Item | Value |
---|---|
geneid | 9866 |
ensemblid | ENSG00000166436.18 |
hgncid | 29005 |
symbol | TRIM66 |
name | tripartite motif containing 66 |
refseq_nuc | NM_001388022.1 |
refseq_prot | NP_001374951.1 |
ensembl_nuc | ENST00000646038.2 |
ensembl_prot | ENSP00000495413.1 |
mane_status | MANE Select |
chr | chr11 |
start | 8612040 |
end | 8682665 |
strand | - |
ver | v1.2 |
region | chr11:8612040-8682665 |
region5000 | chr11:8607040-8687665 |
regionname0 | TRIM66_chr11_8612040_8682665 |
regionname5000 | TRIM66_chr11_8607040_8687665 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1392 | 125 | 37 | 21 | 44 | 5 | 17 | 37 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0002 | 0/0 | 1392 | 78 | 2 | 15 | 48 | 6 | 7 | 39 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0003 | 0/0 | 1392 | 60 | 14 | 10 | 32 | 1 | 3 | 25 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0004 | 0/0 | 1392 | 46 | 5 | 11 | 23 | 2 | 5 | 20 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0005 | 0/0 | 1392 | 9 | 0 | 0 | 9 | 0 | 0 | 8 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0006 | 0/0 | 1392 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0007 | 0/0 | 1392 | 7 | 1 | 2 | 0 | 2 | 2 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0008 | 0/0 | 1392 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0009 | 0/0 | 1392 | 6 | 0 | 0 | 6 | 0 | 0 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0010 | 0/0 | 1392 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0011 | 0/0 | 1392 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0012 | 0/0 | 1392 | 5 | 4 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0013 | 0/0 | 1392 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0014 | 0/0 | 1392 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0015 | 0/0 | 1392 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0016 | 0/0 | 1392 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0017 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0018 | 1/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0019 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0020 | 0/0 | 856 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(851): Show |
chr11 | 8607040 | 8687665 |
a0021 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0022 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0023 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0024 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0025 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0026 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0027 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0028 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
a0029 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | MARLS others(1387): Show |
chr11 | 8607040 | 8687665 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4176 | 123 | 37 | 20 | 44 | 5 | 16 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0001c0023 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0001c0026 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0002c0002 | 0/0 | 4176 | 75 | 2 | 15 | 45 | 6 | 7 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0002c0019 | 0/0 | 4176 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0002c0037 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0003c0003 | 0/0 | 4176 | 58 | 14 | 10 | 30 | 1 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0003c0030 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0003c0031 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0004c0004 | 0/0 | 4176 | 39 | 0 | 11 | 22 | 2 | 4 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0004c0013 | 0/0 | 4176 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0004c0021 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0004c0022 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0005c0005 | 0/0 | 4176 | 9 | 0 | 0 | 9 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0006c0006 | 0/0 | 4176 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0007c0008 | 0/0 | 4176 | 7 | 1 | 2 | 0 | 2 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0008c0007 | 0/0 | 4176 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0009c0009 | 0/0 | 4176 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0010c0010 | 0/0 | 4176 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0011c0012 | 0/0 | 4176 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0012c0011 | 0/0 | 4176 | 5 | 4 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0013c0014 | 0/0 | 4176 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0014c0015 | 0/0 | 4176 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0015c0016 | 0/0 | 4176 | 3 | 0 | 0 | 0 | 0 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0016c0017 | 0/0 | 4176 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0017c0018 | 0/0 | 4176 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0018c0024 | 1/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0019c0025 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0020c0034 | 0/0 | 4186 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4181): Show |
chr11 | 8607040 | 8687665 | ||
a0021c0028 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0022c0036 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0023c0029 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0024c0027 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0025c0033 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0026c0038 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0027c0020 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0028c0035 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 | ||
a0029c0032 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | ATGGC others(4171): Show |
chr11 | 8607040 | 8687665 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 10695 | 102 | 30 | 18 | 39 | 4 | 10 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0005 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0009 | 0/0 | 10695 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0013 | 0/0 | 10695 | 3 | 1 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0017 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0019 | 0/0 | 10695 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0021 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0030 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0031 | 0/0 | 10695 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0032 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0036 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0037 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0038 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0001t0039 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0023t0001 | 0/0 | 10695 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0001c0026t0001 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0002t0002 | 0/0 | 10695 | 62 | 2 | 14 | 34 | 6 | 6 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0002t0008 | 0/0 | 10695 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0002t0012 | 0/0 | 10695 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0002t0025 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0002t0026 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0002t0028 | 0/0 | 10695 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0002t0040 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0019t0002 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0019t0027 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0002c0037t0002 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0003c0003t0003 | 0/0 | 10695 | 42 | 6 | 5 | 29 | 1 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0003c0003t0004 | 0/0 | 10695 | 9 | 7 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0003c0003t0005 | 0/0 | 10695 | 6 | 1 | 3 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0003c0003t0022 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0003c0030t0003 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0003c0031t0003 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0004t0001 | 0/0 | 10695 | 34 | 0 | 11 | 18 | 2 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0004t0014 | 0/0 | 10695 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0004t0029 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0004t0033 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0013t0016 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0013t0018 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0013t0042 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0013t0043 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0021t0035 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0004c0022t0001 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0005c0005t0002 | 0/0 | 10695 | 9 | 0 | 0 | 9 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0006c0006t0002 | 0/0 | 10695 | 9 | 8 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0007c0008t0006 | 0/0 | 10695 | 7 | 1 | 2 | 0 | 2 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0008c0007t0003 | 0/0 | 10695 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0008c0007t0023 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0009c0009t0001 | 0/0 | 10695 | 6 | 0 | 0 | 6 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0010c0010t0001 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0010c0010t0011 | 0/0 | 10692 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10687): Show |
chr11 | 8607040 | 8687665 |
a0011c0012t0007 | 0/0 | 10695 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0012c0011t0001 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0012c0011t0020 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0012c0011t0024 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0012c0011t0041 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0013c0014t0001 | 0/0 | 10695 | 4 | 0 | 3 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0014c0015t0010 | 0/0 | 10695 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0015c0016t0002 | 0/0 | 10695 | 3 | 0 | 0 | 0 | 0 | 3 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0016c0017t0001 | 0/0 | 10695 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0017c0018t0015 | 0/0 | 10695 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0018c0024t0004 | 1/0 | 10695 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0019c0025t0034 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0020c0034t0002 | 0/0 | 10705 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10700): Show |
chr11 | 8607040 | 8687665 |
a0021c0028t0001 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0022c0036t0016 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0023c0029t0007 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0024c0027t0001 | 0/0 | 10695 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0025c0033t0007 | 0/0 | 10695 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0026c0038t0001 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0027c0020t0003 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0028c0035t0002 | 0/0 | 10695 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
a0029c0032t0002 | 0/0 | 10695 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | GCTTC others(10690): Show |
chr11 | 8607040 | 8687665 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0009g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0009g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0009g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0013g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0013g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0013g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0017g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0019g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0019g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0021g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0030g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0031g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0032g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0036g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0037g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0038g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0001t0039g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0023t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0001c0026t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0001 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0012g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0012g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0012g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0025g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0026g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0028g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0002t0040g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0019t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0019t0027g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0002c0037t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0003t0022g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0030t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0003c0031t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0014g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0014g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0014g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0029g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0004t0033g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0013t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0013t0018g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0013t0018g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0013t0042g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0013t0043g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0021t0035g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0004c0022t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0005c0005t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0006c0006t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0008t0006g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0008t0006g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0008t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0008t0006g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0007c0008t0006g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0007t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0007t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0007t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0007t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0007t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0007t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0008c0007t0023g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0009c0009t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0011g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0010c0010t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0012t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0012t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0012t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0012t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0011c0012t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0011t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0011t0020g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0011t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0011t0024g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0012c0011t0041g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0014t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0014t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0014t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0013c0014t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0014c0015t0010g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0014c0015t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0014c0015t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0014c0015t0010g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0015c0016t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0015c0016t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0015c0016t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0016c0017t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0017c0018t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0017c0018t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0018c0024t0004g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0019c0025t0034g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0020c0034t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0021c0028t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0022c0036t0016g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0023c0029t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0024c0027t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0025c0033t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0026c0038t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0027c0020t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0028c0035t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
a0029c0032t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0013 | c0014 | t0001 | g0296 | EUR | GBR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00099 | hp2 | a0007 | c0008 | t0006 | g0007 | EUR | GBR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00140 | hp2 | a0004 | c0004 | t0001 | g0326 | EUR | GBR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0272 | EUR | FIN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00323 | hp1 | a0007 | c0008 | t0006 | g0350 | EUR | FIN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00323 | hp2 | a0003 | c0003 | t0003 | g0114 | EUR | FIN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00408 | hp1 | a0002 | c0002 | t0026 | g0060 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00597 | hp1 | a0003 | c0003 | t0003 | g0158 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00597 | hp2 | a0005 | c0005 | t0002 | g0021 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00609 | hp1 | a0003 | c0003 | t0003 | g0181 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00609 | hp2 | a0019 | c0025 | t0034 | g0236 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00621 | hp1 | a0002 | c0019 | t0002 | g0231 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00621 | hp2 | a0009 | c0009 | t0001 | g0028 | EAS | CHS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00639 | hp1 | a0006 | c0006 | t0002 | g0204 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00642 | hp1 | a0004 | c0004 | t0001 | g0352 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00642 | hp2 | a0003 | c0003 | t0005 | g0182 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00735 | hp1 | a0003 | c0003 | t0003 | g0289 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00735 | hp2 | a0013 | c0014 | t0001 | g0302 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00738 | hp1 | a0004 | c0004 | t0001 | g0323 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00741 | hp1 | a0014 | c0015 | t0010 | g0076 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0338 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01071 | hp2 | a0004 | c0004 | t0001 | g0328 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01081 | hp1 | a0003 | c0003 | t0003 | g0347 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01099 | hp1 | a0013 | c0014 | t0001 | g0299 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0190 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01109 | hp2 | a0003 | c0003 | t0004 | g0206 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0275 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01167 | hp2 | a0001 | c0001 | t0031 | g0151 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01169 | hp1 | a0020 | c0034 | t0002 | g0339 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0249 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0271 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01192 | hp2 | a0004 | c0004 | t0001 | g0293 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01255 | hp2 | a0004 | c0004 | t0001 | g0355 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01256 | hp1 | a0004 | c0004 | t0001 | g0319 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01256 | hp2 | a0002 | c0002 | t0028 | g0276 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01257 | hp1 | a0003 | c0003 | t0003 | g0185 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0248 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01258 | hp1 | a0003 | c0003 | t0003 | g0184 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01258 | hp2 | a0004 | c0004 | t0001 | g0320 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01261 | hp1 | a0003 | c0003 | t0005 | g0187 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01261 | hp2 | a0004 | c0004 | t0001 | g0345 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01346 | hp1 | a0003 | c0003 | t0004 | g0205 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01358 | hp1 | a0004 | c0004 | t0001 | g0329 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01361 | hp2 | a0013 | c0014 | t0001 | g0353 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01433 | hp2 | a0004 | c0004 | t0001 | g0327 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01496 | hp1 | a0004 | c0004 | t0001 | g0027 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0034 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01516 | hp2 | a0001 | c0001 | t0030 | g0096 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0033 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | IBS | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01884 | hp2 | a0010 | c0010 | t0011 | g0002 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01891 | hp1 | a0006 | c0006 | t0002 | g0262 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01943 | hp2 | a0001 | c0001 | t0019 | g0086 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01952 | hp2 | a0007 | c0008 | t0006 | g0007 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01975 | hp1 | a0003 | c0003 | t0003 | g0348 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02015 | hp2 | a0009 | c0009 | t0001 | g0010 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02027 | hp1 | a0003 | c0003 | t0003 | g0229 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02027 | hp2 | a0021 | c0028 | t0001 | g0118 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02040 | hp2 | a0003 | c0003 | t0003 | g0157 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02055 | hp1 | a0010 | c0010 | t0001 | g0134 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02055 | hp2 | a0007 | c0008 | t0006 | g0312 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02056 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02056 | hp2 | a0004 | c0004 | t0001 | g0291 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02071 | hp1 | a0003 | c0003 | t0003 | g0226 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02074 | hp2 | a0004 | c0004 | t0001 | g0294 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02083 | hp1 | a0004 | c0004 | t0001 | g0300 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02132 | hp2 | a0009 | c0009 | t0001 | g0132 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02145 | hp1 | a0006 | c0006 | t0002 | g0263 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02145 | hp2 | a0022 | c0036 | t0016 | g0356 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02148 | hp1 | a0016 | c0017 | t0001 | g0009 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | CDX | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02165 | hp1 | a0003 | c0003 | t0003 | g0235 | EAS | CDX | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | CDX | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02258 | hp1 | a0003 | c0003 | t0003 | g0112 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02258 | hp2 | a0023 | c0029 | t0007 | g0203 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02273 | hp1 | a0016 | c0017 | t0001 | g0009 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02273 | hp2 | a0024 | c0027 | t0001 | g0095 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02293 | hp1 | a0001 | c0023 | t0001 | g0310 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02293 | hp2 | a0007 | c0008 | t0006 | g0007 | AMR | PEL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02451 | hp2 | a0014 | c0015 | t0010 | g0079 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02523 | hp2 | a0002 | c0002 | t0008 | g0123 | EAS | KHV | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02572 | hp1 | a0017 | c0018 | t0015 | g0035 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02572 | hp2 | a0003 | c0003 | t0003 | g0049 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02615 | hp1 | a0004 | c0013 | t0018 | g0121 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02615 | hp2 | a0003 | c0003 | t0003 | g0075 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02622 | hp2 | a0006 | c0006 | t0002 | g0048 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0242 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02683 | hp2 | a0001 | c0001 | t0013 | g0223 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02717 | hp1 | a0017 | c0018 | t0015 | g0119 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02717 | hp2 | a0001 | c0001 | t0036 | g0029 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02723 | hp1 | a0006 | c0006 | t0002 | g0233 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0164 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0261 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02809 | hp1 | a0003 | c0003 | t0003 | g0129 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02818 | hp1 | a0001 | c0001 | t0038 | g0093 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02818 | hp2 | a0001 | c0001 | t0021 | g0025 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02886 | hp2 | a0011 | c0012 | t0007 | g0211 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02895 | hp1 | a0004 | c0013 | t0016 | g0130 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02895 | hp2 | a0011 | c0012 | t0007 | g0221 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02896 | hp1 | a0003 | c0003 | t0004 | g0014 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02896 | hp2 | a0004 | c0013 | t0042 | g0053 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02897 | hp1 | a0003 | c0003 | t0004 | g0014 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02897 | hp2 | a0011 | c0012 | t0007 | g0222 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02922 | hp1 | a0003 | c0003 | t0004 | g0148 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02970 | hp1 | a0012 | c0011 | t0020 | g0052 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02970 | hp2 | a0003 | c0003 | t0004 | g0208 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02976 | hp1 | a0001 | c0001 | t0017 | g0040 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02976 | hp2 | a0001 | c0001 | t0019 | g0087 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03017 | hp1 | a0004 | c0004 | t0029 | g0344 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03017 | hp2 | a0001 | c0001 | t0032 | g0341 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03098 | hp1 | a0012 | c0011 | t0024 | g0215 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03098 | hp2 | a0010 | c0010 | t0011 | g0057 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03130 | hp2 | a0012 | c0011 | t0020 | g0051 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03139 | hp1 | a0014 | c0015 | t0010 | g0078 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03139 | hp2 | a0010 | c0010 | t0011 | g0002 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0207 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03209 | hp1 | a0025 | c0033 | t0007 | g0107 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03209 | hp2 | a0004 | c0013 | t0018 | g0120 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03225 | hp1 | a0010 | c0010 | t0011 | g0002 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03225 | hp2 | a0012 | c0011 | t0041 | g0054 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03491 | hp1 | a0002 | c0002 | t0040 | g0285 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03516 | hp1 | a0014 | c0015 | t0010 | g0077 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03516 | hp2 | a0006 | c0006 | t0002 | g0234 | AFR | ESN | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03540 | hp2 | a0003 | c0003 | t0003 | g0074 | AFR | GWD | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03654 | hp2 | a0004 | c0004 | t0001 | g0317 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03669 | hp2 | a0015 | c0016 | t0002 | g0336 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0314 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03688 | hp2 | a0001 | c0001 | t0013 | g0212 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03704 | hp1 | a0004 | c0004 | t0001 | g0295 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03704 | hp2 | a0001 | c0026 | t0001 | g0036 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03710 | hp1 | a0015 | c0016 | t0002 | g0335 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03710 | hp2 | a0003 | c0003 | t0003 | g0115 | SAS | PJL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03831 | hp1 | a0007 | c0008 | t0006 | g0354 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03831 | hp2 | a0001 | c0001 | t0039 | g0094 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03834 | hp1 | a0004 | c0004 | t0001 | g0106 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03927 | hp1 | a0015 | c0016 | t0002 | g0337 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03927 | hp2 | a0001 | c0001 | t0037 | g0085 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03942 | hp2 | a0007 | c0008 | t0006 | g0194 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04184 | hp1 | a0003 | c0003 | t0005 | g0189 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04184 | hp2 | a0004 | c0021 | t0035 | g0309 | SAS | BEB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04199 | hp1 | a0012 | c0011 | t0001 | g0268 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04204 | hp1 | a0003 | c0003 | t0005 | g0188 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18906 | hp1 | a0003 | c0003 | t0003 | g0113 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18940 | hp2 | a0003 | c0003 | t0003 | g0144 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18944 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18944 | hp2 | a0004 | c0004 | t0001 | g0325 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18950 | hp1 | a0003 | c0003 | t0003 | g0180 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18951 | hp1 | a0009 | c0009 | t0001 | g0047 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18953 | hp1 | a0008 | c0007 | t0003 | g0172 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0349 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18954 | hp1 | a0002 | c0002 | t0012 | g0279 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18956 | hp1 | a0002 | c0002 | t0008 | g0152 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18956 | hp2 | a0004 | c0004 | t0001 | g0298 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18957 | hp1 | a0003 | c0003 | t0022 | g0177 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18959 | hp1 | a0004 | c0004 | t0001 | g0306 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18961 | hp1 | a0002 | c0037 | t0002 | g0265 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18961 | hp2 | a0003 | c0003 | t0003 | g0056 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18962 | hp2 | a0003 | c0003 | t0003 | g0071 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18963 | hp1 | a0003 | c0003 | t0003 | g0346 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18963 | hp2 | a0005 | c0005 | t0002 | g0254 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18964 | hp1 | a0002 | c0002 | t0008 | g0154 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18966 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18973 | hp1 | a0004 | c0004 | t0033 | g0316 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18973 | hp2 | a0003 | c0003 | t0003 | g0174 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18975 | hp1 | a0002 | c0002 | t0012 | g0280 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18975 | hp2 | a0002 | c0002 | t0025 | g0161 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18978 | hp1 | a0008 | c0007 | t0003 | g0170 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18980 | hp2 | a0004 | c0004 | t0001 | g0292 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18981 | hp1 | a0001 | c0001 | t0009 | g0046 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18981 | hp2 | a0005 | c0005 | t0002 | g0253 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18984 | hp1 | a0003 | c0003 | t0003 | g0351 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18984 | hp2 | a0004 | c0004 | t0001 | g0318 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18989 | hp2 | a0001 | c0001 | t0009 | g0043 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18991 | hp1 | a0009 | c0009 | t0001 | g0044 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18991 | hp2 | a0005 | c0005 | t0002 | g0264 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18992 | hp1 | a0003 | c0003 | t0003 | g0150 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18992 | hp2 | a0002 | c0002 | t0008 | g0126 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18994 | hp2 | a0004 | c0004 | t0001 | g0322 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18999 | hp2 | a0004 | c0004 | t0001 | g0321 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19000 | hp2 | a0002 | c0002 | t0008 | g0162 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19003 | hp1 | a0003 | c0003 | t0003 | g0072 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19004 | hp1 | a0004 | c0004 | t0001 | g0303 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19005 | hp1 | a0005 | c0005 | t0002 | g0260 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19005 | hp2 | a0004 | c0004 | t0014 | g0304 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19006 | hp2 | a0003 | c0030 | t0003 | g0178 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19007 | hp1 | a0005 | c0005 | t0002 | g0259 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19007 | hp2 | a0008 | c0007 | t0003 | g0171 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19010 | hp1 | a0002 | c0002 | t0012 | g0286 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19010 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19011 | hp1 | a0004 | c0004 | t0001 | g0324 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19011 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19012 | hp1 | a0003 | c0031 | t0003 | g0176 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19012 | hp2 | a0005 | c0005 | t0002 | g0021 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19030 | hp1 | a0006 | c0006 | t0002 | g0243 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19054 | hp1 | a0002 | c0002 | t0008 | g0201 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19054 | hp2 | a0004 | c0004 | t0014 | g0308 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19055 | hp1 | a0008 | c0007 | t0003 | g0173 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19056 | hp1 | a0004 | c0004 | t0001 | g0334 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19056 | hp2 | a0003 | c0003 | t0003 | g0175 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19058 | hp1 | a0026 | c0038 | t0001 | g0069 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19058 | hp2 | a0002 | c0019 | t0027 | g0357 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19060 | hp1 | a0008 | c0007 | t0023 | g0166 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19063 | hp1 | a0003 | c0003 | t0003 | g0277 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19064 | hp2 | a0004 | c0004 | t0001 | g0169 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19065 | hp1 | a0009 | c0009 | t0001 | g0010 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19066 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19067 | hp2 | a0003 | c0003 | t0003 | g0058 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19068 | hp1 | a0001 | c0001 | t0009 | g0042 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19068 | hp2 | a0003 | c0003 | t0003 | g0143 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19074 | hp1 | a0004 | c0004 | t0001 | g0297 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19077 | hp1 | a0004 | c0004 | t0001 | g0305 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19077 | hp2 | a0027 | c0020 | t0003 | g0191 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19079 | hp1 | a0004 | c0004 | t0001 | g0301 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0179 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19080 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19081 | hp1 | a0028 | c0035 | t0002 | g0244 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19081 | hp2 | a0004 | c0004 | t0001 | g0307 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19084 | hp2 | a0008 | c0007 | t0003 | g0065 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19085 | hp1 | a0003 | c0003 | t0003 | g0213 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19088 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19089 | hp1 | a0005 | c0005 | t0002 | g0255 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19089 | hp2 | a0004 | c0022 | t0001 | g0333 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19090 | hp1 | a0008 | c0007 | t0003 | g0064 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19091 | hp1 | a0005 | c0005 | t0002 | g0284 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19091 | hp2 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20129 | hp2 | a0003 | c0003 | t0004 | g0192 | AFR | ASW | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20752 | hp1 | a0029 | c0032 | t0002 | g0168 | EUR | TSI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | TSI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20805 | hp1 | a0004 | c0004 | t0001 | g0340 | EUR | TSI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0270 | EUR | TSI | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01123 | hp1 | a0003 | c0003 | t0005 | g0183 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02486 | hp2 | a0011 | c0012 | t0007 | g0209 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02559 | hp1 | a0004 | c0013 | t0043 | g0055 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG02559 | hp2 | a0011 | c0012 | t0007 | g0210 | AFR | ACB | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03471 | hp1 | a0001 | c0001 | t0017 | g0039 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG03471 | hp2 | a0010 | c0010 | t0001 | g0137 | AFR | MSL | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG06807 | hp1 | a0003 | c0003 | t0005 | g0167 | AFR | USA | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | USA | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18955 | hp1 | a0004 | c0004 | t0014 | g0313 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20300 | hp1 | a0003 | c0003 | t0004 | g0149 | AFR | USA | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA20300 | hp2 | a0006 | c0006 | t0002 | g0041 | AFR | USA | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA21309 | hp1 | a0006 | c0006 | t0002 | g0269 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0343 | AFR | LWK | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0186 | REF | REF | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
homoSapiens | grch38p0 | a0018 | c0024 | t0004 | g0127 | REF | REF | TRIM66_chr11_8607040_8687665 | TRIM66 | chr11 | 8607040 | 8687665 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:8618903 | C | G | 1 | a0015 | 3 | HG03669.hp2 HG03710.hp1 HG03927.hp1 |
missense_variant | MODERATE | c.3966G>C | p.Glu1322Asp | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/25 | 4578/10695 | 3966/4179 | 1322/1392 | chr11 | 8618903 | |||
chr11:8619490 | T | C | 2 | a0013 a0024 |
5 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(2): Show |
missense_variant | MODERATE | c.3793A>G | p.Ile1265Val | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 23/25 | 4405/10695 | 3793/4179 | 1265/1392 | chr11 | 8619490 | |||
chr11:8624530 | G | C | 1 | a0022 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2848C>G | p.Arg950Gly | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/25 | 3460/10695 | 2848/4179 | 950/1392 | chr11 | 8624530 | |||
chr11:8624811 | G | T | 1 | a0006 | 9 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(6): Show |
missense_variant | MODERATE | c.2728C>A | p.Gln910Lys | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3340/10695 | 2728/4179 | 910/1392 | chr11 | 8624811 | |||
chr11:8624903 | T | G | 1 | a0005 | 9 | HG00597.hp2 NA18963.hp2 NA18981.hp2 others(6): Show |
missense_variant | MODERATE | c.2636A>C | p.Gln879Pro | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3248/10695 | 2636/4179 | 879/1392 | chr11 | 8624903 | |||
chr11:8624990 | C | T | 3 | a0011 a0023 a0025 |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
missense_variant | MODERATE | c.2549G>A | p.Ser850Asn | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3161/10695 | 2549/4179 | 850/1392 | chr11 | 8624990 | |||
chr11:8625020 | A | AGGCTGGG others(3): Show |
1 | a0020 | 1 | HG01169.hp1 | frameshift_variant | HIGH | c.2509_2518dupATGCCC others(4): Show |
p.Leu840fs | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3130/10695 | 2518/4179 | 840/1392 | chr11 | 8625020 | |||
chr11:8625123 | T | G | 10 | a0002 a0005 a0006 others(7): Show |
109 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
missense_variant | MODERATE | c.2416A>C | p.Asn806His | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3028/10695 | 2416/4179 | 806/1392 | chr11 | 8625123 | |||
chr11:8625216 | G | C | 12 | a0002 a0005 a0006 others(9): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
missense_variant | MODERATE | c.2323C>G | p.Leu775Val | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 2935/10695 | 2323/4179 | 775/1392 | chr11 | 8625216 | |||
chr11:8640416 | C | T | 1 | a0027 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.1959G>A | p.Met653Ile | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2571/10695 | 1959/4179 | 653/1392 | chr11 | 8640416 | |||
chr11:8640543 | T | C | 21 | a0001 a0002 a0004 others(18): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
missense_variant | MODERATE | c.1832A>G | p.His611Arg | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2444/10695 | 1832/4179 | 611/1392 | chr11 | 8640543 | |||
chr11:8640738 | C | T | 1 | a0023 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1637G>A | p.Arg546Gln | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2249/10695 | 1637/4179 | 546/1392 | chr11 | 8640738 | |||
chr11:8640763 | C | T | 1 | a0016 | 2 | HG02148.hp1 HG02273.hp1 |
missense_variant | MODERATE | c.1612G>A | p.Val538Met | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2224/10695 | 1612/4179 | 538/1392 | chr11 | 8640763 | |||
chr11:8640906 | T | A | 1 | a0021 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.1469A>T | p.His490Leu | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2081/10695 | 1469/4179 | 490/1392 | chr11 | 8640906 | |||
chr11:8640948 | G | A | 1 | a0028 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.1427C>T | p.Ser476Phe | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2039/10695 | 1427/4179 | 476/1392 | chr11 | 8640948 | |||
chr11:8640969 | T | C | 11 | a0001 a0004 a0009 others(8): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
missense_variant | MODERATE | c.1406A>G | p.His469Arg | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2018/10695 | 1406/4179 | 469/1392 | chr11 | 8640969 | |||
chr11:8641102 | A | G | 1 | a0007 | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
missense_variant | MODERATE | c.1273T>C | p.Tyr425His | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 1885/10695 | 1273/4179 | 425/1392 | chr11 | 8641102 | |||
chr11:8645796 | A | G | 1 | a0010 | 6 | HG01884.hp2 HG02055.hp1 HG03098.hp2 others(3): Show |
missense_variant | MODERATE | c.1049T>C | p.Ile350Thr | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/25 | 1661/10695 | 1049/4179 | 350/1392 | chr11 | 8645796 | |||
chr11:8646469 | T | G | 1 | a0014 | 4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.935A>C | p.Asn312Thr | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 11/25 | 1547/10695 | 935/4179 | 312/1392 | chr11 | 8646469 | |||
chr11:8646535 | C | T | 1 | a0007 | 7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
missense_variant | MODERATE | c.869G>A | p.Arg290Lys | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 11/25 | 1481/10695 | 869/4179 | 290/1392 | chr11 | 8646535 | |||
chr11:8648461 | A | C | 1 | a0016 | 2 | HG02148.hp1 HG02273.hp1 |
missense_variant | MODERATE | c.680T>G | p.Met227Arg | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/25 | 1292/10695 | 680/4179 | 227/1392 | chr11 | 8648461 | |||
chr11:8671858 | G | A | 19 | a0002 a0003 a0004 others(16): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
missense_variant | MODERATE | c.268C>T | p.Arg90Cys | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 880/10695 | 268/4179 | 90/1392 | chr11 | 8671858 | |||
chr11:8671858 | G | T | 2 | a0004 a0013 |
45 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(42): Show |
missense_variant | MODERATE | c.268C>A | p.Arg90Ser | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 880/10695 | 268/4179 | 90/1392 | chr11 | 8671858 | |||
chr11:8671891 | C | A | 1 | a0026 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.235G>T | p.Gly79Cys | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 847/10695 | 235/4179 | 79/1392 | chr11 | 8671891 | |||
chr11:8672022 | C | T | 2 | a0008 a0027 |
8 | NA18953.hp1 NA18978.hp1 NA19007.hp2 others(5): Show |
missense_variant | MODERATE | c.104G>A | p.Gly35Asp | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 716/10695 | 104/4179 | 35/1392 | chr11 | 8672022 | |||
chr11:8672028 | C | T | 1 | a0009 | 6 | HG00621.hp2 HG02015.hp2 HG02132.hp2 others(3): Show |
missense_variant | MODERATE | c.98G>A | p.Gly33Asp | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 710/10695 | 98/4179 | 33/1392 | chr11 | 8672028 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:8624731 | C | G | 1 | a0003c0031 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.2808G>C | p.Leu936Leu | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3420/10695 | 2808/4179 | 936/1392 | chr11 | 8624731 | |||
chr11:8624782 | A | C | 1 | a0001c0026 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.2757T>G | p.Ser919Ser | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3369/10695 | 2757/4179 | 919/1392 | chr11 | 8624782 | |||
chr11:8625058 | G | A | 3 | a0011c0012 a0023c0029 a0025c0033 |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
synonymous_variant | LOW | c.2481C>T | p.Ser827Ser | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3093/10695 | 2481/4179 | 827/1392 | chr11 | 8625058 | |||
chr11:8625112 | A | T | 1 | a0003c0030 | 1 | NA19006.hp2 | synonymous_variant | LOW | c.2427T>A | p.Ala809Ala | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/25 | 3039/10695 | 2427/4179 | 809/1392 | chr11 | 8625112 | |||
chr11:8640578 | C | T | 1 | a0004c0021 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1797G>A | p.Gln599Gln | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/25 | 2409/10695 | 1797/4179 | 599/1392 | chr11 | 8640578 | |||
chr11:8648532 | G | A | 1 | a0002c0019 | 2 | HG00621.hp1 NA19058.hp2 |
synonymous_variant | LOW | c.609C>T | p.Pro203Pro | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/25 | 1221/10695 | 609/4179 | 203/1392 | chr11 | 8648532 | |||
chr11:8649822 | C | T | 4 | a0001c0023 a0004c0004 a0004c0021 others(1): Show |
45 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(42): Show |
synonymous_variant | LOW | c.510G>A | p.Leu170Leu | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/25 | 1122/10695 | 510/4179 | 170/1392 | chr11 | 8649822 | |||
chr11:8671850 | G | A | 1 | a0002c0037 | 1 | NA18961.hp1 | synonymous_variant | LOW | c.276C>T | p.Asp92Asp | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/25 | 888/10695 | 276/4179 | 92/1392 | chr11 | 8671850 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:8612045 | A | G | 2 | a0004c0013t0018 a0004c0013t0043 |
3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5899T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5899 | chr11 | 8612045 | ||||||
chr11:8612081 | A | G | 1 | a0002c0002t0026 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5863T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5863 | chr11 | 8612081 | ||||||
chr11:8612141 | G | A | 1 | a0001c0001t0019 | 2 | HG01943.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5803C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5803 | chr11 | 8612141 | ||||||
chr11:8612734 | C | T | 1 | a0001c0001t0032 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5210G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5210 | chr11 | 8612734 | ||||||
chr11:8612735 | G | A | 1 | a0002c0019t0027 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5209C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5209 | chr11 | 8612735 | ||||||
chr11:8612741 | TATC | T | 1 | a0010c0010t0011 | 4 | HG01884.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5200_*5202delGAT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5200 | chr11 | 8612741 | ||||||
chr11:8612861 | G | A | 1 | a0002c0002t0008 | 6 | HG02523.hp2 NA18956.hp1 NA18964.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5083C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 5083 | chr11 | 8612861 | ||||||
chr11:8612971 | C | A | 3 | a0004c0013t0016 a0004c0013t0042 a0022c0036t0016 |
3 | HG02145.hp2 HG02895.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4973G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4973 | chr11 | 8612971 | ||||||
chr11:8613116 | G | C | 2 | a0003c0003t0022 a0004c0004t0033 |
2 | NA18957.hp1 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4828C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4828 | chr11 | 8613116 | ||||||
chr11:8613595 | T | C | 3 | a0011c0012t0007 a0023c0029t0007 a0025c0033t0007 |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4349A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4349 | chr11 | 8613595 | ||||||
chr11:8613649 | T | A | 2 | a0001c0001t0005 a0003c0003t0005 |
7 | HG00642.hp2 HG01123.hp1 HG01261.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4295A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4295 | chr11 | 8613649 | ||||||
chr11:8613929 | T | A | 1 | a0004c0021t0035 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4015A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 4015 | chr11 | 8613929 | ||||||
chr11:8613948 | G | A | 1 | a0019c0025t0034 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3996C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3996 | chr11 | 8613948 | ||||||
chr11:8614350 | A | AAAAT | 2 | a0005c0005t0002 a0017c0018t0015 |
4 | HG00597.hp2 HG02717.hp1 NA19012.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3590_*3593dupATTT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3593 | chr11 | 8614350 | ||||||
chr11:8614350 | A | T | 10 | a0001c0023t0001 a0004c0004t0001 a0004c0004t0014 others(7): Show |
52 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3594T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3594 | chr11 | 8614350 | ||||||
chr11:8614558 | T | C | 37 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(34): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*3386A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3386 | chr11 | 8614558 | ||||||
chr11:8614581 | T | C | 3 | a0011c0012t0007 a0023c0029t0007 a0025c0033t0007 |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3363A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3363 | chr11 | 8614581 | ||||||
chr11:8614609 | T | A | 52 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(49): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3335A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3335 | chr11 | 8614609 | ||||||
chr11:8614758 | G | A | 1 | a0004c0021t0035 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3186C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3186 | chr11 | 8614758 | ||||||
chr11:8614792 | G | C | 34 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(31): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*3152C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3152 | chr11 | 8614792 | ||||||
chr11:8614796 | A | C | 70 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(67): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
3_prime_UTR_variant | MODIFIER | c.*3148T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3148 | chr11 | 8614796 | ||||||
chr11:8614803 | A | G | 52 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(49): Show |
299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*3141T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3141 | chr11 | 8614803 | ||||||
chr11:8614861 | T | C | 3 | a0011c0012t0007 a0023c0029t0007 a0025c0033t0007 |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3083A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 3083 | chr11 | 8614861 | ||||||
chr11:8614951 | C | T | 1 | a0001c0001t0031 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2993G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2993 | chr11 | 8614951 | ||||||
chr11:8615398 | C | A | 1 | a0001c0001t0036 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2546G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2546 | chr11 | 8615398 | ||||||
chr11:8615506 | C | A | 1 | a0001c0001t0037 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2438G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2438 | chr11 | 8615506 | ||||||
chr11:8615644 | G | C | 51 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(48): Show |
298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*2300C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2300 | chr11 | 8615644 | ||||||
chr11:8615675 | T | C | 1 | a0001c0001t0038 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2269 | chr11 | 8615675 | ||||||
chr11:8615745 | G | A | 1 | a0017c0018t0015 | 2 | HG02572.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2199C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 2199 | chr11 | 8615745 | ||||||
chr11:8615990 | G | C | 1 | a0001c0001t0039 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1954C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1954 | chr11 | 8615990 | ||||||
chr11:8615998 | T | C | 3 | a0011c0012t0007 a0023c0029t0007 a0025c0033t0007 |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1946A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1946 | chr11 | 8615998 | ||||||
chr11:8616265 | A | G | 1 | a0001c0001t0030 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1679T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1679 | chr11 | 8616265 | ||||||
chr11:8616311 | T | C | 1 | a0002c0002t0028 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1633A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1633 | chr11 | 8616311 | ||||||
chr11:8616379 | G | C | 51 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(48): Show |
298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*1565C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1565 | chr11 | 8616379 | ||||||
chr11:8616702 | C | T | 1 | a0004c0004t0029 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1242G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1242 | chr11 | 8616702 | ||||||
chr11:8616726 | C | A | 1 | a0001c0001t0009 | 5 | NA18981.hp1 NA18989.hp2 NA18998.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1218G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1218 | chr11 | 8616726 | ||||||
chr11:8616819 | C | T | 1 | a0012c0011t0020 | 2 | HG02970.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1125G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 1125 | chr11 | 8616819 | ||||||
chr11:8617283 | C | G | 1 | a0012c0011t0024 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*661G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 661 | chr11 | 8617283 | ||||||
chr11:8617566 | G | A | 1 | a0001c0001t0013 | 3 | HG02683.hp2 HG03688.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*378C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 378 | chr11 | 8617566 | ||||||
chr11:8617653 | T | C | 35 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(32): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*291A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 291 | chr11 | 8617653 | ||||||
chr11:8617778 | G | A | 32 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(29): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*166C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 166 | chr11 | 8617778 | ||||||
chr11:8617784 | C | T | 9 | a0001c0001t0005 a0003c0003t0003 a0003c0003t0005 others(6): Show |
60 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*160G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 25/25 | 160 | chr11 | 8617784 | ||||||
chr11:8672321 | A | G | 1 | a0017c0018t0015 | 2 | HG02572.hp1 HG02717.hp1 |
5_prime_UTR_variant | MODIFIER | c.-47T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 5/25 | 47 | chr11 | 8672321 | ||||||
chr11:8672349 | G | A | 1 | a0004c0004t0014 | 3 | NA18955.hp1 NA19005.hp2 NA19054.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-75C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 5/25 | chr11 | 8672349 | |||||||
chr11:8674836 | T | C | 1 | a0002c0002t0040 | 1 | HG03491.hp1 | 5_prime_UTR_variant | MODIFIER | c.-142A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/25 | 2562 | chr11 | 8674836 | ||||||
chr11:8680060 | T | A | 4 | a0004c0013t0042 a0004c0013t0043 a0012c0011t0020 others(1): Show |
5 | HG02559.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-544A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 2/25 | 7786 | chr11 | 8680060 | ||||||
chr11:8682619 | C | G | 1 | a0001c0001t0021 | 1 | HG02818.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-566G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/25 | chr11 | 8682619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:8618119 | G | A | 1 | a0004c0004t0001g0327 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4120-116C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618119 | |||||||
chr11:8618447 | G | C | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(166): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.4119+303C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618447 | |||||||
chr11:8618521 | C | G | 1 | a0002c0002t0002g0160 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4119+229G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618521 | |||||||
chr11:8618526 | GCA | G | 4 | a0001c0001t0017g0039 a0001c0001t0017g0040 a0017c0018t0015g0035 others(1): Show |
4 | HG02572.hp1 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.4119+222_4119+223d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618526 | |||||||
chr11:8618662 | C | T | 2 | a0001c0001t0009g0042 a0001c0001t0009g0046 |
2 | NA18981.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4119+88G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 24/24 | chr11 | 8618662 | |||||||
chr11:8619191 | C | G | 1 | a0001c0001t0021g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3900+192G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 23/24 | chr11 | 8619191 | |||||||
chr11:8619223 | G | T | 1 | a0022c0036t0016g0356 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3900+160C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 23/24 | chr11 | 8619223 | |||||||
chr11:8619349 | G | A | 13 | a0002c0002t0002g0032 a0002c0002t0002g0033 a0002c0002t0002g0034 others(10): Show |
13 | HG00408.hp1 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.3900+34C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 23/24 | chr11 | 8619349 | |||||||
chr11:8619555 | G | A | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3748-20C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8619555 | |||||||
chr11:8619767 | G | C | 3 | a0004c0004t0001g0321 a0004c0004t0001g0322 a0004c0004t0001g0334 |
3 | NA18994.hp2 NA18999.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.3748-232C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8619767 | |||||||
chr11:8619935 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3747+115T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8619935 | |||||||
chr11:8619954 | C | A | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.3747+96G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8619954 | |||||||
chr11:8620028 | A | G | 3 | a0004c0004t0014g0304 a0004c0004t0014g0308 a0004c0004t0014g0313 |
3 | NA18955.hp1 NA19005.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.3747+22T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8620028 | |||||||
chr11:8620036 | G | A | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3747+14C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 22/24 | chr11 | 8620036 | |||||||
chr11:8620192 | T | G | 39 | a0002c0002t0025g0161 a0003c0003t0003g0005 a0003c0003t0003g0008 others(36): Show |
43 | HG00597.hp1 HG00609.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.3673-68A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 21/24 | chr11 | 8620192 | |||||||
chr11:8620335 | G | A | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.3672+111C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 21/24 | chr11 | 8620335 | |||||||
chr11:8620342 | T | C | 2 | a0001c0001t0001g0103 a0024c0027t0001g0095 |
2 | HG01175.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.3672+104A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 21/24 | chr11 | 8620342 | |||||||
chr11:8620671 | C | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.3546-99G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 20/24 | chr11 | 8620671 | |||||||
chr11:8620782 | T | C | 12 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(9): Show |
12 | HG00140.hp1 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.3546-210A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 20/24 | chr11 | 8620782 | |||||||
chr11:8621478 | C | A | 1 | a0012c0011t0024g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3256-157G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 19/24 | chr11 | 8621478 | |||||||
chr11:8621504 | C | CAGCAGGG others(32): Show |
1 | a0003c0030t0003g0178 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3255+102_3255+140d others(41): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 19/24 | chr11 | 8621504 | |||||||
chr11:8621909 | T | A | 1 | a0003c0030t0003g0178 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3081-90A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8621909 | |||||||
chr11:8621980 | C | A | 13 | a0002c0002t0002g0017 a0002c0002t0002g0018 a0002c0002t0002g0066 others(10): Show |
15 | NA18946.hp1 NA18950.hp2 NA18966.hp2 others(12): Show |
intron_variant | MODIFIER | c.3081-161G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8621980 | |||||||
chr11:8622048 | A | C | 1 | a0001c0001t0039g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3081-229T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622048 | |||||||
chr11:8622255 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3081-436G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622255 | |||||||
chr11:8622280 | CATATATA others(5): Show |
C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3081-473_3081-462d others(14): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622280 | |||||||
chr11:8622296 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3081-477A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622296 | |||||||
chr11:8622321 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+495C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622321 | |||||||
chr11:8622336 | CACA | C | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080+477_3080+479d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622336 | |||||||
chr11:8622339 | AACACAC | A | 6 | a0003c0003t0003g0213 a0003c0030t0003g0178 a0012c0011t0020g0051 others(3): Show |
6 | HG02970.hp1 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3080+471_3080+476d others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622339 | |||||||
chr11:8622339 | AACACACA others(1): Show |
A | 59 | a0003c0003t0003g0005 a0003c0003t0003g0008 a0003c0003t0003g0049 others(56): Show |
63 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.3080+469_3080+476d others(10): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622339 | |||||||
chr11:8622346 | AC | A | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080+469delG | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622346 | |||||||
chr11:8622357 | CACACACA others(3): Show |
C | 1 | a0023c0029t0007g0203 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3080+449_3080+458d others(12): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622357 | |||||||
chr11:8622365 | C | CACACACA others(37): Show |
1 | a0004c0013t0018g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(45): Show |
1 | a0004c0021t0035g0309 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(54): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(49): Show |
1 | a0004c0004t0001g0318 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(58): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(53): Show |
1 | a0004c0004t0001g0325 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(62): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(27): Show |
1 | a0012c0011t0001g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(31): Show |
1 | a0004c0004t0001g0317 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(33): Show |
1 | a0004c0013t0043g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(37): Show |
5 | a0004c0004t0001g0292 a0004c0004t0001g0297 a0004c0004t0001g0306 others(2): Show |
5 | HG03209.hp2 NA18959.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(45): Show |
2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(54): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(47): Show |
1 | a0001c0001t0001g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(56): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(49): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0218 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(58): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(23): Show |
1 | a0001c0001t0001g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(27): Show |
1 | a0001c0001t0001g0023 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(29): Show |
1 | a0001c0001t0001g0023 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(33): Show |
1 | a0009c0009t0001g0044 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(35): Show |
4 | a0013c0014t0001g0296 a0013c0014t0001g0299 a0013c0014t0001g0302 others(1): Show |
4 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(37): Show |
1 | a0004c0004t0001g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(41): Show |
1 | a0001c0001t0036g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(50): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(43): Show |
1 | a0001c0001t0001g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(52): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(47): Show |
1 | a0004c0004t0001g0322 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(56): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(25): Show |
1 | a0001c0001t0009g0011 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(27): Show |
3 | a0001c0001t0001g0045 a0001c0001t0009g0042 a0001c0026t0001g0036 |
3 | HG03704.hp2 NA19068.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(29): Show |
1 | a0001c0001t0001g0116 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(33): Show |
1 | a0001c0001t0001g0088 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(35): Show |
3 | a0001c0001t0001g0128 a0001c0023t0001g0310 a0004c0004t0001g0303 |
3 | HG02293.hp1 NA19004.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(37): Show |
3 | a0001c0001t0001g0067 a0004c0004t0001g0293 a0004c0004t0001g0340 |
3 | HG00639.hp2 HG01192.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(39): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0037 |
3 | HG03486.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(48): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(41): Show |
1 | a0001c0001t0001g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(50): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(45): Show |
1 | a0004c0004t0001g0334 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(54): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(47): Show |
1 | a0004c0004t0001g0321 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(56): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(51): Show |
1 | a0001c0001t0001g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(60): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(9): Show |
1 | a0004c0004t0001g0326 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(18): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(19): Show |
1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(23): Show |
1 | a0001c0001t0009g0011 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(25): Show |
4 | a0001c0001t0001g0282 a0001c0001t0009g0046 a0009c0009t0001g0028 others(1): Show |
4 | HG00621.hp2 HG02132.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(27): Show |
2 | a0001c0001t0009g0043 a0001c0001t0013g0343 |
2 | NA18989.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(29): Show |
3 | a0001c0001t0001g0117 a0009c0009t0001g0010 a0009c0009t0001g0047 |
3 | HG02015.hp2 NA18951.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(31): Show |
3 | a0004c0004t0014g0304 a0004c0004t0033g0316 a0016c0017t0001g0009 |
3 | HG02273.hp1 NA18973.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(33): Show |
3 | a0001c0001t0001g0059 a0004c0004t0001g0300 a0004c0004t0001g0324 |
3 | HG02083.hp1 HG02257.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(35): Show |
10 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0111 others(7): Show |
10 | HG00642.hp1 HG01071.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(37): Show |
3 | a0004c0004t0001g0106 a0004c0004t0001g0298 a0004c0004t0001g0355 |
3 | HG01255.hp2 HG03834.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(39): Show |
1 | a0004c0004t0029g0344 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(48): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(41): Show |
1 | a0001c0001t0001g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(50): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(43): Show |
1 | a0001c0001t0001g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(52): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(21): Show |
2 | a0001c0001t0001g0287 a0001c0001t0032g0341 |
2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(23): Show |
1 | a0004c0022t0001g0333 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(25): Show |
4 | a0001c0001t0001g0135 a0001c0001t0001g0219 a0001c0001t0001g0237 others(1): Show |
4 | HG01496.hp2 HG01884.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(27): Show |
3 | a0001c0001t0001g0139 a0004c0004t0001g0301 a0010c0010t0001g0137 |
3 | HG00280.hp1 HG03471.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(29): Show |
2 | a0016c0017t0001g0009 a0021c0028t0001g0118 |
2 | HG02027.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(31): Show |
6 | a0001c0001t0001g0108 a0001c0001t0013g0223 a0004c0004t0001g0027 others(3): Show |
7 | HG01261.hp2 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(33): Show |
10 | a0001c0001t0001g0003 a0001c0001t0001g0109 a0001c0001t0001g0198 others(7): Show |
10 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(35): Show |
1 | a0004c0004t0001g0291 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(37): Show |
2 | a0001c0001t0001g0068 a0004c0004t0001g0329 |
2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(46): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(39): Show |
1 | a0001c0001t0037g0085 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(48): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(41): Show |
1 | a0001c0001t0001g0006 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(50): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(43): Show |
1 | a0001c0001t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(52): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(11): Show |
1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(20): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(17): Show |
1 | a0001c0001t0001g0091 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(19): Show |
2 | a0001c0001t0030g0096 a0004c0004t0001g0169 |
2 | HG01516.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(21): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0163 others(4): Show |
9 | HG00609.hp2 HG00741.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(23): Show |
4 | a0001c0001t0001g0080 a0001c0001t0001g0100 a0001c0001t0001g0140 others(1): Show |
4 | HG01070.hp1 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(25): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0146 |
2 | HG02015.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(27): Show |
3 | a0001c0001t0001g0098 a0001c0001t0001g0195 a0001c0001t0038g0093 |
3 | HG01081.hp2 HG01168.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(29): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0090 a0001c0001t0001g0165 others(2): Show |
5 | HG00738.hp1 HG00738.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(31): Show |
5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0240 others(2): Show |
5 | HG02040.hp1 HG02074.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(33): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0230 |
2 | HG03490.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(42): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(35): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0227 |
2 | NA19070.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(44): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(39): Show |
1 | a0001c0001t0001g0016 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(48): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(11): Show |
1 | a0001c0001t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(20): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(17): Show |
1 | a0001c0001t0001g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(19): Show |
5 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
5 | HG01175.hp1 HG02273.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(21): Show |
5 | a0001c0001t0001g0238 a0001c0001t0001g0288 a0001c0001t0001g0330 others(2): Show |
5 | HG01167.hp2 NA18946.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(23): Show |
4 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0332 others(1): Show |
5 | HG02080.hp1 HG02155.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(25): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0104 |
2 | HG02074.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(27): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0092 others(3): Show |
7 | HG02698.hp1 HG03486.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(29): Show |
2 | a0001c0001t0001g0136 a0010c0010t0011g0057 |
2 | HG03098.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(31): Show |
1 | a0001c0001t0021g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(43): Show |
1 | a0001c0001t0001g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(52): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(17): Show |
1 | a0001c0001t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(25): Show |
1 | a0001c0001t0001g0022 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(27): Show |
1 | a0001c0001t0001g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3080+450_3080+451i others(36): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(29): Show |
1 | a0001c0001t0001g0197 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACACA others(31): Show |
2 | a0001c0001t0001g0290 a0001c0001t0017g0039 |
2 | HG03471.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3080+450_3080+451i others(40): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CACACATA others(29): Show |
1 | a0001c0001t0017g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3080+450_3080+451i others(38): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | CAT | 7 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0190 others(4): Show |
11 | HG00280.hp2 HG01106.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.3080+449_3080+450d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622365 | C | T | 11 | a0003c0003t0003g0213 a0003c0030t0003g0178 a0004c0013t0016g0130 others(8): Show |
11 | HG02145.hp1 HG02895.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.3080+451G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622365 | |||||||
chr11:8622367 | T | C | 10 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(7): Show |
12 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.3080+449A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622367 | |||||||
chr11:8622369 | T | C | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080+447A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622369 | |||||||
chr11:8622424 | C | T | 1 | a0004c0004t0033g0316 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3080+392G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622424 | |||||||
chr11:8622442 | T | C | 283 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(280): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.3080+374A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622442 | |||||||
chr11:8622633 | G | T | 1 | a0003c0030t0003g0178 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3080+183C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622633 | |||||||
chr11:8622637 | C | G | 1 | a0003c0030t0003g0178 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3080+179G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622637 | |||||||
chr11:8622704 | C | T | 1 | a0003c0003t0003g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3080+112G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 18/24 | chr11 | 8622704 | |||||||
chr11:8622983 | T | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.3020-107A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8622983 | |||||||
chr11:8623015 | TCATA | T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.3020-143_3020-140d others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623015 | |||||||
chr11:8623052 | T | C | 1 | a0026c0038t0001g0069 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3020-176A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623052 | |||||||
chr11:8623053 | C | T | 1 | a0004c0004t0029g0344 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3020-177G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623053 | |||||||
chr11:8623443 | A | G | 1 | a0002c0002t0008g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3020-567T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623443 | |||||||
chr11:8623447 | A | G | 2 | a0004c0013t0016g0130 a0004c0013t0042g0053 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3020-571T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623447 | |||||||
chr11:8623534 | A | C | 1 | a0001c0001t0038g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3020-658T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623534 | |||||||
chr11:8623558 | G | A | 1 | a0001c0001t0039g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3020-682C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623558 | |||||||
chr11:8623685 | C | G | 1 | a0001c0001t0009g0046 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3019+674G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623685 | |||||||
chr11:8623854 | T | A | 4 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3019+505A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623854 | |||||||
chr11:8623862 | T | C | 1 | a0023c0029t0007g0203 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3019+497A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623862 | |||||||
chr11:8623908 | G | A | 1 | a0001c0001t0039g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3019+451C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623908 | |||||||
chr11:8623917 | C | A | 2 | a0003c0003t0003g0112 a0003c0003t0003g0113 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3019+442G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623917 | |||||||
chr11:8623963 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0105 a0001c0001t0001g0133 others(92): Show |
107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.3019+396G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623963 | |||||||
chr11:8623993 | C | T | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.3019+366G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8623993 | |||||||
chr11:8624057 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3019+302A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8624057 | |||||||
chr11:8624182 | G | A | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3019+177C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8624182 | |||||||
chr11:8624305 | G | C | 7 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3019+54C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 17/24 | chr11 | 8624305 | |||||||
chr11:8624690 | G | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2826+23C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 16/24 | chr11 | 8624690 | |||||||
chr11:8625249 | G | C | 1 | a0017c0018t0015g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2311-21C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625249 | |||||||
chr11:8625344 | TCTGGTAG others(3): Show |
T | 106 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(103): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2311-126_2311-117d others(12): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625344 | |||||||
chr11:8625453 | C | T | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2311-225G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625453 | |||||||
chr11:8625463 | T | TTGTGTG | 10 | a0002c0002t0002g0024 a0002c0002t0002g0249 a0002c0002t0002g0338 others(7): Show |
11 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.2311-241_2311-236d others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(3): Show |
1 | a0002c0002t0002g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2311-245_2311-236d others(12): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(5): Show |
5 | a0002c0002t0002g0019 a0002c0002t0002g0314 a0002c0002t0025g0161 others(2): Show |
6 | HG01255.hp1 HG01891.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2311-247_2311-236d others(14): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(7): Show |
8 | a0002c0002t0002g0032 a0002c0002t0002g0156 a0002c0002t0002g0247 others(5): Show |
8 | HG00408.hp2 HG01358.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2311-249_2311-236d others(16): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(9): Show |
40 | a0002c0002t0002g0017 a0002c0002t0002g0020 a0002c0002t0002g0033 others(37): Show |
43 | HG00597.hp2 HG00639.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.2311-251_2311-236d others(18): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(11): Show |
17 | a0002c0002t0002g0001 a0002c0002t0002g0124 a0002c0002t0002g0159 others(14): Show |
20 | HG00280.hp2 HG01106.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.2311-253_2311-236d others(20): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(13): Show |
11 | a0002c0002t0002g0015 a0002c0002t0002g0018 a0002c0002t0002g0125 others(8): Show |
13 | HG00408.hp1 HG03491.hp1 HG03491.hp2 others(10): Show |
intron_variant | MODIFIER | c.2311-255_2311-236d others(22): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(15): Show |
1 | a0002c0019t0002g0231 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2311-257_2311-236d others(24): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(17): Show |
1 | a0002c0002t0002g0273 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2311-259_2311-236d others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | T | TTGTGTGT others(19): Show |
2 | a0002c0002t0002g0315 a0002c0002t0008g0154 |
2 | NA18964.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2311-261_2311-236d others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | TTG | T | 74 | a0001c0001t0001g0098 a0001c0001t0013g0212 a0001c0001t0038g0093 others(71): Show |
80 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.2311-237_2311-236d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | TTGTG | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0023 others(85): Show |
95 | HG00099.hp1 HG00609.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2311-239_2311-236d others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625463 | TTGTGTG | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(74): Show |
86 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.2311-241_2311-236d others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625463 | |||||||
chr11:8625541 | TACACACA others(21): Show |
T | 2 | a0003c0003t0004g0014 a0003c0003t0004g0149 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2311-341_2311-314d others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625541 | |||||||
chr11:8625543 | CACACACA others(5): Show |
C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(76): Show |
88 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.2311-327_2311-316d others(14): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625543 | |||||||
chr11:8625577 | C | T | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(167): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2311-349G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625577 | |||||||
chr11:8625624 | C | A | 282 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(279): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2311-396G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625624 | |||||||
chr11:8625750 | C | T | 1 | a0002c0002t0002g0251 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2311-522G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625750 | |||||||
chr11:8625841 | C | T | 1 | a0016c0017t0001g0009 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2311-613G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625841 | |||||||
chr11:8625972 | C | T | 1 | a0012c0011t0024g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2311-744G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8625972 | |||||||
chr11:8626491 | G | T | 346 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(343): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.2311-1263C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626491 | |||||||
chr11:8626592 | C | T | 1 | a0006c0006t0002g0204 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2311-1364G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626592 | |||||||
chr11:8626650 | T | C | 1 | a0008c0007t0003g0064 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2311-1422A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626650 | |||||||
chr11:8626836 | T | A | 1 | a0001c0001t0017g0040 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2311-1608A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626836 | |||||||
chr11:8626856 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0080 a0001c0001t0001g0081 others(22): Show |
26 | HG00280.hp1 HG01070.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.2311-1628C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8626856 | |||||||
chr11:8627020 | G | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
15 | HG02040.hp1 HG02132.hp1 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.2311-1792C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627020 | |||||||
chr11:8627143 | C | T | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2311-1915G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627143 | |||||||
chr11:8627145 | A | G | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-1917T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627145 | |||||||
chr11:8627168 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0038 others(6): Show |
11 | HG01884.hp1 HG02257.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.2311-1940G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627168 | |||||||
chr11:8627249 | GT | G | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-2022delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627249 | |||||||
chr11:8627295 | A | C | 4 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0247 others(1): Show |
6 | HG01192.hp1 HG01255.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-2067T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627295 | |||||||
chr11:8627545 | G | A | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-2317C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627545 | |||||||
chr11:8627596 | C | T | 1 | a0017c0018t0015g0035 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2311-2368G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627596 | |||||||
chr11:8627709 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2311-2481A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627709 | |||||||
chr11:8627743 | T | C | 3 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0079 |
3 | HG00741.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2311-2515A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627743 | |||||||
chr11:8627950 | G | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(283): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2311-2722C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627950 | |||||||
chr11:8627974 | G | A | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-2746C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8627974 | |||||||
chr11:8628080 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0288 a0001c0001t0001g0290 others(3): Show |
7 | NA18939.hp1 NA18946.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-2852G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628080 | |||||||
chr11:8628144 | C | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.2311-2916G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628144 | |||||||
chr11:8628150 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2311-2922A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628150 | |||||||
chr11:8628160 | A | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(169): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2311-2932T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628160 | |||||||
chr11:8628341 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2311-3113C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628341 | |||||||
chr11:8628529 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2311-3301G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628529 | |||||||
chr11:8628612 | C | CA | 82 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(79): Show |
92 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2311-3385dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628612 | |||||||
chr11:8628612 | C | CAA | 8 | a0002c0002t0002g0160 a0002c0002t0002g0261 a0002c0002t0002g0281 others(5): Show |
8 | HG01891.hp1 HG02738.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.2311-3386_2311-338 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628612 | |||||||
chr11:8628612 | C | CAAAA | 32 | a0002c0002t0025g0161 a0003c0003t0003g0005 a0003c0003t0003g0008 others(29): Show |
36 | HG00597.hp1 HG00609.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2311-3388_2311-338 others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628612 | |||||||
chr11:8628612 | C | CAAAAA | 7 | a0003c0003t0003g0056 a0003c0003t0003g0143 a0003c0003t0003g0150 others(4): Show |
7 | HG00735.hp1 HG02071.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-3389_2311-338 others(9): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628612 | |||||||
chr11:8628630 | A | AAG | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
133 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.2311-3403_2311-340 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628630 | |||||||
chr11:8628630 | A | AG | 5 | a0001c0001t0001g0026 a0001c0001t0001g0140 a0001c0001t0001g0216 others(2): Show |
5 | HG01070.hp1 HG02922.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-3403_2311-340 others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628630 | |||||||
chr11:8628632 | A | AGAG | 3 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0004c0004t0001g0317 |
4 | HG02080.hp1 HG02155.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2311-3405_2311-340 others(7): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628632 | |||||||
chr11:8628632 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(120): Show |
138 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.2311-3404T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628632 | |||||||
chr11:8628634 | A | AGAGAG | 3 | a0004c0013t0018g0120 a0004c0013t0018g0121 a0004c0013t0043g0055 |
3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2311-3407_2311-340 others(9): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628634 | |||||||
chr11:8628634 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(131): Show |
150 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.2311-3406T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628634 | |||||||
chr11:8628636 | A | AAAAAAAA others(24): Show |
1 | a0004c0004t0001g0298 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(35): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(23): Show |
1 | a0004c0004t0001g0305 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(34): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(21): Show |
1 | a0004c0004t0001g0325 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(32): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(19): Show |
1 | a0004c0004t0001g0318 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(30): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(18): Show |
2 | a0001c0023t0001g0310 a0004c0004t0001g0293 |
2 | HG01192.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(29): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(17): Show |
6 | a0001c0001t0001g0342 a0004c0004t0001g0301 a0004c0004t0001g0322 others(3): Show |
6 | HG00741.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(16): Show |
19 | a0004c0004t0001g0027 a0004c0004t0001g0106 a0004c0004t0001g0169 others(16): Show |
19 | HG00099.hp1 HG00735.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(27): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(15): Show |
4 | a0004c0004t0001g0294 a0004c0004t0001g0323 a0004c0013t0016g0130 others(1): Show |
4 | HG00738.hp1 HG02074.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(26): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(17): Show |
4 | a0004c0004t0001g0292 a0004c0004t0001g0297 a0004c0004t0001g0306 others(1): Show |
4 | NA18959.hp1 NA18980.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(28): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(14): Show |
1 | a0004c0004t0001g0327 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(25): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(16): Show |
2 | a0004c0004t0001g0345 a0004c0004t0014g0313 |
2 | HG01261.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(27): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0165 a0004c0021t0035g0309 |
2 | HG00738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2311-3409_2311-340 others(24): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(16): Show |
1 | a0017c0018t0015g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(27): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAAAA others(13): Show |
1 | a0017c0018t0015g0035 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(24): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAAAAGAG others(4): Show |
1 | a0004c0004t0001g0326 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2311-3409_2311-340 others(15): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | AAGAGAG | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-3414_2311-340 others(10): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628636 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
155 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.2311-3408T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628636 | |||||||
chr11:8628713 | T | G | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-3485A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628713 | |||||||
chr11:8628787 | T | C | 1 | a0004c0004t0001g0324 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2311-3559A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628787 | |||||||
chr11:8628945 | A | G | 2 | a0001c0023t0001g0310 a0004c0004t0001g0340 |
2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2311-3717T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8628945 | |||||||
chr11:8629061 | A | T | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311-3833T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629061 | |||||||
chr11:8629189 | C | T | 1 | a0003c0003t0005g0182 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2311-3961G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629189 | |||||||
chr11:8629270 | C | T | 1 | a0006c0006t0002g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2311-4042G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629270 | |||||||
chr11:8629348 | T | C | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.2311-4120A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629348 | |||||||
chr11:8629357 | C | T | 5 | a0004c0004t0001g0295 a0013c0014t0001g0296 a0013c0014t0001g0299 others(2): Show |
5 | HG00099.hp1 HG00735.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.2311-4129G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629357 | |||||||
chr11:8629358 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2311-4130C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629358 | |||||||
chr11:8629584 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0195 a0001c0001t0031g0151 |
3 | HG01167.hp2 HG01168.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2311-4356G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629584 | |||||||
chr11:8629623 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0038g0093 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2311-4395C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629623 | |||||||
chr11:8629684 | T | C | 1 | a0014c0015t0010g0078 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2311-4456A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629684 | |||||||
chr11:8629913 | C | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0116 others(17): Show |
23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.2311-4685G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629913 | |||||||
chr11:8629991 | T | C | 1 | a0027c0020t0003g0191 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2311-4763A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8629991 | |||||||
chr11:8630506 | T | C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-5278A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630506 | |||||||
chr11:8630531 | G | A | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2311-5303C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630531 | |||||||
chr11:8630697 | G | A | 1 | a0006c0006t0002g0262 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2311-5469C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630697 | |||||||
chr11:8630711 | C | T | 1 | a0004c0004t0001g0355 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2311-5483G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630711 | |||||||
chr11:8630763 | T | C | 1 | a0019c0025t0034g0236 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2311-5535A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8630763 | |||||||
chr11:8631045 | T | C | 96 | a0001c0001t0001g0241 a0002c0002t0002g0001 a0002c0002t0002g0015 others(93): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2311-5817A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631045 | |||||||
chr11:8631065 | T | A | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311-5837A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631065 | |||||||
chr11:8631140 | A | G | 1 | a0003c0003t0003g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2311-5912T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631140 | |||||||
chr11:8631142 | A | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0068 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311-5914T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631142 | |||||||
chr11:8631189 | A | G | 14 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(11): Show |
16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2311-5961T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631189 | |||||||
chr11:8631686 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2311-6458A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631686 | |||||||
chr11:8631768 | T | C | 1 | a0017c0018t0015g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2311-6540A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631768 | |||||||
chr11:8631812 | T | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(289): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.2311-6584A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631812 | |||||||
chr11:8631951 | T | C | 1 | a0010c0010t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2310+6703A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631951 | |||||||
chr11:8631960 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0136 |
2 | HG03490.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2310+6694C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8631960 | |||||||
chr11:8632079 | G | A | 2 | a0012c0011t0020g0051 a0012c0011t0020g0052 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310+6575C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632079 | |||||||
chr11:8632119 | C | T | 4 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310+6535G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632119 | |||||||
chr11:8632451 | AT | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(166): Show |
188 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.2310+6202delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632451 | |||||||
chr11:8632451 | ATT | A | 156 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0081 others(153): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.2310+6201_2310+620 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632451 | |||||||
chr11:8632451 | ATTT | A | 6 | a0004c0013t0018g0120 a0004c0013t0018g0121 a0004c0013t0043g0055 others(3): Show |
6 | HG00323.hp1 HG01099.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2310+6200_2310+620 others(7): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632451 | |||||||
chr11:8632451 | ATTTT | A | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+6199_2310+620 others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632451 | |||||||
chr11:8632472 | T | C | 2 | a0003c0003t0003g0184 a0003c0003t0003g0185 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2310+6182A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632472 | |||||||
chr11:8632527 | C | T | 2 | a0004c0004t0001g0318 a0004c0004t0001g0325 |
2 | NA18944.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2310+6127G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632527 | |||||||
chr11:8632640 | T | G | 2 | a0010c0010t0011g0002 a0010c0010t0011g0057 |
4 | HG01884.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2310+6014A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632640 | |||||||
chr11:8632697 | G | T | 1 | a0001c0001t0036g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2310+5957C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632697 | |||||||
chr11:8632712 | C | T | 3 | a0012c0011t0020g0051 a0012c0011t0020g0052 a0012c0011t0024g0215 |
3 | HG02970.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310+5942G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632712 | |||||||
chr11:8632981 | T | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(191): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2310+5673A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632981 | |||||||
chr11:8632991 | C | A | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310+5663G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8632991 | |||||||
chr11:8633124 | C | T | 2 | a0003c0003t0003g0184 a0003c0003t0003g0185 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2310+5530G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633124 | |||||||
chr11:8633133 | T | C | 1 | a0006c0006t0002g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2310+5521A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633133 | |||||||
chr11:8633263 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0088 others(2): Show |
5 | NA18960.hp2 NA19006.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310+5391C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633263 | |||||||
chr11:8633322 | C | CA | 64 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0163 others(61): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.2310+5331dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633322 | |||||||
chr11:8633378 | C | T | 1 | a0022c0036t0016g0356 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2310+5276G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633378 | |||||||
chr11:8633427 | G | A | 1 | a0011c0012t0007g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2310+5227C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633427 | |||||||
chr11:8633482 | A | C | 1 | a0008c0007t0003g0172 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2310+5172T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633482 | |||||||
chr11:8633500 | A | AGT | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0116 others(17): Show |
23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.2310+5152_2310+515 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633500 | |||||||
chr11:8633640 | C | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2310+5014G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633640 | |||||||
chr11:8633712 | T | C | 1 | a0002c0002t0002g0153 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2310+4942A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633712 | |||||||
chr11:8633805 | T | C | 14 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(11): Show |
16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2310+4849A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633805 | |||||||
chr11:8633878 | C | T | 1 | a0026c0038t0001g0069 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2310+4776G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633878 | |||||||
chr11:8633895 | T | C | 14 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(11): Show |
16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2310+4759A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633895 | |||||||
chr11:8633938 | C | A | 1 | a0021c0028t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2310+4716G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633938 | |||||||
chr11:8633971 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2310+4683T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633971 | |||||||
chr11:8633990 | G | C | 3 | a0004c0013t0018g0120 a0004c0013t0018g0121 a0004c0013t0043g0055 |
3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2310+4664C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8633990 | |||||||
chr11:8634212 | T | C | 1 | a0002c0002t0002g0066 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2310+4442A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634212 | |||||||
chr11:8634319 | C | T | 1 | a0002c0002t0002g0202 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2310+4335G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634319 | |||||||
chr11:8634375 | C | T | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+4279G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634375 | |||||||
chr11:8634453 | G | C | 1 | a0001c0001t0030g0096 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2310+4201C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634453 | |||||||
chr11:8634488 | T | C | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+4166A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634488 | |||||||
chr11:8634491 | T | C | 2 | a0010c0010t0001g0134 a0010c0010t0001g0137 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2310+4163A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634491 | |||||||
chr11:8634796 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2310+3858A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634796 | |||||||
chr11:8634895 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0038g0093 |
2 | HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2310+3759T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8634895 | |||||||
chr11:8635036 | A | G | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+3618T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635036 | |||||||
chr11:8635043 | G | A | 1 | a0003c0003t0003g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2310+3611C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635043 | |||||||
chr11:8635288 | T | C | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310+3366A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635288 | |||||||
chr11:8635322 | T | C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+3332A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635322 | |||||||
chr11:8635455 | C | A | 7 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(4): Show |
9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.2310+3199G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635455 | |||||||
chr11:8635643 | T | A | 2 | a0001c0001t0019g0086 a0001c0001t0019g0087 |
2 | HG01943.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2310+3011A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635643 | |||||||
chr11:8635739 | G | A | 1 | a0002c0002t0002g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2310+2915C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635739 | |||||||
chr11:8635774 | A | G | 93 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(90): Show |
103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.2310+2880T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635774 | |||||||
chr11:8635969 | T | C | 2 | a0002c0002t0012g0279 a0002c0002t0012g0280 |
2 | NA18954.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2310+2685A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8635969 | |||||||
chr11:8636053 | G | T | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.2310+2601C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636053 | |||||||
chr11:8636183 | G | A | 5 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2310+2471C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636183 | |||||||
chr11:8636376 | G | A | 7 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(4): Show |
9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.2310+2278C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636376 | |||||||
chr11:8636447 | A | G | 6 | a0003c0003t0003g0058 a0003c0003t0003g0070 a0003c0003t0003g0071 others(3): Show |
6 | NA18940.hp2 NA18962.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.2310+2207T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636447 | |||||||
chr11:8636486 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2310+2168A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636486 | |||||||
chr11:8636815 | C | T | 3 | a0012c0011t0020g0051 a0012c0011t0020g0052 a0012c0011t0024g0215 |
3 | HG02970.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2310+1839G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636815 | |||||||
chr11:8636829 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2310+1825G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636829 | |||||||
chr11:8636938 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2310+1716T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8636938 | |||||||
chr11:8637321 | CAT | C | 71 | a0001c0001t0001g0006 a0001c0001t0001g0216 a0001c0001t0001g0217 others(68): Show |
77 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.2310+1331_2310+133 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637321 | |||||||
chr11:8637321 | CATAT | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(266): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2310+1329_2310+133 others(8): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637321 | |||||||
chr11:8637345 | T | TTA | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+1307_2310+130 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637345 | |||||||
chr11:8637560 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2310+1094G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637560 | |||||||
chr11:8637587 | G | A | 287 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(284): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2310+1067C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637587 | |||||||
chr11:8637661 | C | T | 1 | a0001c0001t0036g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2310+993G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637661 | |||||||
chr11:8637741 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2310+913G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637741 | |||||||
chr11:8637857 | G | C | 92 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(89): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2310+797C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637857 | |||||||
chr11:8637878 | G | A | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2310+776C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637878 | |||||||
chr11:8637905 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2310+749C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637905 | |||||||
chr11:8637920 | G | T | 1 | a0004c0021t0035g0309 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2310+734C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8637920 | |||||||
chr11:8638361 | G | A | 4 | a0003c0003t0003g0049 a0003c0003t0003g0074 a0003c0003t0003g0075 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2310+293C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638361 | |||||||
chr11:8638410 | C | G | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2310+244G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638410 | |||||||
chr11:8638414 | T | C | 1 | a0004c0004t0014g0304 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2310+240A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638414 | |||||||
chr11:8638434 | A | C | 1 | a0012c0011t0001g0268 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2310+220T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638434 | |||||||
chr11:8638457 | G | A | 1 | a0004c0004t0001g0352 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2310+197C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638457 | |||||||
chr11:8638514 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2310+140T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638514 | |||||||
chr11:8638570 | C | G | 69 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(66): Show |
79 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.2310+84G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 15/24 | chr11 | 8638570 | |||||||
chr11:8638917 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2149-102G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8638917 | |||||||
chr11:8639417 | G | A | 2 | a0003c0003t0004g0014 a0003c0003t0004g0149 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2149-602C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639417 | |||||||
chr11:8639498 | T | C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2149-683A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639498 | |||||||
chr11:8639714 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2148+513G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639714 | |||||||
chr11:8639850 | C | T | 7 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0190 others(4): Show |
11 | HG00280.hp2 HG01106.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.2148+377G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639850 | |||||||
chr11:8639942 | C | T | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+285G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639942 | |||||||
chr11:8639943 | G | A | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+284C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639943 | |||||||
chr11:8639998 | G | A | 8 | a0003c0003t0003g0150 a0011c0012t0007g0209 a0011c0012t0007g0210 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2148+229C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8639998 | |||||||
chr11:8640081 | T | C | 1 | a0006c0006t0002g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2148+146A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8640081 | |||||||
chr11:8640112 | C | A | 1 | a0004c0004t0033g0316 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2148+115G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8640112 | |||||||
chr11:8640204 | C | T | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0116 others(17): Show |
23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.2148+23G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 14/24 | chr11 | 8640204 | |||||||
chr11:8641219 | T | C | 2 | a0004c0004t0001g0319 a0004c0004t0001g0320 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1223-67A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641219 | |||||||
chr11:8641488 | C | G | 62 | a0001c0023t0001g0310 a0004c0004t0001g0027 a0004c0004t0001g0106 others(59): Show |
64 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.1223-336G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641488 | |||||||
chr11:8641551 | C | T | 287 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(284): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1223-399G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641551 | |||||||
chr11:8641620 | G | T | 2 | a0002c0002t0002g0061 a0002c0002t0002g0156 |
2 | NA18955.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1223-468C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641620 | |||||||
chr11:8641886 | C | T | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1223-734G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641886 | |||||||
chr11:8641887 | G | A | 1 | a0001c0026t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1223-735C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8641887 | |||||||
chr11:8642083 | G | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0073 a0001c0001t0001g0090 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1222+926C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642083 | |||||||
chr11:8642087 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1222+922G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642087 | |||||||
chr11:8642106 | G | A | 1 | a0003c0003t0003g0346 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1222+903C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642106 | |||||||
chr11:8642222 | T | A | 1 | a0008c0007t0003g0172 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1222+787A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642222 | |||||||
chr11:8642423 | C | T | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+586G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642423 | |||||||
chr11:8642472 | A | G | 8 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0190 others(5): Show |
12 | HG00280.hp2 HG01106.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+537T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642472 | |||||||
chr11:8642570 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0196 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1222+439C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642570 | |||||||
chr11:8642610 | C | A | 3 | a0012c0011t0020g0051 a0012c0011t0020g0052 a0012c0011t0024g0215 |
3 | HG02970.hp1 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1222+399G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642610 | |||||||
chr11:8642832 | C | G | 2 | a0003c0003t0003g0112 a0003c0003t0003g0113 |
2 | HG02258.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1222+177G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642832 | |||||||
chr11:8642843 | C | CA | 6 | a0003c0003t0003g0072 a0003c0003t0003g0150 a0003c0003t0003g0179 others(3): Show |
6 | HG00735.hp1 NA18953.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.1222+165dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | |||||||
chr11:8642843 | C | CAA | 7 | a0002c0002t0002g0034 a0002c0002t0002g0050 a0002c0002t0002g0066 others(4): Show |
7 | HG01516.hp1 HG02451.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+164_1222+165d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | |||||||
chr11:8642843 | C | CAAA | 76 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(73): Show |
84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1222+163_1222+165d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | |||||||
chr11:8642843 | C | CAAAA | 13 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0159 others(10): Show |
15 | HG01167.hp1 HG01169.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1222+162_1222+165d others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | |||||||
chr11:8642843 | CA | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(158): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1222+165delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | |||||||
chr11:8642843 | CAA | C | 10 | a0001c0001t0001g0090 a0001c0001t0001g0195 a0001c0001t0001g0330 others(7): Show |
12 | HG00099.hp2 HG00323.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1222+164_1222+165d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | |||||||
chr11:8642843 | CAAA | C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+163_1222+165d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642843 | |||||||
chr11:8642907 | A | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1222+102T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 13/24 | chr11 | 8642907 | |||||||
chr11:8643287 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1105-161A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643287 | |||||||
chr11:8643322 | C | T | 288 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(285): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1105-196G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643322 | |||||||
chr11:8643337 | C | CTTT | 6 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(3): Show |
8 | HG00099.hp2 HG01952.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1105-214_1105-212d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643337 | |||||||
chr11:8643337 | CT | C | 55 | a0001c0001t0019g0087 a0002c0002t0002g0160 a0003c0003t0003g0005 others(52): Show |
59 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1105-212delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643337 | |||||||
chr11:8643363 | G | A | 36 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(33): Show |
44 | HG00280.hp2 HG00597.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1105-237C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643363 | |||||||
chr11:8643496 | C | G | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105-370G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643496 | |||||||
chr11:8643603 | A | C | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1105-477T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643603 | |||||||
chr11:8643732 | C | T | 3 | a0004c0004t0001g0300 a0004c0004t0001g0301 a0004c0004t0001g0324 |
3 | HG02083.hp1 NA19011.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1105-606G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643732 | |||||||
chr11:8643848 | C | T | 1 | a0004c0013t0016g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1105-722G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643848 | |||||||
chr11:8643949 | C | T | 7 | a0002c0002t0002g0066 a0002c0002t0002g0251 a0002c0002t0002g0252 others(4): Show |
7 | NA18950.hp2 NA18969.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.1105-823G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8643949 | |||||||
chr11:8644162 | T | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0099 others(3): Show |
7 | HG01175.hp1 HG02080.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105-1036A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644162 | |||||||
chr11:8644219 | A | C | 2 | a0004c0013t0016g0130 a0004c0013t0042g0053 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1105-1093T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644219 | |||||||
chr11:8644221 | C | T | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105-1095G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644221 | |||||||
chr11:8644442 | G | GA | 5 | a0001c0001t0001g0090 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1104+1298dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644442 | |||||||
chr11:8644494 | C | A | 1 | a0001c0001t0032g0341 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1104+1247G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644494 | |||||||
chr11:8644769 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1104+972G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644769 | |||||||
chr11:8644843 | A | G | 3 | a0006c0006t0002g0234 a0006c0006t0002g0243 a0006c0006t0002g0263 |
3 | HG02145.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1104+898T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644843 | |||||||
chr11:8644864 | G | A | 1 | a0004c0004t0001g0323 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1104+877C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8644864 | |||||||
chr11:8645230 | T | G | 1 | a0001c0001t0039g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1104+511A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8645230 | |||||||
chr11:8645429 | C | G | 45 | a0001c0023t0001g0310 a0004c0004t0001g0027 a0004c0004t0001g0106 others(42): Show |
45 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1104+312G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8645429 | |||||||
chr11:8645432 | G | C | 2 | a0001c0001t0019g0086 a0001c0001t0019g0087 |
2 | HG01943.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1104+309C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8645432 | |||||||
chr11:8645477 | TC | T | 10 | a0002c0002t0002g0061 a0002c0002t0002g0153 a0002c0002t0002g0155 others(7): Show |
10 | HG00408.hp2 HG02083.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1104+263delG | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 12/24 | chr11 | 8645477 | |||||||
chr11:8645968 | T | C | 4 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.958-81A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 11/24 | chr11 | 8645968 | |||||||
chr11:8646133 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.958-246A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 11/24 | chr11 | 8646133 | |||||||
chr11:8646633 | A | G | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.843-72T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8646633 | |||||||
chr11:8646803 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.843-242C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8646803 | |||||||
chr11:8646855 | G | A | 1 | a0006c0006t0002g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843-294C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8646855 | |||||||
chr11:8646941 | TGCCTC | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(283): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.843-385_843-381del others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8646941 | |||||||
chr11:8647022 | A | G | 92 | a0001c0001t0001g0241 a0002c0002t0002g0001 a0002c0002t0002g0015 others(89): Show |
102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.843-461T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647022 | |||||||
chr11:8647089 | CAT | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.843-530_843-529del others(2): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647089 | |||||||
chr11:8647173 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.843-612C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647173 | |||||||
chr11:8647445 | GAA | G | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.842+523_842+524del others(2): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647445 | |||||||
chr11:8647460 | A | T | 1 | a0002c0002t0002g0017 | 2 | NA19009.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.842+510T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647460 | |||||||
chr11:8647537 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.842+433G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647537 | |||||||
chr11:8647585 | C | A | 1 | a0001c0001t0001g0290 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.842+385G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647585 | |||||||
chr11:8647612 | A | G | 3 | a0004c0013t0018g0120 a0004c0013t0018g0121 a0004c0013t0043g0055 |
3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.842+358T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647612 | |||||||
chr11:8647695 | C | T | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+275G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647695 | |||||||
chr11:8647870 | T | C | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.842+100A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647870 | |||||||
chr11:8647890 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.842+80T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647890 | |||||||
chr11:8647897 | G | A | 1 | a0002c0002t0002g0283 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.842+73C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647897 | |||||||
chr11:8647963 | G | A | 2 | a0012c0011t0020g0051 a0012c0011t0020g0052 |
2 | HG02970.hp1 HG03130.hp2 |
splice_region_variant&intron_variant | LOW | c.842+7C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 10/24 | chr11 | 8647963 | |||||||
chr11:8648147 | C | T | 142 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(139): Show |
156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.726-61G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648147 | |||||||
chr11:8648301 | C | T | 1 | a0024c0027t0001g0095 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.725+115G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648301 | |||||||
chr11:8648327 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0097 |
2 | HG06807.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.725+89C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648327 | |||||||
chr11:8648360 | C | G | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.725+56G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648360 | |||||||
chr11:8648376 | A | G | 1 | a0006c0006t0002g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.725+40T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 9/24 | chr11 | 8648376 | |||||||
chr11:8648625 | T | C | 333 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(330): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.593-77A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648625 | |||||||
chr11:8648720 | T | G | 2 | a0002c0002t0002g0033 a0002c0002t0002g0034 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.593-172A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648720 | |||||||
chr11:8648784 | A | G | 4 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-236T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648784 | |||||||
chr11:8648796 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0237 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.593-248G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648796 | |||||||
chr11:8648970 | G | A | 6 | a0003c0003t0003g0049 a0003c0003t0003g0074 a0003c0003t0003g0075 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-422C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8648970 | |||||||
chr11:8649184 | C | T | 1 | a0001c0001t0039g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.592+556G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649184 | |||||||
chr11:8649200 | G | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(181): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.592+540C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649200 | |||||||
chr11:8649229 | C | T | 1 | a0004c0004t0001g0293 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.592+511G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649229 | |||||||
chr11:8649265 | G | A | 3 | a0004c0013t0018g0120 a0004c0013t0018g0121 a0004c0013t0043g0055 |
3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.592+475C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649265 | |||||||
chr11:8649442 | G | T | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.592+298C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649442 | |||||||
chr11:8649507 | T | C | 1 | a0002c0002t0002g0315 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.592+233A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649507 | |||||||
chr11:8649563 | G | A | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.592+177C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649563 | |||||||
chr11:8649659 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02922.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+81G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649659 | |||||||
chr11:8649716 | G | GGCAGGGA others(14): Show |
7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+3_592+23dupACC others(18): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 8/24 | chr11 | 8649716 | |||||||
chr11:8649897 | G | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0105 a0001c0001t0001g0133 |
3 | NA19000.hp1 NA19063.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.445-10C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8649897 | |||||||
chr11:8649944 | C | G | 1 | a0017c0018t0015g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.445-57G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8649944 | |||||||
chr11:8649957 | C | T | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.445-70G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8649957 | |||||||
chr11:8650000 | G | A | 149 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(146): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.445-113C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650000 | |||||||
chr11:8650041 | C | T | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-154G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650041 | |||||||
chr11:8650115 | G | A | 1 | a0012c0011t0024g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.445-228C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650115 | |||||||
chr11:8650229 | C | T | 6 | a0003c0003t0003g0049 a0003c0003t0003g0074 a0003c0003t0003g0075 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-342G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650229 | |||||||
chr11:8650450 | G | A | 3 | a0004c0013t0018g0120 a0004c0013t0018g0121 a0004c0013t0043g0055 |
3 | HG02559.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.445-563C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650450 | |||||||
chr11:8650517 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.445-630C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650517 | |||||||
chr11:8650564 | C | T | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-677G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650564 | |||||||
chr11:8650713 | G | A | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-826C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650713 | |||||||
chr11:8650793 | G | T | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-906C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8650793 | |||||||
chr11:8651253 | A | G | 2 | a0004c0013t0016g0130 a0004c0013t0042g0053 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.444+547T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8651253 | |||||||
chr11:8651443 | T | C | 2 | a0002c0002t0002g0250 a0002c0002t0002g0283 |
2 | HG02071.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.444+357A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 7/24 | chr11 | 8651443 | |||||||
chr11:8651933 | G | A | 1 | a0012c0011t0020g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.341-30C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8651933 | |||||||
chr11:8652041 | C | T | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.341-138G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652041 | |||||||
chr11:8652169 | A | G | 33 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0061 others(30): Show |
35 | HG00408.hp2 HG00621.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.341-266T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652169 | |||||||
chr11:8652179 | A | G | 1 | a0008c0007t0023g0166 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.341-276T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652179 | |||||||
chr11:8652186 | A | C | 1 | a0004c0004t0033g0316 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.341-283T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652186 | |||||||
chr11:8652392 | C | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(173): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.341-489G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652392 | |||||||
chr11:8652502 | A | T | 337 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(334): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.341-599T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652502 | |||||||
chr11:8652541 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.341-638A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652541 | |||||||
chr11:8652653 | A | T | 9 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(6): Show |
9 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-750T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652653 | |||||||
chr11:8652834 | C | T | 1 | a0006c0006t0002g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.341-931G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652834 | |||||||
chr11:8652835 | G | A | 1 | a0003c0003t0003g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.341-932C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652835 | |||||||
chr11:8652903 | C | T | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.341-1000G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8652903 | |||||||
chr11:8653058 | T | C | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.341-1155A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653058 | |||||||
chr11:8653107 | C | T | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1204G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653107 | |||||||
chr11:8653464 | T | C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1561A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653464 | |||||||
chr11:8653519 | G | C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1616C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653519 | |||||||
chr11:8653539 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.341-1636A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653539 | |||||||
chr11:8653735 | T | C | 1 | a0002c0002t0002g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-1832A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653735 | |||||||
chr11:8653781 | C | T | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1878G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653781 | |||||||
chr11:8653787 | C | CAA | 9 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(6): Show |
9 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-1886_341-1885d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653787 | |||||||
chr11:8653897 | C | CAAGAACA others(2307): Show |
1 | a0011c0012t0007g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2316): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653897 | C | CAAGAACA others(2306): Show |
1 | a0011c0012t0007g0222 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2315): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653897 | C | CAAGAACA others(2307): Show |
1 | a0011c0012t0007g0221 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2316): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653897 | C | CAAGAACA others(2309): Show |
1 | a0025c0033t0007g0107 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2318): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653897 | C | CAAGAACA others(2306): Show |
1 | a0011c0012t0007g0210 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2315): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653897 | C | CAAGAACA others(2305): Show |
1 | a0011c0012t0007g0211 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2314): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653897 | C | CAAGAACA others(2307): Show |
1 | a0023c0029t0007g0203 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2316): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653897 | C | CAAGAACA others(2254): Show |
1 | a0017c0018t0015g0035 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2263): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653897 | C | CAAGAACA others(2008): Show |
1 | a0017c0018t0015g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.341-1995_341-1994i others(2017): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653897 | |||||||
chr11:8653928 | C | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(187): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.341-2025G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8653928 | |||||||
chr11:8654282 | G | A | 5 | a0009c0009t0001g0010 a0009c0009t0001g0028 a0009c0009t0001g0044 others(2): Show |
6 | HG00621.hp2 HG02015.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-2379C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654282 | |||||||
chr11:8654637 | T | C | 12 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(9): Show |
12 | HG00140.hp1 HG01243.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.341-2734A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654637 | |||||||
chr11:8654691 | C | T | 142 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(139): Show |
156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.341-2788G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654691 | |||||||
chr11:8654741 | T | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0090 a0001c0001t0001g0197 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-2838A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654741 | |||||||
chr11:8654918 | C | T | 5 | a0002c0002t0002g0018 a0002c0002t0002g0214 a0002c0002t0002g0273 others(2): Show |
6 | HG03209.hp1 NA18946.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-3015G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8654918 | |||||||
chr11:8655035 | T | C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-3132A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655035 | |||||||
chr11:8655092 | T | C | 1 | a0002c0002t0002g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-3189A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655092 | |||||||
chr11:8655178 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0038 others(8): Show |
13 | HG01884.hp1 HG01943.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-3275C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655178 | |||||||
chr11:8655361 | T | C | 1 | a0005c0005t0002g0255 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.341-3458A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655361 | |||||||
chr11:8655484 | C | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0196 |
3 | HG01099.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.341-3581G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655484 | |||||||
chr11:8655485 | G | GT | 11 | a0001c0001t0001g0101 a0001c0001t0001g0228 a0001c0001t0001g0330 others(8): Show |
11 | HG02145.hp2 HG02258.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-3583dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655485 | |||||||
chr11:8655516 | C | A | 141 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(138): Show |
155 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.341-3613G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655516 | |||||||
chr11:8655638 | T | C | 156 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(153): Show |
172 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.341-3735A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655638 | |||||||
chr11:8655654 | G | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(168): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.341-3751C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655654 | |||||||
chr11:8655674 | C | T | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.341-3771G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655674 | |||||||
chr11:8655724 | G | A | 3 | a0009c0009t0001g0010 a0009c0009t0001g0044 a0009c0009t0001g0047 |
4 | HG02015.hp2 NA18951.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-3821C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655724 | |||||||
chr11:8655966 | AGAGCAGA others(4): Show |
A | 1 | a0008c0007t0003g0173 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.341-4074_341-4064d others(13): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8655966 | |||||||
chr11:8656314 | T | A | 1 | a0004c0004t0001g0326 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.341-4411A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8656314 | |||||||
chr11:8656345 | T | C | 2 | a0003c0003t0003g0184 a0003c0003t0003g0185 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.341-4442A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8656345 | |||||||
chr11:8656729 | C | G | 1 | a0001c0001t0021g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.341-4826G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8656729 | |||||||
chr11:8656973 | T | C | 5 | a0002c0002t0002g0267 a0002c0002t0002g0315 a0002c0002t0012g0279 others(2): Show |
5 | NA18954.hp1 NA18964.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-5070A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8656973 | |||||||
chr11:8657085 | C | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.341-5182G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657085 | |||||||
chr11:8657209 | G | A | 165 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(162): Show |
180 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.341-5306C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657209 | |||||||
chr11:8657321 | C | T | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-5418G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657321 | |||||||
chr11:8657444 | C | T | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-5541G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657444 | |||||||
chr11:8657469 | G | A | 179 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(176): Show |
196 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.341-5566C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657469 | |||||||
chr11:8657559 | G | A | 1 | a0004c0004t0001g0323 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.341-5656C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657559 | |||||||
chr11:8657781 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0290 |
3 | NA18939.hp1 NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.341-5878G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657781 | |||||||
chr11:8657999 | C | T | 9 | a0006c0006t0002g0041 a0006c0006t0002g0048 a0006c0006t0002g0204 others(6): Show |
9 | HG00639.hp1 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-6096G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8657999 | |||||||
chr11:8658077 | G | A | 1 | a0006c0006t0002g0233 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.341-6174C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658077 | |||||||
chr11:8658229 | C | T | 1 | a0001c0001t0017g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.341-6326G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658229 | |||||||
chr11:8658480 | C | G | 1 | a0004c0013t0042g0053 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.341-6577G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658480 | |||||||
chr11:8658537 | G | A | 2 | a0001c0001t0013g0223 a0001c0001t0013g0343 |
2 | HG02683.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.341-6634C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658537 | |||||||
chr11:8658834 | G | A | 4 | a0010c0010t0001g0134 a0010c0010t0001g0137 a0010c0010t0011g0002 others(1): Show |
6 | HG01884.hp2 HG02055.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-6931C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658834 | |||||||
chr11:8658917 | T | C | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.341-7014A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8658917 | |||||||
chr11:8659269 | T | G | 8 | a0003c0003t0004g0014 a0003c0003t0004g0148 a0003c0003t0004g0149 others(5): Show |
9 | HG01109.hp2 HG01346.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-7366A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659269 | |||||||
chr11:8659338 | T | G | 62 | a0002c0002t0002g0349 a0002c0002t0025g0161 a0003c0003t0003g0005 others(59): Show |
66 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.341-7435A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659338 | |||||||
chr11:8659344 | T | C | 165 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(162): Show |
180 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.341-7441A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659344 | |||||||
chr11:8659466 | G | C | 1 | a0004c0013t0042g0053 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.341-7563C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659466 | |||||||
chr11:8659891 | G | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0080 others(28): Show |
34 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.341-7988C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659891 | |||||||
chr11:8659894 | T | C | 1 | a0016c0017t0001g0009 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.341-7991A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8659894 | |||||||
chr11:8660014 | A | T | 1 | a0021c0028t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.341-8111T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660014 | |||||||
chr11:8660312 | G | A | 1 | a0004c0013t0016g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.341-8409C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660312 | |||||||
chr11:8660471 | C | T | 170 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(167): Show |
184 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.341-8568G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660471 | |||||||
chr11:8660731 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.341-8828G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660731 | |||||||
chr11:8660822 | G | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0038 others(8): Show |
13 | HG01884.hp1 HG01943.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.341-8919C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660822 | |||||||
chr11:8660918 | T | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0081 others(64): Show |
69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.341-9015A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8660918 | |||||||
chr11:8661092 | G | A | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-9189C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661092 | |||||||
chr11:8661253 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.341-9350C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661253 | |||||||
chr11:8661272 | G | A | 1 | a0003c0003t0003g0213 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.341-9369C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661272 | |||||||
chr11:8661406 | C | A | 1 | a0014c0015t0010g0076 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.341-9503G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661406 | |||||||
chr11:8661428 | C | T | 1 | a0002c0002t0002g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.341-9525G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661428 | |||||||
chr11:8661672 | C | T | 1 | a0001c0001t0013g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.341-9769G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661672 | |||||||
chr11:8661807 | A | T | 14 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0282 others(11): Show |
17 | HG00609.hp2 HG00621.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.341-9904T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8661807 | |||||||
chr11:8662000 | T | C | 1 | a0012c0011t0020g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.340+9786A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662000 | |||||||
chr11:8662092 | C | T | 170 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(167): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.340+9694G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662092 | |||||||
chr11:8662212 | C | T | 8 | a0003c0003t0004g0014 a0003c0003t0004g0148 a0003c0003t0004g0149 others(5): Show |
9 | HG01109.hp2 HG01346.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+9574G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662212 | |||||||
chr11:8662490 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.340+9296C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662490 | |||||||
chr11:8662504 | C | T | 6 | a0003c0003t0003g0049 a0003c0003t0003g0074 a0003c0003t0003g0075 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+9282G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662504 | |||||||
chr11:8662903 | G | T | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.340+8883C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662903 | |||||||
chr11:8662991 | T | G | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+8795A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8662991 | |||||||
chr11:8663205 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.340+8581T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663205 | |||||||
chr11:8663374 | T | C | 2 | a0001c0001t0019g0086 a0001c0001t0019g0087 |
2 | HG01943.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.340+8412A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663374 | |||||||
chr11:8663434 | C | T | 1 | a0003c0003t0003g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.340+8352G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663434 | |||||||
chr11:8663477 | T | TAAGAATA others(342): Show |
1 | a0001c0001t0001g0099 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.340+8308_340+8309i others(351): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663477 | |||||||
chr11:8663564 | T | A | 1 | a0012c0011t0024g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340+8222A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663564 | |||||||
chr11:8663783 | T | C | 1 | a0002c0002t0002g0281 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.340+8003A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663783 | |||||||
chr11:8663805 | A | G | 9 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(6): Show |
9 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+7981T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663805 | |||||||
chr11:8663846 | C | T | 160 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(157): Show |
175 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.340+7940G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663846 | |||||||
chr11:8663904 | C | A | 13 | a0002c0002t0002g0032 a0002c0002t0002g0033 a0002c0002t0002g0034 others(10): Show |
13 | HG00408.hp1 HG00408.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+7882G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8663904 | |||||||
chr11:8664101 | T | C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+7685A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664101 | |||||||
chr11:8664138 | A | C | 143 | a0001c0001t0001g0122 a0002c0002t0002g0001 a0002c0002t0002g0015 others(140): Show |
157 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.340+7648T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664138 | |||||||
chr11:8664154 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.340+7632G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664154 | |||||||
chr11:8664204 | C | T | 1 | a0004c0021t0035g0309 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.340+7582G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664204 | |||||||
chr11:8664206 | T | C | 1 | a0003c0003t0003g0180 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.340+7580A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664206 | |||||||
chr11:8664271 | A | T | 1 | a0012c0011t0024g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340+7515T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664271 | |||||||
chr11:8664471 | G | A | 3 | a0004c0004t0001g0300 a0004c0004t0001g0301 a0004c0004t0001g0324 |
3 | HG02083.hp1 NA19011.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.340+7315C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664471 | |||||||
chr11:8664486 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.340+7300A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664486 | |||||||
chr11:8664521 | A | G | 60 | a0002c0002t0002g0349 a0002c0002t0025g0161 a0003c0003t0003g0005 others(57): Show |
64 | HG00323.hp2 HG00609.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.340+7265T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664521 | |||||||
chr11:8664787 | G | A | 1 | a0002c0002t0040g0285 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.340+6999C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8664787 | |||||||
chr11:8665116 | T | TA | 10 | a0002c0002t0002g0159 a0003c0003t0003g0049 a0003c0003t0003g0074 others(7): Show |
10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+6669dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665116 | |||||||
chr11:8665300 | C | A | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+6486G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665300 | |||||||
chr11:8665637 | A | G | 1 | a0023c0029t0007g0203 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.340+6149T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665637 | |||||||
chr11:8665691 | C | T | 1 | a0008c0007t0003g0064 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.340+6095G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665691 | |||||||
chr11:8665744 | T | G | 1 | a0001c0001t0021g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.340+6042A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665744 | |||||||
chr11:8665805 | C | T | 1 | a0001c0001t0021g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.340+5981G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665805 | |||||||
chr11:8665806 | G | A | 5 | a0002c0002t0002g0024 a0002c0002t0002g0242 a0002c0002t0002g0261 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+5980C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665806 | |||||||
chr11:8665886 | T | C | 1 | a0003c0003t0003g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340+5900A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8665886 | |||||||
chr11:8666095 | G | A | 3 | a0002c0002t0002g0032 a0002c0002t0002g0033 a0002c0002t0002g0034 |
3 | HG01516.hp1 HG01517.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.340+5691C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666095 | |||||||
chr11:8666158 | G | A | 160 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(157): Show |
175 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.340+5628C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666158 | |||||||
chr11:8666163 | C | G | 142 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(139): Show |
156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.340+5623G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666163 | |||||||
chr11:8666251 | A | C | 1 | a0012c0011t0024g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340+5535T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666251 | |||||||
chr11:8666272 | G | A | 5 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+5514C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666272 | |||||||
chr11:8666294 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0045 |
3 | NA18962.hp1 NA18990.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.340+5492C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666294 | |||||||
chr11:8666341 | G | GA | 43 | a0001c0001t0001g0089 a0001c0001t0001g0100 a0001c0001t0001g0104 others(40): Show |
43 | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.340+5444dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | |||||||
chr11:8666341 | GA | G | 32 | a0001c0001t0001g0022 a0001c0001t0001g0059 a0001c0001t0001g0082 others(29): Show |
34 | HG01168.hp1 HG01496.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.340+5444delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | |||||||
chr11:8666341 | GAA | G | 19 | a0001c0001t0001g0145 a0003c0003t0003g0049 a0003c0003t0003g0074 others(16): Show |
20 | HG01109.hp2 HG01346.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.340+5443_340+5444d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | |||||||
chr11:8666341 | GAAAAAAA others(3): Show |
G | 2 | a0017c0018t0015g0035 a0017c0018t0015g0119 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.340+5435_340+5444d others(12): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | |||||||
chr11:8666341 | GAAAAAAA others(6): Show |
G | 4 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(1): Show |
4 | HG00741.hp1 HG02145.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+5432_340+5444d others(15): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | |||||||
chr11:8666341 | GAAAAAAA others(7): Show |
G | 1 | a0014c0015t0010g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.340+5431_340+5444d others(16): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666341 | |||||||
chr11:8666355 | A | AG | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+5430_340+5431i others(3): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666355 | |||||||
chr11:8666370 | G | C | 1 | a0001c0001t0021g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.340+5416C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666370 | |||||||
chr11:8666469 | C | T | 184 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(181): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.340+5317G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666469 | |||||||
chr11:8666538 | G | A | 1 | a0003c0003t0003g0181 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.340+5248C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666538 | |||||||
chr11:8666578 | C | A | 179 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(176): Show |
194 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.340+5208G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666578 | |||||||
chr11:8666744 | A | T | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+5042T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666744 | |||||||
chr11:8666772 | T | C | 10 | a0003c0003t0003g0049 a0003c0003t0003g0074 a0003c0003t0003g0075 others(7): Show |
10 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+5014A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8666772 | |||||||
chr11:8667190 | AT | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0195 a0001c0001t0031g0151 |
3 | HG01167.hp2 HG01168.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.340+4595delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667190 | |||||||
chr11:8667375 | A | C | 13 | a0002c0002t0002g0032 a0002c0002t0002g0033 a0002c0002t0002g0034 others(10): Show |
13 | HG00408.hp1 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.340+4411T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667375 | |||||||
chr11:8667465 | A | G | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+4321T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667465 | |||||||
chr11:8667620 | A | C | 1 | a0001c0001t0001g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.340+4166T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667620 | |||||||
chr11:8667653 | A | C | 5 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+4133T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667653 | |||||||
chr11:8667700 | T | C | 1 | a0002c0002t0002g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340+4086A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667700 | |||||||
chr11:8667789 | C | T | 184 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(181): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.340+3997G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667789 | |||||||
chr11:8667882 | C | A | 3 | a0003c0003t0003g0074 a0003c0003t0003g0075 a0003c0003t0003g0129 |
3 | HG02615.hp2 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.340+3904G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667882 | |||||||
chr11:8667967 | C | T | 19 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(16): Show |
21 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.340+3819G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8667967 | |||||||
chr11:8668158 | C | G | 1 | a0011c0012t0007g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340+3628G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668158 | |||||||
chr11:8668199 | T | C | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+3587A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668199 | |||||||
chr11:8668264 | GT | G | 8 | a0001c0001t0001g0038 a0011c0012t0007g0209 a0011c0012t0007g0210 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.340+3521delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668264 | |||||||
chr11:8668364 | G | A | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+3422C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668364 | |||||||
chr11:8668541 | T | C | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.340+3245A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668541 | |||||||
chr11:8668565 | T | A | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+3221A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668565 | |||||||
chr11:8668590 | A | T | 1 | a0014c0015t0010g0076 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.340+3196T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668590 | |||||||
chr11:8668590 | AT | A | 15 | a0003c0003t0003g0144 a0007c0008t0006g0007 a0007c0008t0006g0194 others(12): Show |
17 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.340+3195delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668590 | |||||||
chr11:8668594 | T | A | 11 | a0001c0001t0001g0038 a0003c0003t0003g0049 a0003c0003t0003g0074 others(8): Show |
11 | HG02258.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.340+3192A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668594 | |||||||
chr11:8668595 | T | A | 7 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(4): Show |
9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+3191A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668595 | |||||||
chr11:8668671 | C | T | 36 | a0003c0003t0003g0005 a0003c0003t0003g0008 a0003c0003t0003g0056 others(33): Show |
40 | HG00609.hp1 HG00735.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.340+3115G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668671 | |||||||
chr11:8668710 | C | G | 142 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(139): Show |
156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.340+3076G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668710 | |||||||
chr11:8668743 | G | A | 1 | a0014c0015t0010g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.340+3043C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8668743 | |||||||
chr11:8669027 | T | C | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+2759A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669027 | |||||||
chr11:8669159 | T | C | 1 | a0001c0001t0009g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.340+2627A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669159 | |||||||
chr11:8669171 | T | C | 142 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(139): Show |
156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.340+2615A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669171 | |||||||
chr11:8669225 | C | T | 5 | a0006c0006t0002g0234 a0006c0006t0002g0243 a0006c0006t0002g0262 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+2561G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669225 | |||||||
chr11:8669311 | T | C | 1 | a0004c0013t0042g0053 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.340+2475A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669311 | |||||||
chr11:8669317 | C | T | 1 | a0004c0004t0001g0355 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.340+2469G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669317 | |||||||
chr11:8669367 | G | A | 3 | a0002c0002t0012g0279 a0002c0002t0012g0280 a0002c0002t0012g0286 |
3 | NA18954.hp1 NA18975.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.340+2419C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669367 | |||||||
chr11:8669465 | G | A | 170 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(167): Show |
185 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.340+2321C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669465 | |||||||
chr11:8669530 | G | A | 1 | a0003c0003t0003g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340+2256C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669530 | |||||||
chr11:8669547 | G | A | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+2239C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669547 | |||||||
chr11:8669597 | C | A | 10 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(7): Show |
10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+2189G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669597 | |||||||
chr11:8669611 | C | A | 1 | a0004c0013t0043g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.340+2175G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669611 | |||||||
chr11:8669642 | C | CA | 17 | a0001c0001t0001g0031 a0001c0001t0001g0101 a0001c0001t0001g0102 others(14): Show |
17 | HG00140.hp2 HG01175.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.340+2143dupT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669642 | |||||||
chr11:8669642 | CA | C | 172 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(169): Show |
189 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.340+2143delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669642 | |||||||
chr11:8669657 | A | C | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+2129T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669657 | |||||||
chr11:8669801 | C | T | 1 | a0008c0007t0023g0166 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.340+1985G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669801 | |||||||
chr11:8669805 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.340+1981G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669805 | |||||||
chr11:8669855 | T | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0282 others(4): Show |
9 | NA18962.hp1 NA18981.hp1 NA18989.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+1931A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669855 | |||||||
chr11:8669984 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.340+1802T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8669984 | |||||||
chr11:8670007 | G | GT | 3 | a0002c0002t0008g0126 a0002c0002t0008g0152 a0002c0002t0008g0154 |
3 | NA18956.hp1 NA18964.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.340+1778dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670007 | |||||||
chr11:8670012 | TA | T | 70 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(67): Show |
78 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.340+1773delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670012 | |||||||
chr11:8670013 | A | AT | 9 | a0003c0003t0004g0014 a0003c0003t0004g0148 a0003c0003t0004g0149 others(6): Show |
10 | HG01109.hp2 HG01346.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.340+1772dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670013 | |||||||
chr11:8670013 | A | T | 19 | a0002c0002t0002g0001 a0002c0002t0002g0018 a0002c0002t0002g0032 others(16): Show |
20 | HG00408.hp1 HG01515.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.340+1773T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670013 | |||||||
chr11:8670017 | A | AT | 61 | a0001c0001t0001g0016 a0002c0002t0002g0190 a0002c0002t0002g0349 others(58): Show |
66 | HG00323.hp2 HG00609.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.340+1768dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670017 | |||||||
chr11:8670017 | A | T | 122 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(119): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.340+1769T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670017 | |||||||
chr11:8670019 | T | A | 17 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(14): Show |
19 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.340+1767A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670019 | |||||||
chr11:8670166 | C | A | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1620G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670166 | |||||||
chr11:8670172 | C | T | 10 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(7): Show |
10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+1614G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670172 | |||||||
chr11:8670173 | C | T | 12 | a0002c0002t0002g0032 a0002c0002t0002g0033 a0002c0002t0002g0034 others(9): Show |
12 | HG00408.hp1 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.340+1613G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670173 | |||||||
chr11:8670233 | G | A | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1553C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670233 | |||||||
chr11:8670264 | G | T | 5 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(2): Show |
7 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+1522C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670264 | |||||||
chr11:8670301 | T | C | 10 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(7): Show |
10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+1485A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670301 | |||||||
chr11:8670414 | T | C | 1 | a0006c0006t0002g0269 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.340+1372A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670414 | |||||||
chr11:8670792 | G | A | 184 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(181): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.340+994C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8670792 | |||||||
chr11:8671019 | C | T | 14 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(11): Show |
16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.340+767G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671019 | |||||||
chr11:8671067 | G | A | 1 | a0003c0003t0003g0115 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.340+719C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671067 | |||||||
chr11:8671217 | GATATTCA others(4): Show |
G | 1 | a0001c0001t0001g0240 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.340+558_340+568del others(11): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671217 | |||||||
chr11:8671369 | CA | C | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+416delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671369 | |||||||
chr11:8671408 | T | C | 10 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(7): Show |
10 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.340+378A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671408 | |||||||
chr11:8671627 | C | T | 1 | a0002c0019t0027g0357 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.340+159G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671627 | |||||||
chr11:8671722 | C | T | 1 | a0012c0011t0024g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.340+64G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671722 | |||||||
chr11:8671785 | C | G | 2 | a0015c0016t0002g0335 a0015c0016t0002g0336 |
2 | HG03669.hp2 HG03710.hp1 |
splice_donor_variant&intron_variant | HIGH | c.340+1G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 6/24 | chr11 | 8671785 | |||||||
chr11:8672526 | G | C | 185 | a0001c0001t0001g0067 a0002c0002t0002g0001 a0002c0002t0002g0015 others(182): Show |
202 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-111-141C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672526 | |||||||
chr11:8672619 | C | CT | 4 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(1): Show |
6 | HG00099.hp2 HG01952.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-235dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672619 | |||||||
chr11:8672619 | CT | C | 276 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.-111-235delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672619 | |||||||
chr11:8672619 | CTT | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0332 a0004c0004t0001g0334 others(5): Show |
8 | HG01099.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-111-236_-111-235d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672619 | |||||||
chr11:8672637 | T | C | 6 | a0003c0003t0005g0167 a0003c0003t0005g0182 a0003c0003t0005g0183 others(3): Show |
6 | HG00642.hp2 HG01123.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-111-252A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672637 | |||||||
chr11:8672701 | G | A | 6 | a0011c0012t0007g0210 a0011c0012t0007g0211 a0011c0012t0007g0221 others(3): Show |
6 | HG02258.hp2 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-316C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672701 | |||||||
chr11:8672935 | C | CTA | 4 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(1): Show |
6 | HG00099.hp2 HG01952.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-111-551_-111-550i others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672935 | |||||||
chr11:8672936 | T | TA | 3 | a0007c0008t0006g0350 a0017c0018t0015g0035 a0017c0018t0015g0119 |
3 | HG00323.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-111-552_-111-551i others(3): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672936 | |||||||
chr11:8672937 | C | T | 7 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(4): Show |
9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-552G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672937 | |||||||
chr11:8672937 | CT | C | 155 | a0001c0001t0001g0023 a0001c0001t0001g0045 a0001c0001t0001g0105 others(152): Show |
171 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-111-553delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672937 | |||||||
chr11:8672937 | CTT | C | 27 | a0001c0001t0009g0046 a0002c0002t0002g0050 a0002c0002t0002g0160 others(24): Show |
27 | HG01167.hp1 HG01169.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.-111-554_-111-553d others(4): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672937 | |||||||
chr11:8672974 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-111-589G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8672974 | |||||||
chr11:8673095 | G | A | 2 | a0004c0013t0016g0130 a0004c0013t0042g0053 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-111-710C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673095 | |||||||
chr11:8673166 | G | A | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-111-781C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673166 | |||||||
chr11:8673179 | C | T | 84 | a0002c0002t0002g0017 a0002c0002t0002g0018 a0002c0002t0002g0019 others(81): Show |
90 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-111-794G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673179 | |||||||
chr11:8673210 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-111-825C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673210 | |||||||
chr11:8673218 | G | A | 1 | a0004c0021t0035g0309 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-111-833C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673218 | |||||||
chr11:8673283 | G | A | 141 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(138): Show |
155 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-111-898C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673283 | |||||||
chr11:8673335 | T | C | 7 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0270 others(4): Show |
11 | HG00280.hp2 HG01106.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-111-950A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673335 | |||||||
chr11:8673452 | C | A | 14 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(11): Show |
16 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.-111-1067G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673452 | |||||||
chr11:8673499 | T | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0116 others(17): Show |
23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.-111-1114A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673499 | |||||||
chr11:8673586 | T | C | 4 | a0002c0002t0002g0190 a0003c0003t0003g0184 a0003c0003t0003g0185 others(1): Show |
4 | HG01106.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-1201A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673586 | |||||||
chr11:8673664 | A | G | 5 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(2): Show |
5 | HG00741.hp1 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112+1142T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673664 | |||||||
chr11:8673679 | T | C | 1 | a0012c0011t0024g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-112+1127A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673679 | |||||||
chr11:8673829 | T | C | 4 | a0004c0004t0001g0327 a0004c0004t0001g0328 a0004c0004t0001g0329 others(1): Show |
4 | HG01071.hp2 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112+977A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673829 | |||||||
chr11:8673925 | G | T | 6 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(3): Show |
8 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+881C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8673925 | |||||||
chr11:8674140 | G | A | 2 | a0001c0023t0001g0310 a0004c0004t0001g0340 |
2 | HG02293.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-112+666C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8674140 | |||||||
chr11:8674325 | T | C | 1 | a0016c0017t0001g0009 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-112+481A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8674325 | |||||||
chr11:8674443 | G | A | 7 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-112+363C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8674443 | |||||||
chr11:8674515 | C | A | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-112+291G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 4/24 | chr11 | 8674515 | |||||||
chr11:8674980 | T | A | 1 | a0002c0002t0002g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-189-97A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8674980 | |||||||
chr11:8675185 | C | G | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-302G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675185 | |||||||
chr11:8675285 | T | C | 2 | a0002c0002t0012g0279 a0002c0002t0012g0280 |
2 | NA18954.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-189-402A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675285 | |||||||
chr11:8675325 | A | T | 66 | a0001c0023t0001g0310 a0004c0004t0001g0027 a0004c0004t0001g0106 others(63): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-189-442T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675325 | |||||||
chr11:8675458 | T | C | 1 | a0001c0001t0021g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-189-575A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675458 | |||||||
chr11:8675469 | ACCTCCCA others(8): Show |
A | 1 | a0001c0001t0001g0282 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-189-601_-189-587d others(17): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675469 | |||||||
chr11:8675493 | C | T | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-610G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675493 | |||||||
chr11:8675507 | C | T | 88 | a0002c0002t0002g0001 a0002c0002t0002g0015 a0002c0002t0002g0017 others(85): Show |
98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-189-624G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675507 | |||||||
chr11:8675642 | A | C | 1 | a0003c0003t0005g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-189-759T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675642 | |||||||
chr11:8675680 | C | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
134 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.-189-797G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675680 | |||||||
chr11:8675731 | AATT | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0116 others(17): Show |
23 | HG01167.hp2 HG01168.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.-189-851_-189-849d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675731 | |||||||
chr11:8675735 | A | C | 1 | a0002c0002t0008g0152 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-189-852T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675735 | |||||||
chr11:8675825 | G | A | 7 | a0007c0008t0006g0007 a0007c0008t0006g0194 a0007c0008t0006g0312 others(4): Show |
9 | HG00099.hp2 HG00323.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-189-942C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675825 | |||||||
chr11:8675927 | C | T | 1 | a0008c0007t0023g0166 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-189-1044G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8675927 | |||||||
chr11:8676234 | CT | C | 29 | a0001c0001t0001g0165 a0001c0001t0001g0195 a0001c0001t0001g0218 others(26): Show |
30 | HG00323.hp1 HG00738.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.-189-1352delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676234 | |||||||
chr11:8676291 | C | T | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-1408G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676291 | |||||||
chr11:8676428 | C | T | 1 | a0002c0002t0002g0242 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-189-1545G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676428 | |||||||
chr11:8676520 | G | A | 4 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189-1637C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676520 | |||||||
chr11:8676673 | T | C | 2 | a0002c0002t0002g0033 a0002c0002t0002g0034 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-189-1790A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676673 | |||||||
chr11:8676679 | A | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0196 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-189-1796T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676679 | |||||||
chr11:8676709 | C | T | 2 | a0003c0003t0003g0229 a0003c0003t0003g0235 |
2 | HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-189-1826G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676709 | |||||||
chr11:8676711 | C | A | 5 | a0004c0013t0016g0130 a0004c0013t0018g0120 a0004c0013t0018g0121 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-189-1828G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676711 | |||||||
chr11:8676781 | T | C | 96 | a0001c0001t0001g0122 a0002c0002t0002g0001 a0002c0002t0002g0015 others(93): Show |
106 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-189-1898A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676781 | |||||||
chr11:8676904 | A | G | 4 | a0014c0015t0010g0076 a0014c0015t0010g0077 a0014c0015t0010g0078 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-189-2021T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676904 | |||||||
chr11:8676991 | C | T | 1 | a0006c0006t0002g0234 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-189-2108G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8676991 | |||||||
chr11:8677194 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-189-2311T>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677194 | |||||||
chr11:8677353 | A | G | 354 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(351): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.-190+2267T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677353 | |||||||
chr11:8677442 | C | A | 1 | a0002c0002t0008g0162 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-190+2178G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677442 | |||||||
chr11:8677469 | T | C | 1 | a0002c0002t0002g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-190+2151A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677469 | |||||||
chr11:8677478 | G | T | 7 | a0001c0001t0001g0016 a0003c0003t0003g0074 a0003c0003t0003g0075 others(4): Show |
8 | HG00621.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-190+2142C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677478 | |||||||
chr11:8677572 | A | G | 1 | a0001c0001t0032g0341 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-190+2048T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677572 | |||||||
chr11:8677624 | CA | C | 13 | a0001c0001t0001g0073 a0003c0003t0003g0129 a0003c0003t0004g0205 others(10): Show |
13 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190+1995delT | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677624 | |||||||
chr11:8677678 | T | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(158): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-190+1942A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677678 | |||||||
chr11:8677747 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0163 a0001c0001t0001g0165 others(2): Show |
7 | HG00738.hp2 HG00741.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190+1873A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677747 | |||||||
chr11:8677859 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02922.hp2 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-190+1761G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8677859 | |||||||
chr11:8678053 | A | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0003c0003t0003g0226 |
3 | HG02040.hp1 HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-190+1567T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678053 | |||||||
chr11:8678115 | A | G | 76 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0287 others(73): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.-190+1505T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678115 | |||||||
chr11:8678163 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0290 |
3 | NA18939.hp1 NA19057.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-190+1457T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678163 | |||||||
chr11:8678258 | T | TC | 4 | a0004c0013t0042g0053 a0012c0011t0020g0051 a0012c0011t0020g0052 others(1): Show |
4 | HG02896.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1361_-190+136 others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678258 | |||||||
chr11:8678263 | T | A | 4 | a0004c0013t0042g0053 a0012c0011t0020g0051 a0012c0011t0020g0052 others(1): Show |
4 | HG02896.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190+1357A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678263 | |||||||
chr11:8678611 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0216 others(15): Show |
21 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-190+1009T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678611 | |||||||
chr11:8678620 | C | T | 200 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0022 others(197): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.-190+1000G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678620 | |||||||
chr11:8678737 | T | G | 33 | a0002c0002t0002g0015 a0002c0002t0002g0066 a0002c0002t0002g0190 others(30): Show |
36 | HG00609.hp1 HG00642.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.-190+883A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678737 | |||||||
chr11:8678779 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0013g0343 |
2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-190+841A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678779 | |||||||
chr11:8678780 | G | C | 71 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0227 others(68): Show |
79 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.-190+840C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678780 | |||||||
chr11:8678965 | A | C | 2 | a0001c0001t0001g0227 a0002c0002t0002g0281 |
2 | NA18957.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-190+655T>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8678965 | |||||||
chr11:8679113 | C | A | 6 | a0006c0006t0002g0204 a0011c0012t0007g0209 a0011c0012t0007g0210 others(3): Show |
6 | HG00639.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-190+507G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679113 | |||||||
chr11:8679176 | C | T | 1 | a0026c0038t0001g0069 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-190+444G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679176 | |||||||
chr11:8679344 | C | T | 1 | a0004c0004t0001g0355 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-190+276G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679344 | |||||||
chr11:8679455 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-190+165C>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679455 | |||||||
chr11:8679501 | G | A | 1 | a0004c0013t0043g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-190+119C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679501 | |||||||
chr11:8679527 | C | A | 4 | a0002c0002t0002g0278 a0002c0002t0012g0279 a0002c0002t0012g0280 others(1): Show |
4 | HG02165.hp2 NA18954.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-190+93G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679527 | |||||||
chr11:8679582 | A | G | 5 | a0004c0013t0042g0053 a0004c0013t0043g0055 a0012c0011t0020g0051 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190+38T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 3/24 | chr11 | 8679582 | |||||||
chr11:8680273 | G | A | 1 | a0003c0003t0003g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-547-210C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680273 | |||||||
chr11:8680289 | C | T | 86 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0287 others(83): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.-547-226G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680289 | |||||||
chr11:8680330 | G | A | 1 | a0004c0004t0029g0344 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-547-267C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680330 | |||||||
chr11:8680341 | G | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(6): Show |
10 | HG01243.hp1 HG01496.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-547-278C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680341 | |||||||
chr11:8680457 | A | AG | 201 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0022 others(198): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.-547-395dupC | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680457 | |||||||
chr11:8680457 | A | G | 1 | a0022c0036t0016g0356 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-547-394T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680457 | |||||||
chr11:8680469 | C | T | 7 | a0006c0006t0002g0204 a0011c0012t0007g0209 a0011c0012t0007g0210 others(4): Show |
7 | HG00639.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-547-406G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680469 | |||||||
chr11:8680489 | T | C | 8 | a0002c0002t0002g0349 a0003c0003t0003g0008 a0003c0003t0003g0289 others(5): Show |
10 | HG00735.hp1 HG01081.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-547-426A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680489 | |||||||
chr11:8680505 | C | G | 1 | a0001c0001t0001g0016 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-547-442G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680505 | |||||||
chr11:8680509 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0003c0003t0003g0226 |
3 | HG02040.hp1 HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.-547-446T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680509 | |||||||
chr11:8680526 | T | C | 3 | a0002c0002t0002g0050 a0003c0003t0003g0049 a0006c0006t0002g0048 |
3 | HG02451.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-547-463A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680526 | |||||||
chr11:8680595 | C | T | 106 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0030 others(103): Show |
119 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.-547-532G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680595 | |||||||
chr11:8680666 | G | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0007c0008t0006g0194 |
3 | HG01168.hp1 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-547-603C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680666 | |||||||
chr11:8680682 | C | G | 10 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01243.hp1 HG01496.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.-547-619G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680682 | |||||||
chr11:8680708 | G | A | 1 | a0003c0003t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-547-645C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680708 | |||||||
chr11:8680754 | G | A | 1 | a0002c0002t0002g0202 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-547-691C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680754 | |||||||
chr11:8680922 | A | G | 202 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0022 others(199): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.-547-859T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680922 | |||||||
chr11:8680926 | C | G | 1 | a0001c0001t0013g0223 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-547-863G>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8680926 | |||||||
chr11:8681028 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0007c0008t0006g0194 |
3 | HG01168.hp1 HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-547-965G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681028 | |||||||
chr11:8681043 | C | T | 1 | a0009c0009t0001g0028 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-547-980G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681043 | |||||||
chr11:8681122 | G | C | 5 | a0011c0012t0007g0209 a0011c0012t0007g0210 a0011c0012t0007g0211 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-547-1059C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681122 | |||||||
chr11:8681134 | A | AT | 76 | a0001c0001t0001g0059 a0001c0001t0001g0224 a0001c0001t0001g0225 others(73): Show |
84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-547-1072dupA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681134 | |||||||
chr11:8681134 | AT | A | 11 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0196 others(8): Show |
11 | HG00323.hp1 HG01168.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.-547-1072delA | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681134 | |||||||
chr11:8681134 | ATT | A | 33 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(30): Show |
38 | HG00621.hp2 HG01243.hp1 HG01516.hp1 others(35): Show |
intron_variant | MODIFIER | c.-547-1073_-547-107 others(6): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681134 | |||||||
chr11:8681179 | G | A | 11 | a0003c0003t0004g0205 a0003c0003t0004g0206 a0003c0003t0004g0207 others(8): Show |
11 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.-547-1116C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681179 | |||||||
chr11:8681184 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-547-1121T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681184 | |||||||
chr11:8681186 | T | C | 77 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0227 others(74): Show |
85 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-547-1123A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681186 | |||||||
chr11:8681262 | T | G | 11 | a0003c0003t0004g0205 a0003c0003t0004g0206 a0003c0003t0004g0207 others(8): Show |
11 | HG00639.hp1 HG01109.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.-547-1199A>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681262 | |||||||
chr11:8681278 | C | T | 1 | a0010c0010t0011g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-547-1215G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681278 | |||||||
chr11:8681376 | G | A | 1 | a0004c0004t0001g0352 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-548+1225C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681376 | |||||||
chr11:8681379 | C | A | 1 | a0001c0001t0013g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-548+1222G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681379 | |||||||
chr11:8681446 | T | C | 2 | a0002c0002t0002g0214 a0003c0003t0003g0213 |
2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-548+1155A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681446 | |||||||
chr11:8681594 | G | A | 1 | a0013c0014t0001g0353 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-548+1007C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681594 | |||||||
chr11:8681647 | ATGC | A | 75 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0287 others(72): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.-548+951_-548+953d others(5): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681647 | |||||||
chr11:8681661 | G | A | 1 | a0007c0008t0006g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-548+940C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681661 | |||||||
chr11:8681683 | G | C | 1 | a0004c0004t0001g0355 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-548+918C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681683 | |||||||
chr11:8681884 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0216 others(4): Show |
10 | HG01884.hp1 HG02622.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-548+717A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681884 | |||||||
chr11:8681949 | C | CGGGGGGG others(24): Show |
1 | a0003c0003t0003g0056 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-548+651_-548+652i others(33): Show |
TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681949 | |||||||
chr11:8681951 | A | G | 1 | a0003c0003t0003g0056 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-548+650T>C | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8681951 | |||||||
chr11:8682055 | C | A | 2 | a0011c0012t0007g0221 a0011c0012t0007g0222 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-548+546G>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682055 | |||||||
chr11:8682394 | T | C | 107 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(104): Show |
118 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.-548+207A>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682394 | |||||||
chr11:8682426 | G | GC | 73 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0288 others(70): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.-548+174dupG | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682426 | |||||||
chr11:8682440 | G | C | 1 | a0022c0036t0016g0356 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-548+161C>G | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682440 | |||||||
chr11:8682459 | T | A | 1 | a0002c0019t0027g0357 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-548+142A>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682459 | |||||||
chr11:8682472 | G | A | 1 | a0002c0002t0002g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-548+129C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682472 | |||||||
chr11:8682491 | C | T | 5 | a0004c0013t0042g0053 a0004c0013t0043g0055 a0012c0011t0020g0051 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-548+110G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682491 | |||||||
chr11:8682492 | G | A | 29 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(26): Show |
32 | HG00621.hp2 HG01243.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-548+109C>T | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682492 | |||||||
chr11:8682544 | C | T | 29 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0031 others(26): Show |
32 | HG00621.hp2 HG01243.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-548+57G>A | TRIM66 | ENSG00000166436.18 | transcript | ENST00000646038.2 | protein_coding | 1/24 | chr11 | 8682544 |