045 | t0001 | g0059 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18977 | hp1 | a0006 | c0007 | t0001 | g0220 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18979 | hp1 | a0019 | c0033 | t0001 | g0049 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18982 | hp2 | a0017 | c0015 | t0001 | g0179 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18984 | hp1 | a0009 | c0006 | t0001 | g0078 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0096 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18990 | hp1 | a0005 | c0019 | t0001 | g0175 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18993 | hp2 | a0019 | c0033 | t0001 | g0046 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18995 | hp1 | a0009 | c0006 | t0001 | g0087 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18995 | hp2 | a0019 | c0032 | t0001 | g0167 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18997 | hp1 | a0006 | c0029 | t0001 | g0055 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19000 | hp1 | a0005 | c0008 | t0001 | g0214 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19005 | hp1 | a0006 | c0007 | t0001 | g0246 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19005 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19030 | hp1 | a0037 | c0044 | t0001 | g0252 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19043 | hp1 | a0001 | c0013 | t0001 | g0277 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19043 | hp2 | a0008 | c0057 | t0001 | g0210 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19056 | hp1 | a0005 | c0008 | t0001 | g0173 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19060 | hp1 | a0007 | c0005 | t0001 | g0234 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19064 | hp1 | a0007 | c0005 | t0001 | g0248 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19064 | hp2 | a0005 | c0008 | t0001 | g0023 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19070 | hp2 | a0006 | c0007 | t0001 | g0245 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19074 | hp2 | a0005 | c0008 | t0001 | g0023 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19077 | hp1 | a0005 | c0008 | t0001 | g0132 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19077 | hp2 | a0009 | c0006 | t0001 | g0084 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19078 | hp1 | a0017 | c0015 | t0001 | g0143 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19078 | hp2 | a0005 | c0008 | t0001 | g0176 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19086 | hp2 | a0013 | c0011 | t0001 | g0235 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19240 | hp1 | a0038 | c0042 | t0001 | g0162 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA19240 | hp2 | a0008 | c0020 | t0001 | g0033 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA20129 | hp1 | a0001 | c0031 | t0001 | g0025 | AFR | ASW | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA20129 | hp2 | a0016 | c0017 | t0001 | g0026 | AFR | ASW | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0185 | EUR | TSI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA20752 | hp2 | a0007 | c0005 | t0001 | g0018 | EUR | TSI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0187 | EUR | TSI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA20805 | hp2 | a0009 | c0006 | t0001 | g0005 | EUR | TSI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02109 | hp1 | a0016 | c0017 | t0001 | g0027 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02109 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02486 | hp1 | a0001 | c0013 | t0001 | g0274 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02486 | hp2 | a0007 | c0005 | t0001 | g0122 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG02559 | hp2 | a0012 | c0024 | t0001 | g0239 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03471 | hp1 | a0001 | c0013 | t0001 | g0276 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG06807 | hp1 | a0012 | c0014 | t0001 | g0011 | AFR | USA | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
HG06807 | hp2 | a0004 | c0004 | t0001 | g0004 | AFR | USA | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA20300 | hp1 | a0001 | c0038 | t0001 | g0119 | AFR | USA | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA20300 | hp2 | a0010 | c0009 | t0001 | g0012 | AFR | USA | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
NA21309 | hp2 | a0012 | c0014 | t0001 | g0196 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
homoSapiens | chm13v2 | a0007 | c0005 | t0001 | g0093 | REF | REF | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
homoSapiens | grch38p0 | a0012 | c0014 | t0001 | g0211 | REF | REF | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:9148976 | A | G | 1 | a0030 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.4445T>C | p.Val1482Ala | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 36/36 | 4499/4635 | 4445/4449 | 1482/1482 | chr12 | 9148976 | |||
chr12:9150700 | A | T | 8 | a0004 a0005 a0013 others(5): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
missense_variant | MODERATE | c.4328T>A | p.Ile1443Asn | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/36 | 4382/4635 | 4328/4449 | 1443/1482 | chr12 | 9150700 | |||
chr12:9151647 | C | T | 1 | a0036 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.4238G>A | p.Arg1413Gln | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/36 | 4292/4635 | 4238/4449 | 1413/1482 | chr12 | 9151647 | |||
chr12:9154620 | G | A | 1 | a0028 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.3770C>T | p.Thr1257Ile | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/36 | 3824/4635 | 3770/4449 | 1257/1482 | chr12 | 9154620 | |||
chr12:9154777 | T | G | 37 | a0001 a0002 a0003 others(34): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
missense_variant | MODERATE | c.3613A>C | p.Thr1205Pro | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/36 | 3667/4635 | 3613/4449 | 1205/1482 | chr12 | 9154777 | |||
chr12:9157223 | G | A | 2 | a0021 a0037 |
3 | HG02622.hp1 HG02723.hp1 NA19030.hp1 |
stop_gained | HIGH | c.3502C>T | p.Gln1168* | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/36 | 3556/4635 | 3502/4449 | 1168/1482 | chr12 | 9157223 | |||
chr12:9157285 | C | T | 2 | a0021 a0037 |
3 | HG02622.hp1 HG02723.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.3440G>A | p.Gly1147Glu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/36 | 3494/4635 | 3440/4449 | 1147/1482 | chr12 | 9157285 | |||
chr12:9157287 | A | T | 1 | a0029 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.3438T>A | p.His1146Gln | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/36 | 3492/4635 | 3438/4449 | 1146/1482 | chr12 | 9157287 | |||
chr12:9160355 | G | A | 13 | a0002 a0005 a0006 others(10): Show |
111 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
missense_variant | MODERATE | c.3008C>T | p.Thr1003Met | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/36 | 3062/4635 | 3008/4449 | 1003/1482 | chr12 | 9160355 | |||
chr12:9164177 | T | C | 17 | a0001 a0009 a0011 others(14): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
missense_variant | MODERATE | c.2570A>G | p.Asn857Ser | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 20/36 | 2624/4635 | 2570/4449 | 857/1482 | chr12 | 9164177 | |||
chr12:9165188 | A | G | 14 | a0002 a0003 a0005 others(11): Show |
139 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
missense_variant | MODERATE | c.2438T>C | p.Val813Ala | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/36 | 2492/4635 | 2438/4449 | 813/1482 | chr12 | 9165188 | |||
chr12:9165363 | A | C | 1 | a0038 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.2263T>G | p.Ser755Ala | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/36 | 2317/4635 | 2263/4449 | 755/1482 | chr12 | 9165363 | |||
chr12:9168905 | C | T | 6 | a0003 a0019 a0022 others(3): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
missense_variant | MODERATE | c.2071G>A | p.Val691Met | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/36 | 2125/4635 | 2071/4449 | 691/1482 | chr12 | 9168905 | |||
chr12:9169485 | C | T | 1 | a0024 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.1946G>A | p.Gly649Glu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/36 | 2000/4635 | 1946/4449 | 649/1482 | chr12 | 9169485 | |||
chr12:9169506 | C | T | 1 | a0033 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1925G>A | p.Arg642His | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/36 | 1979/4635 | 1925/4449 | 642/1482 | chr12 | 9169506 | |||
chr12:9181030 | G | A | 1 | a0005 | 17 | HG00423.hp1 HG02074.hp1 HG02083.hp2 others(14): Show |
stop_gained | HIGH | c.1792C>T | p.Gln598* | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/36 | 1846/4635 | 1792/4449 | 598/1482 | chr12 | 9181030 | |||
chr12:9181062 | G | A | 1 | a0021 | 2 | HG02622.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.1760C>T | p.Pro587Leu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/36 | 1814/4635 | 1760/4449 | 587/1482 | chr12 | 9181062 | |||
chr12:9192228 | G | C | 1 | a0032 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1511C>G | p.Ser504Cys | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/36 | 1565/4635 | 1511/4449 | 504/1482 | chr12 | 9192228 | |||
chr12:9194196 | G | C | 13 | a0002 a0005 a0014 others(10): Show |
91 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
missense_variant | MODERATE | c.1135C>G | p.Leu379Val | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/36 | 1189/4635 | 1135/4449 | 379/1482 | chr12 | 9194196 | |||
chr12:9197118 | G | A | 1 | a0011 | 8 | HG01884.hp1 HG02280.hp2 HG02809.hp1 others(5): Show |
missense_variant | MODERATE | c.761C>T | p.Thr254Ile | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/36 | 815/4635 | 761/4449 | 254/1482 | chr12 | 9197118 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:9152877 | T | C | 40 | a0001c0001 a0001c0013 a0001c0021 others(37): Show |
233 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
synonymous_variant | LOW | c.4068A>G | p.Gln1356Gln | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/36 | 4122/4635 | 4068/4449 | 1356/1482 | chr12 | 9152877 | |||
chr12:9152901 | A | C | 1 | a0001c0046 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.4044T>G | p.Ala1348Ala | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/36 | 4098/4635 | 4044/4449 | 1348/1482 | chr12 | 9152901 | |||
chr12:9157350 | A | G | 1 | a0008c0039 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.3375T>C | p.Pro1125Pro | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/36 | 3429/4635 | 3375/4449 | 1125/1482 | chr12 | 9157350 | |||
chr12:9158429 | A | G | 4 | a0008c0020 a0008c0043 a0018c0030 others(1): Show |
7 | HG02258.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
synonymous_variant | LOW | c.3285T>C | p.Asn1095Asn | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/36 | 3339/4635 | 3285/4449 | 1095/1482 | chr12 | 9158429 | |||
chr12:9162613 | A | G | 30 | a0001c0001 a0001c0013 a0001c0021 others(27): Show |
138 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(135): Show |
synonymous_variant | LOW | c.2772T>C | p.Ser924Ser | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/36 | 2826/4635 | 2772/4449 | 924/1482 | chr12 | 9162613 | |||
chr12:9165289 | G | A | 16 | a0001c0001 a0001c0046 a0001c0058 others(13): Show |
107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
synonymous_variant | LOW | c.2337C>T | p.Ser779Ser | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/36 | 2391/4635 | 2337/4449 | 779/1482 | chr12 | 9165289 | |||
chr12:9168879 | T | C | 7 | a0001c0013 a0001c0021 a0001c0038 others(4): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
synonymous_variant | LOW | c.2097A>G | p.Gly699Gly | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/36 | 2151/4635 | 2097/4449 | 699/1482 | chr12 | 9168879 | |||
chr12:9168924 | C | T | 1 | a0033c0036 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.2052G>A | p.Ser684Ser | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/36 | 2106/4635 | 2052/4449 | 684/1482 | chr12 | 9168924 | |||
chr12:9181019 | C | A | 1 | a0002c0065 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.1803G>T | p.Leu601Leu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/36 | 1857/4635 | 1803/4449 | 601/1482 | chr12 | 9181019 | |||
chr12:9181975 | C | T | 11 | a0001c0055 a0003c0003 a0003c0022 others(8): Show |
37 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(34): Show |
splice_region_variant&synonymous_variant | LOW | c.1689G>A | p.Lys563Lys | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/36 | 1743/4635 | 1689/4449 | 563/1482 | chr12 | 9181975 | |||
chr12:9181999 | C | T | 4 | a0001c0021 a0001c0038 a0011c0010 others(1): Show |
12 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(9): Show |
synonymous_variant | LOW | c.1665G>A | p.Glu555Glu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/36 | 1719/4635 | 1665/4449 | 555/1482 | chr12 | 9181999 | |||
chr12:9192677 | A | G | 49 | a0001c0001 a0001c0013 a0001c0021 others(46): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
synonymous_variant | LOW | c.1317T>C | p.Gly439Gly | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 12/36 | 1371/4635 | 1317/4449 | 439/1482 | chr12 | 9192677 | |||
chr12:9197114 | A | G | 2 | a0008c0020 a0033c0036 |
4 | HG02258.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
synonymous_variant | LOW | c.765T>C | p.Tyr255Tyr | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/36 | 819/4635 | 765/4449 | 255/1482 | chr12 | 9197114 | |||
chr12:9202610 | C | T | 1 | a0006c0035 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.342G>A | p.Arg114Arg | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 3/36 | 396/4635 | 342/4449 | 114/1482 | chr12 | 9202610 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:9149459 | G | A | 1 | a0004c0004t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4426+102C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 35/35 | chr12 | 9149459 | |||||||
chr12:9149717 | A | G | 32 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(29): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.4385-115T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9149717 | |||||||
chr12:9149860 | A | G | 1 | a0012c0024t0001g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4385-258T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9149860 | |||||||
chr12:9150107 | T | G | 1 | a0008c0039t0001g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4385-505A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150107 | |||||||
chr12:9150118 | T | A | 1 | a0010c0009t0001g0237 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4385-516A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150118 | |||||||
chr12:9150119 | A | C | 1 | a0011c0066t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4385-517T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150119 | |||||||
chr12:9150294 | T | G | 1 | a0001c0001t0001g0065 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4384+350A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150294 | |||||||
chr12:9150310 | T | G | 1 | a0008c0039t0001g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4384+334A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150310 | |||||||
chr12:9150314 | G | T | 7 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0001c0031t0001g0025 others(4): Show |
8 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4384+330C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150314 | |||||||
chr12:9150329 | C | T | 2 | a0021c0027t0001g0028 a0037c0044t0001g0252 |
3 | HG02622.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4384+315G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150329 | |||||||
chr12:9150344 | G | A | 32 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(29): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.4384+300C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150344 | |||||||
chr12:9150385 | C | T | 1 | a0014c0016t0001g0153 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.4384+259G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150385 | |||||||
chr12:9150753 | G | C | 40 | a0001c0038t0001g0119 a0003c0003t0001g0002 a0003c0003t0001g0019 others(37): Show |
45 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
splice_region_variant&intron_variant | LOW | c.4282-7C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9150753 | |||||||
chr12:9150759 | G | C | 1 | a0005c0008t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4282-13C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9150759 | |||||||
chr12:9150844 | A | G | 92 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(89): Show |
107 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.4282-98T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9150844 | |||||||
chr12:9150917 | C | A | 1 | a0001c0021t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4282-171G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9150917 | |||||||
chr12:9151337 | G | T | 1 | a0008c0020t0001g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4281+267C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151337 | |||||||
chr12:9151432 | A | G | 7 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0001c0031t0001g0025 others(4): Show |
8 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4281+172T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151432 | |||||||
chr12:9151504 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4281+100G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151504 | |||||||
chr12:9151524 | G | A | 1 | a0011c0066t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4281+80C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151524 | |||||||
chr12:9151549 | C | G | 1 | a0022c0028t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4281+55G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151549 | |||||||
chr12:9152375 | C | T | 1 | a0002c0002t0001g0215 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4122-65G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/35 | chr12 | 9152375 | |||||||
chr12:9152412 | G | A | 1 | a0015c0018t0001g0170 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4122-102C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/35 | chr12 | 9152412 | |||||||
chr12:9152444 | T | A | 2 | a0001c0021t0001g0255 a0018c0037t0001g0254 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4122-134A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/35 | chr12 | 9152444 | |||||||
chr12:9152701 | T | C | 1 | a0010c0009t0001g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4121+123A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/35 | chr12 | 9152701 | |||||||
chr12:9153096 | C | T | 1 | a0028c0048t0001g0265 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3993+29G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 30/35 | chr12 | 9153096 | |||||||
chr12:9153354 | C | T | 1 | a0001c0058t0001g0201 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3775-11G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9153354 | |||||||
chr12:9153390 | A | G | 5 | a0008c0020t0001g0033 a0008c0020t0001g0268 a0008c0043t0001g0270 others(2): Show |
7 | HG02258.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3775-47T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9153390 | |||||||
chr12:9153639 | A | T | 1 | a0031c0060t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3775-296T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9153639 | |||||||
chr12:9153984 | G | A | 1 | a0007c0005t0001g0271 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3774+632C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9153984 | |||||||
chr12:9154180 | G | A | 1 | a0005c0008t0001g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3774+436C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9154180 | |||||||
chr12:9154222 | T | C | 1 | a0003c0041t0001g0088 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3774+394A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9154222 | |||||||
chr12:9154399 | C | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
237 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.3774+217G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9154399 | |||||||
chr12:9155042 | G | A | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3551-203C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155042 | |||||||
chr12:9155156 | C | T | 1 | a0037c0044t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3551-317G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155156 | |||||||
chr12:9155166 | C | T | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3551-327G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155166 | |||||||
chr12:9155326 | G | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3551-487C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155326 | |||||||
chr12:9155345 | C | G | 1 | a0002c0002t0001g0147 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3551-506G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155345 | |||||||
chr12:9155492 | A | G | 1 | a0008c0025t0001g0232 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3551-653T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155492 | |||||||
chr12:9155492 | ATTG | A | 93 | a0001c0001t0001g0070 a0002c0002t0001g0003 a0002c0002t0001g0010 others(90): Show |
108 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.3551-656_3551-654d others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155492 | |||||||
chr12:9155623 | A | G | 2 | a0001c0021t0001g0123 a0001c0021t0001g0193 |
2 | HG01993.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.3551-784T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155623 | |||||||
chr12:9155916 | A | G | 1 | a0008c0039t0001g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3551-1077T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155916 | |||||||
chr12:9155929 | A | G | 41 | a0001c0038t0001g0119 a0003c0003t0001g0002 a0003c0003t0001g0019 others(38): Show |
47 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.3551-1090T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155929 | |||||||
chr12:9155955 | G | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(225): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.3551-1116C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155955 | |||||||
chr12:9156233 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3550+942T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156233 | |||||||
chr12:9156266 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG02976.hp1 HG03453.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3550+909C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156266 | |||||||
chr12:9156928 | T | A | 1 | a0015c0018t0001g0166 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3550+247A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156928 | |||||||
chr12:9156935 | G | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3550+240C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156935 | |||||||
chr12:9156970 | G | A | 7 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0001c0031t0001g0025 others(4): Show |
8 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3550+205C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156970 | |||||||
chr12:9157085 | G | C | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3550+90C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9157085 | |||||||
chr12:9157399 | G | A | 32 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(29): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3370-44C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 27/35 | chr12 | 9157399 | |||||||
chr12:9157412 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.3370-57A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 27/35 | chr12 | 9157412 | |||||||
chr12:9157555 | C | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
236 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.3370-200G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 27/35 | chr12 | 9157555 | |||||||
chr12:9157929 | C | A | 2 | a0001c0055t0001g0212 a0035c0052t0001g0106 |
2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3295-88G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9157929 | |||||||
chr12:9157969 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
236 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.3295-128G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9157969 | |||||||
chr12:9157979 | GT | G | 93 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(90): Show |
108 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.3295-139delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9157979 | |||||||
chr12:9157980 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.3295-139A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9157980 | |||||||
chr12:9158076 | A | C | 1 | a0002c0002t0001g0188 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3295-235T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9158076 | |||||||
chr12:9158363 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.3294+57G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9158363 | |||||||
chr12:9158581 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG01255.hp1 | splice_region_variant&intron_variant | LOW | c.3138-5C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158581 | |||||||
chr12:9158655 | C | G | 32 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(29): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3138-79G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158655 | |||||||
chr12:9158669 | A | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(225): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.3138-93T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158669 | |||||||
chr12:9158685 | C | T | 32 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(29): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3138-109G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158685 | |||||||
chr12:9158752 | C | CT | 30 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(27): Show |
35 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.3138-177dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158752 | |||||||
chr12:9158757 | C | T | 32 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(29): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3138-181G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | |||||||
chr12:9158757 | CT | C | 36 | a0001c0038t0001g0119 a0003c0003t0001g0002 a0003c0003t0001g0019 others(33): Show |
41 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.3138-182delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | |||||||
chr12:9158757 | CTT | C | 8 | a0001c0026t0001g0035 a0008c0020t0001g0033 a0008c0020t0001g0268 others(5): Show |
10 | HG02258.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.3138-183_3138-182d others(4): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | |||||||
chr12:9158757 | CTTT | C | 101 | a0001c0001t0001g0073 a0001c0001t0001g0183 a0001c0026t0001g0126 others(98): Show |
118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.3138-184_3138-182d others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | |||||||
chr12:9158757 | CTTTT | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
114 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.3138-185_3138-182d others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | |||||||
chr12:9159077 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3138-501T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159077 | |||||||
chr12:9159082 | G | A | 32 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(29): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3138-506C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159082 | |||||||
chr12:9159134 | G | T | 5 | a0010c0009t0001g0038 a0010c0009t0001g0101 a0016c0017t0001g0026 others(2): Show |
7 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3138-558C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159134 | |||||||
chr12:9159372 | C | A | 1 | a0001c0021t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3137+566G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159372 | |||||||
chr12:9159428 | T | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.3137+510A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159428 | |||||||
chr12:9159505 | T | C | 2 | a0013c0011t0001g0278 a0013c0011t0001g0279 |
2 | HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3137+433A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159505 | |||||||
chr12:9159885 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3137+53T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159885 | |||||||
chr12:9160141 | A | G | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3050-116T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/35 | chr12 | 9160141 | |||||||
chr12:9160150 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3050-125A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/35 | chr12 | 9160150 | |||||||
chr12:9160183 | A | G | 1 | a0008c0039t0001g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3049+131T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/35 | chr12 | 9160183 | |||||||
chr12:9160276 | T | C | 3 | a0017c0015t0001g0128 a0017c0015t0001g0129 a0017c0015t0001g0133 |
3 | HG02735.hp2 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.3049+38A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/35 | chr12 | 9160276 | |||||||
chr12:9160573 | CAG | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
235 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.2873-85_2873-84del others(2): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160573 | |||||||
chr12:9160708 | A | G | 33 | a0002c0065t0001g0138 a0004c0004t0001g0004 a0004c0004t0001g0030 others(30): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.2873-218T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160708 | |||||||
chr12:9160781 | G | A | 92 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(89): Show |
107 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2872+252C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160781 | |||||||
chr12:9160783 | C | T | 1 | a0001c0001t0001g0007 | 3 | HG00140.hp2 HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2872+250G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160783 | |||||||
chr12:9160788 | G | A | 1 | a0004c0004t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2872+245C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160788 | |||||||
chr12:9160840 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2872+193T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160840 | |||||||
chr12:9160887 | C | G | 4 | a0002c0002t0001g0136 a0002c0002t0001g0145 a0002c0002t0001g0146 others(1): Show |
4 | NA18967.hp1 NA18975.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2872+146G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160887 | |||||||
chr12:9160922 | T | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2872+111A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160922 | |||||||
chr12:9160924 | A | G | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2872+109T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160924 | |||||||
chr12:9161020 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2872+13C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9161020 | |||||||
chr12:9161212 | C | T | 1 | a0037c0044t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2789-96G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161212 | |||||||
chr12:9161277 | A | G | 1 | a0007c0005t0001g0271 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2789-161T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161277 | |||||||
chr12:9161363 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2789-247C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161363 | |||||||
chr12:9161471 | G | C | 1 | a0001c0001t0001g0225 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2789-355C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161471 | |||||||
chr12:9161611 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0044 others(78): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2789-495T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161611 | |||||||
chr12:9161862 | G | A | 1 | a0002c0002t0001g0157 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2788+735C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161862 | |||||||
chr12:9162013 | G | A | 4 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0001c0031t0001g0025 others(1): Show |
5 | HG02258.hp1 HG02280.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2788+584C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162013 | |||||||
chr12:9162032 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2788+565C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162032 | |||||||
chr12:9162074 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2788+523C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162074 | |||||||
chr12:9162106 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2788+491G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162106 | |||||||
chr12:9162209 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2788+388C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162209 | |||||||
chr12:9162261 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2788+336A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162261 | |||||||
chr12:9162392 | G | A | 3 | a0001c0001t0001g0192 a0013c0011t0001g0278 a0013c0011t0001g0279 |
3 | HG02735.hp1 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2788+205C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162392 | |||||||
chr12:9162909 | C | A | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.2737-261G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9162909 | |||||||
chr12:9162948 | C | T | 1 | a0005c0008t0001g0023 | 2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2737-300G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9162948 | |||||||
chr12:9163009 | T | C | 1 | a0037c0044t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2737-361A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163009 | |||||||
chr12:9163072 | G | T | 89 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(86): Show |
99 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.2737-424C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163072 | |||||||
chr12:9163162 | G | A | 3 | a0017c0015t0001g0128 a0017c0015t0001g0129 a0017c0015t0001g0133 |
3 | HG02735.hp2 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2736+506C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163162 | |||||||
chr12:9163280 | G | A | 1 | a0014c0016t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2736+388C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163280 | |||||||
chr12:9163296 | CA | C | 89 | a0001c0013t0001g0275 a0001c0026t0001g0035 a0001c0026t0001g0126 others(86): Show |
101 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.2736+371delT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163296 | |||||||
chr12:9163296 | CAA | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
162 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.2736+370_2736+371d others(4): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163296 | |||||||
chr12:9163296 | CAAAA | C | 44 | a0004c0004t0001g0004 a0004c0004t0001g0030 a0004c0004t0001g0031 others(41): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.2736+368_2736+371d others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163296 | |||||||
chr12:9163411 | A | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2736+257T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163411 | |||||||
chr12:9163452 | CA | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
129 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.2736+215delT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163452 | |||||||
chr12:9163531 | GC | G | 8 | a0003c0003t0001g0019 a0003c0003t0001g0043 a0003c0003t0001g0052 others(5): Show |
9 | NA18953.hp1 NA18970.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.2736+136delG | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163531 | |||||||
chr12:9163882 | G | T | 2 | a0008c0012t0001g0257 a0008c0012t0001g0260 |
2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2615-93C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 20/35 | chr12 | 9163882 | |||||||
chr12:9164311 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2488-52G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/35 | chr12 | 9164311 | |||||||
chr12:9164563 | A | T | 1 | a0013c0011t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2488-304T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/35 | chr12 | 9164563 | |||||||
chr12:9164807 | G | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
131 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2487+332C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/35 | chr12 | 9164807 | |||||||
chr12:9165050 | C | T | 1 | a0012c0024t0001g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2487+89G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/35 | chr12 | 9165050 | |||||||
chr12:9165405 | T | C | 2 | a0001c0001t0001g0062 a0009c0006t0001g0078 |
2 | NA18984.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.2259-38A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165405 | |||||||
chr12:9165573 | ACAAATGA others(8): Show |
A | 1 | a0009c0006t0001g0079 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2259-221_2259-207d others(17): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165573 | |||||||
chr12:9165683 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2259-316A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165683 | |||||||
chr12:9165692 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2259-325T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165692 | |||||||
chr12:9165900 | T | C | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2258+152A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165900 | |||||||
chr12:9166613 | G | A | 18 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(15): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.2108-411C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166613 | |||||||
chr12:9166629 | T | C | 2 | a0001c0021t0001g0255 a0018c0037t0001g0254 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2108-427A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166629 | |||||||
chr12:9166672 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(218): Show |
261 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2108-470G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166672 | |||||||
chr12:9166772 | G | A | 1 | a0016c0017t0001g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2108-570C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166772 | |||||||
chr12:9166820 | A | G | 1 | a0003c0041t0001g0088 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2108-618T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166820 | |||||||
chr12:9166881 | G | A | 1 | a0004c0004t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2108-679C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166881 | |||||||
chr12:9166924 | T | G | 1 | a0008c0039t0001g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2108-722A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166924 | |||||||
chr12:9166934 | T | C | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2108-732A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166934 | |||||||
chr12:9167119 | G | A | 18 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(15): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.2108-917C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167119 | |||||||
chr12:9167238 | C | T | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2108-1036G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167238 | |||||||
chr12:9167273 | G | A | 1 | a0019c0033t0001g0049 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2108-1071C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167273 | |||||||
chr12:9167534 | G | T | 46 | a0002c0002t0001g0172 a0002c0002t0001g0184 a0002c0002t0001g0185 others(43): Show |
51 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.2108-1332C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167534 | |||||||
chr12:9167615 | T | C | 1 | a0014c0016t0001g0153 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2107+1254A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167615 | |||||||
chr12:9167665 | T | C | 1 | a0037c0044t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2107+1204A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167665 | |||||||
chr12:9168065 | C | T | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2107+804G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168065 | |||||||
chr12:9168242 | A | G | 1 | a0035c0052t0001g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2107+627T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168242 | |||||||
chr12:9168265 | C | T | 6 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(3): Show |
6 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+604G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168265 | |||||||
chr12:9168303 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2107+566C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168303 | |||||||
chr12:9168364 | G | A | 18 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(15): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.2107+505C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168364 | |||||||
chr12:9168493 | T | C | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2107+376A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168493 | |||||||
chr12:9168529 | T | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2107+340A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168529 | |||||||
chr12:9168671 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2107+198G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168671 | |||||||
chr12:9168689 | A | T | 1 | a0005c0008t0001g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2107+180T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168689 | |||||||
chr12:9169081 | C | T | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.2002-107G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169081 | |||||||
chr12:9169176 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2002-202C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169176 | |||||||
chr12:9169177 | C | CA | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2002-204dupT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169177 | |||||||
chr12:9169180 | AT | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.2002-207delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169180 | |||||||
chr12:9169181 | T | A | 54 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(51): Show |
59 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.2002-207A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169181 | |||||||
chr12:9169300 | G | A | 1 | a0003c0022t0001g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2001+130C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169300 | |||||||
chr12:9169311 | G | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.2001+119C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169311 | |||||||
chr12:9169697 | G | T | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1840-106C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169697 | |||||||
chr12:9169702 | T | C | 6 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(3): Show |
6 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1840-111A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169702 | |||||||
chr12:9169798 | A | T | 5 | a0010c0009t0001g0038 a0016c0017t0001g0026 a0016c0017t0001g0027 others(2): Show |
7 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-207T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169798 | |||||||
chr12:9169816 | A | C | 1 | a0012c0024t0001g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1840-225T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169816 | |||||||
chr12:9169885 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1840-294T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169885 | |||||||
chr12:9169889 | G | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1840-298C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169889 | |||||||
chr12:9169923 | C | A | 1 | a0001c0001t0001g0041 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1840-332G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169923 | |||||||
chr12:9170062 | A | G | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-471T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170062 | |||||||
chr12:9170235 | G | A | 2 | a0008c0020t0001g0033 a0008c0020t0001g0268 |
3 | HG02647.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-644C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170235 | |||||||
chr12:9170367 | T | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1840-776A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170367 | |||||||
chr12:9170405 | C | T | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1840-814G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170405 | |||||||
chr12:9170431 | G | C | 2 | a0003c0003t0001g0160 a0003c0003t0001g0264 |
2 | NA18999.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1840-840C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170431 | |||||||
chr12:9170475 | G | A | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-884C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170475 | |||||||
chr12:9170703 | C | T | 2 | a0003c0022t0001g0233 a0003c0022t0001g0236 |
2 | HG00639.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1840-1112G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170703 | |||||||
chr12:9170857 | C | T | 43 | a0002c0002t0001g0172 a0002c0002t0001g0184 a0002c0002t0001g0187 others(40): Show |
48 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.1840-1266G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170857 | |||||||
chr12:9170881 | C | T | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-1290G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170881 | |||||||
chr12:9170944 | G | A | 18 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(15): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-1353C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170944 | |||||||
chr12:9171100 | C | T | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1840-1509G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171100 | |||||||
chr12:9171109 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1840-1518T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171109 | |||||||
chr12:9171201 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1840-1610G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171201 | |||||||
chr12:9171216 | C | T | 1 | a0002c0002t0001g0050 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1840-1625G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171216 | |||||||
chr12:9171358 | A | C | 1 | a0004c0004t0001g0031 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1840-1767T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171358 | |||||||
chr12:9171387 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
268 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.1840-1796A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171387 | |||||||
chr12:9171411 | T | G | 3 | a0008c0020t0001g0033 a0008c0020t0001g0268 a0033c0036t0001g0227 |
4 | HG02258.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1840-1820A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171411 | |||||||
chr12:9171423 | G | A | 6 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(3): Show |
6 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1840-1832C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171423 | |||||||
chr12:9171535 | G | A | 18 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(15): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-1944C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171535 | |||||||
chr12:9171543 | C | T | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-1952G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171543 | |||||||
chr12:9171652 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1840-2061G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171652 | |||||||
chr12:9171774 | G | C | 1 | a0037c0044t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1840-2183C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171774 | |||||||
chr12:9172017 | A | G | 18 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(15): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-2426T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172017 | |||||||
chr12:9172081 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1840-2490T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172081 | |||||||
chr12:9172094 | A | C | 2 | a0001c0001t0001g0125 a0015c0018t0001g0127 |
2 | HG01891.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1840-2503T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172094 | |||||||
chr12:9172245 | C | T | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-2654G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172245 | |||||||
chr12:9172477 | A | G | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-2886T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172477 | |||||||
chr12:9172585 | G | A | 1 | a0023c0053t0001g0195 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1840-2994C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172585 | |||||||
chr12:9172600 | C | T | 20 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(17): Show |
23 | HG00738.hp1 HG00738.hp2 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.1840-3009G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172600 | |||||||
chr12:9172776 | ACTAT | A | 18 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(15): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-3189_1840-318 others(8): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172776 | |||||||
chr12:9172875 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1840-3284C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172875 | |||||||
chr12:9172933 | A | G | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1840-3342T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172933 | |||||||
chr12:9173011 | C | T | 1 | a0005c0008t0001g0023 | 2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1840-3420G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173011 | |||||||
chr12:9173189 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1840-3598T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173189 | |||||||
chr12:9173266 | T | C | 1 | a0037c0044t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1840-3675A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173266 | |||||||
chr12:9173297 | T | C | 1 | a0004c0004t0001g0231 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1840-3706A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173297 | |||||||
chr12:9173416 | G | A | 1 | a0004c0004t0001g0030 | 2 | HG01168.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1840-3825C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173416 | |||||||
chr12:9173450 | A | G | 6 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(3): Show |
6 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1840-3859T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173450 | |||||||
chr12:9173463 | T | C | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-3872A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173463 | |||||||
chr12:9173509 | C | G | 4 | a0007c0005t0001g0122 a0007c0005t0001g0124 a0007c0056t0001g0208 others(1): Show |
5 | HG02486.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1840-3918G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173509 | |||||||
chr12:9173555 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1840-3964T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173555 | |||||||
chr12:9173598 | A | G | 1 | a0006c0007t0001g0037 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1840-4007T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173598 | |||||||
chr12:9173615 | A | G | 1 | a0006c0029t0001g0055 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1840-4024T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173615 | |||||||
chr12:9173646 | A | T | 90 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(87): Show |
101 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1840-4055T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173646 | |||||||
chr12:9173776 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1840-4185T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173776 | |||||||
chr12:9174083 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1840-4492T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174083 | |||||||
chr12:9174192 | C | T | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1840-4601G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174192 | |||||||
chr12:9174203 | A | G | 1 | a0008c0057t0001g0210 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1840-4612T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174203 | |||||||
chr12:9174564 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1840-4973T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174564 | |||||||
chr12:9174575 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1840-4984G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174575 | |||||||
chr12:9174614 | C | A | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-5023G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174614 | |||||||
chr12:9174662 | C | A | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-5071G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174662 | |||||||
chr12:9174845 | A | G | 10 | a0004c0004t0001g0223 a0004c0004t0001g0230 a0004c0004t0001g0258 others(7): Show |
10 | HG00642.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1840-5254T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174845 | |||||||
chr12:9174879 | A | G | 1 | a0005c0008t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1840-5288T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174879 | |||||||
chr12:9174906 | A | G | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1840-5315T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174906 | |||||||
chr12:9174955 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1840-5364T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174955 | |||||||
chr12:9175035 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1840-5444C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175035 | |||||||
chr12:9175067 | C | A | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1840-5476G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175067 | |||||||
chr12:9175193 | A | G | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-5602T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175193 | |||||||
chr12:9175661 | A | C | 1 | a0007c0005t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1839+5322T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175661 | |||||||
chr12:9175684 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1839+5299G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175684 | |||||||
chr12:9175825 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1839+5158C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175825 | |||||||
chr12:9175841 | GC | G | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+5141delG | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175841 | |||||||
chr12:9175876 | C | T | 2 | a0001c0021t0001g0255 a0018c0037t0001g0254 |
2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1839+5107G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175876 | |||||||
chr12:9176033 | C | T | 1 | a0009c0006t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1839+4950G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176033 | |||||||
chr12:9176132 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1839+4851T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176132 | |||||||
chr12:9176149 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1839+4834G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176149 | |||||||
chr12:9176411 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0125 a0015c0018t0001g0127 |
3 | HG01891.hp2 HG01952.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1839+4572T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176411 | |||||||
chr12:9176476 | T | G | 8 | a0001c0038t0001g0119 a0001c0055t0001g0212 a0011c0010t0001g0021 others(5): Show |
9 | HG01884.hp1 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1839+4507A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176476 | |||||||
chr12:9176554 | T | C | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+4429A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176554 | |||||||
chr12:9176624 | C | T | 1 | a0011c0066t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1839+4359G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176624 | |||||||
chr12:9176952 | G | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1839+4031C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176952 | |||||||
chr12:9177003 | T | G | 18 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(15): Show |
19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1839+3980A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177003 | |||||||
chr12:9177134 | T | C | 1 | a0005c0008t0001g0177 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1839+3849A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177134 | |||||||
chr12:9177196 | A | G | 17 | a0002c0002t0001g0172 a0002c0002t0001g0189 a0005c0008t0001g0022 others(14): Show |
19 | HG00423.hp1 HG00673.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1839+3787T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177196 | |||||||
chr12:9177278 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1839+3705A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177278 | |||||||
chr12:9177353 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1839+3630A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177353 | |||||||
chr12:9177552 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1839+3431C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177552 | |||||||
chr12:9177821 | A | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1839+3162T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177821 | |||||||
chr12:9177933 | A | G | 1 | a0007c0005t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1839+3050T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177933 | |||||||
chr12:9178009 | T | C | 90 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(87): Show |
101 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1839+2974A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178009 | |||||||
chr12:9178469 | A | G | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+2514T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178469 | |||||||
chr12:9178576 | G | A | 1 | a0001c0013t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1839+2407C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178576 | |||||||
chr12:9178813 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1839+2170C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178813 | |||||||
chr12:9178905 | TCA | T | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+2076_1839+207 others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178905 | |||||||
chr12:9179288 | T | G | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1839+1695A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179288 | |||||||
chr12:9179486 | A | G | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1839+1497T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179486 | |||||||
chr12:9179593 | A | G | 4 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0011c0066t0001g0209 others(1): Show |
4 | HG02280.hp1 HG02809.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839+1390T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179593 | |||||||
chr12:9179750 | C | T | 1 | a0003c0003t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1839+1233G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179750 | |||||||
chr12:9179983 | C | T | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+1000G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179983 | |||||||
chr12:9180011 | C | T | 32 | a0003c0003t0001g0002 a0003c0003t0001g0019 a0003c0003t0001g0043 others(29): Show |
36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+972G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180011 | |||||||
chr12:9180205 | A | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0125 a0015c0018t0001g0127 |
3 | HG01891.hp2 HG01952.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1839+778T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180205 | |||||||
chr12:9180224 | G | A | 29 | a0001c0001t0001g0029 a0004c0004t0001g0004 a0004c0004t0001g0031 others(26): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+759C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180224 | |||||||
chr12:9180233 | T | C | 3 | a0004c0004t0001g0223 a0004c0004t0001g0258 a0004c0004t0001g0263 |
3 | HG01346.hp1 HG01978.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1839+750A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180233 | |||||||
chr12:9180329 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1839+654G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180329 | |||||||
chr12:9180405 | T | C | 2 | a0006c0007t0001g0037 a0006c0007t0001g0220 |
2 | NA18961.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1839+578A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180405 | |||||||
chr12:9180520 | G | A | 1 | a0012c0024t0001g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1839+463C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180520 | |||||||
chr12:9180724 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1839+259G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180724 | |||||||
chr12:9180745 | G | A | 1 | a0008c0039t0001g0067 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1839+238C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180745 | |||||||
chr12:9180799 | T | C | 1 | a0014c0016t0001g0140 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1839+184A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180799 | |||||||
chr12:9180821 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1839+162C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180821 | |||||||
chr12:9180848 | T | A | 2 | a0003c0022t0001g0233 a0003c0022t0001g0236 |
2 | HG00639.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1839+135A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180848 | |||||||
chr12:9180872 | A | C | 1 | a0037c0044t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1839+111T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180872 | |||||||
chr12:9180889 | G | A | 5 | a0008c0020t0001g0033 a0008c0020t0001g0268 a0008c0039t0001g0067 others(2): Show |
6 | HG02258.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1839+94C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180889 | |||||||
chr12:9181153 | G | A | 91 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0125 others(88): Show |
101 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.1690-21C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181153 | |||||||
chr12:9181311 | C | T | 26 | a0001c0055t0001g0212 a0003c0003t0001g0019 a0003c0003t0001g0043 others(23): Show |
27 | HG00280.hp2 HG01109.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1690-179G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181311 | |||||||
chr12:9181375 | T | C | 1 | a0006c0007t0001g0253 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1690-243A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181375 | |||||||
chr12:9181658 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG00735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1689+317C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181658 | |||||||
chr12:9181725 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1689+250G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181725 | |||||||
chr12:9181903 | T | C | 1 | a0003c0003t0001g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1689+72A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181903 | |||||||
chr12:9181905 | T | C | 1 | a0003c0003t0001g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1689+70A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181905 | |||||||
chr12:9181961 | G | A | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1689+14C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181961 | |||||||
chr12:9182132 | G | GAGTGAGA others(13): Show |
195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
235 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1547-35_1547-16dup others(20): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182132 | |||||||
chr12:9182198 | G | T | 1 | a0027c0051t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1547-81C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182198 | |||||||
chr12:9182225 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1547-108C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182225 | |||||||
chr12:9182419 | C | CAT | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
247 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1547-304_1547-303d others(4): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182419 | |||||||
chr12:9182636 | T | C | 81 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(78): Show |
91 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1547-519A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182636 | |||||||
chr12:9182678 | A | C | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1547-561T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182678 | |||||||
chr12:9182712 | G | A | 3 | a0003c0003t0001g0200 a0003c0003t0001g0203 a0022c0028t0001g0204 |
3 | HG01109.hp2 HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1547-595C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182712 | |||||||
chr12:9182743 | C | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1547-626G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182743 | |||||||
chr12:9182820 | A | T | 34 | a0001c0055t0001g0212 a0003c0003t0001g0002 a0003c0003t0001g0019 others(31): Show |
38 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1547-703T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182820 | |||||||
chr12:9182901 | C | T | 1 | a0001c0013t0001g0276 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1547-784G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182901 | |||||||
chr12:9183050 | C | T | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1547-933G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183050 | |||||||
chr12:9183156 | A | G | 34 | a0001c0055t0001g0212 a0003c0003t0001g0002 a0003c0003t0001g0019 others(31): Show |
38 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1547-1039T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183156 | |||||||
chr12:9183321 | G | T | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1547-1204C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183321 | |||||||
chr12:9183408 | A | AT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
191 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1547-1292dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183408 | |||||||
chr12:9183630 | C | T | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1547-1513G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183630 | |||||||
chr12:9183685 | G | A | 1 | a0007c0005t0001g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1547-1568C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183685 | |||||||
chr12:9183772 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1547-1655C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183772 | |||||||
chr12:9183822 | A | G | 81 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(78): Show |
91 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1547-1705T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183822 | |||||||
chr12:9183905 | T | C | 9 | a0002c0002t0001g0130 a0002c0002t0001g0151 a0002c0002t0001g0154 others(6): Show |
9 | HG00738.hp2 HG01168.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1547-1788A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183905 | |||||||
chr12:9184136 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0083 a0009c0006t0001g0068 others(1): Show |
5 | HG02135.hp2 NA18961.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547-2019A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184136 | |||||||
chr12:9184223 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1547-2106C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184223 | |||||||
chr12:9184347 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1547-2230C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184347 | |||||||
chr12:9184423 | C | T | 1 | a0006c0007t0001g0245 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1547-2306G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184423 | |||||||
chr12:9184561 | G | A | 2 | a0003c0003t0001g0205 a0003c0022t0001g0121 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1547-2444C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184561 | |||||||
chr12:9184713 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1547-2596G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184713 | |||||||
chr12:9184972 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1547-2855C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184972 | |||||||
chr12:9185072 | A | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
225 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.1547-2955T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185072 | |||||||
chr12:9185391 | T | C | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1547-3274A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185391 | |||||||
chr12:9185658 | GAA | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1547-3543_1547-354 others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185658 | |||||||
chr12:9185672 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1547-3555C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185672 | |||||||
chr12:9185790 | A | ATTTCTTT others(3): Show |
3 | a0002c0002t0001g0154 a0002c0002t0001g0215 a0015c0018t0001g0169 |
3 | HG01256.hp2 HG02080.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1547-3683_1547-367 others(14): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(8): Show |
12 | a0001c0001t0001g0072 a0002c0002t0001g0117 a0002c0002t0001g0130 others(9): Show |
12 | HG01433.hp2 HG02717.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547-3688_1547-367 others(19): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(13): Show |
50 | a0001c0001t0001g0071 a0001c0021t0001g0193 a0002c0002t0001g0003 others(47): Show |
56 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1547-3693_1547-367 others(24): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(18): Show |
49 | a0001c0038t0001g0119 a0001c0046t0001g0051 a0002c0002t0001g0145 others(46): Show |
60 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1547-3698_1547-367 others(29): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(23): Show |
24 | a0001c0001t0001g0029 a0001c0026t0001g0035 a0001c0026t0001g0126 others(21): Show |
26 | HG00609.hp1 HG00639.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(34): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(28): Show |
9 | a0004c0004t0001g0243 a0006c0007t0001g0037 a0006c0007t0001g0220 others(6): Show |
9 | HG01074.hp1 HG02074.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(39): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(33): Show |
4 | a0001c0021t0001g0123 a0008c0020t0001g0033 a0008c0020t0001g0268 others(1): Show |
5 | HG01993.hp1 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(44): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(38): Show |
3 | a0001c0013t0001g0276 a0021c0027t0001g0028 a0032c0050t0001g0168 |
4 | HG02145.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(49): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(48): Show |
1 | a0001c0013t0001g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1547-3674_1547-367 others(59): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(53): Show |
3 | a0001c0013t0001g0275 a0001c0013t0001g0277 a0001c0059t0001g0197 |
3 | HG02572.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(64): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185790 | A | ATTTCTTT others(58): Show |
1 | a0001c0013t0001g0274 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1547-3674_1547-367 others(69): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | |||||||
chr12:9185814 | C | CTTTTCTT others(19): Show |
1 | a0005c0008t0001g0190 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1547-3698_1547-369 others(30): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185814 | |||||||
chr12:9185815 | T | TTTTCTTT others(22): Show |
1 | a0007c0005t0001g0269 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1547-3699_1547-369 others(33): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185815 | |||||||
chr12:9185819 | T | C | 1 | a0010c0009t0001g0242 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1547-3702A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185819 | |||||||
chr12:9185938 | G | A | 2 | a0014c0016t0001g0155 a0014c0016t0001g0156 |
2 | HG00099.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1547-3821C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185938 | |||||||
chr12:9185953 | G | A | 1 | a0004c0004t0001g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1547-3836C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185953 | |||||||
chr12:9186020 | A | C | 1 | a0001c0001t0001g0013 | 2 | NA18942.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1547-3903T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186020 | |||||||
chr12:9186039 | T | C | 1 | a0006c0007t0001g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1547-3922A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186039 | |||||||
chr12:9186059 | A | G | 165 | a0001c0001t0001g0029 a0001c0001t0001g0071 a0001c0001t0001g0072 others(162): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1547-3942T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186059 | |||||||
chr12:9186067 | A | G | 1 | a0002c0002t0001g0213 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1547-3950T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186067 | |||||||
chr12:9186079 | T | A | 1 | a0007c0005t0001g0045 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1547-3962A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186079 | |||||||
chr12:9186113 | T | G | 1 | a0002c0002t0001g0158 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1547-3996A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186113 | |||||||
chr12:9186143 | C | A | 1 | a0027c0051t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1547-4026G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186143 | |||||||
chr12:9186264 | G | A | 1 | a0004c0004t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1547-4147C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186264 | |||||||
chr12:9186383 | G | T | 6 | a0010c0009t0001g0012 a0010c0009t0001g0221 a0010c0009t0001g0237 others(3): Show |
8 | HG01106.hp2 HG01109.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1547-4266C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186383 | |||||||
chr12:9186429 | T | C | 3 | a0001c0001t0001g0017 a0009c0006t0001g0068 a0009c0006t0001g0084 |
4 | HG02135.hp2 NA18961.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-4312A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186429 | |||||||
chr12:9186543 | T | A | 1 | a0006c0007t0001g0250 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1547-4426A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186543 | |||||||
chr12:9186603 | C | A | 153 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(150): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1547-4486G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186603 | |||||||
chr12:9186688 | C | A | 4 | a0003c0003t0001g0002 a0003c0003t0001g0102 a0003c0003t0001g0103 others(1): Show |
7 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-4571G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186688 | |||||||
chr12:9186859 | G | A | 1 | a0003c0022t0001g0236 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1547-4742C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186859 | |||||||
chr12:9186904 | A | G | 85 | a0001c0021t0001g0123 a0002c0002t0001g0003 a0002c0002t0001g0010 others(82): Show |
94 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1547-4787T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186904 | |||||||
chr12:9187048 | G | A | 1 | a0001c0046t0001g0051 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1547-4931C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187048 | |||||||
chr12:9187077 | C | CAA | 80 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(77): Show |
89 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1547-4962_1547-496 others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187077 | |||||||
chr12:9187077 | CA | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1547-4961delT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187077 | |||||||
chr12:9187215 | A | G | 3 | a0003c0003t0001g0095 a0003c0003t0001g0097 a0003c0003t0001g0105 |
3 | HG02965.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1546+4978T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187215 | |||||||
chr12:9187226 | A | G | 152 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+4967T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187226 | |||||||
chr12:9187408 | C | A | 1 | a0013c0011t0001g0086 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1546+4785G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187408 | |||||||
chr12:9187413 | A | G | 51 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1546+4780T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187413 | |||||||
chr12:9187672 | A | G | 85 | a0001c0021t0001g0123 a0002c0002t0001g0003 a0002c0002t0001g0010 others(82): Show |
94 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1546+4521T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187672 | |||||||
chr12:9187681 | G | A | 5 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546+4512C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187681 | |||||||
chr12:9187693 | G | A | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1546+4500C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187693 | |||||||
chr12:9187762 | G | A | 152 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+4431C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187762 | |||||||
chr12:9187816 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1546+4377G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187816 | |||||||
chr12:9187882 | C | A | 1 | a0011c0010t0001g0110 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1546+4311G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187882 | |||||||
chr12:9188000 | A | C | 152 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+4193T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188000 | |||||||
chr12:9188033 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG00408.hp1 NA19004.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+4160C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188033 | |||||||
chr12:9188046 | G | A | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1546+4147C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188046 | |||||||
chr12:9188108 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1546+4085A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188108 | |||||||
chr12:9188113 | C | T | 152 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+4080G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188113 | |||||||
chr12:9188445 | C | T | 6 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(3): Show |
7 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+3748G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188445 | |||||||
chr12:9188559 | C | A | 152 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+3634G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188559 | |||||||
chr12:9188832 | A | T | 1 | a0006c0029t0001g0055 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1546+3361T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188832 | |||||||
chr12:9189016 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1546+3177T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189016 | |||||||
chr12:9189117 | C | T | 152 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+3076G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189117 | |||||||
chr12:9189333 | T | G | 152 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+2860A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189333 | |||||||
chr12:9189447 | G | T | 88 | a0001c0021t0001g0123 a0001c0021t0001g0193 a0001c0038t0001g0119 others(85): Show |
97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1546+2746C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189447 | |||||||
chr12:9189690 | T | C | 1 | a0015c0018t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1546+2503A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189690 | |||||||
chr12:9189924 | A | G | 88 | a0001c0021t0001g0123 a0001c0021t0001g0193 a0001c0038t0001g0119 others(85): Show |
97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1546+2269T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189924 | |||||||
chr12:9190063 | C | G | 1 | a0006c0035t0001g0042 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1546+2130G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190063 | |||||||
chr12:9190227 | A | G | 1 | a0002c0002t0001g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1546+1966T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190227 | |||||||
chr12:9190254 | C | T | 6 | a0003c0003t0001g0019 a0003c0003t0001g0043 a0003c0003t0001g0052 others(3): Show |
7 | NA18953.hp1 NA18970.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+1939G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190254 | |||||||
chr12:9190294 | C | T | 152 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(149): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+1899G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190294 | |||||||
chr12:9190422 | C | T | 3 | a0001c0021t0001g0193 a0001c0038t0001g0119 a0032c0050t0001g0168 |
3 | HG02055.hp1 HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1546+1771G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190422 | |||||||
chr12:9190488 | C | T | 1 | a0007c0005t0001g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1546+1705G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190488 | |||||||
chr12:9190696 | T | C | 1 | a0009c0006t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1546+1497A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190696 | |||||||
chr12:9190726 | A | T | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1546+1467T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190726 | |||||||
chr12:9190908 | T | C | 6 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0008c0020t0001g0033 others(3): Show |
7 | HG02258.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+1285A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190908 | |||||||
chr12:9190924 | G | C | 1 | a0037c0044t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546+1269C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190924 | |||||||
chr12:9190989 | A | T | 2 | a0002c0002t0001g0010 a0002c0002t0001g0139 |
4 | HG01081.hp2 HG01192.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+1204T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190989 | |||||||
chr12:9190990 | T | G | 88 | a0001c0021t0001g0123 a0001c0021t0001g0193 a0001c0038t0001g0119 others(85): Show |
97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1546+1203A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190990 | |||||||
chr12:9191057 | A | T | 6 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(3): Show |
7 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+1136T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9191057 | |||||||
chr12:9191297 | G | A | 1 | a0002c0002t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1546+896C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9191297 | |||||||
chr12:9191403 | A | T | 1 | a0007c0005t0001g0069 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1546+790T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9191403 | |||||||
chr12:9191778 | C | A | 1 | a0008c0020t0001g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1546+415G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9191778 | |||||||
chr12:9192282 | A | G | 86 | a0001c0021t0001g0123 a0002c0002t0001g0003 a0002c0002t0001g0010 others(83): Show |
95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1483-26T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 12/35 | chr12 | 9192282 | |||||||
chr12:9192366 | A | G | 51 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1483-110T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 12/35 | chr12 | 9192366 | |||||||
chr12:9192754 | A | G | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1255-15T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9192754 | |||||||
chr12:9192784 | T | G | 1 | a0007c0005t0001g0018 | 2 | HG01516.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1255-45A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9192784 | |||||||
chr12:9192812 | A | G | 156 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(153): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1255-73T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9192812 | |||||||
chr12:9192868 | G | A | 1 | a0003c0041t0001g0088 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1255-129C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9192868 | |||||||
chr12:9193054 | C | G | 1 | a0011c0010t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1255-315G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193054 | |||||||
chr12:9193221 | T | C | 156 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0089 others(153): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1255-482A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193221 | |||||||
chr12:9193226 | G | A | 86 | a0001c0021t0001g0123 a0002c0002t0001g0003 a0002c0002t0001g0010 others(83): Show |
95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1255-487C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193226 | |||||||
chr12:9193506 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1254+571A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193506 | |||||||
chr12:9193606 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1254+471A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193606 | |||||||
chr12:9193696 | C | T | 3 | a0001c0021t0001g0193 a0001c0038t0001g0119 a0032c0050t0001g0168 |
3 | HG02055.hp1 HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1254+381G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193696 | |||||||
chr12:9193727 | G | A | 5 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+350C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193727 | |||||||
chr12:9193869 | ATGAT | A | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+204_1254+207d others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193869 | |||||||
chr12:9193875 | G | A | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+202C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193875 | |||||||
chr12:9193877 | GAAA | G | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+197_1254+199d others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193877 | |||||||
chr12:9193883 | ATCAGGCA others(3): Show |
A | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+184_1254+193d others(12): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193883 | |||||||
chr12:9193895 | T | A | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+182A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193895 | |||||||
chr12:9193897 | C | T | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+180G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193897 | |||||||
chr12:9193899 | G | A | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+178C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193899 | |||||||
chr12:9193900 | T | A | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+177A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193900 | |||||||
chr12:9193902 | C | G | 6 | a0002c0002t0001g0047 a0002c0002t0001g0137 a0002c0002t0001g0144 others(3): Show |
6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+175G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193902 | |||||||
chr12:9194297 | A | T | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1093-59T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194297 | |||||||
chr12:9194318 | G | T | 1 | a0004c0004t0001g0273 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1093-80C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194318 | |||||||
chr12:9194462 | G | GT | 7 | a0001c0055t0001g0212 a0003c0003t0001g0102 a0003c0003t0001g0264 others(4): Show |
7 | HG01175.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1093-225dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194462 | |||||||
chr12:9194462 | GT | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1093-225delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194462 | |||||||
chr12:9194474 | T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1093-236A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194474 | |||||||
chr12:9194475 | T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1093-237A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194475 | |||||||
chr12:9194560 | A | G | 1 | a0003c0003t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1093-322T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194560 | |||||||
chr12:9194561 | C | T | 1 | a0003c0003t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1093-323G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194561 | |||||||
chr12:9194564 | A | C | 1 | a0003c0003t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1093-326T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194564 | |||||||
chr12:9194580 | T | G | 1 | a0002c0002t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1093-342A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194580 | |||||||
chr12:9194603 | T | C | 2 | a0001c0001t0001g0044 a0007c0005t0001g0045 |
2 | HG02155.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1093-365A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194603 | |||||||
chr12:9194638 | G | A | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1093-400C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194638 | |||||||
chr12:9194745 | T | A | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1093-507A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194745 | |||||||
chr12:9194798 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1093-560G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194798 | |||||||
chr12:9195143 | A | G | 1 | a0030c0061t0001g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1093-905T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195143 | |||||||
chr12:9195180 | A | G | 1 | a0007c0005t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1093-942T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195180 | |||||||
chr12:9195295 | A | T | 1 | a0004c0004t0001g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1092+1035T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195295 | |||||||
chr12:9195443 | C | G | 1 | a0004c0004t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1092+887G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195443 | |||||||
chr12:9195611 | A | AT | 64 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0054 others(61): Show |
77 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1092+718dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195611 | |||||||
chr12:9195611 | A | ATT | 12 | a0004c0004t0001g0223 a0004c0004t0001g0230 a0004c0004t0001g0231 others(9): Show |
13 | HG00642.hp2 HG01346.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1092+717_1092+718d others(4): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195611 | |||||||
chr12:9195611 | AT | A | 7 | a0001c0001t0001g0090 a0001c0013t0001g0277 a0001c0021t0001g0193 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+718delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195611 | |||||||
chr12:9195629 | T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1092+701A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195629 | |||||||
chr12:9195702 | C | G | 82 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(79): Show |
91 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1092+628G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195702 | |||||||
chr12:9195730 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1092+600T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195730 | |||||||
chr12:9195736 | G | A | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1092+594C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195736 | |||||||
chr12:9195756 | A | G | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1092+574T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195756 | |||||||
chr12:9195824 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1092+506A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195824 | |||||||
chr12:9195845 | A | G | 1 | a0010c0054t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1092+485T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195845 | |||||||
chr12:9195867 | TATA | T | 88 | a0001c0021t0001g0123 a0001c0021t0001g0193 a0001c0038t0001g0119 others(85): Show |
97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1092+460_1092+462d others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195867 | |||||||
chr12:9195903 | A | T | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1092+427T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195903 | |||||||
chr12:9195904 | T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1092+426A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195904 | |||||||
chr12:9196019 | G | A | 1 | a0004c0004t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1092+311C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9196019 | |||||||
chr12:9196687 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.868-2A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196687 | |||||||
chr12:9196774 | C | CT | 153 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0116 others(150): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.868-90dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196774 | |||||||
chr12:9196808 | C | T | 12 | a0001c0001t0001g0116 a0001c0046t0001g0051 a0003c0022t0001g0233 others(9): Show |
13 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.868-123G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196808 | |||||||
chr12:9196891 | C | A | 3 | a0008c0020t0001g0033 a0008c0020t0001g0268 a0033c0036t0001g0227 |
4 | HG02258.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+121G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196891 | |||||||
chr12:9196892 | G | A | 1 | a0016c0017t0001g0027 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.867+120C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196892 | |||||||
chr12:9196970 | T | C | 4 | a0003c0003t0001g0002 a0003c0003t0001g0102 a0003c0003t0001g0103 others(1): Show |
7 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.867+42A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196970 | |||||||
chr12:9197139 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.756-16A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197139 | |||||||
chr12:9197359 | A | G | 89 | a0001c0021t0001g0123 a0001c0021t0001g0193 a0001c0038t0001g0119 others(86): Show |
98 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.756-236T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197359 | |||||||
chr12:9197416 | A | G | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.756-293T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197416 | |||||||
chr12:9197418 | TAAAATAA others(93): Show |
T | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.756-395_756-296del others(100): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197418 | |||||||
chr12:9197425 | A | C | 47 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0116 others(44): Show |
56 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.756-302T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197425 | |||||||
chr12:9197480 | TATA | T | 6 | a0001c0013t0001g0111 a0001c0013t0001g0274 a0001c0013t0001g0275 others(3): Show |
7 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-360_756-358del others(3): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197480 | |||||||
chr12:9197595 | TA | T | 60 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0116 others(57): Show |
71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.756-473delT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197595 | |||||||
chr12:9197606 | T | C | 1 | a0005c0008t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.756-483A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197606 | |||||||
chr12:9197611 | T | G | 1 | a0032c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.756-488A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197611 | |||||||
chr12:9197632 | A | C | 3 | a0003c0003t0001g0019 a0003c0003t0001g0043 a0003c0003t0001g0052 |
4 | NA18970.hp2 NA18974.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-509T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197632 | |||||||
chr12:9197632 | ATATATTA others(3): Show |
A | 3 | a0001c0026t0001g0035 a0001c0026t0001g0126 a0038c0042t0001g0162 |
3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.756-519_756-510del others(10): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197632 | |||||||
chr12:9197642 | T | TTA | 149 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0116 others(146): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.756-521_756-520dup others(2): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197642 | |||||||
chr12:9197643 | T | A | 7 | a0011c0010t0001g0021 a0011c0010t0001g0036 a0011c0010t0001g0107 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.756-520A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197643 | |||||||
chr12:9197643 | TATATAAT others(3): Show |
T | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.756-530_756-521del others(10): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197643 | |||||||
chr12:9197649 | A | T | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.756-526T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197649 | |||||||
chr12:9197650 | T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.756-527A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197650 | |||||||
chr12:9197663 | TATTATAT others(26): Show |
T | 4 | a0006c0007t0001g0228 a0008c0020t0001g0033 a0008c0020t0001g0268 others(1): Show |
5 | HG02074.hp2 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-573_756-541del others(33): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197663 | |||||||
chr12:9197667 | ATATATAT others(24): Show |
A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(164): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.756-575_756-545del others(31): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197667 | |||||||
chr12:9197684 | C | T | 11 | a0001c0001t0001g0032 a0004c0004t0001g0223 a0004c0004t0001g0258 others(8): Show |
12 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.756-561G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197684 | |||||||
chr12:9197715 | C | T | 54 | a0001c0001t0001g0029 a0001c0001t0001g0116 a0001c0013t0001g0111 others(51): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.756-592G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197715 | |||||||
chr12:9197715 | CATAATAT others(117): Show |
C | 4 | a0001c0021t0001g0123 a0003c0022t0001g0121 a0007c0005t0001g0122 others(1): Show |
4 | HG01993.hp1 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-716_756-593del | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197715 | |||||||
chr12:9197718 | AATATATA others(26): Show |
A | 1 | a0011c0010t0001g0021 | 2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.756-628_756-596del others(33): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197718 | |||||||
chr12:9197726 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0070 |
2 | NA19067.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.756-603A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197726 | |||||||
chr12:9197777 | CATAATAT others(55): Show |
C | 78 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0047 others(75): Show |
87 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.756-716_756-655del others(62): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197777 | |||||||
chr12:9197780 | AATATATA others(26): Show |
A | 1 | a0001c0031t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756-690_756-658del others(33): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197780 | |||||||
chr12:9197808 | CATAATAT others(24): Show |
C | 4 | a0002c0002t0001g0130 a0002c0002t0001g0137 a0002c0065t0001g0138 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-716_756-686del others(31): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197808 | |||||||
chr12:9197826 | A | G | 1 | a0010c0009t0001g0241 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.756-703T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197826 | |||||||
chr12:9197934 | ATATAT | A | 4 | a0001c0021t0001g0123 a0003c0022t0001g0121 a0007c0005t0001g0122 others(1): Show |
4 | HG01993.hp1 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-816_756-812del others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197934 | |||||||
chr12:9198045 | CAT | C | 155 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0116 others(152): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.756-924_756-923del others(2): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9198045 | |||||||
chr12:9198178 | A | G | 155 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0116 others(152): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.756-1055T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9198178 | |||||||
chr12:9198258 | A | G | 4 | a0016c0017t0001g0026 a0016c0017t0001g0027 a0016c0017t0001g0217 others(1): Show |
6 | HG01884.hp2 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.756-1135T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9198258 | |||||||
chr12:9198473 | A | G | 86 | a0001c0021t0001g0123 a0002c0002t0001g0003 a0002c0002t0001g0010 others(83): Show |
95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.756-1350T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9198473 | |||||||
chr12:9199050 | A | G | 2 | a0017c0015t0001g0128 a0017c0015t0001g0129 |
2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.755+1314T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199050 | |||||||
chr12:9199052 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.755+1312T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199052 | |||||||
chr12:9199414 | A | G | 1 | a0012c0014t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755+950T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199414 | |||||||
chr12:9199625 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.755+739G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199625 | |||||||
chr12:9199725 | T | C | 1 | a0001c0026t0001g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.755+639A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199725 | |||||||
chr12:9199756 | T | C | 1 | a0027c0051t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.755+608A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199756 | |||||||
chr12:9199863 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.755+501C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199863 | |||||||
chr12:9199881 | A | G | 52 | a0001c0021t0001g0123 a0001c0026t0001g0126 a0002c0002t0001g0003 others(49): Show |
57 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.755+483T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199881 | |||||||
chr12:9199887 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.755+477T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199887 | |||||||
chr12:9200047 | A | G | 6 | a0011c0010t0001g0021 a0011c0010t0001g0036 a0011c0010t0001g0107 others(3): Show |
7 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+317T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200047 | |||||||
chr12:9200117 | C | T | 44 | a0002c0002t0001g0003 a0002c0002t0001g0010 a0002c0002t0001g0130 others(41): Show |
49 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.755+247G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200117 | |||||||
chr12:9200194 | T | C | 1 | a0002c0002t0001g0163 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.755+170A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200194 | |||||||
chr12:9200195 | A | G | 13 | a0001c0001t0001g0198 a0001c0001t0001g0206 a0001c0055t0001g0212 others(10): Show |
13 | HG00280.hp2 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.755+169T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200195 | |||||||
chr12:9200312 | C | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.755+52G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200312 | |||||||
chr12:9200349 | A | C | 5 | a0002c0002t0001g0184 a0002c0002t0001g0185 a0002c0002t0001g0186 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+15T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200349 | |||||||
chr12:9200569 | A | G | 3 | a0001c0001t0001g0044 a0003c0003t0001g0043 a0007c0005t0001g0045 |
3 | HG02155.hp1 NA18970.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.671-121T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 6/35 | chr12 | 9200569 | |||||||
chr12:9200636 | C | T | 1 | a0001c0059t0001g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.671-188G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 6/35 | chr12 | 9200636 | |||||||
chr12:9201232 | A | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.501+95T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 5/35 | chr12 | 9201232 | |||||||
chr12:9201279 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.501+48A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 5/35 | chr12 | 9201279 | |||||||
chr12:9201690 | T | G | 1 | a0015c0018t0001g0166 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.481-343A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201690 | |||||||
chr12:9201757 | A | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.481-410T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201757 | |||||||
chr12:9201817 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.481-470G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201817 | |||||||
chr12:9201921 | C | T | 1 | a0002c0002t0001g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480+398G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201921 | |||||||
chr12:9201988 | G | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.480+331C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201988 | |||||||
chr12:9202125 | T | A | 1 | a0035c0052t0001g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480+194A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9202125 | |||||||
chr12:9202249 | C | A | 1 | a0001c0021t0001g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.480+70G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9202249 | |||||||
chr12:9202424 | G | C | 1 | a0001c0021t0001g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.428-53C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 3/35 | chr12 | 9202424 | |||||||
chr12:9202792 | G | C | 1 | a0013c0011t0001g0279 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.268-108C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9202792 | |||||||
chr12:9202892 | A | G | 1 | a0015c0018t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.268-208T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9202892 | |||||||
chr12:9203017 | G | A | 1 | a0002c0002t0001g0164 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.268-333C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203017 | |||||||
chr12:9203265 | T | TA | 63 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0116 others(60): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.267+502dupT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203265 | |||||||
chr12:9203271 | A | T | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.267+497T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203271 | |||||||
chr12:9203318 | T | C | 1 | a0001c0026t0001g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.267+450A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203318 | |||||||
chr12:9203337 | C | CT | 29 | a0001c0001t0001g0183 a0001c0038t0001g0119 a0002c0002t0001g0130 others(26): Show |
31 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.267+430dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | |||||||
chr12:9203337 | CT | C | 13 | a0001c0013t0001g0274 a0001c0013t0001g0275 a0001c0013t0001g0276 others(10): Show |
14 | HG00738.hp2 HG01106.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.267+430delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | |||||||
chr12:9203337 | CTT | C | 55 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0116 others(52): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.267+429_267+430del others(2): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | |||||||
chr12:9203337 | CTTT | C | 5 | a0007c0005t0001g0034 a0007c0005t0001g0269 a0008c0020t0001g0033 others(2): Show |
7 | HG02083.hp1 HG02647.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+428_267+430del others(3): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | |||||||
chr12:9203337 | CTTTTT | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
96 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.267+426_267+430del others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | |||||||
chr12:9203337 | CTTTTTT | C | 25 | a0001c0001t0001g0020 a0001c0013t0001g0111 a0002c0002t0001g0094 others(22): Show |
31 | HG01884.hp1 HG02015.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.267+425_267+430del others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | |||||||
chr12:9203368 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
130 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.267+400C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203368 | |||||||
chr12:9203451 | C | T | 2 | a0015c0018t0001g0169 a0015c0018t0001g0170 |
2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.267+317G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203451 | |||||||
chr12:9203502 | C | T | 1 | a0015c0018t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.267+266G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203502 | |||||||
chr12:9203524 | G | A | 7 | a0001c0013t0001g0111 a0011c0010t0001g0021 a0011c0010t0001g0036 others(4): Show |
8 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.267+244C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203524 | |||||||
chr12:9203563 | G | A | 31 | a0001c0001t0001g0183 a0001c0001t0001g0192 a0001c0021t0001g0193 others(28): Show |
35 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.267+205C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203563 | |||||||
chr12:9204007 | T | C | 33 | a0001c0001t0001g0183 a0001c0001t0001g0192 a0001c0021t0001g0193 others(30): Show |
37 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.84-56A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204007 | |||||||
chr12:9204063 | A | G | 1 | a0001c0026t0001g0126 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84-112T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204063 | |||||||
chr12:9204085 | T | G | 1 | a0001c0055t0001g0212 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.84-134A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204085 | |||||||
chr12:9204156 | T | C | 1 | a0007c0005t0001g0271 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.84-205A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204156 | |||||||
chr12:9204340 | A | T | 1 | a0006c0007t0001g0037 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.84-389T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204340 | |||||||
chr12:9204410 | C | T | 5 | a0001c0001t0001g0125 a0001c0021t0001g0123 a0003c0022t0001g0121 others(2): Show |
5 | HG01891.hp2 HG01993.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-459G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204410 | |||||||
chr12:9204844 | C | T | 2 | a0001c0013t0001g0274 a0001c0013t0001g0275 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.84-893G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204844 | |||||||
chr12:9204854 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG00408.hp1 NA19004.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-903C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204854 | |||||||
chr12:9204906 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.84-955T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204906 | |||||||
chr12:9204981 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.84-1030G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204981 | |||||||
chr12:9205139 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.84-1188A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205139 | |||||||
chr12:9205223 | AC | A | 4 | a0001c0013t0001g0274 a0001c0013t0001g0275 a0001c0013t0001g0276 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-1273delG | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205223 | |||||||
chr12:9205271 | C | T | 1 | a0011c0010t0001g0036 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.84-1320G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205271 | |||||||
chr12:9205330 | C | G | 1 | a0015c0018t0001g0120 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.84-1379G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205330 | |||||||
chr12:9205543 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.84-1592T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205543 | |||||||
chr12:9205622 | A | G | 1 | a0021c0027t0001g0028 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.84-1671T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205622 | |||||||
chr12:9205627 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.84-1676C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205627 | |||||||
chr12:9205676 | T | C | 1 | a0006c0007t0001g0118 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.84-1725A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205676 | |||||||
chr12:9205677 | T | C | 1 | a0004c0004t0001g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.84-1726A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205677 | |||||||
chr12:9205702 | A | G | 53 | a0001c0001t0001g0125 a0001c0021t0001g0123 a0001c0026t0001g0126 others(50): Show |
58 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.84-1751T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205702 | |||||||
chr12:9205878 | A | T | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.84-1927T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205878 | |||||||
chr12:9206152 | G | A | 3 | a0002c0002t0001g0213 a0002c0002t0001g0215 a0005c0008t0001g0214 |
3 | HG02080.hp2 NA19000.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.83+2107C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206152 | |||||||
chr12:9206185 | T | C | 4 | a0016c0017t0001g0026 a0016c0017t0001g0027 a0016c0017t0001g0217 others(1): Show |
6 | HG01884.hp2 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2074A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206185 | |||||||
chr12:9206399 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
131 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.83+1860T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206399 | |||||||
chr12:9206476 | T | G | 4 | a0001c0013t0001g0274 a0001c0013t0001g0275 a0001c0013t0001g0276 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+1783A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206476 | |||||||
chr12:9206648 | T | C | 2 | a0004c0004t0001g0004 a0004c0004t0001g0273 |
5 | HG00140.hp1 HG00280.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+1611A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206648 | |||||||
chr12:9206783 | T | C | 4 | a0001c0013t0001g0274 a0001c0013t0001g0275 a0001c0013t0001g0276 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+1476A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206783 | |||||||
chr12:9206887 | C | T | 1 | a0010c0054t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.83+1372G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206887 | |||||||
chr12:9206976 | A | G | 1 | a0001c0026t0001g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83+1283T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206976 | |||||||
chr12:9207613 | C | A | 1 | a0009c0006t0001g0218 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.83+646G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9207613 | |||||||
chr12:9207884 | G | A | 68 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0225 others(65): Show |
80 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.83+375C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9207884 | |||||||
chr12:9208210 | G | A | 2 | a0013c0011t0001g0278 a0013c0011t0001g0279 |
2 | HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.83+49C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9208210 |