Item | Value |
---|---|
geneid | 10346 |
ensemblid | ENSG00000132274.17 |
hgncid | 16379 |
symbol | TRIM22 |
name | tripartite motif containing 22 |
refseq_nuc | NM_006074.5 |
refseq_prot | NP_006065.2 |
ensembl_nuc | ENST00000379965.8 |
ensembl_prot | ENSP00000369299.3 |
mane_status | MANE Select |
chr | chr11 |
start | 5689790 |
end | 5710863 |
strand | + |
ver | v1.2 |
region | chr11:5689790-5710863 |
region5000 | chr11:5684790-5715863 |
regionname0 | TRIM22_chr11_5689790_5710863 |
regionname5000 | TRIM22_chr11_5684790_5715863 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 498 | 211 | 32 | 23 | 144 | 2 | 9 | 108 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0002 | 0/0 | 498 | 73 | 7 | 17 | 32 | 8 | 9 | 31 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0003 | 0/1 | 498 | 72 | 19 | 26 | 6 | 4 | 16 | 5 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0004 | 0/0 | 498 | 66 | 14 | 14 | 22 | 2 | 14 | 15 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0005 | 0/0 | 498 | 18 | 0 | 0 | 18 | 0 | 0 | 16 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0006 | 0/0 | 498 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0007 | 0/0 | 498 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0008 | 0/0 | 498 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0009 | 0/0 | 498 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0010 | 0/0 | 498 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0011 | 0/0 | 498 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0012 | 0/0 | 498 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0013 | 0/0 | 454 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(449): Show |
chr11 | 5684790 | 5715863 |
a0014 | 0/0 | 498 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0015 | 0/0 | 498 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0016 | 0/0 | 498 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0017 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0018 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0019 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0020 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0021 | 0/0 | 498 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0022 | 0/0 | 498 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
a0023 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | MDFSV others(493): Show |
chr11 | 5684790 | 5715863 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1494 | 126 | 10 | 15 | 93 | 2 | 5 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0001c0002 | 0/0 | 1494 | 73 | 13 | 6 | 51 | 0 | 3 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0001c0010 | 0/0 | 1494 | 7 | 7 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0001c0024 | 0/0 | 1494 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0001c0046 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0001c0052 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0001c0054 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0005 | 0/0 | 1494 | 33 | 1 | 12 | 12 | 4 | 4 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0006 | 0/0 | 1494 | 30 | 2 | 3 | 20 | 3 | 2 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0014 | 0/0 | 1494 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0020 | 0/0 | 1494 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0029 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0033 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0038 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0039 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0002c0042 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0003c0003 | 0/1 | 1494 | 51 | 16 | 16 | 2 | 1 | 15 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0003c0009 | 0/0 | 1494 | 14 | 1 | 8 | 4 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0003c0011 | 0/0 | 1494 | 4 | 1 | 2 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0003c0017 | 0/0 | 1494 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0003c0030 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0004c0004 | 0/0 | 1494 | 47 | 6 | 13 | 18 | 2 | 8 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0004c0008 | 0/0 | 1494 | 15 | 7 | 0 | 4 | 0 | 4 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0004c0025 | 0/0 | 1494 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0004c0044 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0004c0048 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0005c0007 | 0/0 | 1494 | 16 | 0 | 0 | 16 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0005c0023 | 0/0 | 1494 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0006c0013 | 0/0 | 1494 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0006c0022 | 0/0 | 1494 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0007c0012 | 0/0 | 1494 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0007c0034 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0007c0037 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0008c0016 | 0/0 | 1494 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0008c0049 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0009c0031 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0009c0036 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0009c0041 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0010c0019 | 0/0 | 1494 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0010c0040 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0011c0015 | 0/0 | 1494 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0012c0021 | 0/0 | 1494 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0013c0018 | 0/0 | 1494 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0014c0045 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0014c0050 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0015c0027 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0016c0035 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0017c0043 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0018c0028 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0019c0053 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0020c0032 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0021c0047 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0022c0051 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 | ||
a0023c0026 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATGGA others(1489): Show |
chr11 | 5684790 | 5715863 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2888 | 48 | 2 | 8 | 33 | 2 | 2 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0002 | 0/0 | 2888 | 49 | 6 | 4 | 39 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0003 | 0/0 | 2887 | 18 | 0 | 1 | 17 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0004 | 0/0 | 2888 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0007 | 0/0 | 2888 | 3 | 0 | 2 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0009 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0010 | 0/0 | 2888 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0012 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0014 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0001t0015 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0001 | 0/0 | 2888 | 21 | 0 | 3 | 17 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0002 | 0/0 | 2888 | 24 | 3 | 1 | 20 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0003 | 0/0 | 2887 | 19 | 4 | 1 | 12 | 0 | 2 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0004 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0006 | 0/0 | 2888 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0008 | 0/0 | 2888 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0009 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0016 | 0/0 | 2887 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0001c0002t0021 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0010t0006 | 0/0 | 2888 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0010t0018 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0024t0004 | 0/0 | 2888 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0046t0004 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0052t0001 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0001c0054t0002 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0005t0001 | 0/0 | 2888 | 13 | 0 | 3 | 3 | 4 | 3 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0005t0002 | 0/0 | 2888 | 18 | 1 | 9 | 7 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0005t0003 | 0/0 | 2887 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0002c0006t0001 | 0/0 | 2888 | 12 | 1 | 3 | 4 | 3 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0006t0002 | 0/0 | 2888 | 13 | 0 | 0 | 12 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0006t0003 | 0/0 | 2887 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0002c0006t0013 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0014t0001 | 0/0 | 2888 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0020t0004 | 0/0 | 2888 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0029t0004 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0033t0004 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0038t0001 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0039t0004 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0002c0042t0001 | 0/0 | 2888 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0003t0001 | 0/1 | 2888 | 34 | 9 | 11 | 1 | 1 | 11 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0003t0002 | 0/0 | 2888 | 15 | 6 | 4 | 1 | 0 | 4 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0003t0003 | 0/0 | 2887 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0003c0003t0008 | 0/0 | 2888 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0009t0001 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0009t0002 | 0/0 | 2888 | 13 | 1 | 8 | 4 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0011t0001 | 0/0 | 2888 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0011t0002 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0017t0001 | 0/0 | 2888 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0003c0030t0001 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0004t0001 | 0/0 | 2888 | 32 | 2 | 9 | 13 | 2 | 6 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0004t0002 | 0/0 | 2888 | 11 | 4 | 2 | 3 | 0 | 2 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0004t0003 | 0/0 | 2887 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0004c0004t0007 | 0/0 | 2888 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0004t0017 | 0/0 | 2888 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0008t0001 | 0/0 | 2888 | 8 | 3 | 0 | 3 | 0 | 2 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0008t0002 | 0/0 | 2888 | 3 | 1 | 0 | 0 | 0 | 2 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0008t0003 | 0/0 | 2887 | 4 | 3 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0004c0025t0001 | 0/0 | 2888 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0044t0001 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0004c0048t0004 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0005c0007t0001 | 0/0 | 2888 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0005c0007t0002 | 0/0 | 2888 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0005c0007t0003 | 0/0 | 2887 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0005c0023t0002 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0005c0023t0003 | 0/0 | 2887 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0006c0013t0002 | 0/0 | 2888 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0006c0022t0001 | 0/0 | 2888 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0007c0012t0001 | 0/0 | 2888 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0007c0034t0001 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0007c0037t0002 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0008c0016t0001 | 0/0 | 2888 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0008c0049t0001 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0009c0031t0005 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0009c0036t0005 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0009c0041t0005 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0010c0019t0005 | 0/0 | 2888 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0010c0040t0005 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0011c0015t0002 | 0/0 | 2888 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0011c0015t0003 | 0/0 | 2887 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0012c0021t0001 | 0/0 | 2888 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0013c0018t0001 | 0/0 | 2888 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0014c0045t0005 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0014c0050t0005 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0015c0027t0020 | 0/0 | 2887 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0016c0035t0001 | 0/0 | 2888 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0017c0043t0005 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0018c0028t0019 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0019c0053t0011 | 0/0 | 2887 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0020c0032t0011 | 0/0 | 2887 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2882): Show |
chr11 | 5684790 | 5715863 |
a0021c0047t0001 | 0/0 | 2888 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0022c0051t0001 | 0/0 | 2888 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
a0023c0026t0001 | 0/0 | 2888 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | ATTTG others(2883): Show |
chr11 | 5684790 | 5715863 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0001g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0003g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0007g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0009g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0010g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0012g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0014g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0002g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0006g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0008g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0009g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0016g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0002t0021g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0010t0006g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0010t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0010t0018g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0024t0004g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0046t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0052t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0001c0054t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0005t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0006t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0014t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0014t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0020t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0020t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0029t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0033t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0038t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0039t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0002c0042t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0006 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0003t0008g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0009t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0011t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0011t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0011t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0011t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0017t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0017t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0003c0030t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0002g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0007g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0004t0017g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0008t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0025t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0025t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0044t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0004c0048t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0007t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0023t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0005c0023t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0006c0013t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0006c0013t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0006c0013t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0006c0013t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0006c0022t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0007c0012t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0007c0012t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0007c0034t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0007c0037t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0008c0016t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0008c0016t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0008c0049t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0009c0031t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0009c0036t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0009c0041t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0010c0019t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0010c0019t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0010c0040t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0011c0015t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0011c0015t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0011c0015t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0012c0021t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0012c0021t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0013c0018t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0014c0045t0005g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0014c0050t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0015c0027t0020g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0016c0035t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0017c0043t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0018c0028t0019g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0019c0053t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0020c0032t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0021c0047t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0022c0051t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
a0023c0026t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0001 | g0145 | EUR | GBR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00099 | hp2 | a0004 | c0004 | t0001 | g0369 | EUR | GBR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00140 | hp1 | a0002 | c0006 | t0001 | g0137 | EUR | GBR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0374 | EUR | GBR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00280 | hp1 | a0012 | c0021 | t0001 | g0278 | EUR | FIN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00280 | hp2 | a0003 | c0011 | t0001 | g0276 | EUR | FIN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00323 | hp1 | a0002 | c0006 | t0001 | g0144 | EUR | FIN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00323 | hp2 | a0002 | c0005 | t0001 | g0153 | EUR | FIN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00423 | hp1 | a0005 | c0007 | t0002 | g0157 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00438 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00544 | hp1 | a0002 | c0005 | t0001 | g0074 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00609 | hp2 | a0004 | c0004 | t0001 | g0310 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00621 | hp2 | a0001 | c0001 | t0012 | g0366 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00639 | hp1 | a0002 | c0020 | t0004 | g0148 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00639 | hp2 | a0002 | c0042 | t0001 | g0066 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00642 | hp1 | a0003 | c0003 | t0008 | g0268 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0360 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00673 | hp1 | a0005 | c0023 | t0002 | g0093 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0354 | EAS | CHS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00733 | hp1 | a0004 | c0025 | t0001 | g0293 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00733 | hp2 | a0002 | c0005 | t0001 | g0004 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00735 | hp1 | a0001 | c0024 | t0004 | g0042 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00735 | hp2 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00738 | hp1 | a0012 | c0021 | t0001 | g0277 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00741 | hp1 | a0002 | c0005 | t0001 | g0139 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG00741 | hp2 | a0003 | c0011 | t0001 | g0272 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01069 | hp1 | a0003 | c0009 | t0002 | g0022 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01069 | hp2 | a0004 | c0004 | t0001 | g0227 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01070 | hp1 | a0002 | c0006 | t0001 | g0030 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01070 | hp2 | a0003 | c0009 | t0002 | g0285 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01071 | hp1 | a0002 | c0006 | t0001 | g0030 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01071 | hp2 | a0003 | c0009 | t0002 | g0138 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01074 | hp2 | a0002 | c0005 | t0002 | g0118 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0006 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01099 | hp1 | a0003 | c0003 | t0001 | g0121 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01099 | hp2 | a0004 | c0004 | t0001 | g0358 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01106 | hp1 | a0002 | c0005 | t0001 | g0004 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0385 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01109 | hp1 | a0013 | c0018 | t0001 | g0021 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01109 | hp2 | a0001 | c0024 | t0004 | g0042 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01167 | hp2 | a0003 | c0009 | t0002 | g0143 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01168 | hp1 | a0003 | c0009 | t0002 | g0022 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0114 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01169 | hp1 | a0003 | c0009 | t0002 | g0080 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0096 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01175 | hp2 | a0003 | c0003 | t0002 | g0147 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0379 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0223 | AMR | PUR | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0100 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01255 | hp2 | a0003 | c0003 | t0002 | g0029 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01257 | hp1 | a0002 | c0006 | t0001 | g0146 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01261 | hp1 | a0003 | c0003 | t0002 | g0029 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01261 | hp2 | a0004 | c0004 | t0007 | g0357 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01346 | hp1 | a0002 | c0005 | t0002 | g0011 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01346 | hp2 | a0015 | c0027 | t0020 | g0233 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01358 | hp1 | a0004 | c0004 | t0002 | g0057 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01361 | hp1 | a0016 | c0035 | t0001 | g0098 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01361 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01433 | hp1 | a0003 | c0009 | t0002 | g0131 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01433 | hp2 | a0003 | c0003 | t0002 | g0225 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01496 | hp1 | a0003 | c0011 | t0001 | g0274 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01496 | hp2 | a0002 | c0005 | t0002 | g0108 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01515 | hp1 | a0003 | c0017 | t0001 | g0110 | EUR | IBS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01515 | hp2 | a0002 | c0005 | t0001 | g0012 | EUR | IBS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01516 | hp1 | a0002 | c0005 | t0001 | g0012 | EUR | IBS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01516 | hp2 | a0004 | c0004 | t0001 | g0372 | EUR | IBS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01517 | hp1 | a0002 | c0005 | t0001 | g0012 | EUR | IBS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01517 | hp2 | a0003 | c0017 | t0001 | g0111 | EUR | IBS | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01884 | hp1 | a0009 | c0031 | t0005 | g0231 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0362 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01891 | hp1 | a0006 | c0013 | t0002 | g0338 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01891 | hp2 | a0001 | c0002 | t0008 | g0036 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01928 | hp2 | a0002 | c0005 | t0002 | g0024 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01934 | hp1 | a0004 | c0004 | t0001 | g0015 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01934 | hp2 | a0003 | c0003 | t0001 | g0142 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01943 | hp1 | a0001 | c0002 | t0006 | g0047 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01943 | hp2 | a0004 | c0004 | t0002 | g0262 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01952 | hp1 | a0002 | c0005 | t0002 | g0094 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01952 | hp2 | a0002 | c0005 | t0002 | g0024 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01975 | hp2 | a0002 | c0005 | t0002 | g0107 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01978 | hp1 | a0004 | c0004 | t0001 | g0251 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01978 | hp2 | a0002 | c0005 | t0002 | g0109 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01993 | hp1 | a0003 | c0009 | t0002 | g0011 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01993 | hp2 | a0002 | c0005 | t0002 | g0011 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0097 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02004 | hp2 | a0004 | c0004 | t0001 | g0049 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0382 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02027 | hp2 | a0003 | c0009 | t0002 | g0117 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02040 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02055 | hp1 | a0006 | c0022 | t0001 | g0045 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02055 | hp2 | a0001 | c0052 | t0001 | g0364 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02074 | hp1 | a0001 | c0001 | t0009 | g0055 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0342 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02129 | hp2 | a0004 | c0004 | t0001 | g0043 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0013 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0351 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02145 | hp1 | a0002 | c0005 | t0002 | g0123 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02145 | hp2 | a0013 | c0018 | t0001 | g0021 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02148 | hp1 | a0004 | c0004 | t0001 | g0009 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02148 | hp2 | a0004 | c0004 | t0017 | g0072 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02155 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | CDX | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02155 | hp2 | a0008 | c0049 | t0001 | g0161 | EAS | CDX | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02165 | hp1 | a0004 | c0008 | t0003 | g0341 | EAS | CDX | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02165 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | CDX | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02257 | hp1 | a0004 | c0008 | t0003 | g0205 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02257 | hp2 | a0003 | c0030 | t0001 | g0132 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0006 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02258 | hp2 | a0003 | c0003 | t0002 | g0039 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02280 | hp1 | a0017 | c0043 | t0005 | g0063 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02280 | hp2 | a0004 | c0004 | t0001 | g0323 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02293 | hp2 | a0004 | c0004 | t0001 | g0015 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02300 | hp1 | a0004 | c0004 | t0001 | g0015 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02300 | hp2 | a0001 | c0002 | t0003 | g0037 | AMR | PEL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02451 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02451 | hp2 | a0003 | c0003 | t0002 | g0127 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02523 | hp2 | a0004 | c0004 | t0003 | g0197 | EAS | KHV | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02572 | hp1 | a0019 | c0053 | t0011 | g0069 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02602 | hp1 | a0002 | c0005 | t0001 | g0086 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0371 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02615 | hp1 | a0001 | c0010 | t0006 | g0007 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02615 | hp2 | a0003 | c0003 | t0001 | g0226 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02622 | hp1 | a0001 | c0010 | t0006 | g0007 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02622 | hp2 | a0006 | c0013 | t0002 | g0337 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02630 | hp1 | a0002 | c0006 | t0013 | g0129 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02630 | hp2 | a0006 | c0013 | t0002 | g0336 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02647 | hp1 | a0014 | c0045 | t0005 | g0368 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02647 | hp2 | a0004 | c0008 | t0001 | g0258 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02683 | hp1 | a0002 | c0006 | t0002 | g0031 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02683 | hp2 | a0002 | c0005 | t0001 | g0154 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02698 | hp1 | a0003 | c0009 | t0001 | g0119 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0136 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0202 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02717 | hp2 | a0001 | c0010 | t0006 | g0007 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02723 | hp1 | a0009 | c0041 | t0005 | g0020 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02723 | hp2 | a0001 | c0010 | t0006 | g0007 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02735 | hp1 | a0003 | c0003 | t0002 | g0081 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02735 | hp2 | a0002 | c0005 | t0002 | g0112 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02818 | hp1 | a0009 | c0036 | t0005 | g0027 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02818 | hp2 | a0001 | c0010 | t0018 | g0301 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02886 | hp1 | a0014 | c0050 | t0005 | g0263 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02886 | hp2 | a0007 | c0012 | t0001 | g0010 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02895 | hp1 | a0001 | c0010 | t0006 | g0046 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0339 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0052 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02896 | hp2 | a0020 | c0032 | t0011 | g0076 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02897 | hp1 | a0001 | c0010 | t0006 | g0046 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0052 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02922 | hp1 | a0001 | c0002 | t0021 | g0280 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02922 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0381 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02965 | hp2 | a0004 | c0004 | t0002 | g0206 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02970 | hp1 | a0002 | c0014 | t0001 | g0133 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02970 | hp2 | a0002 | c0006 | t0001 | g0230 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02976 | hp1 | a0002 | c0014 | t0001 | g0028 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0292 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03017 | hp2 | a0002 | c0033 | t0004 | g0287 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03041 | hp1 | a0003 | c0003 | t0002 | g0128 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03041 | hp2 | a0002 | c0014 | t0001 | g0028 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03098 | hp1 | a0004 | c0004 | t0002 | g0238 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03098 | hp2 | a0004 | c0008 | t0001 | g0333 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03130 | hp1 | a0007 | c0012 | t0001 | g0010 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03130 | hp2 | a0001 | c0002 | t0008 | g0036 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03139 | hp1 | a0010 | c0019 | t0005 | g0027 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03139 | hp2 | a0001 | c0002 | t0006 | g0279 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03195 | hp1 | a0007 | c0012 | t0001 | g0010 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0257 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03209 | hp1 | a0004 | c0008 | t0003 | g0044 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03239 | hp1 | a0002 | c0005 | t0001 | g0120 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03239 | hp2 | a0001 | c0046 | t0004 | g0346 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03453 | hp1 | a0004 | c0025 | t0001 | g0294 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03486 | hp1 | a0001 | c0002 | t0003 | g0234 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03490 | hp1 | a0002 | c0020 | t0004 | g0309 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03490 | hp2 | a0003 | c0003 | t0002 | g0048 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03491 | hp1 | a0001 | c0001 | t0010 | g0383 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03491 | hp2 | a0003 | c0003 | t0001 | g0299 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03492 | hp1 | a0001 | c0001 | t0010 | g0053 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03492 | hp2 | a0003 | c0003 | t0002 | g0048 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03516 | hp1 | a0006 | c0013 | t0002 | g0059 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03516 | hp2 | a0004 | c0004 | t0002 | g0155 | AFR | ESN | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03540 | hp1 | a0007 | c0034 | t0001 | g0075 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03540 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | GWD | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03579 | hp1 | a0004 | c0008 | t0002 | g0067 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03579 | hp2 | a0003 | c0003 | t0002 | g0039 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03654 | hp1 | a0001 | c0001 | t0007 | g0018 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0026 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0126 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03669 | hp2 | a0003 | c0003 | t0001 | g0296 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03688 | hp1 | a0004 | c0008 | t0001 | g0196 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03688 | hp2 | a0004 | c0004 | t0001 | g0363 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03704 | hp1 | a0003 | c0003 | t0001 | g0295 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03704 | hp2 | a0004 | c0004 | t0001 | g0355 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03710 | hp1 | a0002 | c0029 | t0004 | g0102 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03710 | hp2 | a0004 | c0044 | t0001 | g0343 | SAS | PJL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03831 | hp1 | a0004 | c0008 | t0002 | g0340 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03834 | hp1 | a0003 | c0003 | t0001 | g0078 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03834 | hp2 | a0003 | c0003 | t0002 | g0297 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03927 | hp1 | a0004 | c0004 | t0001 | g0319 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03927 | hp2 | a0004 | c0004 | t0002 | g0332 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03942 | hp1 | a0003 | c0003 | t0001 | g0298 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0235 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04115 | hp1 | a0002 | c0006 | t0001 | g0130 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04115 | hp2 | a0004 | c0048 | t0004 | g0221 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04184 | hp1 | a0004 | c0004 | t0001 | g0380 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0320 | SAS | BEB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04199 | hp1 | a0004 | c0004 | t0002 | g0269 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0101 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04204 | hp1 | a0003 | c0003 | t0001 | g0006 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04204 | hp2 | a0004 | c0004 | t0001 | g0203 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04228 | hp1 | a0004 | c0008 | t0001 | g0211 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | YRI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18522 | hp2 | a0001 | c0002 | t0004 | g0260 | AFR | YRI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18612 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | CHB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | CHB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | CHB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18906 | hp1 | a0003 | c0003 | t0002 | g0134 | AFR | YRI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0038 | AFR | YRI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18939 | hp1 | a0005 | c0007 | t0002 | g0194 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18939 | hp2 | a0004 | c0004 | t0001 | g0283 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18941 | hp1 | a0002 | c0006 | t0003 | g0140 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18942 | hp1 | a0005 | c0007 | t0003 | g0013 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18942 | hp2 | a0005 | c0007 | t0002 | g0345 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18943 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18944 | hp1 | a0002 | c0006 | t0002 | g0005 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18944 | hp2 | a0005 | c0007 | t0001 | g0183 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18946 | hp2 | a0004 | c0004 | t0003 | g0068 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18947 | hp1 | a0004 | c0004 | t0001 | g0200 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18950 | hp2 | a0005 | c0007 | t0003 | g0184 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18953 | hp2 | a0002 | c0005 | t0003 | g0104 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18956 | hp1 | a0003 | c0009 | t0002 | g0105 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18956 | hp2 | a0011 | c0015 | t0002 | g0149 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18957 | hp2 | a0001 | c0002 | t0003 | g0267 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18959 | hp1 | a0005 | c0007 | t0002 | g0033 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18960 | hp2 | a0005 | c0007 | t0003 | g0013 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18961 | hp1 | a0002 | c0006 | t0002 | g0286 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18966 | hp1 | a0002 | c0006 | t0001 | g0073 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18966 | hp2 | a0004 | c0004 | t0001 | g0387 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18967 | hp2 | a0002 | c0005 | t0001 | g0099 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18968 | hp1 | a0002 | c0006 | t0002 | g0005 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18970 | hp2 | a0002 | c0006 | t0002 | g0005 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0158 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18972 | hp1 | a0008 | c0016 | t0001 | g0058 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18975 | hp1 | a0001 | c0002 | t0016 | g0062 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18975 | hp2 | a0002 | c0006 | t0001 | g0089 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0377 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0376 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18978 | hp2 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18979 | hp1 | a0005 | c0007 | t0002 | g0195 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18983 | hp2 | a0004 | c0008 | t0001 | g0213 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18987 | hp2 | a0002 | c0006 | t0002 | g0005 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18989 | hp2 | a0002 | c0005 | t0002 | g0003 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18990 | hp2 | a0002 | c0006 | t0003 | g0060 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18991 | hp1 | a0002 | c0005 | t0002 | g0092 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18993 | hp2 | a0002 | c0005 | t0002 | g0003 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18994 | hp2 | a0004 | c0004 | t0002 | g0179 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18995 | hp1 | a0005 | c0007 | t0002 | g0322 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18997 | hp1 | a0001 | c0002 | t0003 | g0228 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18997 | hp2 | a0008 | c0016 | t0001 | g0050 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18999 | hp2 | a0003 | c0009 | t0002 | g0103 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0367 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19001 | hp1 | a0002 | c0006 | t0002 | g0284 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19002 | hp1 | a0005 | c0023 | t0003 | g0321 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19002 | hp2 | a0002 | c0005 | t0001 | g0088 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19003 | hp2 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19004 | hp1 | a0008 | c0016 | t0001 | g0050 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19004 | hp2 | a0002 | c0006 | t0002 | g0106 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19006 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19009 | hp1 | a0001 | c0002 | t0009 | g0212 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19009 | hp2 | a0005 | c0007 | t0002 | g0316 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19010 | hp1 | a0001 | c0002 | t0003 | g0219 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19010 | hp2 | a0002 | c0005 | t0002 | g0091 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19011 | hp2 | a0005 | c0007 | t0002 | g0349 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19012 | hp1 | a0002 | c0006 | t0002 | g0095 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19030 | hp1 | a0004 | c0008 | t0001 | g0240 | AFR | LWK | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19030 | hp2 | a0003 | c0009 | t0002 | g0122 | AFR | LWK | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19043 | hp1 | a0007 | c0037 | t0002 | g0115 | AFR | LWK | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19043 | hp2 | a0010 | c0019 | t0005 | g0135 | AFR | LWK | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19056 | hp2 | a0002 | c0006 | t0002 | g0113 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19057 | hp1 | a0005 | c0007 | t0002 | g0041 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0386 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19062 | hp1 | a0002 | c0006 | t0002 | g0116 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19063 | hp1 | a0002 | c0006 | t0002 | g0087 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19063 | hp2 | a0002 | c0005 | t0003 | g0090 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19064 | hp1 | a0011 | c0015 | t0002 | g0288 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0378 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19065 | hp1 | a0002 | c0006 | t0001 | g0151 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19065 | hp2 | a0002 | c0006 | t0003 | g0289 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0388 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19067 | hp2 | a0004 | c0004 | t0001 | g0016 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19068 | hp2 | a0001 | c0001 | t0014 | g0191 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19070 | hp1 | a0002 | c0005 | t0002 | g0003 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19070 | hp2 | a0005 | c0007 | t0002 | g0041 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19076 | hp1 | a0011 | c0015 | t0003 | g0291 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19076 | hp2 | a0004 | c0004 | t0001 | g0001 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19077 | hp1 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19078 | hp1 | a0002 | c0006 | t0001 | g0150 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19078 | hp2 | a0002 | c0006 | t0003 | g0290 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0375 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19080 | hp1 | a0004 | c0004 | t0002 | g0353 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19082 | hp1 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19082 | hp2 | a0005 | c0007 | t0001 | g0023 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19083 | hp1 | a0004 | c0004 | t0002 | g0389 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19083 | hp2 | a0004 | c0008 | t0001 | g0359 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19084 | hp1 | a0004 | c0004 | t0001 | g0002 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19084 | hp2 | a0002 | c0005 | t0002 | g0003 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19085 | hp1 | a0004 | c0008 | t0001 | g0188 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19086 | hp1 | a0002 | c0005 | t0002 | g0085 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19086 | hp2 | a0004 | c0004 | t0001 | g0373 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19087 | hp1 | a0003 | c0009 | t0002 | g0282 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19089 | hp2 | a0003 | c0003 | t0002 | g0141 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19091 | hp2 | a0005 | c0007 | t0002 | g0350 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | YRI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA19240 | hp2 | a0010 | c0040 | t0005 | g0020 | AFR | YRI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0229 | AFR | ASW | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20129 | hp2 | a0003 | c0003 | t0002 | g0224 | AFR | ASW | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20752 | hp1 | a0002 | c0006 | t0001 | g0082 | EUR | TSI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0352 | EUR | TSI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20805 | hp1 | a0022 | c0051 | t0001 | g0356 | EUR | TSI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20805 | hp2 | a0002 | c0038 | t0001 | g0273 | EUR | TSI | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20905 | hp1 | a0001 | c0002 | t0003 | g0330 | SAS | GIH | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20905 | hp2 | a0004 | c0008 | t0002 | g0193 | SAS | GIH | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01123 | hp1 | a0004 | c0004 | t0001 | g0344 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0026 | AMR | CLM | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02109 | hp1 | a0006 | c0022 | t0001 | g0045 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02109 | hp2 | a0001 | c0002 | t0006 | g0047 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02486 | hp1 | a0018 | c0028 | t0019 | g0232 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02486 | hp2 | a0007 | c0012 | t0001 | g0064 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02559 | hp1 | a0002 | c0039 | t0004 | g0065 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG02559 | hp2 | a0003 | c0003 | t0003 | g0222 | AFR | ACB | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03471 | hp1 | a0004 | c0004 | t0002 | g0204 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG03471 | hp2 | a0004 | c0008 | t0003 | g0044 | AFR | MSL | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | USA | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
HG06807 | hp2 | a0003 | c0011 | t0002 | g0275 | AFR | USA | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18955 | hp1 | a0021 | c0047 | t0001 | g0058 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA18955 | hp2 | a0002 | c0006 | t0002 | g0031 | EAS | JPT | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0079 | AFR | USA | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA20300 | hp2 | a0004 | c0004 | t0001 | g0317 | AFR | USA | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA21309 | hp1 | a0023 | c0026 | t0001 | g0125 | AFR | LWK | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
NA21309 | hp2 | a0001 | c0054 | t0002 | g0370 | AFR | LWK | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0152 | REF | REF | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0043 | REF | REF | TRIM22_chr11_5684790_5715863 | TRIM22 | chr11 | 5684790 | 5715863 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:5696414 | C | A | 1 | a0023 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.182C>A | p.Thr61Asn | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/8 | 358/2888 | 182/1497 | 61/498 | chr11 | 5696414 | |||
chr11:5697273 | G | C | 2 | a0015 a0018 |
2 | HG01346.hp2 HG02486.hp1 |
missense_variant | MODERATE | c.449G>C | p.Arg150Thr | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/8 | 625/2888 | 449/1497 | 150/498 | chr11 | 5697273 | |||
chr11:5697287 | G | A | 14 | a0002 a0003 a0007 others(11): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
missense_variant | MODERATE | c.463G>A | p.Asp155Asn | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/8 | 639/2888 | 463/1497 | 155/498 | chr11 | 5697287 | |||
chr11:5698489 | A | G | 3 | a0005 a0011 a0021 |
22 | HG00423.hp1 HG00673.hp1 NA18939.hp1 others(19): Show |
missense_variant | MODERATE | c.694A>G | p.Thr232Ala | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/8 | 870/2888 | 694/1497 | 232/498 | chr11 | 5698489 | |||
chr11:5698520 | G | C | 6 | a0003 a0004 a0010 others(3): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
missense_variant | MODERATE | c.725G>C | p.Arg242Thr | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/8 | 901/2888 | 725/1497 | 242/498 | chr11 | 5698520 | |||
chr11:5698526 | C | T | 4 | a0006 a0007 a0017 others(1): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
missense_variant | MODERATE | c.731C>T | p.Ser244Leu | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/8 | 907/2888 | 731/1497 | 244/498 | chr11 | 5698526 | |||
chr11:5706606 | G | A | 2 | a0008 a0021 |
5 | HG02155.hp2 NA18955.hp1 NA18972.hp1 others(2): Show |
missense_variant | MODERATE | c.763G>A | p.Val255Ile | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/8 | 939/2888 | 763/1497 | 255/498 | chr11 | 5706606 | |||
chr11:5708583 | C | A | 4 | a0009 a0010 a0014 others(1): Show |
9 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
missense_variant | MODERATE | c.881C>A | p.Thr294Lys | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/8 | 1057/2888 | 881/1497 | 294/498 | chr11 | 5708583 | |||
chr11:5709113 | G | A | 2 | a0016 a0022 |
2 | HG01361.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.962G>A | p.Arg321Lys | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1138/2888 | 962/1497 | 321/498 | chr11 | 5709113 | |||
chr11:5709395 | C | T | 3 | a0015 a0019 a0020 |
3 | HG01346.hp2 HG02572.hp1 HG02896.hp2 |
missense_variant | MODERATE | c.1244C>T | p.Thr415Ile | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1420/2888 | 1244/1497 | 415/498 | chr11 | 5709395 | |||
chr11:5709475 | C | T | 1 | a0012 | 2 | HG00280.hp1 HG00738.hp1 |
missense_variant | MODERATE | c.1324C>T | p.Arg442Cys | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1500/2888 | 1324/1497 | 442/498 | chr11 | 5709475 | |||
chr11:5709515 | C | A | 1 | a0013 | 2 | HG01109.hp1 HG02145.hp2 |
stop_gained | HIGH | c.1364C>A | p.Ser455* | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1540/2888 | 1364/1497 | 455/498 | chr11 | 5709515 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:5696532 | T | C | 22 | a0002c0005 a0002c0006 a0002c0014 others(19): Show |
153 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(150): Show |
synonymous_variant | LOW | c.300T>C | p.His100His | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/8 | 476/2888 | 300/1497 | 100/498 | chr11 | 5696532 | |||
chr11:5696550 | C | T | 1 | a0004c0025 | 2 | HG00733.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.318C>T | p.Ile106Ile | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/8 | 494/2888 | 318/1497 | 106/498 | chr11 | 5696550 | |||
chr11:5698404 | A | G | 1 | a0001c0054 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.609A>G | p.Gln203Gln | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/8 | 785/2888 | 609/1497 | 203/498 | chr11 | 5698404 | |||
chr11:5698419 | T | C | 5 | a0001c0010 a0002c0014 a0002c0029 others(2): Show |
13 | HG02257.hp2 HG02615.hp1 HG02622.hp1 others(10): Show |
synonymous_variant | LOW | c.624T>C | p.Gly208Gly | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/8 | 800/2888 | 624/1497 | 208/498 | chr11 | 5698419 | |||
chr11:5698437 | T | C | 22 | a0001c0002 a0001c0046 a0001c0054 others(19): Show |
160 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(157): Show |
synonymous_variant | LOW | c.642T>C | p.Asp214Asp | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/8 | 818/2888 | 642/1497 | 214/498 | chr11 | 5698437 | |||
chr11:5709064 | C | T | 7 | a0001c0024 a0001c0046 a0002c0020 others(4): Show |
9 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(6): Show |
synonymous_variant | LOW | c.913C>T | p.Leu305Leu | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1089/2888 | 913/1497 | 305/498 | chr11 | 5709064 | |||
chr11:5709087 | G | A | 1 | a0003c0017 | 2 | HG01515.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.936G>A | p.Ser312Ser | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1112/2888 | 936/1497 | 312/498 | chr11 | 5709087 | |||
chr11:5709354 | T | C | 1 | a0001c0052 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1203T>C | p.Tyr401Tyr | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1379/2888 | 1203/1497 | 401/498 | chr11 | 5709354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:5689836 | A | G | 3 | a0001c0002t0006 a0001c0002t0021 a0001c0010t0006 |
10 | HG01943.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-130A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/8 | 6397 | chr11 | 5689836 | ||||||
chr11:5689847 | C | T | 2 | a0015c0027t0020 a0018c0028t0019 |
2 | HG01346.hp2 HG02486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-119C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/8 | 6386 | chr11 | 5689847 | ||||||
chr11:5709684 | C | T | 21 | a0001c0001t0004 a0001c0002t0004 a0001c0010t0018 others(18): Show |
25 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*36C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 36 | chr11 | 5709684 | ||||||
chr11:5709778 | T | C | 1 | a0001c0001t0012 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 130 | chr11 | 5709778 | ||||||
chr11:5709978 | T | C | 1 | a0002c0006t0013 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*330T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 330 | chr11 | 5709978 | ||||||
chr11:5709992 | A | G | 8 | a0009c0031t0005 a0009c0036t0005 a0009c0041t0005 others(5): Show |
9 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*344A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 344 | chr11 | 5709992 | ||||||
chr11:5710059 | T | G | 8 | a0009c0031t0005 a0009c0036t0005 a0009c0041t0005 others(5): Show |
9 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*411T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 411 | chr11 | 5710059 | ||||||
chr11:5710095 | C | T | 2 | a0001c0010t0018 a0004c0004t0017 |
2 | HG02148.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*447C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 447 | chr11 | 5710095 | ||||||
chr11:5710225 | T | A | 23 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(20): Show |
176 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*577T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 577 | chr11 | 5710225 | ||||||
chr11:5710266 | TA | T | 11 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0016 others(8): Show |
56 | HG00438.hp2 HG00609.hp1 HG02040.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*619delA | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 619 | chr11 | 5710266 | ||||||
chr11:5710286 | A | G | 8 | a0009c0031t0005 a0009c0036t0005 a0009c0041t0005 others(5): Show |
9 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*638A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 638 | chr11 | 5710286 | ||||||
chr11:5710319 | CA | C | 3 | a0015c0027t0020 a0019c0053t0011 a0020c0032t0011 |
3 | HG01346.hp2 HG02572.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*672delA | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 672 | chr11 | 5710319 | ||||||
chr11:5710352 | C | T | 18 | a0001c0001t0004 a0001c0002t0004 a0001c0010t0018 others(15): Show |
22 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*704C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 704 | chr11 | 5710352 | ||||||
chr11:5710375 | T | C | 1 | a0001c0002t0016 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*727T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 727 | chr11 | 5710375 | ||||||
chr11:5710408 | C | T | 2 | a0001c0001t0007 a0004c0004t0007 |
4 | HG00735.hp2 HG01081.hp1 HG01261.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*760C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 760 | chr11 | 5710408 | ||||||
chr11:5710519 | T | C | 18 | a0001c0001t0004 a0001c0002t0004 a0001c0010t0018 others(15): Show |
22 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*871T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 871 | chr11 | 5710519 | ||||||
chr11:5710602 | A | G | 2 | a0001c0001t0009 a0001c0002t0009 |
2 | HG02074.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*954A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 954 | chr11 | 5710602 | ||||||
chr11:5710624 | T | C | 1 | a0001c0001t0010 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*976T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 976 | chr11 | 5710624 | ||||||
chr11:5710646 | A | G | 1 | a0001c0001t0015 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*998A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 998 | chr11 | 5710646 | ||||||
chr11:5710669 | T | C | 3 | a0001c0002t0008 a0002c0006t0013 a0003c0003t0008 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1021T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1021 | chr11 | 5710669 | ||||||
chr11:5710671 | T | C | 1 | a0001c0001t0014 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1023T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1023 | chr11 | 5710671 | ||||||
chr11:5710797 | C | T | 21 | a0001c0001t0004 a0001c0002t0004 a0001c0010t0018 others(18): Show |
25 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1149C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1149 | chr11 | 5710797 | ||||||
chr11:5710798 | T | A | 21 | a0001c0001t0004 a0001c0002t0004 a0001c0010t0018 others(18): Show |
25 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1150T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 8/8 | 1150 | chr11 | 5710798 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:5689947 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0049 others(133): Show |
154 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-67+48A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5689947 | |||||||
chr11:5690034 | C | G | 1 | a0001c0001t0002g0281 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-67+135C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690034 | |||||||
chr11:5690034 | C | T | 1 | a0003c0009t0002g0282 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-67+135C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690034 | |||||||
chr11:5690283 | G | A | 1 | a0006c0013t0002g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-67+384G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690283 | |||||||
chr11:5690348 | T | C | 1 | a0004c0004t0001g0283 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-67+449T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690348 | |||||||
chr11:5690561 | A | G | 12 | a0001c0002t0006g0047 a0001c0002t0006g0279 a0001c0002t0021g0280 others(9): Show |
17 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-67+662A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690561 | |||||||
chr11:5690590 | G | A | 11 | a0001c0002t0006g0047 a0001c0002t0006g0279 a0001c0010t0006g0007 others(8): Show |
16 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-67+691G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690590 | |||||||
chr11:5690617 | G | A | 1 | a0002c0006t0003g0060 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-67+718G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690617 | |||||||
chr11:5690734 | T | A | 7 | a0002c0038t0001g0273 a0003c0011t0001g0272 a0003c0011t0001g0274 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+835T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690734 | |||||||
chr11:5690989 | T | A | 2 | a0001c0002t0003g0061 a0001c0002t0016g0062 |
2 | HG00438.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-67+1090T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5690989 | |||||||
chr11:5691010 | G | A | 7 | a0002c0039t0004g0065 a0002c0042t0001g0066 a0007c0012t0001g0010 others(4): Show |
9 | HG00639.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67+1111G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691010 | |||||||
chr11:5691030 | G | A | 93 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(90): Show |
101 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.-67+1131G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691030 | |||||||
chr11:5691177 | G | A | 1 | a0004c0008t0002g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-67+1278G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691177 | |||||||
chr11:5691295 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(104): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-67+1396C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691295 | |||||||
chr11:5691296 | G | A | 215 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(212): Show |
250 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.-67+1397G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691296 | |||||||
chr11:5691329 | G | C | 1 | a0004c0004t0001g0310 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-67+1430G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691329 | |||||||
chr11:5691336 | G | A | 1 | a0004c0004t0003g0068 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-67+1437G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691336 | |||||||
chr11:5691357 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-67+1458C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691357 | |||||||
chr11:5691400 | G | GCTTTTCT others(48): Show |
1 | a0001c0002t0003g0228 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-67+1503_-67+1557d others(57): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5691400 | ||||||
chr11:5691421 | A | T | 14 | a0002c0038t0001g0273 a0002c0039t0004g0065 a0002c0042t0001g0066 others(11): Show |
16 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.-67+1522A>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691421 | |||||||
chr11:5691424 | C | G | 3 | a0002c0006t0001g0230 a0003c0003t0001g0229 a0009c0031t0005g0231 |
3 | HG01884.hp1 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-67+1525C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691424 | |||||||
chr11:5691488 | C | T | 7 | a0002c0038t0001g0273 a0003c0011t0001g0272 a0003c0011t0001g0274 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67+1589C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691488 | |||||||
chr11:5691502 | G | A | 5 | a0001c0002t0002g0070 a0002c0006t0001g0230 a0003c0003t0001g0229 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67+1603G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691502 | |||||||
chr11:5691617 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0049 others(133): Show |
156 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.-67+1718C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691617 | |||||||
chr11:5691684 | C | G | 7 | a0002c0039t0004g0065 a0002c0042t0001g0066 a0007c0012t0001g0010 others(4): Show |
9 | HG00639.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67+1785C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691684 | |||||||
chr11:5691767 | G | T | 226 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(223): Show |
264 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-67+1868G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691767 | |||||||
chr11:5691927 | C | T | 7 | a0003c0003t0001g0038 a0003c0003t0001g0223 a0003c0003t0001g0226 others(4): Show |
9 | HG01243.hp2 HG01433.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67+2028C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5691927 | |||||||
chr11:5692049 | G | A | 2 | a0002c0005t0001g0074 a0002c0006t0001g0073 |
2 | HG00544.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.-67+2150G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692049 | |||||||
chr11:5692118 | A | C | 14 | a0002c0038t0001g0273 a0002c0039t0004g0065 a0002c0042t0001g0066 others(11): Show |
16 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.-67+2219A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692118 | |||||||
chr11:5692120 | T | C | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-67+2221T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692120 | |||||||
chr11:5692258 | A | G | 1 | a0004c0004t0002g0389 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-67+2359A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692258 | |||||||
chr11:5692307 | C | A | 14 | a0002c0038t0001g0273 a0002c0039t0004g0065 a0002c0042t0001g0066 others(11): Show |
16 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.-67+2408C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692307 | |||||||
chr11:5692319 | GCAGTCT | G | 3 | a0007c0034t0001g0075 a0013c0018t0001g0021 a0020c0032t0011g0076 |
4 | HG01109.hp1 HG02145.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+2421_-67+2426d others(8): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692319 | |||||||
chr11:5692326 | T | A | 3 | a0007c0034t0001g0075 a0013c0018t0001g0021 a0020c0032t0011g0076 |
4 | HG01109.hp1 HG02145.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+2427T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692326 | |||||||
chr11:5692428 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0049 others(136): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.-67+2529T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692428 | |||||||
chr11:5692479 | T | C | 1 | a0003c0003t0001g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-67+2580T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692479 | |||||||
chr11:5692558 | C | T | 86 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(83): Show |
92 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-67+2659C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692558 | |||||||
chr11:5692587 | A | C | 115 | a0001c0001t0001g0084 a0001c0001t0002g0083 a0001c0001t0003g0124 others(112): Show |
140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-67+2688A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692587 | |||||||
chr11:5692749 | G | C | 120 | a0001c0001t0001g0084 a0001c0001t0002g0083 a0001c0001t0003g0124 others(117): Show |
145 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-67+2850G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692749 | |||||||
chr11:5692775 | C | T | 1 | a0020c0032t0011g0076 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-67+2876C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692775 | |||||||
chr11:5692793 | C | CAAAA | 10 | a0001c0001t0001g0300 a0001c0001t0001g0384 a0001c0001t0002g0382 others(7): Show |
10 | HG00741.hp2 HG01346.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67+2907_-67+2910d others(6): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5692793 | ||||||
chr11:5692793 | C | CAAAAA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(113): Show |
136 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-67+2906_-67+2910d others(7): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5692793 | ||||||
chr11:5692808 | A | AT | 114 | a0001c0001t0001g0084 a0001c0001t0002g0083 a0001c0001t0003g0124 others(111): Show |
139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-67+2909_-67+2910i others(3): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692808 | |||||||
chr11:5692808 | A | T | 1 | a0002c0006t0002g0286 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-67+2909A>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692808 | |||||||
chr11:5692876 | C | CT | 97 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(94): Show |
103 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-67+2992dupT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5692876 | ||||||
chr11:5692876 | C | CTT | 135 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(132): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-67+2991_-67+2992d others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5692876 | ||||||
chr11:5692876 | CT | C | 7 | a0001c0002t0003g0234 a0002c0006t0001g0082 a0002c0033t0004g0287 others(4): Show |
8 | HG01069.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67+2992delT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5692876 | ||||||
chr11:5692961 | C | T | 1 | a0003c0009t0002g0282 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-67+3062C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692961 | |||||||
chr11:5692970 | G | T | 93 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(90): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-67+3071G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5692970 | |||||||
chr11:5693000 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(257): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.-67+3101A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693000 | |||||||
chr11:5693011 | G | C | 4 | a0001c0001t0001g0084 a0001c0001t0002g0083 a0001c0002t0001g0023 others(1): Show |
4 | NA18979.hp2 NA19080.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67+3112G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693011 | |||||||
chr11:5693060 | A | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(240): Show |
276 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-66-3107A>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693060 | |||||||
chr11:5693092 | G | A | 1 | a0004c0004t0001g0235 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-66-3075G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693092 | |||||||
chr11:5693134 | G | A | 62 | a0001c0001t0001g0084 a0001c0001t0002g0083 a0001c0001t0003g0124 others(59): Show |
76 | HG00323.hp2 HG00673.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.-66-3033G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693134 | |||||||
chr11:5693171 | G | A | 112 | a0001c0001t0001g0084 a0001c0001t0002g0083 a0001c0002t0001g0023 others(109): Show |
136 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-66-2996G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693171 | |||||||
chr11:5693179 | G | A | 114 | a0001c0001t0001g0084 a0001c0001t0002g0083 a0001c0002t0001g0023 others(111): Show |
139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-66-2988G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693179 | |||||||
chr11:5693180 | C | A | 1 | a0002c0006t0002g0286 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-66-2987C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693180 | |||||||
chr11:5693189 | C | CT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(127): Show |
149 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-66-2958dupT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693189 | ||||||
chr11:5693189 | C | CTT | 80 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0049 others(77): Show |
86 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-66-2959_-66-2958d others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693189 | ||||||
chr11:5693189 | C | CTTT | 21 | a0001c0001t0001g0014 a0001c0001t0001g0216 a0001c0001t0002g0214 others(18): Show |
22 | HG00438.hp2 HG00558.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-66-2960_-66-2958d others(5): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693189 | ||||||
chr11:5693189 | CT | C | 10 | a0001c0002t0006g0047 a0001c0002t0006g0279 a0001c0010t0006g0007 others(7): Show |
15 | HG01943.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-66-2958delT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693189 | ||||||
chr11:5693189 | CTT | C | 95 | a0001c0001t0001g0084 a0001c0001t0002g0083 a0001c0002t0001g0023 others(92): Show |
119 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.-66-2959_-66-2958d others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693189 | ||||||
chr11:5693189 | CTTT | C | 15 | a0002c0005t0001g0086 a0002c0005t0001g0088 a0002c0005t0002g0085 others(12): Show |
16 | HG01109.hp1 HG01169.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-66-2960_-66-2958d others(5): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693189 | ||||||
chr11:5693189 | CTTTTTTT others(3): Show |
C | 7 | a0002c0038t0001g0273 a0003c0011t0001g0272 a0003c0011t0001g0274 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-66-2967_-66-2958d others(12): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693189 | ||||||
chr11:5693189 | CTTTTTTT others(4): Show |
C | 7 | a0002c0039t0004g0065 a0002c0042t0001g0066 a0007c0012t0001g0010 others(4): Show |
9 | HG00639.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-66-2968_-66-2958d others(13): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693189 | ||||||
chr11:5693221 | C | T | 355 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(352): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.-66-2946C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693221 | |||||||
chr11:5693264 | A | C | 7 | a0002c0038t0001g0273 a0003c0011t0001g0272 a0003c0011t0001g0274 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-66-2903A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693264 | |||||||
chr11:5693279 | G | A | 1 | a0001c0002t0002g0236 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-66-2888G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693279 | |||||||
chr11:5693321 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-66-2846C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693321 | |||||||
chr11:5693322 | G | A | 1 | a0003c0003t0001g0126 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-66-2845G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693322 | |||||||
chr11:5693385 | C | G | 1 | a0001c0001t0001g0379 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-66-2782C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693385 | |||||||
chr11:5693385 | C | T | 1 | a0003c0003t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-66-2782C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693385 | |||||||
chr11:5693447 | G | A | 3 | a0003c0003t0002g0127 a0003c0003t0002g0128 a0003c0003t0008g0268 |
3 | HG00642.hp1 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-66-2720G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693447 | |||||||
chr11:5693458 | C | T | 2 | a0001c0001t0003g0163 a0004c0004t0003g0068 |
2 | HG02080.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-66-2709C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693458 | |||||||
chr11:5693479 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-66-2688G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693479 | |||||||
chr11:5693487 | G | A | 2 | a0009c0036t0005g0027 a0010c0019t0005g0027 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-66-2680G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693487 | |||||||
chr11:5693492 | G | A | 5 | a0001c0002t0006g0047 a0001c0002t0006g0279 a0001c0010t0006g0007 others(2): Show |
10 | HG01943.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-66-2675G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693492 | |||||||
chr11:5693537 | A | G | 119 | a0001c0001t0002g0378 a0001c0002t0001g0377 a0002c0005t0001g0004 others(116): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-66-2630A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693537 | |||||||
chr11:5693545 | C | T | 7 | a0002c0038t0001g0273 a0003c0011t0001g0272 a0003c0011t0001g0274 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-66-2622C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693545 | |||||||
chr11:5693582 | G | T | 2 | a0001c0001t0002g0376 a0001c0002t0003g0375 |
2 | NA18978.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-66-2585G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693582 | |||||||
chr11:5693638 | C | A | 1 | a0002c0005t0002g0085 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-66-2529C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693638 | |||||||
chr11:5693648 | A | G | 363 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(360): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.-66-2519A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693648 | |||||||
chr11:5693694 | C | A | 12 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0178 others(9): Show |
13 | NA18946.hp1 NA18948.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.-66-2473C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693694 | |||||||
chr11:5693721 | C | CA | 8 | a0001c0001t0001g0237 a0001c0001t0002g0239 a0001c0002t0002g0236 others(5): Show |
8 | HG00423.hp2 HG02135.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-2424dupA | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693721 | ||||||
chr11:5693721 | C | CAA | 16 | a0001c0001t0004g0302 a0001c0002t0021g0280 a0001c0010t0018g0301 others(13): Show |
17 | HG01346.hp2 HG01516.hp2 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.-66-2425_-66-2424d others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693721 | ||||||
chr11:5693721 | C | CAAA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(78): Show |
94 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-66-2426_-66-2424d others(5): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693721 | ||||||
chr11:5693721 | C | CAAAA | 29 | a0001c0001t0001g0311 a0001c0001t0001g0328 a0001c0001t0001g0334 others(26): Show |
35 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-66-2427_-66-2424d others(6): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693721 | ||||||
chr11:5693721 | CA | C | 77 | a0001c0001t0001g0170 a0001c0001t0001g0261 a0001c0001t0002g0259 others(74): Show |
94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-66-2424delA | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693721 | ||||||
chr11:5693721 | CAA | C | 141 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(138): Show |
162 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.-66-2425_-66-2424d others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693721 | ||||||
chr11:5693721 | CAAA | C | 16 | a0001c0001t0001g0084 a0002c0038t0001g0273 a0002c0039t0004g0065 others(13): Show |
18 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.-66-2426_-66-2424d others(5): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5693721 | ||||||
chr11:5693784 | T | G | 1 | a0004c0008t0001g0211 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-66-2383T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693784 | |||||||
chr11:5693954 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(128): Show |
151 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-66-2213T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693954 | |||||||
chr11:5693977 | T | C | 1 | a0002c0005t0001g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-66-2190T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5693977 | |||||||
chr11:5694019 | C | A | 2 | a0001c0002t0002g0070 a0019c0053t0011g0069 |
2 | HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-66-2148C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694019 | |||||||
chr11:5694128 | A | T | 104 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(101): Show |
112 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-66-2039A>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694128 | |||||||
chr11:5694265 | A | G | 1 | a0002c0005t0002g0118 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-66-1902A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694265 | |||||||
chr11:5694380 | C | T | 2 | a0001c0001t0003g0182 a0001c0001t0003g0208 |
2 | HG00609.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-66-1787C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694380 | |||||||
chr11:5694488 | A | G | 14 | a0002c0038t0001g0273 a0002c0039t0004g0065 a0002c0042t0001g0066 others(11): Show |
16 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.-66-1679A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694488 | |||||||
chr11:5694532 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-66-1635T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694532 | |||||||
chr11:5694766 | A | T | 1 | a0004c0004t0001g0373 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-66-1401A>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694766 | |||||||
chr11:5694786 | G | A | 3 | a0001c0001t0001g0159 a0001c0002t0003g0158 a0005c0007t0002g0157 |
3 | HG00408.hp1 HG00423.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-66-1381G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694786 | |||||||
chr11:5694870 | T | C | 14 | a0002c0038t0001g0273 a0002c0039t0004g0065 a0002c0042t0001g0066 others(11): Show |
16 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.-66-1297T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5694870 | |||||||
chr11:5695012 | G | A | 1 | a0003c0003t0001g0100 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-66-1155G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695012 | |||||||
chr11:5695040 | T | C | 3 | a0006c0013t0002g0336 a0006c0013t0002g0337 a0006c0013t0002g0338 |
3 | HG01891.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-66-1127T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695040 | |||||||
chr11:5695076 | A | C | 119 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(116): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-66-1091A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695076 | |||||||
chr11:5695101 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(118): Show |
141 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-66-1066G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695101 | |||||||
chr11:5695283 | G | A | 99 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(96): Show |
105 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-66-884G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695283 | |||||||
chr11:5695480 | T | C | 5 | a0002c0014t0001g0028 a0002c0014t0001g0133 a0003c0030t0001g0132 others(2): Show |
6 | HG01346.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-687T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695480 | |||||||
chr11:5695492 | C | T | 119 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(116): Show |
144 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-66-675C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695492 | |||||||
chr11:5695556 | T | C | 1 | a0001c0001t0002g0040 | 2 | HG01192.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-66-611T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695556 | |||||||
chr11:5695566 | G | GTTT | 105 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(102): Show |
129 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-66-592_-66-590dup others(3): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5695566 | ||||||
chr11:5695566 | G | GTTTT | 13 | a0002c0005t0002g0092 a0002c0005t0002g0123 a0002c0006t0002g0284 others(10): Show |
14 | HG01109.hp1 HG02027.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-593_-66-590dup others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5695566 | ||||||
chr11:5695591 | T | C | 3 | a0002c0006t0001g0230 a0003c0003t0001g0229 a0009c0031t0005g0231 |
3 | HG01884.hp1 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-66-576T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695591 | |||||||
chr11:5695633 | G | A | 374 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(371): Show |
434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.-66-534G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695633 | |||||||
chr11:5695679 | T | A | 14 | a0002c0038t0001g0273 a0002c0039t0004g0065 a0002c0042t0001g0066 others(11): Show |
16 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.-66-488T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695679 | |||||||
chr11:5695692 | G | T | 1 | a0001c0001t0004g0302 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-66-475G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695692 | |||||||
chr11:5695703 | A | G | 1 | a0001c0002t0004g0260 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-66-464A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695703 | |||||||
chr11:5695726 | G | A | 5 | a0002c0014t0001g0028 a0002c0014t0001g0133 a0003c0030t0001g0132 others(2): Show |
6 | HG01346.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-441G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695726 | |||||||
chr11:5695737 | T | C | 127 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(124): Show |
153 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-66-430T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695737 | |||||||
chr11:5695818 | T | A | 7 | a0002c0038t0001g0273 a0003c0011t0001g0272 a0003c0011t0001g0274 others(4): Show |
7 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-66-349T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695818 | |||||||
chr11:5695833 | G | A | 127 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(124): Show |
153 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-66-334G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695833 | |||||||
chr11:5695887 | G | A | 4 | a0001c0002t0006g0047 a0001c0002t0006g0279 a0001c0010t0006g0007 others(1): Show |
9 | HG01943.hp1 HG02109.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-66-280G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695887 | |||||||
chr11:5695929 | A | C | 1 | a0002c0020t0004g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-66-238A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695929 | |||||||
chr11:5695938 | TAAC | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0254 a0001c0001t0001g0256 others(2): Show |
6 | NA18954.hp2 NA18983.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-226_-66-224del others(3): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5695938 | ||||||
chr11:5695959 | G | A | 1 | a0001c0002t0003g0267 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-66-208G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 1/7 | chr11 | 5695959 | |||||||
chr11:5696764 | G | C | 3 | a0001c0001t0004g0315 a0001c0002t0003g0052 a0001c0002t0003g0339 |
4 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+109G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5696764 | |||||||
chr11:5696871 | G | A | 141 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(138): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.423+216G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5696871 | |||||||
chr11:5696919 | C | G | 1 | a0002c0006t0002g0116 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.423+264C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5696919 | |||||||
chr11:5696921 | A | G | 141 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(138): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.423+266A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5696921 | |||||||
chr11:5696929 | C | T | 119 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(116): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.423+274C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5696929 | |||||||
chr11:5696983 | C | A | 134 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(131): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.424-265C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5696983 | |||||||
chr11:5697026 | A | G | 1 | a0003c0003t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.424-222A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5697026 | |||||||
chr11:5697172 | A | G | 3 | a0003c0011t0001g0272 a0012c0021t0001g0277 a0012c0021t0001g0278 |
3 | HG00280.hp1 HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.424-76A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5697172 | |||||||
chr11:5697176 | C | A | 1 | a0001c0002t0003g0166 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.424-72C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5697176 | |||||||
chr11:5697214 | A | G | 2 | a0015c0027t0020g0233 a0018c0028t0019g0232 |
2 | HG01346.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.424-34A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5697214 | |||||||
chr11:5697221 | T | C | 1 | a0003c0003t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.424-27T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 2/7 | chr11 | 5697221 | |||||||
chr11:5697345 | C | T | 1 | a0001c0002t0001g0308 | 1 | NA19054.hp1 | splice_donor_variant&intron_variant | HIGH | c.519+2C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697345 | |||||||
chr11:5697430 | G | T | 5 | a0002c0014t0001g0028 a0002c0014t0001g0133 a0003c0030t0001g0132 others(2): Show |
6 | HG01346.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+87G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697430 | |||||||
chr11:5697482 | C | T | 135 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(132): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.519+139C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697482 | |||||||
chr11:5697512 | G | A | 129 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(126): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.519+169G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697512 | |||||||
chr11:5697534 | C | A | 5 | a0002c0014t0001g0028 a0002c0014t0001g0133 a0003c0030t0001g0132 others(2): Show |
6 | HG01346.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+191C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697534 | |||||||
chr11:5697534 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.519+191C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697534 | |||||||
chr11:5697579 | C | T | 1 | a0001c0001t0002g0252 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.519+236C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697579 | |||||||
chr11:5697587 | G | A | 130 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(127): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.519+244G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697587 | |||||||
chr11:5697593 | C | G | 1 | a0001c0001t0002g0378 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.519+250C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697593 | |||||||
chr11:5697699 | T | TTTTG | 134 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0074 others(131): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.519+372_519+375dup others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5697699 | ||||||
chr11:5697699 | TTTTG | T | 4 | a0001c0001t0001g0300 a0001c0001t0004g0302 a0001c0010t0018g0301 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+372_519+375del others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5697699 | ||||||
chr11:5697745 | A | C | 136 | a0001c0002t0002g0180 a0002c0005t0001g0004 a0002c0005t0001g0012 others(133): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.519+402A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697745 | |||||||
chr11:5697764 | C | T | 7 | a0002c0039t0004g0065 a0002c0042t0001g0066 a0007c0012t0001g0010 others(4): Show |
9 | HG00639.hp2 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+421C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697764 | |||||||
chr11:5697774 | G | A | 1 | a0003c0003t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.519+431G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697774 | |||||||
chr11:5697787 | T | A | 52 | a0002c0005t0001g0004 a0002c0005t0001g0012 a0002c0005t0001g0086 others(49): Show |
66 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.519+444T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697787 | |||||||
chr11:5697807 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.519+464G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697807 | |||||||
chr11:5697807 | G | T | 2 | a0001c0002t0002g0070 a0019c0053t0011g0069 |
2 | HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.519+464G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697807 | |||||||
chr11:5697828 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0053 others(106): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.519+485C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697828 | |||||||
chr11:5697843 | A | G | 2 | a0001c0001t0004g0302 a0001c0010t0018g0301 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.520-472A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697843 | |||||||
chr11:5697865 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(240): Show |
275 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.520-450A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697865 | |||||||
chr11:5697871 | T | G | 1 | a0002c0020t0004g0309 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.520-444T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697871 | |||||||
chr11:5697919 | G | A | 2 | a0001c0001t0004g0302 a0001c0010t0018g0301 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.520-396G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697919 | |||||||
chr11:5697947 | C | T | 1 | a0002c0006t0001g0130 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.520-368C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697947 | |||||||
chr11:5697998 | A | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0049 others(194): Show |
227 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(224): Show |
intron_variant | MODIFIER | c.520-317A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5697998 | |||||||
chr11:5698021 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(324): Show |
376 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.520-294T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5698021 | |||||||
chr11:5698255 | C | T | 2 | a0003c0003t0001g0097 a0016c0035t0001g0098 |
2 | HG01361.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.520-60C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5698255 | |||||||
chr11:5698274 | A | G | 1 | a0003c0003t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.520-41A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5698274 | |||||||
chr11:5698296 | T | C | 1 | a0017c0043t0005g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.520-19T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 3/7 | chr11 | 5698296 | |||||||
chr11:5698547 | T | C | 2 | a0001c0010t0006g0007 a0001c0010t0006g0046 |
6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
splice_donor_variant&intron_variant | HIGH | c.750+2T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698547 | |||||||
chr11:5698558 | A | G | 33 | a0001c0001t0001g0207 a0001c0001t0002g0253 a0001c0001t0002g0259 others(30): Show |
40 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.750+13A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698558 | |||||||
chr11:5698559 | T | G | 4 | a0001c0001t0001g0379 a0002c0006t0001g0137 a0004c0004t0001g0344 others(1): Show |
4 | HG00140.hp1 HG01123.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+14T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698559 | |||||||
chr11:5698562 | A | G | 3 | a0001c0002t0021g0280 a0015c0027t0020g0233 a0018c0028t0019g0232 |
3 | HG01346.hp2 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.750+17A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698562 | |||||||
chr11:5698585 | GA | G | 16 | a0001c0002t0003g0052 a0001c0002t0003g0339 a0001c0002t0006g0047 others(13): Show |
23 | HG01109.hp1 HG01943.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.750+45delA | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5698585 | ||||||
chr11:5698605 | T | C | 197 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0016 others(194): Show |
232 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.750+60T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698605 | |||||||
chr11:5698618 | C | T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0014 others(341): Show |
406 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.750+73C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698618 | |||||||
chr11:5698656 | G | A | 3 | a0015c0027t0020g0233 a0018c0028t0019g0232 a0019c0053t0011g0069 |
3 | HG01346.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.750+111G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698656 | |||||||
chr11:5698669 | G | A | 14 | a0001c0002t0002g0257 a0001c0002t0003g0052 a0001c0002t0003g0234 others(11): Show |
15 | HG01070.hp2 HG01496.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.750+124G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698669 | |||||||
chr11:5698691 | C | T | 1 | a0005c0007t0002g0157 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.750+146C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698691 | |||||||
chr11:5698730 | G | C | 87 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0053 others(84): Show |
106 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.750+185G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698730 | |||||||
chr11:5698790 | G | C | 103 | a0001c0001t0001g0084 a0001c0001t0001g0175 a0001c0001t0001g0242 others(100): Show |
115 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.750+245G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698790 | |||||||
chr11:5698810 | A | T | 1 | a0003c0003t0001g0296 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.750+265A>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698810 | |||||||
chr11:5698811 | T | A | 3 | a0001c0001t0001g0300 a0018c0028t0019g0232 a0019c0053t0011g0069 |
3 | HG02486.hp1 HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.750+266T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698811 | |||||||
chr11:5698919 | T | C | 2 | a0001c0002t0008g0036 a0002c0006t0013g0129 |
3 | HG01891.hp2 HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.750+374T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5698919 | |||||||
chr11:5699020 | A | G | 1 | a0019c0053t0011g0069 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.750+475A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699020 | |||||||
chr11:5699096 | T | C | 1 | a0004c0004t0001g0323 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.750+551T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699096 | |||||||
chr11:5699224 | TAAGAGTG others(336): Show |
T | 29 | a0001c0001t0004g0302 a0001c0001t0004g0315 a0001c0002t0002g0070 others(26): Show |
30 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.750+698_750+1040de others(1): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699224 | ||||||
chr11:5699291 | G | A | 1 | a0019c0053t0011g0069 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.750+746G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699291 | |||||||
chr11:5699295 | C | T | 1 | a0003c0003t0001g0026 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.750+750C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699295 | |||||||
chr11:5699321 | G | C | 1 | a0004c0004t0001g0355 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.750+776G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699321 | |||||||
chr11:5699392 | C | T | 17 | a0001c0001t0003g0054 a0001c0001t0003g0124 a0001c0001t0003g0164 others(14): Show |
17 | HG00609.hp1 HG02132.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.750+847C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699392 | |||||||
chr11:5699397 | G | A | 53 | a0001c0001t0003g0037 a0001c0001t0003g0054 a0001c0001t0003g0124 others(50): Show |
56 | HG00438.hp2 HG00609.hp1 HG02040.hp1 others(53): Show |
intron_variant | MODIFIER | c.750+852G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699397 | |||||||
chr11:5699449 | G | A | 1 | a0002c0006t0002g0116 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.750+904G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699449 | |||||||
chr11:5699466 | A | G | 280 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0159 others(277): Show |
323 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.750+921A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699466 | |||||||
chr11:5699486 | T | C | 8 | a0001c0001t0002g0056 a0001c0001t0002g0381 a0004c0004t0002g0238 others(5): Show |
9 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.750+941T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699486 | |||||||
chr11:5699500 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.750+955C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699500 | |||||||
chr11:5699530 | C | CA | 16 | a0001c0001t0001g0053 a0001c0001t0001g0084 a0001c0001t0001g0159 others(13): Show |
18 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.750+1024dupA | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAA | 7 | a0001c0001t0001g0049 a0001c0001t0001g0307 a0001c0001t0010g0383 others(4): Show |
7 | HG01981.hp1 HG01981.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.750+1023_750+1024d others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAA | 6 | a0001c0001t0003g0054 a0001c0001t0003g0163 a0001c0001t0003g0217 others(3): Show |
7 | HG02040.hp1 HG02080.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.750+1021_750+1024d others(6): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(1): Show |
8 | a0001c0002t0003g0166 a0001c0002t0003g0228 a0001c0002t0003g0375 others(5): Show |
8 | HG02523.hp2 NA18950.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.750+1017_750+1024d others(10): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0037 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.750+1015_750+1024d others(12): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(4): Show |
2 | a0001c0002t0003g0037 a0005c0007t0003g0013 |
2 | HG02300.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.750+1014_750+1024d others(13): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0003g0347 a0011c0015t0003g0291 |
2 | NA18962.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.750+1013_750+1024d others(14): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0216 a0001c0002t0001g0329 a0001c0002t0003g0171 others(2): Show |
5 | NA18957.hp1 NA18975.hp1 NA19082.hp1 others(2): Show |
intron_variant | MODIFIER | c.750+1012_750+1024d others(15): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(7): Show |
2 | a0001c0002t0001g0023 a0001c0002t0003g0320 |
2 | HG04184.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.750+1011_750+1024d others(16): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0261 a0001c0002t0001g0001 a0001c0002t0001g0014 others(1): Show |
4 | NA18970.hp1 NA18992.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+1010_750+1024d others(17): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0314 |
2 | NA19001.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.750+1009_750+1024d others(18): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(10): Show |
2 | a0001c0002t0001g0051 a0001c0002t0001g0367 |
2 | HG02027.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.750+1008_750+1024d others(19): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(11): Show |
1 | a0001c0002t0003g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.750+1007_750+1024d others(20): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0001g0210 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.750+1006_750+1024d others(21): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0313 a0001c0002t0001g0220 |
3 | NA18747.hp2 NA18993.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.750+1005_750+1024d others(22): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | C | CAAAAAAA others(22): Show |
1 | a0004c0004t0001g0283 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.750+996_750+1024du others(30): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CA | C | 23 | a0001c0001t0001g0009 a0001c0001t0001g0237 a0001c0001t0001g0247 others(20): Show |
24 | HG00140.hp2 HG00558.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.750+1024delA | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAA | C | 12 | a0001c0001t0001g0328 a0001c0001t0001g0379 a0001c0002t0001g0348 others(9): Show |
12 | HG00099.hp2 HG01192.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.750+1023_750+1024d others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAA | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0300 a0001c0002t0001g0377 others(7): Show |
11 | HG00140.hp1 HG00323.hp2 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.750+1022_750+1024d others(5): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAA | C | 14 | a0001c0001t0002g0056 a0001c0001t0002g0270 a0001c0001t0002g0326 others(11): Show |
14 | HG00423.hp1 HG01346.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.750+1020_750+1024d others(7): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAA | C | 53 | a0001c0001t0002g0019 a0001c0001t0002g0040 a0001c0001t0002g0055 others(50): Show |
56 | HG00423.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.750+1019_750+1024d others(8): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA | C | 95 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0178 others(92): Show |
100 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.750+1018_750+1024d others(9): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(1): Show |
C | 66 | a0001c0001t0001g0034 a0001c0001t0001g0170 a0001c0001t0001g0242 others(63): Show |
78 | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.750+1017_750+1024d others(10): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0003g0124 a0001c0001t0003g0172 a0001c0001t0003g0208 others(4): Show |
8 | HG00609.hp1 HG01943.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.750+1016_750+1024d others(11): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(3): Show |
C | 16 | a0001c0001t0001g0312 a0001c0001t0003g0054 a0001c0001t0003g0164 others(13): Show |
16 | HG02040.hp2 HG02132.hp1 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.750+1015_750+1024d others(12): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(4): Show |
C | 1 | a0004c0004t0001g0323 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.750+1014_750+1024d others(13): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(6): Show |
C | 1 | a0019c0053t0011g0069 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.750+1012_750+1024d others(15): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(7): Show |
C | 1 | a0018c0028t0019g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.750+1011_750+1024d others(16): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0311 a0003c0003t0001g0006 |
2 | HG02258.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.750+1010_750+1024d others(17): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(11): Show |
C | 2 | a0001c0002t0003g0234 a0004c0008t0001g0258 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.750+1007_750+1024d others(20): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699530 | CAAAAAAA others(12): Show |
C | 1 | a0004c0008t0001g0240 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.750+1006_750+1024d others(21): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699530 | ||||||
chr11:5699570 | G | T | 4 | a0001c0001t0002g0218 a0001c0002t0002g0248 a0001c0002t0002g0388 others(1): Show |
4 | HG00438.hp1 HG00673.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+1025G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699570 | |||||||
chr11:5699608 | C | T | 1 | a0004c0004t0001g0387 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.750+1063C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699608 | |||||||
chr11:5699609 | G | A | 8 | a0001c0002t0002g0070 a0001c0002t0021g0280 a0003c0003t0002g0134 others(5): Show |
8 | HG01346.hp2 HG02572.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.750+1064G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699609 | |||||||
chr11:5699635 | C | T | 29 | a0001c0001t0004g0302 a0001c0001t0004g0315 a0001c0002t0002g0070 others(26): Show |
30 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.750+1090C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699635 | |||||||
chr11:5699724 | C | CT | 13 | a0001c0001t0002g0259 a0001c0001t0003g0217 a0001c0002t0002g0257 others(10): Show |
13 | HG00140.hp1 HG00323.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.750+1196dupT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699724 | ||||||
chr11:5699724 | CT | C | 44 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(41): Show |
49 | HG00423.hp1 HG00597.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.750+1196delT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699724 | ||||||
chr11:5699724 | CTT | C | 30 | a0001c0001t0004g0302 a0001c0001t0004g0315 a0001c0002t0002g0070 others(27): Show |
31 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.750+1195_750+1196d others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5699724 | ||||||
chr11:5699741 | T | C | 4 | a0001c0001t0002g0318 a0001c0001t0002g0324 a0001c0001t0002g0382 others(1): Show |
4 | HG00597.hp2 HG02015.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+1196T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699741 | |||||||
chr11:5699766 | A | G | 30 | a0001c0001t0004g0302 a0001c0001t0004g0315 a0001c0002t0002g0070 others(27): Show |
31 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.750+1221A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699766 | |||||||
chr11:5699787 | T | G | 1 | a0002c0006t0001g0146 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.750+1242T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699787 | |||||||
chr11:5699806 | A | G | 1 | a0002c0006t0002g0106 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.750+1261A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699806 | |||||||
chr11:5699815 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.750+1270A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699815 | |||||||
chr11:5699862 | A | G | 30 | a0001c0001t0004g0302 a0001c0001t0004g0315 a0001c0002t0002g0070 others(27): Show |
31 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.750+1317A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699862 | |||||||
chr11:5699935 | T | A | 2 | a0001c0002t0003g0320 a0001c0002t0003g0330 |
2 | HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.750+1390T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5699935 | |||||||
chr11:5700018 | G | GT | 13 | a0001c0001t0004g0302 a0001c0001t0004g0315 a0001c0002t0004g0260 others(10): Show |
14 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.750+1483dupT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700018 | ||||||
chr11:5700056 | T | C | 189 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(186): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.750+1511T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700056 | |||||||
chr11:5700066 | T | C | 50 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0057 others(47): Show |
56 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.750+1521T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700066 | |||||||
chr11:5700114 | G | GT | 40 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0057 others(37): Show |
46 | HG00408.hp2 HG00621.hp2 HG01358.hp1 others(43): Show |
intron_variant | MODIFIER | c.750+1581dupT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700114 | ||||||
chr11:5700186 | A | G | 241 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(238): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.750+1641A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700186 | |||||||
chr11:5700260 | C | T | 239 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(236): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.750+1715C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700260 | |||||||
chr11:5700322 | C | T | 2 | a0006c0013t0002g0337 a0006c0013t0002g0338 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.750+1777C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700322 | |||||||
chr11:5700390 | A | C | 260 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(257): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.750+1845A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700390 | |||||||
chr11:5700399 | G | C | 23 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0328 others(20): Show |
29 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.750+1854G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700399 | |||||||
chr11:5700400 | C | A | 239 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(236): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.750+1855C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700400 | |||||||
chr11:5700405 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.750+1860G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700405 | |||||||
chr11:5700410 | T | C | 239 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(236): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.750+1865T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700410 | |||||||
chr11:5700439 | T | C | 1 | a0004c0004t0001g0323 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.750+1894T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700439 | |||||||
chr11:5700440 | C | G | 2 | a0002c0006t0002g0284 a0002c0006t0002g0286 |
2 | NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.750+1895C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700440 | |||||||
chr11:5700487 | A | G | 239 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(236): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.750+1942A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700487 | |||||||
chr11:5700488 | C | T | 239 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(236): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.750+1943C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700488 | |||||||
chr11:5700540 | G | A | 12 | a0001c0001t0004g0302 a0001c0001t0004g0315 a0001c0002t0004g0260 others(9): Show |
13 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.750+1995G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700540 | |||||||
chr11:5700584 | C | CTTTTTTT | 14 | a0001c0001t0002g0249 a0001c0001t0002g0271 a0001c0002t0002g0162 others(11): Show |
14 | HG01074.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.750+2054_750+2060d others(9): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700584 | ||||||
chr11:5700584 | C | CTTTTTTT others(1): Show |
50 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(47): Show |
56 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.750+2053_750+2060d others(10): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700584 | ||||||
chr11:5700584 | C | CTTTTTTT others(2): Show |
77 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0019 others(74): Show |
92 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.750+2052_750+2060d others(11): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700584 | ||||||
chr11:5700584 | C | CTTTTTTT others(3): Show |
17 | a0001c0001t0002g0186 a0001c0001t0002g0190 a0001c0001t0002g0218 others(14): Show |
18 | HG00438.hp1 HG00621.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.750+2051_750+2060d others(12): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700584 | ||||||
chr11:5700584 | C | CTTTTTTT others(4): Show |
2 | a0001c0002t0004g0260 a0002c0005t0002g0109 |
2 | HG01978.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.750+2050_750+2060d others(13): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700584 | ||||||
chr11:5700584 | CT | C | 11 | a0001c0001t0001g0216 a0001c0001t0001g0312 a0001c0001t0004g0302 others(8): Show |
12 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.750+2060delT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700584 | ||||||
chr11:5700605 | T | C | 2 | a0003c0003t0001g0078 a0003c0003t0001g0126 |
2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.750+2060T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700605 | |||||||
chr11:5700605 | T | TTTTTC | 18 | a0001c0002t0003g0013 a0001c0002t0003g0339 a0002c0005t0001g0139 others(15): Show |
20 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.750+2060_750+2061i others(7): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700605 | |||||||
chr11:5700605 | T | TTTTTTC | 96 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(93): Show |
114 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.750+2060_750+2061i others(8): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700605 | |||||||
chr11:5700605 | T | TTTTTTTC | 15 | a0001c0001t0003g0163 a0001c0001t0003g0306 a0001c0002t0003g0166 others(12): Show |
15 | HG02080.hp1 HG02615.hp2 HG03139.hp2 others(12): Show |
intron_variant | MODIFIER | c.750+2060_750+2061i others(9): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700605 | |||||||
chr11:5700658 | G | A | 1 | a0001c0001t0003g0331 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.750+2113G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700658 | |||||||
chr11:5700727 | C | T | 3 | a0001c0001t0004g0302 a0001c0002t0004g0260 a0001c0010t0018g0301 |
3 | HG02809.hp2 HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.750+2182C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700727 | |||||||
chr11:5700766 | G | T | 50 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0057 others(47): Show |
56 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.750+2221G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700766 | |||||||
chr11:5700796 | G | C | 233 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(230): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.750+2251G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700796 | |||||||
chr11:5700870 | C | A | 236 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(233): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.750+2325C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700870 | |||||||
chr11:5700905 | A | AG | 3 | a0001c0002t0008g0036 a0002c0006t0013g0129 a0003c0003t0008g0268 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2360_750+2361i others(3): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700905 | |||||||
chr11:5700906 | C | G | 232 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(229): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.750+2361C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700906 | |||||||
chr11:5700906 | C | T | 3 | a0001c0002t0008g0036 a0002c0006t0013g0129 a0003c0003t0008g0268 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2361C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700906 | |||||||
chr11:5700934 | T | TCGAATAG | 69 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(66): Show |
75 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.750+2391_750+2397d others(9): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5700934 | ||||||
chr11:5700977 | T | G | 1 | a0004c0025t0001g0293 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.750+2432T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5700977 | |||||||
chr11:5701107 | C | T | 1 | a0001c0002t0006g0279 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.750+2562C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701107 | |||||||
chr11:5701115 | T | C | 1 | a0002c0006t0001g0030 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.750+2570T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701115 | |||||||
chr11:5701177 | T | G | 235 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(232): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.750+2632T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701177 | |||||||
chr11:5701200 | G | A | 235 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(232): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.750+2655G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701200 | |||||||
chr11:5701214 | A | C | 235 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(232): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.750+2669A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701214 | |||||||
chr11:5701269 | G | A | 48 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0057 others(45): Show |
54 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.750+2724G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701269 | |||||||
chr11:5701278 | A | G | 235 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(232): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.750+2733A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701278 | |||||||
chr11:5701286 | C | T | 3 | a0002c0014t0001g0028 a0002c0014t0001g0133 a0003c0030t0001g0132 |
4 | HG02257.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2741C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701286 | |||||||
chr11:5701382 | T | TCAACAGA | 3 | a0001c0002t0008g0036 a0002c0006t0013g0129 a0003c0003t0008g0268 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2838_750+2839i others(9): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5701382 | ||||||
chr11:5701384 | T | A | 3 | a0001c0002t0008g0036 a0002c0006t0013g0129 a0003c0003t0008g0268 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2839T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701384 | |||||||
chr11:5701386 | T | TAAC | 3 | a0001c0002t0008g0036 a0002c0006t0013g0129 a0003c0003t0008g0268 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2841_750+2842i others(5): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701386 | |||||||
chr11:5701387 | T | A | 3 | a0001c0002t0008g0036 a0002c0006t0013g0129 a0003c0003t0008g0268 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+2842T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701387 | |||||||
chr11:5701389 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.750+2844C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701389 | |||||||
chr11:5701416 | C | T | 235 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(232): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.750+2871C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701416 | |||||||
chr11:5701571 | C | T | 232 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(229): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.750+3026C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701571 | |||||||
chr11:5701577 | C | A | 235 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(232): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.750+3032C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701577 | |||||||
chr11:5701609 | C | T | 304 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(301): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.750+3064C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701609 | |||||||
chr11:5701631 | C | A | 235 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(232): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.750+3086C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701631 | |||||||
chr11:5701718 | A | G | 304 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(301): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.750+3173A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701718 | |||||||
chr11:5701836 | G | A | 175 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0019 others(172): Show |
199 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.750+3291G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701836 | |||||||
chr11:5701877 | G | C | 302 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(299): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.750+3332G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701877 | |||||||
chr11:5701899 | C | T | 1 | a0001c0001t0001g0334 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.750+3354C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701899 | |||||||
chr11:5701938 | C | T | 300 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(297): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.750+3393C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701938 | |||||||
chr11:5701960 | C | T | 33 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0328 others(30): Show |
44 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.750+3415C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5701960 | |||||||
chr11:5702082 | C | CTATATTA others(26): Show |
1 | a0001c0046t0004g0346 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.750+3554_750+3586d others(35): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5702082 | ||||||
chr11:5702086 | ATTAG | A | 48 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(45): Show |
53 | HG00423.hp1 HG00597.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.750+3545_750+3548d others(6): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5702086 | ||||||
chr11:5702146 | G | GAATATAT others(28): Show |
1 | a0001c0002t0002g0176 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.750+3624_750+3658d others(37): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5702146 | ||||||
chr11:5702146 | GAATATAT others(28): Show |
G | 1 | a0001c0001t0001g0385 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.750+3624_750+3658d others(37): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5702146 | ||||||
chr11:5702148 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0003g0244 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.750+3613_750+3623d others(13): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5702148 | ||||||
chr11:5702185 | A | G | 2 | a0002c0006t0002g0284 a0002c0006t0002g0286 |
2 | NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.750+3640A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5702185 | |||||||
chr11:5702320 | ATAAC | A | 4 | a0001c0001t0003g0164 a0001c0002t0003g0158 a0001c0002t0003g0173 others(1): Show |
4 | HG02523.hp1 NA18953.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+3779_750+3782d others(6): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5702320 | ||||||
chr11:5702623 | C | T | 3 | a0003c0003t0002g0029 a0003c0011t0002g0275 a0004c0004t0002g0269 |
4 | HG01255.hp2 HG01261.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-3971C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5702623 | |||||||
chr11:5702688 | C | G | 1 | a0001c0002t0002g0354 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.751-3906C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5702688 | |||||||
chr11:5702688 | C | T | 4 | a0002c0014t0001g0028 a0002c0014t0001g0133 a0003c0030t0001g0132 others(1): Show |
6 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.751-3906C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5702688 | |||||||
chr11:5702837 | G | A | 171 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0019 others(168): Show |
194 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.751-3757G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5702837 | |||||||
chr11:5703109 | T | C | 1 | a0011c0015t0003g0291 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.751-3485T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703109 | |||||||
chr11:5703112 | G | T | 298 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(295): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.751-3482G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703112 | |||||||
chr11:5703344 | A | G | 65 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(62): Show |
75 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.751-3250A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703344 | |||||||
chr11:5703392 | C | T | 106 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0019 others(103): Show |
124 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.751-3202C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703392 | |||||||
chr11:5703392 | CT | C | 193 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(190): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.751-3191delT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5703392 | ||||||
chr11:5703393 | T | C | 106 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0019 others(103): Show |
124 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.751-3201T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703393 | |||||||
chr11:5703447 | G | A | 230 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(227): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.751-3147G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703447 | |||||||
chr11:5703464 | C | T | 300 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(297): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.751-3130C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703464 | |||||||
chr11:5703487 | G | A | 50 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0057 others(47): Show |
56 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.751-3107G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703487 | |||||||
chr11:5703530 | C | T | 1 | a0001c0002t0003g0219 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.751-3064C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703530 | |||||||
chr11:5703562 | T | A | 230 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(227): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.751-3032T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703562 | |||||||
chr11:5703573 | G | A | 69 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(66): Show |
75 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.751-3021G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703573 | |||||||
chr11:5703607 | G | A | 6 | a0001c0001t0001g0385 a0001c0001t0007g0018 a0002c0006t0001g0144 others(3): Show |
9 | HG00323.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-2987G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703607 | |||||||
chr11:5703618 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.751-2976C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703618 | |||||||
chr11:5703627 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.751-2967C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703627 | |||||||
chr11:5703665 | A | G | 342 | a0001c0001t0001g0016 a0001c0001t0001g0034 a0001c0001t0001g0071 others(339): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.751-2929A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703665 | |||||||
chr11:5703680 | C | T | 1 | a0004c0004t0001g0200 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.751-2914C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703680 | |||||||
chr11:5703681 | G | A | 4 | a0002c0014t0001g0028 a0002c0014t0001g0133 a0003c0030t0001g0132 others(1): Show |
5 | HG01123.hp1 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-2913G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703681 | |||||||
chr11:5703690 | A | AT | 297 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(294): Show |
336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.751-2896dupT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5703690 | ||||||
chr11:5703899 | T | C | 48 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(45): Show |
53 | HG00423.hp1 HG00597.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.751-2695T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703899 | |||||||
chr11:5703939 | C | T | 2 | a0001c0010t0006g0046 a0018c0028t0019g0232 |
3 | HG02486.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.751-2655C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5703939 | |||||||
chr11:5704209 | A | T | 2 | a0003c0009t0002g0282 a0005c0007t0002g0195 |
2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.751-2385A>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704209 | |||||||
chr11:5704253 | C | CT | 69 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(66): Show |
75 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.751-2332dupT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5704253 | ||||||
chr11:5704370 | A | G | 53 | a0001c0001t0003g0037 a0001c0001t0003g0054 a0001c0001t0003g0124 others(50): Show |
56 | HG00438.hp2 HG00609.hp1 HG02040.hp1 others(53): Show |
intron_variant | MODIFIER | c.751-2224A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704370 | |||||||
chr11:5704422 | T | C | 69 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(66): Show |
75 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.751-2172T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704422 | |||||||
chr11:5704729 | A | G | 48 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(45): Show |
53 | HG00423.hp1 HG00597.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.751-1865A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704729 | |||||||
chr11:5704784 | G | A | 2 | a0001c0010t0006g0046 a0018c0028t0019g0232 |
3 | HG02486.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.751-1810G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704784 | |||||||
chr11:5704902 | G | A | 1 | a0002c0006t0001g0073 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.751-1692G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704902 | |||||||
chr11:5704909 | G | T | 1 | a0004c0004t0003g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.751-1685G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704909 | |||||||
chr11:5704980 | G | A | 48 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(45): Show |
53 | HG00423.hp1 HG00597.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.751-1614G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704980 | |||||||
chr11:5704986 | T | C | 69 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(66): Show |
75 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.751-1608T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5704986 | |||||||
chr11:5705158 | T | G | 16 | a0002c0005t0001g0139 a0002c0006t0001g0030 a0002c0006t0001g0082 others(13): Show |
18 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.751-1436T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705158 | |||||||
chr11:5705182 | T | A | 69 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(66): Show |
75 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.751-1412T>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705182 | |||||||
chr11:5705216 | G | A | 1 | a0017c0043t0005g0063 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.751-1378G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705216 | |||||||
chr11:5705307 | C | G | 3 | a0001c0002t0008g0036 a0002c0006t0013g0129 a0003c0003t0008g0268 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-1287C>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705307 | |||||||
chr11:5705423 | G | A | 1 | a0004c0004t0002g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.751-1171G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705423 | |||||||
chr11:5705457 | A | C | 1 | a0001c0001t0001g0314 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.751-1137A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705457 | |||||||
chr11:5705581 | G | T | 102 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0019 others(99): Show |
119 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.751-1013G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705581 | |||||||
chr11:5705606 | AC | A | 95 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0019 others(92): Show |
111 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.751-987delC | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705606 | |||||||
chr11:5705795 | C | T | 1 | a0001c0001t0004g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.751-799C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705795 | |||||||
chr11:5705806 | G | C | 1 | a0009c0031t0005g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.751-788G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705806 | |||||||
chr11:5705890 | T | G | 174 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0019 others(171): Show |
198 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.751-704T>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705890 | |||||||
chr11:5705937 | A | C | 120 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(117): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.751-657A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705937 | |||||||
chr11:5705981 | G | C | 1 | a0001c0002t0003g0171 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.751-613G>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5705981 | |||||||
chr11:5706031 | A | T | 4 | a0003c0003t0002g0147 a0003c0009t0002g0022 a0003c0009t0002g0080 others(1): Show |
5 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.751-563A>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5706031 | |||||||
chr11:5706074 | C | T | 1 | a0004c0004t0001g0203 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.751-520C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5706074 | |||||||
chr11:5706153 | A | C | 2 | a0004c0008t0001g0188 a0004c0008t0001g0359 |
2 | NA19083.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.751-441A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5706153 | |||||||
chr11:5706199 | T | C | 48 | a0001c0001t0002g0040 a0001c0001t0002g0055 a0001c0001t0002g0083 others(45): Show |
53 | HG00423.hp1 HG00597.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.751-395T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5706199 | |||||||
chr11:5706315 | T | C | 1 | a0002c0014t0001g0133 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.751-279T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5706315 | |||||||
chr11:5706541 | T | C | 1 | a0004c0004t0001g0323 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.751-53T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 4/7 | chr11 | 5706541 | |||||||
chr11:5706748 | T | C | 8 | a0001c0001t0002g0056 a0001c0001t0002g0381 a0004c0004t0002g0238 others(5): Show |
9 | HG01891.hp1 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.773+132T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5706748 | |||||||
chr11:5706777 | G | T | 1 | a0002c0005t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.773+161G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5706777 | |||||||
chr11:5706846 | A | G | 3 | a0002c0014t0001g0028 a0002c0014t0001g0133 a0003c0030t0001g0132 |
4 | HG02257.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.773+230A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5706846 | |||||||
chr11:5706972 | C | T | 1 | a0004c0004t0001g0358 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.773+356C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5706972 | |||||||
chr11:5706982 | G | A | 124 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(121): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.773+366G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5706982 | |||||||
chr11:5706983 | C | A | 1 | a0001c0001t0002g0360 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.773+367C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5706983 | |||||||
chr11:5707135 | G | A | 3 | a0015c0027t0020g0233 a0019c0053t0011g0069 a0020c0032t0011g0076 |
3 | HG01346.hp2 HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.773+519G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707135 | |||||||
chr11:5707186 | G | T | 1 | a0003c0003t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.773+570G>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707186 | |||||||
chr11:5707208 | C | T | 3 | a0001c0002t0008g0036 a0002c0006t0013g0129 a0003c0003t0008g0268 |
4 | HG00642.hp1 HG01891.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.773+592C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707208 | |||||||
chr11:5707435 | C | T | 21 | a0001c0001t0004g0302 a0001c0001t0004g0315 a0001c0002t0004g0260 others(18): Show |
22 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.774-738C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707435 | |||||||
chr11:5707464 | A | G | 1 | a0002c0006t0001g0130 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.774-709A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707464 | |||||||
chr11:5707621 | C | A | 1 | a0001c0010t0018g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.774-552C>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707621 | |||||||
chr11:5707668 | T | C | 299 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(296): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.774-505T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707668 | |||||||
chr11:5707749 | T | C | 1 | a0003c0003t0001g0078 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.774-424T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707749 | |||||||
chr11:5707799 | G | A | 9 | a0009c0031t0005g0231 a0009c0036t0005g0027 a0009c0041t0005g0020 others(6): Show |
9 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.774-374G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | chr11 | 5707799 | |||||||
chr11:5707812 | A | AAAAC | 55 | a0001c0001t0001g0300 a0001c0001t0002g0019 a0001c0001t0002g0056 others(52): Show |
66 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.774-337_774-334dup others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5707812 | ||||||
chr11:5707812 | A | AAAACAAA others(1): Show |
49 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0057 others(46): Show |
55 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.774-341_774-334dup others(8): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5707812 | ||||||
chr11:5707940 | TGAAGACC others(21): Show |
T | 1 | a0001c0002t0009g0212 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.774-209_774-182del others(28): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr11 | 5707940 | ||||||
chr11:5708337 | C | T | 1 | a0015c0027t0020g0233 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.874+64C>T | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 6/7 | chr11 | 5708337 | |||||||
chr11:5708350 | T | C | 40 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(37): Show |
43 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.874+77T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 6/7 | chr11 | 5708350 | |||||||
chr11:5708362 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.874+89T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 6/7 | chr11 | 5708362 | |||||||
chr11:5708389 | G | A | 3 | a0015c0027t0020g0233 a0019c0053t0011g0069 a0020c0032t0011g0076 |
3 | HG01346.hp2 HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.874+116G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 6/7 | chr11 | 5708389 | |||||||
chr11:5708550 | A | G | 9 | a0009c0031t0005g0231 a0009c0036t0005g0027 a0009c0041t0005g0020 others(6): Show |
9 | HG01884.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.875-27A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 6/7 | chr11 | 5708550 | |||||||
chr11:5708713 | GTTCT | G | 41 | a0001c0001t0002g0019 a0001c0001t0002g0186 a0001c0001t0002g0214 others(38): Show |
50 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.901+113_901+116del others(4): Show |
TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 5708713 | ||||||
chr11:5708716 | CT | C | 189 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0170 others(186): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.901+130delT | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 5708716 | ||||||
chr11:5708778 | G | A | 9 | a0001c0001t0004g0315 a0001c0024t0004g0042 a0001c0046t0004g0346 others(6): Show |
10 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.901+175G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/7 | chr11 | 5708778 | |||||||
chr11:5708780 | G | A | 49 | a0001c0001t0002g0008 a0001c0001t0002g0017 a0001c0001t0002g0057 others(46): Show |
55 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.901+177G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/7 | chr11 | 5708780 | |||||||
chr11:5708784 | T | C | 5 | a0001c0001t0001g0385 a0001c0001t0007g0018 a0002c0006t0001g0144 others(2): Show |
8 | HG00323.hp1 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.901+181T>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/7 | chr11 | 5708784 | |||||||
chr11:5708946 | G | A | 2 | a0004c0008t0001g0240 a0004c0008t0001g0258 |
2 | HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.902-107G>A | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/7 | chr11 | 5708946 | |||||||
chr11:5709018 | A | C | 3 | a0015c0027t0020g0233 a0019c0053t0011g0069 a0020c0032t0011g0076 |
3 | HG01346.hp2 HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.902-35A>C | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/7 | chr11 | 5709018 | |||||||
chr11:5709018 | A | G | 172 | a0001c0001t0001g0300 a0001c0001t0002g0008 a0001c0001t0002g0017 others(169): Show |
196 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.902-35A>G | TRIM22 | ENSG00000132274.17 | transcript | ENST00000379965.8 | protein_coding | 7/7 | chr11 | 5709018 |