Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 140691 |
| ensemblid | ENSG00000185880.13 |
| hgncid | 17857 |
| symbol | TRIM69 |
| name | tripartite motif containing 69 |
| refseq_nuc | NM_182985.5 |
| refseq_prot | NP_892030.3 |
| ensembl_nuc | ENST00000329464.9 |
| ensembl_prot | ENSP00000332284.3 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 44736528 |
| end | 44767827 |
| strand | + |
| ver | v1.2 |
| region | chr15:44736528-44767827 |
| region5000 | chr15:44731528-44772827 |
| regionname0 | TRIM69_chr15_44736528_44767827 |
| regionname5000 | TRIM69_chr15_44731528_44772827 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 500 | 189 | 39 | 40 | 77 | 12 | 21 | 53 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0002 | 0/1 | 500 | 54 | 10 | 6 | 30 | 1 | 6 | 21 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0003 | 0/0 | 500 | 45 | 2 | 8 | 25 | 1 | 9 | 19 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0004 | 0/0 | 500 | 34 | 14 | 4 | 12 | 1 | 3 | 9 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0005 | 0/0 | 500 | 9 | 4 | 1 | 0 | 3 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0006 | 0/0 | 500 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0007 | 0/0 | 500 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0008 | 0/0 | 500 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0009 | 0/0 | 500 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0010 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| a0011 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | MEVST others(495): Show |
chr15 | 44731528 | 44772827 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1500 | 185 | 39 | 40 | 73 | 12 | 21 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0001c0008 | 0/0 | 1500 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0001c0014 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0002c0002 | 0/1 | 1500 | 54 | 10 | 6 | 30 | 1 | 6 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0003c0003 | 0/0 | 1500 | 45 | 2 | 8 | 25 | 1 | 9 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0004c0004 | 0/0 | 1500 | 31 | 11 | 4 | 12 | 1 | 3 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0004c0009 | 0/0 | 1500 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0005c0005 | 0/0 | 1500 | 9 | 4 | 1 | 0 | 3 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0006c0006 | 0/0 | 1500 | 6 | 4 | 2 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0007c0007 | 0/0 | 1500 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0008c0011 | 0/0 | 1500 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0009c0010 | 0/0 | 1500 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0010c0012 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 | ||
| a0011c0013 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | ATGGA others(1495): Show |
chr15 | 44731528 | 44772827 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1735 | 183 | 38 | 40 | 72 | 12 | 21 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0001c0001t0002 | 0/0 | 1735 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0001c0001t0003 | 0/0 | 1735 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0001c0008t0001 | 0/0 | 1735 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0001c0014t0001 | 0/0 | 1735 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0002c0002t0001 | 0/1 | 1735 | 46 | 10 | 6 | 22 | 1 | 6 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0002c0002t0002 | 0/0 | 1735 | 8 | 0 | 0 | 8 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0003c0003t0001 | 0/0 | 1735 | 12 | 0 | 7 | 5 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0003c0003t0002 | 0/0 | 1735 | 33 | 2 | 1 | 20 | 1 | 9 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0004c0004t0001 | 0/0 | 1735 | 30 | 10 | 4 | 12 | 1 | 3 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0004c0004t0002 | 0/0 | 1735 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0004c0009t0001 | 0/0 | 1735 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0005c0005t0002 | 0/0 | 1735 | 9 | 4 | 1 | 0 | 3 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0006c0006t0001 | 0/0 | 1735 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0006c0006t0002 | 0/0 | 1735 | 5 | 3 | 2 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0007c0007t0002 | 0/0 | 1735 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0008c0011t0001 | 0/0 | 1735 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0009c0010t0001 | 0/0 | 1735 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0010c0012t0001 | 0/0 | 1735 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| a0011c0013t0001 | 0/0 | 1735 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | AGACC others(1730): Show |
chr15 | 44731528 | 44772827 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 2 | 7 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 3 | 6 | 2 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 4 | 4 | 1 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0008t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0008t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0001c0014t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0004t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0009t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0009t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0004c0009t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0005c0005t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0005c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0005c0005t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0005c0005t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0005c0005t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0005c0005t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0005c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0005c0005t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0006c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0006c0006t0002g0007 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0006c0006t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0007c0007t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0007c0007t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0007c0007t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0007c0007t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0007c0007t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0008c0011t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0008c0011t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0009c0010t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0009c0010t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0010c0012t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| a0011c0013t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00099 | hp2 | a0004 | c0004 | t0001 | g0248 | EUR | GBR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00140 | hp1 | a0005 | c0005 | t0002 | g0084 | EUR | GBR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | FIN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0051 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0059 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00558 | hp1 | a0004 | c0004 | t0001 | g0245 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00642 | hp2 | a0006 | c0006 | t0002 | g0007 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00738 | hp1 | a0004 | c0004 | t0001 | g0237 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01070 | hp2 | a0005 | c0005 | t0002 | g0081 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01099 | hp1 | a0006 | c0006 | t0002 | g0007 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01255 | hp1 | a0008 | c0011 | t0001 | g0082 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01256 | hp2 | a0004 | c0004 | t0001 | g0239 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01257 | hp1 | a0004 | c0004 | t0001 | g0032 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0061 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01258 | hp1 | a0004 | c0004 | t0001 | g0032 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01515 | hp2 | a0005 | c0005 | t0002 | g0023 | EUR | IBS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01517 | hp1 | a0005 | c0005 | t0002 | g0023 | EUR | IBS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0056 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0053 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0052 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0057 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02004 | hp2 | a0003 | c0003 | t0001 | g0012 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02027 | hp1 | a0001 | c0008 | t0001 | g0227 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02040 | hp1 | a0003 | c0003 | t0002 | g0048 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02055 | hp1 | a0004 | c0009 | t0001 | g0077 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02056 | hp2 | a0004 | c0004 | t0001 | g0033 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02074 | hp1 | a0003 | c0003 | t0002 | g0058 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02145 | hp1 | a0006 | c0006 | t0001 | g0071 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02148 | hp1 | a0003 | c0003 | t0002 | g0047 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02155 | hp1 | a0004 | c0004 | t0001 | g0033 | EAS | CDX | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0055 | EAS | CDX | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02257 | hp1 | a0007 | c0007 | t0002 | g0022 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0012 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02451 | hp2 | a0007 | c0007 | t0002 | g0066 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0036 | EAS | KHV | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02572 | hp1 | a0004 | c0004 | t0001 | g0094 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02572 | hp2 | a0005 | c0005 | t0002 | g0234 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02602 | hp2 | a0004 | c0004 | t0001 | g0243 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02615 | hp1 | a0004 | c0004 | t0001 | g0035 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02622 | hp1 | a0006 | c0006 | t0002 | g0070 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02630 | hp2 | a0004 | c0004 | t0001 | g0246 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0198 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0085 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02717 | hp1 | a0006 | c0006 | t0002 | g0007 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02738 | hp2 | a0004 | c0004 | t0001 | g0086 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02895 | hp1 | a0005 | c0005 | t0002 | g0236 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02896 | hp1 | a0004 | c0004 | t0002 | g0065 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02922 | hp2 | a0007 | c0007 | t0002 | g0068 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02965 | hp2 | a0003 | c0003 | t0002 | g0072 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03017 | hp2 | a0005 | c0005 | t0002 | g0080 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03195 | hp2 | a0004 | c0004 | t0001 | g0241 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03209 | hp1 | a0004 | c0009 | t0001 | g0078 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0122 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03453 | hp2 | a0007 | c0007 | t0002 | g0069 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03486 | hp2 | a0005 | c0005 | t0002 | g0233 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03490 | hp1 | a0003 | c0003 | t0002 | g0020 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03492 | hp1 | a0003 | c0003 | t0002 | g0020 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03492 | hp2 | a0009 | c0010 | t0001 | g0010 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03516 | hp1 | a0007 | c0007 | t0002 | g0022 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03516 | hp2 | a0004 | c0004 | t0001 | g0095 | AFR | ESN | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03654 | hp2 | a0009 | c0010 | t0001 | g0199 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0196 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03688 | hp2 | a0003 | c0003 | t0002 | g0046 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03704 | hp1 | a0003 | c0003 | t0002 | g0011 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0215 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03942 | hp2 | a0003 | c0003 | t0002 | g0045 | SAS | BEB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04184 | hp2 | a0004 | c0004 | t0001 | g0088 | SAS | BEB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04199 | hp2 | a0003 | c0003 | t0002 | g0064 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04204 | hp2 | a0003 | c0003 | t0002 | g0040 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04228 | hp1 | a0003 | c0003 | t0002 | g0041 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18906 | hp1 | a0004 | c0004 | t0001 | g0250 | AFR | YRI | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18940 | hp1 | a0004 | c0004 | t0001 | g0244 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18943 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18948 | hp2 | a0003 | c0003 | t0002 | g0037 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18951 | hp2 | a0003 | c0003 | t0002 | g0011 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18952 | hp2 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0062 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18963 | hp2 | a0003 | c0003 | t0002 | g0011 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18965 | hp1 | a0001 | c0008 | t0001 | g0001 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18965 | hp2 | a0003 | c0003 | t0002 | g0060 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18966 | hp2 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18967 | hp1 | a0003 | c0003 | t0002 | g0044 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18982 | hp2 | a0010 | c0012 | t0001 | g0116 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18986 | hp1 | a0011 | c0013 | t0001 | g0144 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18988 | hp1 | a0004 | c0004 | t0001 | g0242 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18988 | hp2 | a0001 | c0008 | t0001 | g0001 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19000 | hp1 | a0003 | c0003 | t0002 | g0042 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19004 | hp2 | a0003 | c0003 | t0002 | g0063 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19005 | hp1 | a0004 | c0004 | t0001 | g0089 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19007 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19009 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19030 | hp1 | a0004 | c0004 | t0001 | g0096 | AFR | LWK | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19043 | hp1 | a0008 | c0011 | t0001 | g0083 | AFR | LWK | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | LWK | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19055 | hp2 | a0004 | c0004 | t0001 | g0087 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19058 | hp1 | a0004 | c0004 | t0001 | g0240 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19063 | hp2 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19064 | hp1 | a0004 | c0004 | t0001 | g0251 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19075 | hp1 | a0001 | c0014 | t0001 | g0107 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19075 | hp2 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19085 | hp1 | a0003 | c0003 | t0002 | g0050 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19089 | hp2 | a0003 | c0003 | t0002 | g0043 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19090 | hp2 | a0004 | c0004 | t0001 | g0238 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20129 | hp1 | a0006 | c0006 | t0002 | g0007 | AFR | ASW | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | ASW | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20752 | hp1 | a0003 | c0003 | t0002 | g0039 | EUR | TSI | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02109 | hp1 | a0004 | c0004 | t0001 | g0249 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02109 | hp2 | a0003 | c0003 | t0002 | g0038 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02559 | hp1 | a0007 | c0007 | t0002 | g0067 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03471 | hp1 | a0004 | c0004 | t0001 | g0035 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | MSL | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG06807 | hp1 | a0004 | c0009 | t0001 | g0076 | AFR | USA | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18955 | hp1 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20300 | hp1 | a0005 | c0005 | t0002 | g0235 | AFR | USA | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA20300 | hp2 | a0004 | c0004 | t0001 | g0247 | AFR | USA | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | LWK | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0197 | REF | REF | TRIM69_chr15_44731528_44772827 | TRIM69 | chr15 | 44731528 | 44772827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44754927 | G | A | 1 | a0006 | 6 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(3): Show |
missense_variant | MODERATE | c.34G>A | p.Asp12Asn | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/7 | 211/1735 | 34/1503 | 12/500 | chr15 | 44754927 | |||
| chr15:44754936 | G | A | 3 | a0001 a0010 a0011 |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
missense_variant | MODERATE | c.43G>A | p.Asp15Asn | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/7 | 220/1735 | 43/1503 | 15/500 | chr15 | 44754936 | |||
| chr15:44755204 | A | G | 2 | a0005 a0008 |
11 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(8): Show |
missense_variant | MODERATE | c.311A>G | p.Lys104Arg | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/7 | 488/1735 | 311/1503 | 104/500 | chr15 | 44755204 | |||
| chr15:44755375 | C | T | 5 | a0001 a0002 a0009 others(2): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
missense_variant&splice_region_variant | MODERATE | c.482C>T | p.Thr161Met | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/7 | 659/1735 | 482/1503 | 161/500 | chr15 | 44755375 | |||
| chr15:44756389 | G | T | 1 | a0011 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.505G>T | p.Gly169Cys | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/7 | 682/1735 | 505/1503 | 169/500 | chr15 | 44756389 | |||
| chr15:44756453 | C | T | 3 | a0004 a0005 a0008 |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
missense_variant | MODERATE | c.569C>T | p.Ala190Val | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/7 | 746/1735 | 569/1503 | 190/500 | chr15 | 44756453 | |||
| chr15:44758758 | T | A | 1 | a0008 | 2 | HG01255.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.717T>A | p.Asn239Lys | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/7 | 894/1735 | 717/1503 | 239/500 | chr15 | 44758758 | |||
| chr15:44758817 | C | G | 1 | a0009 | 2 | HG03492.hp2 HG03654.hp2 |
missense_variant | MODERATE | c.776C>G | p.Ala259Gly | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/7 | 953/1735 | 776/1503 | 259/500 | chr15 | 44758817 | |||
| chr15:44758828 | C | A | 1 | a0010 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.787C>A | p.Gln263Lys | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/7 | 964/1735 | 787/1503 | 263/500 | chr15 | 44758828 | |||
| chr15:44767464 | A | T | 1 | a0007 | 6 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
missense_variant | MODERATE | c.1195A>T | p.Ile399Phe | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 7/7 | 1372/1735 | 1195/1503 | 399/500 | chr15 | 44767464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44755143 | C | T | 1 | a0001c0014 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.250C>T | p.Leu84Leu | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/7 | 427/1735 | 250/1503 | 84/500 | chr15 | 44755143 | |||
| chr15:44755352 | C | T | 1 | a0001c0008 | 3 | HG02027.hp1 NA18965.hp1 NA18988.hp2 |
synonymous_variant | LOW | c.459C>T | p.Ile153Ile | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/7 | 636/1735 | 459/1503 | 153/500 | chr15 | 44755352 | |||
| chr15:44767616 | T | C | 1 | a0004c0009 | 3 | HG02055.hp1 HG03209.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.1347T>C | p.Tyr449Tyr | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 7/7 | 1524/1735 | 1347/1503 | 449/500 | chr15 | 44767616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44736619 | T | C | 1 | a0001c0001t0003 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/7 | 86 | chr15 | 44736619 | ||||||
| chr15:44767816 | A | T | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0008t0001 others(10): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*44A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 7/7 | 44 | chr15 | 44767816 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44736721 | C | CT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.6+22dupT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44736721 | ||||||
| chr15:44736770 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.6+60G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44736770 | |||||||
| chr15:44736806 | G | C | 1 | a0003c0003t0002g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.6+96G>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44736806 | |||||||
| chr15:44737449 | A | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
7 | HG01074.hp1 HG01433.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+739A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44737449 | |||||||
| chr15:44737581 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.6+871C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44737581 | |||||||
| chr15:44737594 | G | A | 3 | a0004c0009t0001g0076 a0004c0009t0001g0077 a0004c0009t0001g0078 |
3 | HG02055.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.6+884G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44737594 | |||||||
| chr15:44737700 | C | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA18995.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.6+990C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44737700 | |||||||
| chr15:44737903 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.6+1193A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44737903 | |||||||
| chr15:44738041 | ACTTT | A | 26 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(23): Show |
30 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.6+1344_6+1347delCT others(2): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44738041 | ||||||
| chr15:44738050 | C | CT | 9 | a0002c0002t0001g0073 a0002c0002t0001g0074 a0003c0003t0002g0072 others(6): Show |
13 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.6+1343dupT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44738050 | ||||||
| chr15:44738050 | CTTTCTTT others(2): Show |
C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.6+1344_6+1352delCT others(7): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44738050 | ||||||
| chr15:44738050 | CTTTCTTT others(3): Show |
C | 1 | a0001c0001t0001g0097 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6+1344_6+1353delCT others(8): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44738050 | ||||||
| chr15:44738050 | CTTTCTTT others(6): Show |
C | 1 | a0004c0004t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6+1344_6+1356delCT others(11): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44738050 | ||||||
| chr15:44738051 | TTTC | T | 10 | a0003c0003t0002g0085 a0004c0004t0001g0086 a0004c0004t0001g0088 others(7): Show |
11 | HG00140.hp1 HG01070.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.6+1344_6+1346delCT others(1): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44738051 | ||||||
| chr15:44738053 | T | TTC | 1 | a0002c0002t0001g0014 | 3 | HG01891.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.6+1343_6+1344insTC | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738053 | |||||||
| chr15:44738054 | C | T | 11 | a0002c0002t0001g0014 a0003c0003t0002g0072 a0004c0004t0002g0065 others(8): Show |
17 | HG00642.hp2 HG01099.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.6+1344C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738054 | |||||||
| chr15:44738226 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.6+1516T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738226 | |||||||
| chr15:44738233 | A | AT | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.6+1525dupT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44738233 | ||||||
| chr15:44738233 | A | ATT | 12 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(9): Show |
13 | HG02004.hp1 HG02027.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.6+1524_6+1525dupTT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44738233 | ||||||
| chr15:44738236 | A | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.6+1526A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738236 | |||||||
| chr15:44738239 | A | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.6+1529A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738239 | |||||||
| chr15:44738248 | T | C | 1 | a0003c0003t0002g0037 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.6+1538T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738248 | |||||||
| chr15:44738278 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.6+1568C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738278 | |||||||
| chr15:44738365 | T | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.6+1655T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738365 | |||||||
| chr15:44738473 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.6+1763C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738473 | |||||||
| chr15:44738844 | A | G | 1 | a0002c0002t0001g0223 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.6+2134A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44738844 | |||||||
| chr15:44739112 | T | C | 11 | a0003c0003t0002g0085 a0005c0005t0002g0023 a0005c0005t0002g0080 others(8): Show |
12 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+2402T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739112 | |||||||
| chr15:44739127 | C | A | 1 | a0002c0002t0001g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6+2417C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739127 | |||||||
| chr15:44739149 | A | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.6+2439A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739149 | |||||||
| chr15:44739204 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+2494C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739204 | |||||||
| chr15:44739205 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.6+2495G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739205 | |||||||
| chr15:44739213 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+2503T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739213 | |||||||
| chr15:44739237 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+2527C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739237 | |||||||
| chr15:44739269 | C | G | 1 | a0001c0001t0001g0222 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.6+2559C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739269 | |||||||
| chr15:44739285 | C | T | 5 | a0003c0003t0002g0085 a0005c0005t0002g0233 a0005c0005t0002g0234 others(2): Show |
5 | HG02572.hp2 HG02698.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+2575C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739285 | |||||||
| chr15:44739299 | G | A | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+2589G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739299 | |||||||
| chr15:44739361 | G | A | 1 | a0003c0003t0002g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6+2651G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739361 | |||||||
| chr15:44739396 | G | A | 4 | a0005c0005t0002g0233 a0005c0005t0002g0234 a0005c0005t0002g0235 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+2686G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739396 | |||||||
| chr15:44739421 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.6+2711C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739421 | |||||||
| chr15:44739533 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+2823G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739533 | |||||||
| chr15:44739545 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6+2835C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739545 | |||||||
| chr15:44739558 | C | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.6+2848C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739558 | |||||||
| chr15:44739559 | G | A | 6 | a0004c0004t0002g0065 a0007c0007t0002g0022 a0007c0007t0002g0066 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+2849G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739559 | |||||||
| chr15:44739592 | C | T | 3 | a0004c0004t0001g0094 a0004c0004t0001g0095 a0004c0004t0001g0250 |
3 | HG02572.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6+2882C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739592 | |||||||
| chr15:44739682 | C | T | 1 | a0003c0003t0002g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6+2972C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739682 | |||||||
| chr15:44739724 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.6+3014G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739724 | |||||||
| chr15:44739892 | C | T | 2 | a0001c0001t0001g0219 a0002c0002t0001g0220 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6+3182C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739892 | |||||||
| chr15:44739912 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.6+3202T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739912 | |||||||
| chr15:44739943 | AC | A | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+3237delC | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44739943 | ||||||
| chr15:44739982 | A | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.6+3272A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44739982 | |||||||
| chr15:44740078 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3368T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740078 | |||||||
| chr15:44740097 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.6+3387C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740097 | |||||||
| chr15:44740209 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3499T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740209 | |||||||
| chr15:44740273 | G | A | 1 | a0005c0005t0002g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6+3563G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740273 | |||||||
| chr15:44740321 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3611C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740321 | |||||||
| chr15:44740344 | G | A | 5 | a0001c0001t0001g0099 a0002c0002t0001g0014 a0002c0002t0001g0073 others(2): Show |
7 | HG01891.hp1 HG02970.hp1 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.6+3634G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740344 | |||||||
| chr15:44740423 | C | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.6+3713C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740423 | |||||||
| chr15:44740431 | C | G | 1 | a0005c0005t0002g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6+3721C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740431 | |||||||
| chr15:44740486 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+3776G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740486 | |||||||
| chr15:44740521 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.6+3811C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740521 | |||||||
| chr15:44740632 | C | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.6+3922C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740632 | |||||||
| chr15:44740740 | G | C | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
28 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+4030G>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740740 | |||||||
| chr15:44740761 | G | A | 1 | a0005c0005t0002g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6+4051G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740761 | |||||||
| chr15:44740763 | T | G | 1 | a0004c0004t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.6+4053T>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740763 | |||||||
| chr15:44740880 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.6+4170C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740880 | |||||||
| chr15:44740961 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0232 a0001c0001t0001g0255 others(3): Show |
8 | HG01074.hp1 HG01433.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+4251C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44740961 | |||||||
| chr15:44741135 | T | C | 1 | a0004c0004t0001g0237 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.6+4425T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741135 | |||||||
| chr15:44741288 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.6+4578A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741288 | |||||||
| chr15:44741301 | G | A | 1 | a0002c0002t0001g0100 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.6+4591G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741301 | |||||||
| chr15:44741308 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.6+4598T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741308 | |||||||
| chr15:44741373 | C | T | 4 | a0004c0004t0001g0096 a0004c0009t0001g0076 a0004c0009t0001g0077 others(1): Show |
4 | HG02055.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+4663C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741373 | |||||||
| chr15:44741374 | G | A | 2 | a0004c0004t0001g0096 a0004c0004t0002g0065 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6+4664G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741374 | |||||||
| chr15:44741619 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+4909G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741619 | |||||||
| chr15:44741622 | T | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+4912T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741622 | |||||||
| chr15:44741631 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+4921G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741631 | |||||||
| chr15:44741643 | T | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+4933T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741643 | |||||||
| chr15:44741805 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.6+5095C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741805 | |||||||
| chr15:44741872 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.6+5162G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741872 | |||||||
| chr15:44741880 | C | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+5170C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741880 | |||||||
| chr15:44741996 | C | T | 3 | a0005c0005t0002g0233 a0005c0005t0002g0234 a0005c0005t0002g0236 |
3 | HG02572.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6+5286C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741996 | |||||||
| chr15:44741997 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+5287G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44741997 | |||||||
| chr15:44742085 | T | C | 2 | a0001c0001t0001g0232 a0002c0002t0001g0102 |
2 | HG00639.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.6+5375T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742085 | |||||||
| chr15:44742141 | T | G | 4 | a0005c0005t0002g0233 a0005c0005t0002g0234 a0005c0005t0002g0235 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+5431T>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742141 | |||||||
| chr15:44742166 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+5456C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742166 | |||||||
| chr15:44742240 | A | C | 34 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0010 others(31): Show |
49 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.6+5530A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742240 | |||||||
| chr15:44742268 | C | T | 1 | a0005c0005t0002g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6+5558C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742268 | |||||||
| chr15:44742327 | AAG | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.6+5620_6+5621delAG | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44742327 | ||||||
| chr15:44742361 | A | G | 22 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(19): Show |
25 | HG01243.hp2 HG01981.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.6+5651A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742361 | |||||||
| chr15:44742407 | C | G | 5 | a0003c0003t0002g0085 a0005c0005t0002g0233 a0005c0005t0002g0234 others(2): Show |
5 | HG02572.hp2 HG02698.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.6+5697C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742407 | |||||||
| chr15:44742426 | C | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+5716C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742426 | |||||||
| chr15:44742438 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.6+5728A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742438 | |||||||
| chr15:44742504 | A | G | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
28 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+5794A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742504 | |||||||
| chr15:44742543 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.6+5833T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742543 | |||||||
| chr15:44742544 | G | A | 40 | a0003c0003t0002g0085 a0004c0004t0001g0032 a0004c0004t0001g0033 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.6+5834G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742544 | |||||||
| chr15:44742583 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.6+5873T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742583 | |||||||
| chr15:44742615 | CAA | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.6+5907_6+5908delAA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44742615 | ||||||
| chr15:44742628 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.6+5918C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742628 | |||||||
| chr15:44742641 | T | C | 1 | a0004c0004t0001g0249 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6+5931T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742641 | |||||||
| chr15:44742642 | A | G | 4 | a0003c0003t0002g0072 a0006c0006t0001g0071 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+5932A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742642 | |||||||
| chr15:44742673 | A | AACAG | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.6+5966_6+5967insGA others(2): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44742673 | ||||||
| chr15:44742692 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6+5982C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742692 | |||||||
| chr15:44742767 | T | G | 4 | a0003c0003t0002g0020 a0003c0003t0002g0039 a0003c0003t0002g0040 others(1): Show |
5 | HG03490.hp1 HG03492.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+6057T>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742767 | |||||||
| chr15:44742771 | C | T | 1 | a0004c0004t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6+6061C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742771 | |||||||
| chr15:44742886 | T | C | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+6176T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44742886 | |||||||
| chr15:44743120 | G | T | 1 | a0007c0007t0002g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6+6410G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44743120 | |||||||
| chr15:44743159 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6+6449C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44743159 | |||||||
| chr15:44743290 | C | T | 4 | a0003c0003t0002g0072 a0006c0006t0001g0071 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+6580C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44743290 | |||||||
| chr15:44743437 | G | T | 1 | a0002c0002t0001g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6+6727G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44743437 | |||||||
| chr15:44743465 | C | G | 4 | a0003c0003t0002g0072 a0006c0006t0001g0071 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+6755C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44743465 | |||||||
| chr15:44743691 | A | G | 5 | a0002c0002t0002g0210 a0002c0002t0002g0211 a0002c0002t0002g0212 others(2): Show |
5 | NA18948.hp1 NA18949.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+6981A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44743691 | |||||||
| chr15:44743709 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6+6999C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44743709 | |||||||
| chr15:44744036 | A | G | 4 | a0003c0003t0002g0072 a0006c0006t0001g0071 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+7326A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744036 | |||||||
| chr15:44744183 | A | G | 3 | a0002c0002t0001g0006 a0002c0002t0001g0030 a0002c0002t0001g0209 |
8 | HG00438.hp2 HG02083.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+7473A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744183 | |||||||
| chr15:44744199 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.6+7489T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744199 | |||||||
| chr15:44744248 | T | C | 4 | a0005c0005t0002g0233 a0005c0005t0002g0234 a0005c0005t0002g0235 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+7538T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744248 | |||||||
| chr15:44744294 | T | A | 1 | a0001c0001t0001g0103 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.6+7584T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744294 | |||||||
| chr15:44744315 | G | A | 4 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(1): Show |
5 | HG00140.hp1 HG01070.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+7605G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744315 | |||||||
| chr15:44744318 | A | G | 1 | a0004c0004t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6+7608A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744318 | |||||||
| chr15:44744358 | A | C | 1 | a0005c0005t0002g0081 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.6+7648A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744358 | |||||||
| chr15:44744386 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.6+7676A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744386 | |||||||
| chr15:44744670 | T | C | 34 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0010 others(31): Show |
49 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.6+7960T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744670 | |||||||
| chr15:44744675 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.6+7965G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744675 | |||||||
| chr15:44744719 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.6+8009G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744719 | |||||||
| chr15:44744741 | C | T | 3 | a0004c0004t0001g0094 a0004c0004t0001g0095 a0004c0004t0001g0250 |
3 | HG02572.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6+8031C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744741 | |||||||
| chr15:44744853 | T | TA | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+8144dupA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44744853 | ||||||
| chr15:44744914 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6+8204G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744914 | |||||||
| chr15:44744976 | G | GA | 16 | a0003c0003t0002g0085 a0004c0004t0001g0096 a0004c0004t0001g0249 others(13): Show |
17 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.6+8269dupA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44744976 | ||||||
| chr15:44744976 | G | GAA | 24 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(21): Show |
28 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.6+8268_6+8269dupAA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44744976 | ||||||
| chr15:44744996 | T | C | 1 | a0004c0004t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6+8286T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44744996 | |||||||
| chr15:44745069 | TA | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.6+8375delA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44745069 | ||||||
| chr15:44745218 | T | C | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+8508T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44745218 | |||||||
| chr15:44745227 | TTTG | T | 6 | a0004c0004t0002g0065 a0007c0007t0002g0022 a0007c0007t0002g0066 others(3): Show |
7 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.6+8532_6+8534delGT others(1): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44745227 | ||||||
| chr15:44745409 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.6+8699T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44745409 | |||||||
| chr15:44745522 | G | T | 40 | a0003c0003t0002g0085 a0004c0004t0001g0032 a0004c0004t0001g0033 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.6+8812G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44745522 | |||||||
| chr15:44745773 | A | G | 1 | a0005c0005t0002g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.6+9063A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44745773 | |||||||
| chr15:44746008 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.7-8892G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44746008 | |||||||
| chr15:44746047 | G | GTAAGA | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.7-8849_7-8848insAT others(3): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44746047 | ||||||
| chr15:44746069 | C | CAAGAT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.7-8828_7-8827insAT others(3): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44746069 | ||||||
| chr15:44746216 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.7-8684A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44746216 | |||||||
| chr15:44746671 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.7-8229A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44746671 | |||||||
| chr15:44746750 | G | GCA | 7 | a0001c0001t0001g0108 a0003c0003t0002g0085 a0005c0005t0002g0233 others(4): Show |
7 | HG02572.hp2 HG02698.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-8123_7-8122dupCA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44746750 | ||||||
| chr15:44746750 | GCA | G | 39 | a0001c0001t0001g0105 a0001c0001t0001g0109 a0001c0001t0001g0110 others(36): Show |
44 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.7-8123_7-8122delCA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44746750 | ||||||
| chr15:44746750 | GCACA | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(161): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.7-8125_7-8122delCA others(2): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44746750 | ||||||
| chr15:44746750 | GCACACA | G | 4 | a0001c0001t0001g0174 a0002c0002t0001g0014 a0002c0002t0001g0073 others(1): Show |
6 | HG01891.hp1 HG02970.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-8127_7-8122delCA others(4): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44746750 | ||||||
| chr15:44746794 | A | G | 1 | a0004c0004t0001g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.7-8106A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44746794 | |||||||
| chr15:44747069 | T | C | 1 | a0003c0003t0002g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.7-7831T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44747069 | |||||||
| chr15:44747082 | G | A | 4 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(1): Show |
5 | HG00140.hp1 HG01070.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-7818G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44747082 | |||||||
| chr15:44747126 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-7774C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44747126 | |||||||
| chr15:44747265 | G | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.7-7635G>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44747265 | |||||||
| chr15:44747273 | C | CT | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-7626dupT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44747273 | ||||||
| chr15:44747584 | A | C | 1 | a0003c0003t0001g0079 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.7-7316A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44747584 | |||||||
| chr15:44747650 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
247 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.7-7250G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44747650 | |||||||
| chr15:44747929 | A | C | 1 | a0002c0002t0001g0220 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7-6971A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44747929 | |||||||
| chr15:44747938 | C | T | 41 | a0003c0003t0002g0085 a0004c0004t0001g0032 a0004c0004t0001g0033 others(38): Show |
46 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.7-6962C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44747938 | |||||||
| chr15:44748121 | C | T | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-6779C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748121 | |||||||
| chr15:44748173 | T | C | 1 | a0007c0007t0002g0067 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7-6727T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748173 | |||||||
| chr15:44748314 | G | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(28): Show |
48 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.7-6586G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748314 | |||||||
| chr15:44748386 | A | G | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-6514A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748386 | |||||||
| chr15:44748397 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.7-6503C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748397 | |||||||
| chr15:44748427 | A | AGCCACTT others(6): Show |
1 | a0001c0001t0001g0159 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.7-6457_7-6445dupCA others(11): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44748427 | ||||||
| chr15:44748454 | GC | G | 7 | a0003c0003t0002g0020 a0003c0003t0002g0039 a0003c0003t0002g0040 others(4): Show |
8 | HG03490.hp1 HG03492.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-6445delC | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748454 | |||||||
| chr15:44748486 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.7-6414G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748486 | |||||||
| chr15:44748597 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.7-6303G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748597 | |||||||
| chr15:44748825 | C | CA | 9 | a0003c0003t0001g0079 a0003c0003t0002g0020 a0003c0003t0002g0038 others(6): Show |
10 | HG02109.hp2 HG02148.hp1 HG03490.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-6050dupA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44748825 | ||||||
| chr15:44748825 | CA | C | 31 | a0003c0003t0001g0061 a0003c0003t0002g0060 a0003c0003t0002g0062 others(28): Show |
35 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.7-6050delA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44748825 | ||||||
| chr15:44748825 | CAAA | C | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-6052_7-6050delAA others(1): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44748825 | ||||||
| chr15:44748825 | CAAAAAA | C | 7 | a0001c0001t0001g0111 a0001c0001t0001g0178 a0001c0001t0001g0253 others(4): Show |
7 | HG00673.hp1 HG01243.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-6055_7-6050delAA others(4): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44748825 | ||||||
| chr15:44748825 | CAAAAAAA | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.7-6056_7-6050delAA others(5): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44748825 | ||||||
| chr15:44748825 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
8 | HG01099.hp2 HG01255.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-6057_7-6050delAA others(6): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44748825 | ||||||
| chr15:44748903 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0112 a0001c0001t0001g0113 |
5 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-5997T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748903 | |||||||
| chr15:44748906 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7-5994G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748906 | |||||||
| chr15:44748920 | G | A | 1 | a0003c0003t0002g0037 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.7-5980G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44748920 | |||||||
| chr15:44749003 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.7-5897T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749003 | |||||||
| chr15:44749004 | C | T | 2 | a0004c0004t0001g0096 a0004c0004t0002g0065 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.7-5896C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749004 | |||||||
| chr15:44749013 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-5887C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749013 | |||||||
| chr15:44749021 | C | G | 1 | a0002c0002t0002g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.7-5879C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749021 | |||||||
| chr15:44749031 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.7-5869A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749031 | |||||||
| chr15:44749090 | A | G | 1 | a0004c0004t0001g0251 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.7-5810A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749090 | |||||||
| chr15:44749205 | T | C | 1 | a0002c0002t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.7-5695T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749205 | |||||||
| chr15:44749226 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.7-5674G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749226 | |||||||
| chr15:44749253 | AGATG | A | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-5646_7-5643delGA others(2): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749253 | |||||||
| chr15:44749379 | C | A | 30 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(27): Show |
34 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.7-5521C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749379 | |||||||
| chr15:44749768 | T | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.7-5132T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749768 | |||||||
| chr15:44749847 | T | C | 1 | a0003c0003t0002g0047 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.7-5053T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749847 | |||||||
| chr15:44749857 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.7-5043A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44749857 | |||||||
| chr15:44750231 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0160 |
3 | HG01516.hp1 HG01517.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.7-4669T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750231 | |||||||
| chr15:44750300 | T | A | 1 | a0007c0007t0002g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7-4600T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750300 | |||||||
| chr15:44750530 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-4370C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750530 | |||||||
| chr15:44750582 | A | G | 2 | a0004c0004t0001g0096 a0004c0004t0002g0065 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.7-4318A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750582 | |||||||
| chr15:44750588 | C | T | 3 | a0004c0004t0001g0035 a0004c0004t0001g0246 a0004c0004t0001g0247 |
4 | HG02615.hp1 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-4312C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750588 | |||||||
| chr15:44750657 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(171): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.7-4243T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750657 | |||||||
| chr15:44750706 | T | C | 1 | a0004c0004t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.7-4194T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750706 | |||||||
| chr15:44750709 | C | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.7-4191C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750709 | |||||||
| chr15:44750715 | C | CT | 9 | a0003c0003t0001g0056 a0003c0003t0001g0057 a0003c0003t0001g0059 others(6): Show |
10 | HG00438.hp1 HG01928.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.7-4158dupT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44750715 | ||||||
| chr15:44750715 | CTTT | C | 52 | a0001c0001t0001g0097 a0001c0001t0001g0148 a0001c0001t0001g0149 others(49): Show |
57 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.7-4160_7-4158delTT others(1): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44750715 | ||||||
| chr15:44750715 | CTTTT | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.7-4161_7-4158delTT others(2): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44750715 | ||||||
| chr15:44750722 | T | C | 1 | a0004c0004t0001g0086 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7-4178T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750722 | |||||||
| chr15:44750723 | T | C | 26 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(23): Show |
30 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.7-4177T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750723 | |||||||
| chr15:44750724 | T | C | 2 | a0001c0001t0001g0105 a0004c0004t0001g0239 |
2 | HG01256.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.7-4176T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750724 | |||||||
| chr15:44750726 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG00280.hp1 HG00323.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.7-4174T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750726 | |||||||
| chr15:44750727 | T | C | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-4173T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750727 | |||||||
| chr15:44750748 | G | A | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-4152G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750748 | |||||||
| chr15:44750786 | G | A | 2 | a0001c0008t0001g0227 a0002c0002t0001g0018 |
4 | HG02027.hp1 NA18970.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-4114G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750786 | |||||||
| chr15:44750787 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7-4113C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750787 | |||||||
| chr15:44750905 | T | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.7-3995T>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44750905 | |||||||
| chr15:44750950 | C | CT | 6 | a0003c0003t0001g0059 a0003c0003t0001g0079 a0003c0003t0002g0044 others(3): Show |
6 | HG00438.hp1 HG02074.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-3927dupT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44750950 | ||||||
| chr15:44750950 | CT | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.7-3927delT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44750950 | ||||||
| chr15:44750950 | CTT | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0178 others(3): Show |
6 | HG01243.hp2 HG02809.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-3928_7-3927delTT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44750950 | ||||||
| chr15:44751057 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.7-3843G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751057 | |||||||
| chr15:44751117 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.7-3783A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751117 | |||||||
| chr15:44751147 | G | A | 5 | a0003c0003t0002g0085 a0005c0005t0002g0233 a0005c0005t0002g0234 others(2): Show |
5 | HG02572.hp2 HG02698.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-3753G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751147 | |||||||
| chr15:44751194 | C | T | 3 | a0004c0004t0001g0094 a0004c0004t0001g0095 a0004c0004t0001g0250 |
3 | HG02572.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7-3706C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751194 | |||||||
| chr15:44751228 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.7-3672G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751228 | |||||||
| chr15:44751264 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7-3636C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751264 | |||||||
| chr15:44751265 | G | A | 2 | a0004c0004t0001g0096 a0004c0004t0002g0065 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.7-3635G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751265 | |||||||
| chr15:44751272 | C | T | 1 | a0004c0004t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-3628C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751272 | |||||||
| chr15:44751537 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.7-3363T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751537 | |||||||
| chr15:44751622 | G | C | 2 | a0002c0002t0002g0212 a0002c0002t0002g0213 |
2 | NA18949.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.7-3278G>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751622 | |||||||
| chr15:44751656 | C | A | 1 | a0004c0004t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.7-3244C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751656 | |||||||
| chr15:44751714 | C | T | 4 | a0003c0003t0002g0072 a0006c0006t0001g0071 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-3186C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751714 | |||||||
| chr15:44751774 | C | T | 4 | a0003c0003t0002g0072 a0006c0006t0001g0071 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-3126C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751774 | |||||||
| chr15:44751887 | G | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-3013G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751887 | |||||||
| chr15:44751909 | T | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0117 |
2 | HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.7-2991T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44751909 | |||||||
| chr15:44752210 | G | T | 5 | a0007c0007t0002g0022 a0007c0007t0002g0066 a0007c0007t0002g0067 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-2690G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752210 | |||||||
| chr15:44752258 | C | A | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-2642C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752258 | |||||||
| chr15:44752512 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7-2388A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752512 | |||||||
| chr15:44752588 | G | T | 5 | a0003c0003t0002g0085 a0005c0005t0002g0233 a0005c0005t0002g0234 others(2): Show |
5 | HG02572.hp2 HG02698.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-2312G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752588 | |||||||
| chr15:44752667 | G | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.7-2233G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752667 | |||||||
| chr15:44752721 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.7-2179C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752721 | |||||||
| chr15:44752737 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
247 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.7-2163A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752737 | |||||||
| chr15:44752770 | T | C | 2 | a0003c0003t0002g0048 a0003c0003t0002g0058 |
2 | HG02040.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.7-2130T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752770 | |||||||
| chr15:44752835 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.7-2065G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752835 | |||||||
| chr15:44752855 | C | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0180 others(14): Show |
19 | HG01981.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.7-2045C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752855 | |||||||
| chr15:44752903 | T | C | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-1997T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44752903 | |||||||
| chr15:44753062 | T | C | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-1838T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753062 | |||||||
| chr15:44753144 | T | C | 1 | a0002c0002t0002g0214 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.7-1756T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753144 | |||||||
| chr15:44753212 | AC | A | 6 | a0002c0002t0001g0194 a0002c0002t0002g0210 a0002c0002t0002g0211 others(3): Show |
6 | NA18948.hp1 NA18949.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-1687delC | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753212 | |||||||
| chr15:44753281 | ATTCT | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0160 |
3 | HG01516.hp1 HG01517.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.7-1616_7-1613delCT others(2): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44753281 | ||||||
| chr15:44753351 | C | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
248 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.7-1549C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753351 | |||||||
| chr15:44753365 | A | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-1535A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753365 | |||||||
| chr15:44753407 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.7-1493T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753407 | |||||||
| chr15:44753540 | G | T | 40 | a0003c0003t0002g0085 a0004c0004t0001g0032 a0004c0004t0001g0033 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.7-1360G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753540 | |||||||
| chr15:44753714 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.7-1186T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753714 | |||||||
| chr15:44753722 | T | A | 40 | a0003c0003t0002g0085 a0004c0004t0001g0032 a0004c0004t0001g0033 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.7-1178T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753722 | |||||||
| chr15:44753758 | C | G | 1 | a0001c0001t0001g0145 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.7-1142C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753758 | |||||||
| chr15:44753781 | T | C | 40 | a0003c0003t0002g0085 a0004c0004t0001g0032 a0004c0004t0001g0033 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.7-1119T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753781 | |||||||
| chr15:44753866 | C | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0170 |
2 | HG00741.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.7-1034C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44753866 | |||||||
| chr15:44754124 | CT | C | 6 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 others(3): Show |
8 | HG01891.hp1 HG02970.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-759delT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44754124 | ||||||
| chr15:44754124 | CTT | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.7-760_7-759delTT | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44754124 | ||||||
| chr15:44754124 | CTTTTTTT | C | 40 | a0003c0003t0002g0085 a0004c0004t0001g0032 a0004c0004t0001g0033 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.7-765_7-759delTTTT others(3): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 44754124 | ||||||
| chr15:44754141 | T | C | 1 | a0003c0003t0001g0049 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.7-759T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44754141 | |||||||
| chr15:44754271 | C | T | 1 | a0004c0004t0001g0251 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.7-629C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44754271 | |||||||
| chr15:44754272 | G | A | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.7-628G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44754272 | |||||||
| chr15:44754387 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.7-513G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44754387 | |||||||
| chr15:44754493 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.7-407T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44754493 | |||||||
| chr15:44754728 | C | T | 3 | a0001c0001t0001g0106 a0003c0003t0002g0038 a0004c0004t0001g0095 |
3 | HG02109.hp2 HG03516.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.7-172C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44754728 | |||||||
| chr15:44754760 | G | T | 1 | a0004c0004t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7-140G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 1/6 | chr15 | 44754760 | |||||||
| chr15:44755496 | G | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+120G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | chr15 | 44755496 | |||||||
| chr15:44755527 | C | G | 1 | a0003c0003t0002g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.483+151C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | chr15 | 44755527 | |||||||
| chr15:44755611 | G | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+235G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | chr15 | 44755611 | |||||||
| chr15:44755741 | G | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.483+365G>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | chr15 | 44755741 | |||||||
| chr15:44755896 | CA | C | 3 | a0004c0004t0001g0035 a0004c0004t0001g0246 a0004c0004t0001g0247 |
4 | HG02615.hp1 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-469delA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 44755896 | ||||||
| chr15:44755923 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.484-445G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | chr15 | 44755923 | |||||||
| chr15:44756152 | A | C | 1 | a0011c0013t0001g0144 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.484-216A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | chr15 | 44756152 | |||||||
| chr15:44756219 | A | G | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.484-149A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | chr15 | 44756219 | |||||||
| chr15:44756220 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.484-148C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 2/6 | chr15 | 44756220 | |||||||
| chr15:44756559 | T | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.579+96T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44756559 | |||||||
| chr15:44756576 | C | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0099 others(5): Show |
12 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.579+113C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44756576 | |||||||
| chr15:44756585 | G | A | 28 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(25): Show |
32 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+122G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44756585 | |||||||
| chr15:44756643 | A | G | 28 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(25): Show |
32 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+180A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44756643 | |||||||
| chr15:44756727 | G | A | 5 | a0001c0001t0001g0166 a0005c0005t0002g0233 a0005c0005t0002g0234 others(2): Show |
5 | HG02300.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+264G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44756727 | |||||||
| chr15:44756762 | CA | C | 38 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(35): Show |
43 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.579+311delA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 44756762 | ||||||
| chr15:44756762 | CAA | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.579+310_579+311del others(2): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 44756762 | ||||||
| chr15:44756811 | C | G | 28 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(25): Show |
32 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+348C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44756811 | |||||||
| chr15:44756818 | C | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.579+355C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44756818 | |||||||
| chr15:44756860 | C | T | 1 | a0004c0004t0001g0247 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.579+397C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44756860 | |||||||
| chr15:44757204 | T | C | 5 | a0003c0003t0002g0072 a0003c0003t0002g0085 a0006c0006t0001g0071 others(2): Show |
8 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+741T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757204 | |||||||
| chr15:44757206 | A | T | 1 | a0004c0004t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.579+743A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757206 | |||||||
| chr15:44757252 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(172): Show |
247 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.579+789T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757252 | |||||||
| chr15:44757305 | A | G | 1 | a0003c0003t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+842A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757305 | |||||||
| chr15:44757330 | C | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.579+867C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757330 | |||||||
| chr15:44757341 | G | T | 29 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(26): Show |
33 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.579+878G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757341 | |||||||
| chr15:44757497 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.579+1034T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757497 | |||||||
| chr15:44757646 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.580-975T>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757646 | |||||||
| chr15:44757870 | G | A | 1 | a0004c0004t0001g0241 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.580-751G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757870 | |||||||
| chr15:44757939 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-682C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44757939 | |||||||
| chr15:44758330 | T | G | 1 | a0011c0013t0001g0144 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.580-291T>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44758330 | |||||||
| chr15:44758395 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.580-226G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44758395 | |||||||
| chr15:44758534 | C | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02258.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.580-87C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 3/6 | chr15 | 44758534 | |||||||
| chr15:44758949 | G | GAAAAC | 7 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 others(4): Show |
9 | HG01891.hp1 HG02572.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.813+116_813+120dup others(5): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 44758949 | ||||||
| chr15:44758968 | A | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
7 | HG02015.hp1 NA18940.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.813+114A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/6 | chr15 | 44758968 | |||||||
| chr15:44759071 | C | T | 5 | a0003c0003t0002g0072 a0003c0003t0002g0085 a0006c0006t0001g0071 others(2): Show |
8 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.813+217C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/6 | chr15 | 44759071 | |||||||
| chr15:44759074 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.813+220T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/6 | chr15 | 44759074 | |||||||
| chr15:44759426 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.814-214C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/6 | chr15 | 44759426 | |||||||
| chr15:44759478 | G | A | 39 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(36): Show |
44 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.814-162G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/6 | chr15 | 44759478 | |||||||
| chr15:44759620 | C | T | 4 | a0005c0005t0002g0233 a0005c0005t0002g0234 a0005c0005t0002g0235 others(1): Show |
4 | HG02572.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.814-20C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 4/6 | chr15 | 44759620 | |||||||
| chr15:44760155 | T | C | 10 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(7): Show |
11 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.961+283T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44760155 | |||||||
| chr15:44760403 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.961+531T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44760403 | |||||||
| chr15:44760415 | C | G | 1 | a0004c0004t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.961+543C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44760415 | |||||||
| chr15:44760507 | A | T | 3 | a0004c0004t0001g0094 a0004c0004t0001g0095 a0004c0004t0001g0250 |
3 | HG02572.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.961+635A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44760507 | |||||||
| chr15:44760635 | G | A | 1 | a0004c0004t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.961+763G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44760635 | |||||||
| chr15:44760692 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.961+820A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44760692 | |||||||
| chr15:44760724 | A | T | 27 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(24): Show |
31 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.961+852A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44760724 | |||||||
| chr15:44760731 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.961+859A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44760731 | |||||||
| chr15:44761094 | A | G | 1 | a0004c0004t0001g0249 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.961+1222A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44761094 | |||||||
| chr15:44761198 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.961+1326A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44761198 | |||||||
| chr15:44761342 | C | A | 1 | a0004c0004t0001g0032 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.961+1470C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44761342 | |||||||
| chr15:44761478 | G | A | 1 | a0003c0003t0002g0038 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.961+1606G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44761478 | |||||||
| chr15:44761612 | G | A | 1 | a0003c0003t0002g0051 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.961+1740G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44761612 | |||||||
| chr15:44761713 | C | T | 9 | a0002c0002t0001g0018 a0002c0002t0001g0200 a0002c0002t0002g0201 others(6): Show |
11 | HG02015.hp2 NA18946.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.961+1841C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44761713 | |||||||
| chr15:44761794 | C | T | 1 | a0009c0010t0001g0199 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.961+1922C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44761794 | |||||||
| chr15:44762001 | C | G | 40 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(37): Show |
45 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.961+2129C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762001 | |||||||
| chr15:44762029 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.961+2157A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762029 | |||||||
| chr15:44762034 | C | T | 6 | a0005c0005t0002g0023 a0005c0005t0002g0080 a0005c0005t0002g0081 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.961+2162C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762034 | |||||||
| chr15:44762122 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.961+2250C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762122 | |||||||
| chr15:44762126 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.961+2254C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762126 | |||||||
| chr15:44762127 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0228 |
3 | HG00621.hp2 HG02071.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.961+2255G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762127 | |||||||
| chr15:44762187 | C | T | 1 | a0002c0002t0001g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.961+2315C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762187 | |||||||
| chr15:44762189 | A | G | 2 | a0004c0004t0001g0096 a0004c0004t0002g0065 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.961+2317A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762189 | |||||||
| chr15:44762212 | C | G | 2 | a0004c0004t0001g0096 a0004c0004t0002g0065 |
2 | HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.961+2340C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762212 | |||||||
| chr15:44762212 | C | T | 33 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0010 others(30): Show |
48 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.961+2340C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762212 | |||||||
| chr15:44762367 | G | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.961+2495G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762367 | |||||||
| chr15:44762376 | C | A | 5 | a0007c0007t0002g0022 a0007c0007t0002g0066 a0007c0007t0002g0067 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.961+2504C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762376 | |||||||
| chr15:44762386 | C | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0180 others(14): Show |
19 | HG01981.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.961+2514C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762386 | |||||||
| chr15:44762657 | A | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0180 others(14): Show |
19 | HG01981.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.961+2785A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762657 | |||||||
| chr15:44762692 | T | C | 1 | a0003c0003t0002g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961+2820T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762692 | |||||||
| chr15:44762754 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.961+2882A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762754 | |||||||
| chr15:44762896 | A | G | 28 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(25): Show |
32 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.961+3024A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44762896 | |||||||
| chr15:44763054 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.961+3182C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763054 | |||||||
| chr15:44763146 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0148 |
2 | NA18995.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.961+3274A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763146 | |||||||
| chr15:44763401 | A | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.961+3529A>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763401 | |||||||
| chr15:44763547 | T | A | 27 | a0004c0004t0001g0032 a0004c0004t0001g0033 a0004c0004t0001g0034 others(24): Show |
31 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.961+3675T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763547 | |||||||
| chr15:44763610 | G | A | 1 | a0002c0002t0001g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.962-3621G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763610 | |||||||
| chr15:44763625 | G | T | 5 | a0007c0007t0002g0022 a0007c0007t0002g0066 a0007c0007t0002g0067 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.962-3606G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763625 | |||||||
| chr15:44763914 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 |
5 | HG01891.hp1 HG02970.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-3317C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763914 | |||||||
| chr15:44763915 | G | A | 5 | a0007c0007t0002g0022 a0007c0007t0002g0066 a0007c0007t0002g0067 others(2): Show |
6 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.962-3316G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763915 | |||||||
| chr15:44763934 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.962-3297T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763934 | |||||||
| chr15:44763988 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.962-3243C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44763988 | |||||||
| chr15:44764127 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.962-3104C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44764127 | |||||||
| chr15:44764281 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.962-2950G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44764281 | |||||||
| chr15:44764364 | T | C | 1 | a0004c0004t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.962-2867T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44764364 | |||||||
| chr15:44764398 | T | C | 7 | a0003c0003t0002g0072 a0003c0003t0002g0085 a0004c0004t0001g0096 others(4): Show |
10 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.962-2833T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44764398 | |||||||
| chr15:44764529 | T | TA | 4 | a0003c0003t0002g0072 a0006c0006t0001g0071 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.962-2699dupA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44764529 | ||||||
| chr15:44764699 | T | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.962-2532T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44764699 | |||||||
| chr15:44764772 | G | C | 1 | a0004c0004t0001g0087 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.962-2459G>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44764772 | |||||||
| chr15:44764990 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.962-2241T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44764990 | |||||||
| chr15:44765082 | G | C | 10 | a0002c0002t0002g0201 a0002c0002t0002g0207 a0002c0002t0002g0210 others(7): Show |
11 | HG00140.hp1 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.962-2149G>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765082 | |||||||
| chr15:44765166 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.962-2065G>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765166 | |||||||
| chr15:44765202 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.962-2029G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765202 | |||||||
| chr15:44765239 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.962-1992C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765239 | |||||||
| chr15:44765282 | T | G | 1 | a0004c0004t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.962-1949T>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765282 | |||||||
| chr15:44765306 | G | A | 23 | a0002c0002t0001g0122 a0004c0004t0001g0032 a0004c0004t0001g0033 others(20): Show |
27 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.962-1925G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765306 | |||||||
| chr15:44765613 | G | GC | 23 | a0002c0002t0001g0122 a0004c0004t0001g0032 a0004c0004t0001g0033 others(20): Show |
27 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.962-1617dupC | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44765613 | ||||||
| chr15:44765621 | G | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.962-1610G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765621 | |||||||
| chr15:44765659 | CAGG | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.962-1569_962-1567d others(5): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44765659 | ||||||
| chr15:44765753 | C | A | 3 | a0004c0009t0001g0076 a0004c0009t0001g0077 a0004c0009t0001g0078 |
3 | HG02055.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.962-1478C>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765753 | |||||||
| chr15:44765757 | A | C | 3 | a0004c0009t0001g0076 a0004c0009t0001g0077 a0004c0009t0001g0078 |
3 | HG02055.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.962-1474A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765757 | |||||||
| chr15:44765768 | AAAAC | A | 43 | a0002c0002t0001g0014 a0002c0002t0001g0073 a0002c0002t0001g0074 others(40): Show |
50 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.962-1447_962-1444d others(6): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44765768 | ||||||
| chr15:44765772 | C | CA | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
239 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.962-1456dupA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44765772 | ||||||
| chr15:44765784 | CAAAA | C | 4 | a0003c0003t0002g0072 a0003c0003t0002g0085 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.962-1440_962-1437d others(6): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44765784 | ||||||
| chr15:44765788 | A | C | 2 | a0003c0003t0002g0040 a0004c0009t0001g0077 |
2 | HG02055.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.962-1443A>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765788 | |||||||
| chr15:44765823 | C | T | 1 | a0004c0004t0002g0065 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.962-1408C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765823 | |||||||
| chr15:44765864 | T | A | 1 | a0001c0001t0001g0252 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.962-1367T>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44765864 | |||||||
| chr15:44766014 | C | T | 1 | a0004c0004t0001g0249 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.962-1217C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766014 | |||||||
| chr15:44766287 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.962-944G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766287 | |||||||
| chr15:44766306 | T | C | 3 | a0004c0004t0001g0033 a0004c0004t0001g0089 a0004c0004t0001g0245 |
4 | HG00558.hp1 HG02056.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-925T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766306 | |||||||
| chr15:44766441 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.962-790C>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766441 | |||||||
| chr15:44766507 | G | A | 1 | a0008c0011t0001g0082 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.962-724G>A | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766507 | |||||||
| chr15:44766554 | AC | A | 7 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG00140.hp2 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.962-676delC | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766554 | |||||||
| chr15:44766823 | T | C | 4 | a0003c0003t0002g0072 a0003c0003t0002g0085 a0006c0006t0002g0007 others(1): Show |
7 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.962-408T>C | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766823 | |||||||
| chr15:44766855 | A | G | 3 | a0004c0009t0001g0076 a0004c0009t0001g0077 a0004c0009t0001g0078 |
3 | HG02055.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.962-376A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766855 | |||||||
| chr15:44766966 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.962-265C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44766966 | |||||||
| chr15:44767016 | A | G | 2 | a0004c0004t0001g0035 a0004c0004t0001g0246 |
3 | HG02615.hp1 HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.962-215A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44767016 | |||||||
| chr15:44767053 | C | CA | 10 | a0003c0003t0001g0079 a0003c0003t0002g0039 a0003c0003t0002g0042 others(7): Show |
10 | HG02148.hp1 HG02165.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.962-147dupA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA | 9 | a0004c0004t0001g0032 a0004c0004t0001g0035 a0004c0004t0001g0094 others(6): Show |
11 | HG00099.hp2 HG00558.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.962-153_962-147dup others(7): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(1): Show |
11 | a0001c0001t0001g0154 a0001c0001t0001g0168 a0002c0002t0001g0122 others(8): Show |
13 | HG00738.hp1 HG02056.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.962-154_962-147dup others(8): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0115 others(7): Show |
10 | HG00280.hp1 HG02129.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.962-155_962-147dup others(9): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(3): Show |
34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(31): Show |
58 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.962-156_962-147dup others(10): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(4): Show |
62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(59): Show |
90 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.962-157_962-147dup others(11): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(5): Show |
37 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0028 others(34): Show |
52 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.962-158_962-147dup others(12): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0125 a0001c0001t0001g0150 a0002c0002t0001g0093 others(4): Show |
7 | HG01175.hp1 HG01175.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.962-159_962-147dup others(13): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0129 a0001c0001t0001g0155 a0001c0001t0001g0217 others(1): Show |
4 | HG01928.hp2 NA18949.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-160_962-147dup others(14): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.962-161_962-147dup others(15): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0188 |
2 | HG03486.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.962-162_962-147dup others(16): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0128 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.962-163_962-147dup others(17): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0127 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.962-164_962-147dup others(18): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | CA | C | 5 | a0003c0003t0002g0021 a0003c0003t0002g0038 a0003c0003t0002g0043 others(2): Show |
6 | HG02109.hp2 HG02451.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.962-147delA | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | CAAA | C | 16 | a0001c0001t0001g0183 a0002c0002t0001g0014 a0002c0002t0001g0073 others(13): Show |
19 | HG00140.hp1 HG01070.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.962-149_962-147del others(3): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | CAAAA | C | 3 | a0003c0003t0002g0072 a0006c0006t0002g0007 a0006c0006t0002g0070 |
6 | HG00642.hp2 HG01099.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.962-150_962-147del others(4): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | CAAAAAA | C | 5 | a0001c0001t0001g0133 a0001c0001t0001g0172 a0001c0014t0001g0107 others(2): Show |
7 | HG01978.hp1 HG01978.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.962-152_962-147del others(6): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.962-156_962-147del others(10): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0184 a0004c0009t0001g0078 |
4 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-157_962-147del others(11): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767053 | CAAAAAAA others(5): Show |
C | 2 | a0004c0009t0001g0076 a0004c0009t0001g0077 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.962-158_962-147del others(12): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767053 | ||||||
| chr15:44767060 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0255 a0001c0001t0001g0257 |
2 | HG01433.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.962-160_962-159ins others(12): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767060 | ||||||
| chr15:44767061 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0258 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.962-159_962-158ins others(12): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767061 | ||||||
| chr15:44767061 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0256 |
4 | HG01074.hp1 HG02300.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.962-160_962-159ins others(11): Show |
TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 44767061 | ||||||
| chr15:44767113 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.962-118G>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44767113 | |||||||
| chr15:44767133 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0147 |
3 | HG01256.hp1 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.962-98A>G | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44767133 | |||||||
| chr15:44767192 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.962-39C>T | TRIM69 | ENSG00000185880.13 | transcript | ENST00000329464.9 | protein_coding | 6/6 | chr15 | 44767192 |