Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27315 |
| ensemblid | ENSG00000148985.20 |
| hgncid | 17893 |
| symbol | PGAP2 |
| name | post-GPI attachment to proteins 2 |
| refseq_nuc | NM_014489.4 |
| refseq_prot | NP_055304.1 |
| ensembl_nuc | ENST00000278243.9 |
| ensembl_prot | ENSP00000278243.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 3808560 |
| end | 3826371 |
| strand | + |
| ver | v1.2 |
| region | chr11:3808560-3826371 |
| region5000 | chr11:3803560-3831371 |
| regionname0 | PGAP2_chr11_3808560_3826371 |
| regionname5000 | PGAP2_chr11_3803560_3831371 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 315 | 414 | 96 | 76 | 176 | 18 | 46 | 131 | PGAP2_chr11_3803560_3831371 | PGAP2 | MYQVP others(310): Show |
chr11 | 3803560 | 3831371 |
| a0002 | 0/0 | 315 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | MYQVP others(310): Show |
chr11 | 3803560 | 3831371 |
| a0003 | 0/0 | 248 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | MYQVP others(243): Show |
chr11 | 3803560 | 3831371 |
| a0004 | 0/0 | 315 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | MYQVP others(310): Show |
chr11 | 3803560 | 3831371 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 945 | 413 | 96 | 76 | 175 | 18 | 46 | PGAP2_chr11_3803560_3831371 | PGAP2 | ATGTA others(940): Show |
chr11 | 3803560 | 3831371 | ||
| a0001c0004 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | ATGTA others(940): Show |
chr11 | 3803560 | 3831371 | ||
| a0002c0002 | 0/0 | 945 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | ATGTA others(940): Show |
chr11 | 3803560 | 3831371 | ||
| a0003c0003 | 0/0 | 883 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | ATGTA others(878): Show |
chr11 | 3803560 | 3831371 | ||
| a0004c0005 | 0/0 | 945 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | ATGTA others(940): Show |
chr11 | 3803560 | 3831371 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1964 | 107 | 12 | 26 | 50 | 8 | 11 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0002 | 1/0 | 1963 | 74 | 3 | 10 | 50 | 3 | 7 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0003 | 0/0 | 1960 | 61 | 17 | 15 | 25 | 0 | 4 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1955): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0004 | 0/0 | 1964 | 24 | 1 | 4 | 17 | 0 | 2 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0005 | 0/0 | 1964 | 21 | 0 | 2 | 15 | 2 | 2 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0006 | 0/0 | 1964 | 14 | 12 | 2 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0007 | 0/0 | 1963 | 13 | 3 | 1 | 7 | 1 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0008 | 0/1 | 1963 | 13 | 2 | 3 | 2 | 1 | 4 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0009 | 0/0 | 1964 | 11 | 0 | 7 | 0 | 1 | 3 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0010 | 0/0 | 1961 | 9 | 8 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1956): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0011 | 0/0 | 1960 | 8 | 6 | 1 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1955): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0012 | 0/0 | 1960 | 7 | 6 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1955): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0013 | 0/0 | 1960 | 7 | 5 | 1 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1955): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0014 | 0/0 | 1963 | 6 | 0 | 1 | 1 | 0 | 4 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0015 | 0/0 | 1960 | 6 | 6 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1955): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0016 | 0/0 | 1965 | 5 | 4 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1960): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0017 | 0/0 | 1965 | 4 | 1 | 0 | 2 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1960): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0018 | 0/0 | 1964 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0019 | 0/0 | 1961 | 2 | 0 | 0 | 1 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1956): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0020 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1960): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0021 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1960): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0022 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0024 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0025 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0026 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0028 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0029 | 0/0 | 1963 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0030 | 0/0 | 1963 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0031 | 0/0 | 1963 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0032 | 0/0 | 1963 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0033 | 0/0 | 1961 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1956): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0034 | 0/0 | 1961 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1956): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0035 | 0/0 | 1961 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1956): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0036 | 0/0 | 1960 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1955): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0037 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0038 | 0/0 | 1965 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1960): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0039 | 0/0 | 1964 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0001c0001t0040 | 0/0 | 1963 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1958): Show |
chr11 | 3803560 | 3831371 |
| a0001c0004t0005 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0002c0002t0023 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0002c0002t0027 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| a0003c0003t0001 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1897): Show |
chr11 | 3803560 | 3831371 |
| a0004c0005t0001 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | GTTCG others(1959): Show |
chr11 | 3803560 | 3831371 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 1 | 10 | 7 | 2 | 2 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0002 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 2 | 6 | 0 | 2 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0002 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0003 | 0/0 | 13 | 0 | 3 | 6 | 2 | 2 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0008 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0011 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0002 | 0/0 | 17 | 2 | 4 | 10 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0010 | 0/0 | 6 | 2 | 2 | 1 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0012 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0009g0007 | 0/0 | 6 | 0 | 2 | 0 | 1 | 3 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0009g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0009g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0010g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0010g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0010g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0010g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0011g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0011g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0011g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0011g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0012g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0012g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0013g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0013g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0013g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0014g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0014g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0014g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0014g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0014g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0015g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0015g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0015g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0015g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0016g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0016g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0017g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0017g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0017g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0017g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0018g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0018g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0019g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0019g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0020g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0021g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0022g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0024g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0025g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0026g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0028g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0029g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0030g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0031g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0032g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0033g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0034g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0035g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0036g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0037g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0038g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0039g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0001t0040g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0001c0004t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0002c0002t0023g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0002c0002t0027g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| a0004c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0140 | EUR | GBR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0172 | EUR | GBR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0178 | EUR | GBR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0094 | EUR | FIN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0092 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0206 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0144 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | CHS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0203 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0040 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0202 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0137 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0204 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01109 | hp1 | a0001 | c0001 | t0016 | g0027 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0112 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01168 | hp2 | a0001 | c0001 | t0009 | g0050 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01169 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0019 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0043 | AMR | PUR | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0019 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01433 | hp2 | a0001 | c0001 | t0012 | g0196 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0012 | EUR | IBS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01516 | hp2 | a0001 | c0001 | t0038 | g0007 | EUR | IBS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01517 | hp2 | a0001 | c0001 | t0009 | g0007 | EUR | IBS | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0129 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0207 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01934 | hp1 | a0001 | c0001 | t0008 | g0081 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01943 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01978 | hp1 | a0001 | c0001 | t0013 | g0010 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02145 | hp2 | a0001 | c0001 | t0015 | g0152 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0088 | EAS | CDX | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CDX | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0131 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0128 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0040 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02451 | hp2 | a0001 | c0001 | t0026 | g0048 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02602 | hp1 | a0001 | c0001 | t0008 | g0104 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02622 | hp1 | a0001 | c0001 | t0034 | g0013 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0020 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02630 | hp1 | a0001 | c0001 | t0022 | g0150 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02630 | hp2 | a0001 | c0001 | t0037 | g0043 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0103 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0102 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02738 | hp1 | a0001 | c0001 | t0017 | g0106 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0110 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0054 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02818 | hp1 | a0001 | c0001 | t0028 | g0183 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02886 | hp1 | a0001 | c0001 | t0016 | g0027 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0013 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0027 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0120 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0013 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02922 | hp2 | a0001 | c0001 | t0030 | g0068 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0044 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02965 | hp2 | a0001 | c0001 | t0015 | g0020 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02976 | hp1 | a0002 | c0002 | t0023 | g0214 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0003 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03017 | hp2 | a0001 | c0001 | t0008 | g0069 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0208 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0158 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03130 | hp1 | a0001 | c0001 | t0016 | g0185 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0055 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03195 | hp2 | a0001 | c0001 | t0016 | g0030 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0025 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0013 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03239 | hp2 | a0001 | c0001 | t0014 | g0163 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0184 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03486 | hp2 | a0001 | c0001 | t0033 | g0209 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03491 | hp1 | a0001 | c0001 | t0009 | g0007 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03492 | hp2 | a0001 | c0001 | t0009 | g0007 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0157 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0013 | AFR | GWD | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03579 | hp1 | a0002 | c0002 | t0027 | g0149 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03654 | hp1 | a0001 | c0001 | t0008 | g0012 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03654 | hp2 | a0001 | c0001 | t0009 | g0007 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03688 | hp1 | a0001 | c0001 | t0032 | g0017 | SAS | STU | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | STU | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03710 | hp1 | a0001 | c0001 | t0039 | g0007 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0148 | SAS | PJL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03831 | hp1 | a0001 | c0001 | t0029 | g0017 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0132 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03834 | hp1 | a0001 | c0001 | t0014 | g0133 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03927 | hp1 | a0001 | c0001 | t0013 | g0002 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03942 | hp1 | a0001 | c0001 | t0036 | g0201 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03942 | hp2 | a0001 | c0001 | t0014 | g0195 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0135 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0188 | SAS | BEB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | STU | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG04228 | hp1 | a0001 | c0001 | t0031 | g0070 | SAS | STU | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | YRI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0211 | AFR | YRI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18943 | hp2 | a0001 | c0001 | t0011 | g0018 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18949 | hp1 | a0001 | c0001 | t0035 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18952 | hp2 | a0001 | c0001 | t0019 | g0037 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18956 | hp2 | a0001 | c0004 | t0005 | g0134 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18961 | hp1 | a0004 | c0005 | t0001 | g0023 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18961 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18967 | hp1 | a0001 | c0001 | t0018 | g0065 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18968 | hp2 | a0001 | c0001 | t0017 | g0121 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18983 | hp2 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18987 | hp1 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18987 | hp2 | a0001 | c0001 | t0007 | g0078 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18988 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18989 | hp2 | a0001 | c0001 | t0020 | g0009 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18998 | hp1 | a0001 | c0001 | t0008 | g0138 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | LWK | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0197 | AFR | LWK | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0044 | AFR | LWK | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | LWK | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19062 | hp2 | a0001 | c0001 | t0017 | g0009 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19080 | hp1 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19080 | hp2 | a0001 | c0001 | t0018 | g0006 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0028 | AFR | YRI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | YRI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ASW | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0087 | AFR | ASW | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20752 | hp2 | a0001 | c0001 | t0040 | g0003 | EUR | TSI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | GIH | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20905 | hp2 | a0001 | c0001 | t0019 | g0160 | SAS | GIH | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0051 | AMR | CLM | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0053 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02109 | hp2 | a0001 | c0001 | t0015 | g0200 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0123 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0030 | AFR | ACB | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03471 | hp1 | a0001 | c0001 | t0021 | g0182 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0035 | AFR | MSL | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0213 | AFR | USA | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0125 | AFR | USA | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0151 | AFR | USA | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | USA | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0049 | AFR | LWK | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0073 | REF | REF | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | PGAP2_chr11_3803560_3831371 | PGAP2 | chr11 | 3803560 | 3831371 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:3811311 | C | T | 1 | a0004 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.52C>T | p.Arg18Cys | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/7 | 154/1963 | 52/948 | 18/315 | chr11 | 3811311 | |||
| chr11:3817473 | TTCTTCTG others(82): Show |
T | 1 | a0003 | 1 | HG02155.hp2 | splice_donor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.289_348+29delTTCTG others(84): Show |
p.Phe97_Gly116del | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/7 | 391/1963 | 289/948 | 97/315 | INFO_REALIGN_3_PRIME | chr11 | 3817473 | ||
| chr11:3817513 | A | T | 1 | a0001 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.326A>T | p.Tyr109Phe | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/7 | 428/1963 | 326/948 | 109/315 | chr11 | 3817513 | |||
| chr11:3824078 | G | A | 1 | a0002 | 2 | HG02976.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.544G>A | p.Val182Ile | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 4/7 | 646/1963 | 544/948 | 182/315 | chr11 | 3824078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:3817466 | C | T | 1 | a0001c0004 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.279C>T | p.Phe93Phe | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/7 | 381/1963 | 279/948 | 93/315 | chr11 | 3817466 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:3808567 | C | G | 1 | a0001c0001t0040 | 1 | NA20752.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/7 | 2693 | chr11 | 3808567 | ||||||
| chr11:3808632 | C | G | 3 | a0001c0001t0009 a0001c0001t0038 a0001c0001t0039 |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-30C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/7 | 2628 | chr11 | 3808632 | ||||||
| chr11:3825538 | C | T | 1 | a0001c0001t0037 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*80C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 80 | chr11 | 3825538 | ||||||
| chr11:3825622 | TCTC | T | 11 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(8): Show |
104 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*168_*170delCTC | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 168 | INFO_REALIGN_3_PRIME | chr11 | 3825622 | |||||
| chr11:3825723 | T | TA | 23 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(20): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*276dupA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 277 | INFO_REALIGN_3_PRIME | chr11 | 3825723 | |||||
| chr11:3825723 | T | TAA | 5 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0020 others(2): Show |
12 | HG01109.hp1 HG01516.hp2 HG02738.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*275_*276dupAA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 277 | INFO_REALIGN_3_PRIME | chr11 | 3825723 | |||||
| chr11:3825853 | G | T | 1 | a0001c0001t0028 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*395G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 395 | chr11 | 3825853 | ||||||
| chr11:3825858 | C | T | 1 | a0001c0001t0032 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*400C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 400 | chr11 | 3825858 | ||||||
| chr11:3825864 | T | C | 1 | a0001c0001t0033 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 406 | chr11 | 3825864 | ||||||
| chr11:3825937 | G | C | 1 | a0001c0001t0022 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 479 | chr11 | 3825937 | ||||||
| chr11:3826031 | C | T | 19 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(16): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*573C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 573 | chr11 | 3826031 | ||||||
| chr11:3826063 | A | G | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(13): Show |
154 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*605A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 605 | chr11 | 3826063 | ||||||
| chr11:3826077 | T | C | 1 | a0001c0001t0029 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*619T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 619 | chr11 | 3826077 | ||||||
| chr11:3826130 | C | T | 2 | a0001c0001t0026 a0002c0002t0023 |
2 | HG02451.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*672C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 672 | chr11 | 3826130 | ||||||
| chr11:3826200 | C | T | 12 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(9): Show |
55 | HG00639.hp2 HG00741.hp1 HG01074.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 742 | chr11 | 3826200 | ||||||
| chr11:3826216 | T | C | 1 | a0001c0001t0024 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*758T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 758 | chr11 | 3826216 | ||||||
| chr11:3826344 | T | G | 2 | a0001c0001t0022 a0001c0001t0030 |
2 | HG02630.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*886T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 886 | chr11 | 3826344 | ||||||
| chr11:3826345 | T | G | 2 | a0001c0001t0022 a0001c0001t0030 |
2 | HG02630.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*887T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 7/7 | 887 | chr11 | 3826345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:3808723 | C | T | 1 | a0001c0001t0006g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+72C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3808723 | |||||||
| chr11:3808729 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-11+78G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3808729 | |||||||
| chr11:3808773 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-11+122C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3808773 | |||||||
| chr11:3808848 | G | A | 18 | a0001c0001t0001g0047 a0001c0001t0004g0031 a0001c0001t0006g0031 others(15): Show |
25 | HG01123.hp2 HG01167.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.-11+197G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3808848 | |||||||
| chr11:3809267 | C | G | 15 | a0001c0001t0003g0210 a0001c0001t0006g0028 a0001c0001t0006g0029 others(12): Show |
18 | HG00639.hp2 HG01891.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11+616C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3809267 | |||||||
| chr11:3809425 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-11+774A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3809425 | |||||||
| chr11:3809540 | A | G | 8 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(5): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+889A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3809540 | |||||||
| chr11:3809555 | T | G | 1 | a0001c0001t0012g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-11+904T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3809555 | |||||||
| chr11:3809598 | C | T | 1 | a0001c0001t0036g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-11+947C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3809598 | |||||||
| chr11:3810066 | C | T | 1 | a0001c0001t0013g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-1184C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810066 | |||||||
| chr11:3810074 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-10-1176G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810074 | |||||||
| chr11:3810092 | C | T | 8 | a0001c0001t0004g0031 a0001c0001t0006g0031 a0001c0001t0011g0013 others(5): Show |
10 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-1158C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810092 | |||||||
| chr11:3810098 | A | G | 1 | a0001c0001t0008g0148 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10-1152A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810098 | |||||||
| chr11:3810544 | C | T | 1 | a0001c0001t0003g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-10-706C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810544 | |||||||
| chr11:3810701 | T | G | 1 | a0002c0002t0027g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10-549T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810701 | |||||||
| chr11:3810789 | G | T | 1 | a0001c0001t0002g0147 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-10-461G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810789 | |||||||
| chr11:3810948 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-10-302C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810948 | |||||||
| chr11:3810949 | T | A | 1 | a0001c0001t0003g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-10-301T>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3810949 | |||||||
| chr11:3811027 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-10-223G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3811027 | |||||||
| chr11:3811114 | G | A | 1 | a0001c0001t0006g0206 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-10-136G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 1/6 | chr11 | 3811114 | |||||||
| chr11:3811550 | G | A | 2 | a0001c0001t0004g0056 a0001c0001t0004g0057 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.165+126G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3811550 | |||||||
| chr11:3811663 | AACAGAGT others(5): Show |
A | 1 | a0001c0001t0005g0155 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.165+243_165+254del others(12): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3811663 | ||||||
| chr11:3811684 | C | T | 3 | a0001c0001t0011g0013 a0001c0001t0013g0013 a0001c0001t0034g0013 |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+260C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3811684 | |||||||
| chr11:3812080 | T | C | 5 | a0001c0001t0002g0061 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | NA18977.hp1 NA18979.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+656T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3812080 | |||||||
| chr11:3812424 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.165+1000A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3812424 | |||||||
| chr11:3812537 | G | A | 1 | a0001c0001t0022g0150 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.165+1113G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3812537 | |||||||
| chr11:3812620 | G | A | 2 | a0001c0001t0002g0064 a0001c0001t0005g0063 |
2 | NA18999.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.165+1196G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3812620 | |||||||
| chr11:3812627 | A | C | 2 | a0001c0001t0026g0048 a0002c0002t0023g0214 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.165+1203A>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3812627 | |||||||
| chr11:3812651 | T | TGGGGTCC others(19): Show |
1 | a0001c0001t0003g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.165+1228_165+1253d others(28): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3812651 | ||||||
| chr11:3812809 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.165+1385C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3812809 | |||||||
| chr11:3812849 | T | C | 8 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(5): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+1425T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3812849 | |||||||
| chr11:3813029 | G | A | 3 | a0001c0001t0005g0066 a0001c0001t0005g0067 a0001c0001t0018g0065 |
3 | NA18946.hp1 NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.165+1605G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3813029 | |||||||
| chr11:3813084 | T | C | 21 | a0001c0001t0003g0020 a0001c0001t0004g0031 a0001c0001t0006g0031 others(18): Show |
30 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.165+1660T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3813084 | |||||||
| chr11:3813377 | C | T | 6 | a0001c0001t0003g0210 a0001c0001t0006g0029 a0001c0001t0006g0206 others(3): Show |
8 | HG00639.hp2 HG01943.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+1953C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3813377 | |||||||
| chr11:3813386 | TA | T | 9 | a0001c0001t0003g0193 a0001c0001t0009g0007 a0001c0001t0009g0050 others(6): Show |
14 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+1972delA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3813386 | ||||||
| chr11:3813415 | G | A | 1 | a0001c0001t0030g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.165+1991G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3813415 | |||||||
| chr11:3813712 | G | C | 1 | a0001c0001t0014g0195 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.165+2288G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3813712 | |||||||
| chr11:3813940 | A | G | 2 | a0001c0001t0004g0144 a0001c0001t0004g0145 |
2 | HG00673.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.165+2516A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3813940 | |||||||
| chr11:3813991 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0008g0069 a0001c0001t0031g0070 |
3 | HG02735.hp1 HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.165+2567T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3813991 | |||||||
| chr11:3814106 | A | G | 8 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(5): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+2682A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814106 | |||||||
| chr11:3814199 | C | T | 1 | a0001c0001t0033g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.165+2775C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814199 | |||||||
| chr11:3814331 | A | G | 1 | a0001c0001t0004g0192 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.165+2907A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814331 | |||||||
| chr11:3814417 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.166-2936T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814417 | |||||||
| chr11:3814418 | G | A | 17 | a0001c0001t0003g0153 a0001c0001t0003g0210 a0001c0001t0006g0028 others(14): Show |
20 | HG00639.hp2 HG01891.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.166-2935G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814418 | |||||||
| chr11:3814454 | G | C | 1 | a0001c0001t0002g0072 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.166-2899G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814454 | |||||||
| chr11:3814472 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166-2881G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814472 | |||||||
| chr11:3814477 | G | C | 3 | a0001c0001t0008g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG02055.hp2 HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.166-2876G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814477 | |||||||
| chr11:3814517 | A | G | 1 | a0001c0001t0010g0044 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.166-2836A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814517 | |||||||
| chr11:3814537 | G | A | 21 | a0001c0001t0003g0020 a0001c0001t0004g0031 a0001c0001t0006g0031 others(18): Show |
30 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.166-2816G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814537 | |||||||
| chr11:3814545 | C | T | 6 | a0001c0001t0001g0159 a0001c0001t0010g0043 a0001c0001t0010g0044 others(3): Show |
7 | HG01243.hp2 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-2808C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814545 | |||||||
| chr11:3814674 | G | C | 1 | a0001c0001t0015g0200 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-2679G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814674 | |||||||
| chr11:3814720 | T | TTTCTTTC others(1): Show |
23 | a0001c0001t0001g0022 a0001c0001t0001g0101 a0001c0001t0002g0016 others(20): Show |
29 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.166-2610_166-2603d others(10): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814720 | ||||||
| chr11:3814748 | T | TTTCCTTC others(5): Show |
9 | a0001c0001t0001g0014 a0001c0001t0002g0041 a0001c0001t0002g0061 others(6): Show |
11 | HG00099.hp1 HG01070.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-2603_166-2602i others(14): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | T | TTTCCTTC others(9): Show |
1 | a0001c0001t0001g0014 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.166-2603_166-2602i others(18): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0003g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.166-2603_166-2602i others(13): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | T | TTTTC | 21 | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0001g0177 others(18): Show |
31 | HG00642.hp1 HG00738.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.166-2543_166-2540d others(6): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | T | TTTTCTTT others(1): Show |
17 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0154 others(14): Show |
22 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.166-2547_166-2540d others(10): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | T | TTTTCTTT others(5): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0170 others(3): Show |
7 | HG01358.hp1 HG01496.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-2551_166-2540d others(14): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | T | TTTTCTTT others(9): Show |
2 | a0001c0001t0003g0188 a0001c0001t0003g0193 |
2 | HG04184.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.166-2555_166-2540d others(18): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | T | TTTTCTTT others(13): Show |
1 | a0001c0001t0003g0002 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.166-2559_166-2540d others(22): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | TTTTC | T | 24 | a0001c0001t0001g0005 a0001c0001t0001g0161 a0001c0001t0002g0005 others(21): Show |
26 | HG00639.hp2 HG01169.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.166-2543_166-2540d others(6): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | TTTTCTTT others(1): Show |
T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0045 others(14): Show |
24 | HG01167.hp1 HG01952.hp2 HG03041.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-2547_166-2540d others(10): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | TTTTCTTT others(5): Show |
T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0175 others(9): Show |
13 | HG00735.hp1 HG01106.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-2551_166-2540d others(14): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | TTTTCTTT others(9): Show |
T | 4 | a0001c0001t0009g0050 a0001c0001t0009g0202 a0001c0001t0010g0043 others(1): Show |
4 | HG00741.hp2 HG01168.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-2555_166-2540d others(18): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | TTTTCTTT others(13): Show |
T | 1 | a0002c0002t0027g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.166-2559_166-2540d others(22): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | TTTTCTTT others(17): Show |
T | 4 | a0001c0001t0001g0159 a0001c0001t0010g0044 a0001c0001t0012g0053 others(1): Show |
5 | HG02109.hp1 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-2563_166-2540d others(26): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814748 | TTTTCTTT others(21): Show |
T | 1 | a0001c0001t0008g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.166-2567_166-2540d others(30): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814748 | ||||||
| chr11:3814751 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.166-2602T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814751 | |||||||
| chr11:3814752 | C | CTTCT | 40 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0032 others(37): Show |
60 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.166-2599_166-2598i others(6): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814752 | ||||||
| chr11:3814755 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(77): Show |
140 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.166-2598T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814755 | |||||||
| chr11:3814756 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(77): Show |
140 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.166-2597C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814756 | |||||||
| chr11:3814757 | T | C | 1 | a0001c0001t0005g0105 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.166-2596T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814757 | |||||||
| chr11:3814759 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0017g0106 |
3 | HG02602.hp2 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.166-2594T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814759 | |||||||
| chr11:3814796 | CTTTCTTT others(13): Show |
C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0012g0196 others(1): Show |
4 | HG01261.hp1 HG01433.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-2555_166-2536d others(22): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814796 | ||||||
| chr11:3814800 | CTTTCTTT others(9): Show |
C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0008g0138 |
3 | HG01081.hp1 NA18998.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.166-2551_166-2536d others(18): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814800 | ||||||
| chr11:3814804 | CTTTCTTT others(5): Show |
C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0042 others(6): Show |
10 | HG01255.hp1 HG01255.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.166-2547_166-2536d others(14): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814804 | ||||||
| chr11:3814807 | T | C | 1 | a0001c0001t0002g0072 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.166-2546T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814807 | |||||||
| chr11:3814808 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.166-2545C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814808 | |||||||
| chr11:3814808 | CTTTCTCT others(1): Show |
C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(18): Show |
35 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.166-2543_166-2536d others(10): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814808 | ||||||
| chr11:3814810 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.166-2543T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814810 | |||||||
| chr11:3814812 | CTCTT | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
36 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.166-2531_166-2528d others(6): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814812 | ||||||
| chr11:3814814 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.166-2539C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814814 | |||||||
| chr11:3814815 | T | G | 2 | a0001c0001t0006g0216 a0001c0001t0012g0055 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.166-2538T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814815 | |||||||
| chr11:3814816 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.166-2537T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814816 | |||||||
| chr11:3814819 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.166-2534T>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814819 | |||||||
| chr11:3814826 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0026g0048 |
2 | HG02451.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.166-2527T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814826 | |||||||
| chr11:3814830 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.166-2523C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814830 | |||||||
| chr11:3814832 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.166-2521T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814832 | |||||||
| chr11:3814834 | T | C | 8 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(5): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-2519T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814834 | |||||||
| chr11:3814863 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.166-2490T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814863 | |||||||
| chr11:3814887 | T | TCCCTTTC others(11): Show |
1 | a0001c0001t0002g0108 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.166-2448_166-2431d others(20): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814887 | ||||||
| chr11:3814905 | G | T | 1 | a0001c0001t0013g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.166-2448G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814905 | |||||||
| chr11:3814905 | GCCCTTT | G | 3 | a0001c0001t0004g0141 a0001c0001t0006g0189 a0001c0001t0006g0190 |
3 | HG02258.hp1 HG02293.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.166-2427_166-2422d others(8): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814905 | ||||||
| chr11:3814905 | GCCCTTTC others(5): Show |
G | 1 | a0001c0001t0005g0091 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.166-2433_166-2422d others(14): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3814905 | ||||||
| chr11:3814972 | C | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.166-2381C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3814972 | |||||||
| chr11:3815017 | G | A | 13 | a0001c0001t0003g0020 a0001c0001t0004g0031 a0001c0001t0006g0031 others(10): Show |
17 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.166-2336G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815017 | |||||||
| chr11:3815058 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.166-2295C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815058 | |||||||
| chr11:3815062 | C | T | 1 | a0002c0002t0023g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.166-2291C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815062 | |||||||
| chr11:3815074 | A | C | 1 | a0001c0004t0005g0134 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.166-2279A>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815074 | |||||||
| chr11:3815245 | G | A | 1 | a0001c0001t0033g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.166-2108G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815245 | |||||||
| chr11:3815278 | AC | A | 8 | a0001c0001t0003g0210 a0001c0001t0006g0029 a0001c0001t0006g0206 others(5): Show |
10 | HG00639.hp2 HG01891.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.166-2074delC | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815278 | |||||||
| chr11:3815302 | GTCT | G | 13 | a0001c0001t0003g0020 a0001c0001t0004g0031 a0001c0001t0006g0031 others(10): Show |
17 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.166-2043_166-2041d others(5): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr11 | 3815302 | ||||||
| chr11:3815339 | C | T | 21 | a0001c0001t0003g0020 a0001c0001t0004g0031 a0001c0001t0006g0031 others(18): Show |
30 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.166-2014C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815339 | |||||||
| chr11:3815378 | G | A | 1 | a0002c0002t0027g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.166-1975G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815378 | |||||||
| chr11:3815404 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.166-1949G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815404 | |||||||
| chr11:3815433 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.166-1920C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815433 | |||||||
| chr11:3815463 | C | T | 3 | a0001c0001t0001g0187 a0001c0001t0003g0186 a0001c0001t0003g0188 |
3 | HG01358.hp1 HG01361.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.166-1890C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815463 | |||||||
| chr11:3815526 | T | C | 1 | a0002c0002t0027g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.166-1827T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815526 | |||||||
| chr11:3815547 | C | A | 1 | a0001c0001t0006g0029 | 3 | HG03130.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-1806C>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815547 | |||||||
| chr11:3815640 | G | A | 8 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(5): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-1713G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815640 | |||||||
| chr11:3815762 | A | G | 1 | a0001c0001t0005g0140 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.166-1591A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815762 | |||||||
| chr11:3815794 | A | G | 2 | a0001c0001t0002g0090 a0001c0001t0002g0139 |
2 | HG01346.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.166-1559A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815794 | |||||||
| chr11:3815852 | T | C | 1 | a0001c0001t0004g0092 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.166-1501T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815852 | |||||||
| chr11:3815872 | A | G | 8 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(5): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-1481A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815872 | |||||||
| chr11:3815915 | C | T | 1 | a0001c0001t0016g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.166-1438C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815915 | |||||||
| chr11:3815975 | A | G | 8 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(5): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-1378A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815975 | |||||||
| chr11:3815998 | G | A | 8 | a0001c0001t0003g0210 a0001c0001t0006g0029 a0001c0001t0006g0206 others(5): Show |
10 | HG00639.hp2 HG01891.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.166-1355G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3815998 | |||||||
| chr11:3816127 | G | A | 1 | a0001c0001t0019g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.166-1226G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816127 | |||||||
| chr11:3816135 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0045 others(12): Show |
26 | HG00408.hp2 HG00642.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.166-1218T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816135 | |||||||
| chr11:3816257 | G | A | 1 | a0001c0001t0018g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.166-1096G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816257 | |||||||
| chr11:3816516 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.166-837C>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816516 | |||||||
| chr11:3816536 | C | G | 1 | a0001c0001t0005g0140 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.166-817C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816536 | |||||||
| chr11:3816554 | T | G | 3 | a0001c0001t0003g0015 a0001c0001t0003g0166 a0001c0001t0003g0194 |
7 | HG02615.hp1 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-799T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816554 | |||||||
| chr11:3816608 | T | C | 8 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(5): Show |
13 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-745T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816608 | |||||||
| chr11:3816619 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.166-734A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816619 | |||||||
| chr11:3816652 | A | G | 1 | a0001c0001t0014g0133 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.166-701A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816652 | |||||||
| chr11:3816694 | C | T | 16 | a0001c0001t0003g0210 a0001c0001t0006g0028 a0001c0001t0006g0029 others(13): Show |
19 | HG00639.hp2 HG01891.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.166-659C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3816694 | |||||||
| chr11:3817076 | G | A | 3 | a0001c0001t0008g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG02055.hp2 HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.166-277G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3817076 | |||||||
| chr11:3817098 | C | T | 1 | a0002c0002t0027g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.166-255C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3817098 | |||||||
| chr11:3817132 | G | A | 16 | a0001c0001t0003g0210 a0001c0001t0006g0028 a0001c0001t0006g0029 others(13): Show |
19 | HG00639.hp2 HG01891.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.166-221G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3817132 | |||||||
| chr11:3817259 | C | T | 43 | a0001c0001t0001g0159 a0001c0001t0003g0020 a0001c0001t0003g0210 others(40): Show |
56 | HG00639.hp2 HG00735.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.166-94C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 2/6 | chr11 | 3817259 | |||||||
| chr11:3817582 | T | C | 24 | a0001c0001t0001g0159 a0001c0001t0003g0210 a0001c0001t0006g0028 others(21): Show |
28 | HG00639.hp2 HG01243.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.348+47T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3817582 | |||||||
| chr11:3817669 | A | T | 10 | a0001c0001t0009g0007 a0001c0001t0009g0050 a0001c0001t0009g0051 others(7): Show |
15 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.348+134A>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3817669 | |||||||
| chr11:3817680 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.348+145G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3817680 | |||||||
| chr11:3817723 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.348+188T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3817723 | |||||||
| chr11:3817885 | A | T | 1 | a0001c0001t0012g0054 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.348+350A>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3817885 | |||||||
| chr11:3818057 | C | CAA | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(49): Show |
92 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.348+525_348+526dup others(2): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3818057 | ||||||
| chr11:3818057 | C | CAAA | 6 | a0001c0001t0002g0021 a0001c0001t0002g0074 a0001c0001t0002g0093 others(3): Show |
8 | HG00609.hp2 HG01175.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+524_348+526dup others(3): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3818057 | ||||||
| chr11:3818060 | A | AAC | 3 | a0001c0001t0002g0080 a0001c0001t0002g0099 a0001c0001t0002g0100 |
3 | HG00438.hp2 HG00558.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.348+526_348+527ins others(2): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3818060 | ||||||
| chr11:3818062 | T | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(58): Show |
103 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.348+527T>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818062 | |||||||
| chr11:3818062 | T | TA | 12 | a0001c0001t0007g0131 a0001c0001t0009g0007 a0001c0001t0009g0050 others(9): Show |
17 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.348+540dupA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3818062 | ||||||
| chr11:3818062 | T | TAA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(103): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.348+539_348+540dup others(2): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3818062 | ||||||
| chr11:3818128 | C | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0098 |
2 | NA18966.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.348+593C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818128 | |||||||
| chr11:3818326 | C | CA | 10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0161 others(7): Show |
12 | HG01952.hp2 HG02055.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.348+808dupA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3818326 | ||||||
| chr11:3818326 | CA | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.348+808delA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3818326 | ||||||
| chr11:3818326 | CAA | C | 15 | a0001c0001t0002g0090 a0001c0001t0002g0139 a0001c0001t0003g0020 others(12): Show |
19 | HG01346.hp1 HG01433.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+807_348+808del others(2): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3818326 | ||||||
| chr11:3818404 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.348+869G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818404 | |||||||
| chr11:3818452 | G | C | 1 | a0001c0001t0003g0186 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.348+917G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818452 | |||||||
| chr11:3818600 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.348+1065C>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818600 | |||||||
| chr11:3818713 | T | C | 17 | a0001c0001t0001g0159 a0001c0001t0006g0028 a0001c0001t0006g0216 others(14): Show |
19 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.348+1178T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818713 | |||||||
| chr11:3818784 | C | A | 1 | a0001c0001t0003g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.348+1249C>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818784 | |||||||
| chr11:3818826 | A | T | 1 | a0001c0001t0002g0114 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.348+1291A>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818826 | |||||||
| chr11:3818870 | C | T | 14 | a0001c0001t0002g0090 a0001c0001t0002g0130 a0001c0001t0003g0168 others(11): Show |
15 | HG00639.hp2 HG01109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+1335C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3818870 | |||||||
| chr11:3819308 | G | T | 2 | a0001c0001t0012g0030 a0001c0001t0016g0030 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.348+1773G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819308 | |||||||
| chr11:3819329 | G | A | 7 | a0001c0001t0003g0083 a0001c0001t0016g0027 a0001c0001t0016g0184 others(4): Show |
8 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+1794G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819329 | |||||||
| chr11:3819354 | G | A | 9 | a0001c0001t0003g0083 a0001c0001t0006g0028 a0001c0001t0011g0028 others(6): Show |
11 | HG01109.hp1 HG02559.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.348+1819G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819354 | |||||||
| chr11:3819397 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.348+1862G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819397 | |||||||
| chr11:3819436 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.348+1901G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819436 | |||||||
| chr11:3819461 | A | G | 7 | a0001c0001t0003g0083 a0001c0001t0016g0027 a0001c0001t0016g0184 others(4): Show |
8 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+1926A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819461 | |||||||
| chr11:3819483 | A | G | 1 | a0001c0001t0004g0116 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.348+1948A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819483 | |||||||
| chr11:3819585 | C | T | 46 | a0001c0001t0001g0159 a0001c0001t0002g0090 a0001c0001t0002g0130 others(43): Show |
54 | HG00639.hp2 HG01109.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.348+2050C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819585 | |||||||
| chr11:3819667 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.348+2132C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819667 | |||||||
| chr11:3819866 | A | G | 2 | a0001c0001t0015g0152 a0001c0001t0015g0200 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.348+2331A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3819866 | |||||||
| chr11:3820133 | A | C | 3 | a0001c0001t0002g0090 a0001c0001t0002g0130 a0001c0001t0002g0139 |
3 | HG01346.hp1 HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.348+2598A>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820133 | |||||||
| chr11:3820218 | C | G | 1 | a0001c0001t0033g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.348+2683C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820218 | |||||||
| chr11:3820233 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.348+2698G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820233 | |||||||
| chr11:3820337 | T | G | 7 | a0001c0001t0003g0083 a0001c0001t0016g0027 a0001c0001t0016g0184 others(4): Show |
8 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.348+2802T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820337 | |||||||
| chr11:3820534 | T | C | 49 | a0001c0001t0001g0159 a0001c0001t0002g0090 a0001c0001t0002g0130 others(46): Show |
57 | HG00639.hp2 HG01109.hp1 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.348+2999T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820534 | |||||||
| chr11:3820639 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.348+3104A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820639 | |||||||
| chr11:3820685 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.348+3150C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820685 | |||||||
| chr11:3820747 | T | G | 4 | a0001c0001t0003g0015 a0001c0001t0003g0166 a0001c0001t0003g0173 others(1): Show |
8 | HG02615.hp1 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-3136T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820747 | |||||||
| chr11:3820822 | C | CAAAT | 8 | a0001c0001t0003g0083 a0001c0001t0012g0055 a0001c0001t0016g0027 others(5): Show |
9 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-3045_349-3042d others(6): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3820822 | ||||||
| chr11:3820930 | C | T | 9 | a0001c0001t0001g0159 a0001c0001t0010g0043 a0001c0001t0010g0044 others(6): Show |
10 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-2953C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820930 | |||||||
| chr11:3820986 | G | C | 2 | a0001c0001t0006g0028 a0001c0001t0011g0028 |
3 | HG02559.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.349-2897G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820986 | |||||||
| chr11:3820995 | C | T | 3 | a0001c0001t0002g0090 a0001c0001t0002g0130 a0001c0001t0002g0139 |
3 | HG01346.hp1 HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.349-2888C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3820995 | |||||||
| chr11:3821055 | A | ATATCTCA others(8): Show |
7 | a0001c0001t0003g0083 a0001c0001t0016g0027 a0001c0001t0016g0184 others(4): Show |
8 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-2812_349-2798d others(17): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3821055 | ||||||
| chr11:3821431 | C | G | 1 | a0001c0001t0015g0200 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.349-2452C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3821431 | |||||||
| chr11:3821473 | T | C | 7 | a0001c0001t0003g0083 a0001c0001t0016g0027 a0001c0001t0016g0184 others(4): Show |
8 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-2410T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3821473 | |||||||
| chr11:3821681 | G | A | 1 | a0001c0001t0007g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.349-2202G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3821681 | |||||||
| chr11:3821756 | T | TA | 10 | a0001c0001t0001g0124 a0001c0001t0001g0187 a0001c0001t0009g0007 others(7): Show |
15 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-2127_349-2126i others(3): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3821756 | |||||||
| chr11:3821757 | C | A | 10 | a0001c0001t0001g0124 a0001c0001t0001g0187 a0001c0001t0009g0007 others(7): Show |
15 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-2126C>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3821757 | |||||||
| chr11:3821757 | C | CA | 22 | a0001c0001t0003g0083 a0001c0001t0003g0174 a0001c0001t0004g0031 others(19): Show |
24 | HG00741.hp1 HG01109.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.349-2113dupA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3821757 | ||||||
| chr11:3821830 | AG | A | 30 | a0001c0001t0001g0154 a0001c0001t0003g0083 a0001c0001t0004g0031 others(27): Show |
34 | HG00639.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.349-2047delG | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3821830 | ||||||
| chr11:3821900 | T | TA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(83): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.349-1968dupA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3821900 | ||||||
| chr11:3821997 | G | T | 1 | a0001c0001t0008g0081 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.349-1886G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3821997 | |||||||
| chr11:3822014 | G | T | 18 | a0001c0001t0006g0029 a0001c0001t0006g0206 a0001c0001t0006g0211 others(15): Show |
21 | HG00639.hp2 HG01243.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-1869G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822014 | |||||||
| chr11:3822082 | C | T | 1 | a0001c0001t0016g0184 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.349-1801C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822082 | |||||||
| chr11:3822091 | G | A | 1 | a0001c0001t0005g0066 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.349-1792G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822091 | |||||||
| chr11:3822093 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.349-1790A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822093 | |||||||
| chr11:3822104 | T | C | 1 | a0001c0001t0012g0196 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.349-1779T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822104 | |||||||
| chr11:3822112 | T | C | 30 | a0001c0001t0001g0159 a0001c0001t0003g0083 a0001c0001t0004g0031 others(27): Show |
34 | HG00639.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.349-1771T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822112 | |||||||
| chr11:3822131 | G | A | 17 | a0001c0001t0001g0159 a0001c0001t0006g0029 a0001c0001t0006g0206 others(14): Show |
20 | HG00639.hp2 HG01243.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.349-1752G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822131 | |||||||
| chr11:3822148 | A | C | 2 | a0002c0002t0023g0214 a0002c0002t0027g0149 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.349-1735A>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822148 | |||||||
| chr11:3822160 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(106): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.349-1723T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822160 | |||||||
| chr11:3822161 | G | A | 1 | a0001c0001t0007g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.349-1722G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822161 | |||||||
| chr11:3822167 | A | G | 1 | a0001c0001t0007g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.349-1716A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822167 | |||||||
| chr11:3822171 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(99): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.349-1712T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822171 | |||||||
| chr11:3822181 | G | A | 1 | a0001c0001t0012g0196 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.349-1702G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822181 | |||||||
| chr11:3822224 | C | T | 2 | a0001c0001t0012g0055 a0001c0001t0030g0068 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.349-1659C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822224 | |||||||
| chr11:3822225 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(74): Show |
122 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.349-1658G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822225 | |||||||
| chr11:3822230 | G | A | 1 | a0001c0001t0026g0048 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.349-1653G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822230 | |||||||
| chr11:3822232 | C | T | 10 | a0001c0001t0001g0124 a0001c0001t0001g0187 a0001c0001t0009g0007 others(7): Show |
15 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-1651C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822232 | |||||||
| chr11:3822237 | G | A | 18 | a0001c0001t0006g0029 a0001c0001t0006g0206 a0001c0001t0006g0211 others(15): Show |
21 | HG00639.hp2 HG01243.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-1646G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822237 | |||||||
| chr11:3822241 | G | A | 11 | a0001c0001t0003g0083 a0001c0001t0004g0031 a0001c0001t0006g0031 others(8): Show |
12 | HG01109.hp1 HG02145.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-1642G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822241 | |||||||
| chr11:3822246 | C | T | 8 | a0001c0001t0010g0043 a0001c0001t0010g0044 a0001c0001t0010g0087 others(5): Show |
9 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-1637C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822246 | |||||||
| chr11:3822281 | G | A | 8 | a0001c0001t0003g0083 a0001c0001t0012g0055 a0001c0001t0016g0027 others(5): Show |
9 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-1602G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822281 | |||||||
| chr11:3822281 | G | C | 8 | a0001c0001t0010g0043 a0001c0001t0010g0044 a0001c0001t0010g0087 others(5): Show |
9 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-1602G>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822281 | |||||||
| chr11:3822289 | G | T | 11 | a0001c0001t0003g0083 a0001c0001t0004g0031 a0001c0001t0006g0031 others(8): Show |
12 | HG01109.hp1 HG02145.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-1594G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822289 | |||||||
| chr11:3822300 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.349-1583C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822300 | |||||||
| chr11:3822313 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(128): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.349-1570A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822313 | |||||||
| chr11:3822371 | GA | G | 10 | a0001c0001t0001g0124 a0001c0001t0001g0187 a0001c0001t0009g0007 others(7): Show |
15 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-1504delA | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3822371 | ||||||
| chr11:3822380 | G | T | 1 | a0001c0001t0007g0179 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.349-1503G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822380 | |||||||
| chr11:3822487 | A | G | 2 | a0001c0001t0006g0028 a0001c0001t0011g0028 |
3 | HG02559.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.349-1396A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822487 | |||||||
| chr11:3822612 | C | T | 11 | a0001c0001t0006g0029 a0001c0001t0006g0206 a0001c0001t0006g0211 others(8): Show |
13 | HG00639.hp2 HG01433.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-1271C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822612 | |||||||
| chr11:3822683 | T | C | 1 | a0001c0001t0012g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.349-1200T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822683 | |||||||
| chr11:3822803 | T | C | 1 | a0001c0001t0003g0180 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.349-1080T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822803 | |||||||
| chr11:3822924 | A | C | 1 | a0001c0001t0018g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.349-959A>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3822924 | |||||||
| chr11:3823011 | T | C | 1 | a0001c0001t0017g0106 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.349-872T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823011 | |||||||
| chr11:3823012 | C | G | 1 | a0001c0001t0015g0152 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.349-871C>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823012 | |||||||
| chr11:3823024 | C | CT | 76 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.349-829dupT | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3823024 | ||||||
| chr11:3823024 | C | CTT | 10 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0119 others(7): Show |
10 | HG00597.hp1 HG01891.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.349-830_349-829dup others(2): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3823024 | ||||||
| chr11:3823024 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349-859C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823024 | |||||||
| chr11:3823024 | CT | C | 35 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0071 others(32): Show |
46 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.349-829delT | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3823024 | ||||||
| chr11:3823024 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0003g0018 a0001c0001t0003g0060 a0001c0001t0003g0077 others(1): Show |
6 | HG00621.hp2 HG02080.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-838_349-829del others(10): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3823024 | ||||||
| chr11:3823024 | CTTTTTTT others(5): Show |
C | 11 | a0001c0001t0006g0029 a0001c0001t0006g0206 a0001c0001t0006g0211 others(8): Show |
13 | HG00639.hp2 HG01106.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-840_349-829del others(12): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3823024 | ||||||
| chr11:3823024 | CTTTTTTT others(6): Show |
C | 9 | a0001c0001t0001g0124 a0001c0001t0001g0187 a0001c0001t0003g0174 others(6): Show |
14 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.349-841_349-829del others(13): Show |
PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3823024 | ||||||
| chr11:3823054 | T | TG | 8 | a0001c0001t0004g0031 a0001c0001t0006g0031 a0001c0001t0006g0216 others(5): Show |
9 | HG01109.hp1 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-828dupG | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 3823054 | ||||||
| chr11:3823138 | A | G | 23 | a0001c0001t0003g0083 a0001c0001t0004g0031 a0001c0001t0006g0028 others(20): Show |
27 | HG00639.hp2 HG01109.hp1 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.349-745A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823138 | |||||||
| chr11:3823177 | G | A | 11 | a0001c0001t0006g0029 a0001c0001t0006g0206 a0001c0001t0006g0211 others(8): Show |
13 | HG00639.hp2 HG01433.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-706G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823177 | |||||||
| chr11:3823269 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.349-614C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823269 | |||||||
| chr11:3823325 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.349-558C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823325 | |||||||
| chr11:3823373 | A | G | 43 | a0001c0001t0001g0177 a0001c0001t0003g0020 a0001c0001t0003g0083 others(40): Show |
52 | HG00639.hp2 HG00642.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.349-510A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823373 | |||||||
| chr11:3823508 | G | T | 1 | a0001c0001t0012g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.349-375G>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823508 | |||||||
| chr11:3823526 | G | A | 1 | a0001c0001t0012g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.349-357G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823526 | |||||||
| chr11:3823575 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.349-308A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823575 | |||||||
| chr11:3823629 | G | A | 1 | a0001c0001t0009g0050 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.349-254G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823629 | |||||||
| chr11:3823680 | T | G | 1 | a0003c0003t0001g0088 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.349-203T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 3/6 | chr11 | 3823680 | |||||||
| chr11:3824210 | T | G | 1 | a0001c0001t0005g0178 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.602-60T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 4/6 | chr11 | 3824210 | |||||||
| chr11:3824494 | A | G | 2 | a0001c0001t0012g0207 a0001c0001t0012g0208 |
2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.708+118A>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 5/6 | chr11 | 3824494 | |||||||
| chr11:3824501 | C | T | 3 | a0001c0001t0026g0048 a0002c0002t0023g0214 a0002c0002t0027g0149 |
3 | HG02451.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.708+125C>T | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 5/6 | chr11 | 3824501 | |||||||
| chr11:3824639 | G | A | 1 | a0001c0001t0028g0183 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.708+263G>A | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 5/6 | chr11 | 3824639 | |||||||
| chr11:3824709 | T | C | 2 | a0002c0002t0023g0214 a0002c0002t0027g0149 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.709-311T>C | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 5/6 | chr11 | 3824709 | |||||||
| chr11:3824746 | T | G | 1 | a0001c0001t0003g0083 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.709-274T>G | PGAP2 | ENSG00000148985.20 | transcript | ENST00000278243.9 | protein_coding | 5/6 | chr11 | 3824746 |