Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 53840 |
| ensemblid | ENSG00000258659.7 |
| hgncid | 10063 |
| symbol | TRIM34 |
| name | tripartite motif containing 34 |
| refseq_nuc | NM_021616.6 |
| refseq_prot | NP_067629.2 |
| ensembl_nuc | ENST00000429814.3 |
| ensembl_prot | ENSP00000402595.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 5625001 |
| end | 5644398 |
| strand | + |
| ver | v1.2 |
| region | chr11:5625001-5644398 |
| region5000 | chr11:5620001-5649398 |
| regionname0 | TRIM34_chr11_5625001_5644398 |
| regionname5000 | TRIM34_chr11_5620001_5649398 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 488 | 360 | 76 | 62 | 164 | 13 | 43 | 127 | TRIM34_chr11_5620001_5649398 | TRIM34 | MASKI others(483): Show |
chr11 | 5620001 | 5649398 |
| a0002 | 0/0 | 488 | 30 | 1 | 10 | 19 | 0 | 0 | 12 | TRIM34_chr11_5620001_5649398 | TRIM34 | MASKI others(483): Show |
chr11 | 5620001 | 5649398 |
| a0003 | 0/0 | 488 | 29 | 12 | 5 | 4 | 3 | 5 | 3 | TRIM34_chr11_5620001_5649398 | TRIM34 | MASKI others(483): Show |
chr11 | 5620001 | 5649398 |
| a0004 | 0/0 | 488 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | MASKI others(483): Show |
chr11 | 5620001 | 5649398 |
| a0005 | 0/0 | 488 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | MASKI others(483): Show |
chr11 | 5620001 | 5649398 |
| a0006 | 0/0 | 146 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | MASKI others(141): Show |
chr11 | 5620001 | 5649398 |
| a0007 | 0/0 | 488 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | MASKI others(483): Show |
chr11 | 5620001 | 5649398 |
| a0008 | 0/0 | 488 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | MASKI others(483): Show |
chr11 | 5620001 | 5649398 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1464 | 205 | 51 | 36 | 85 | 12 | 19 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0001c0002 | 0/0 | 1464 | 149 | 20 | 25 | 79 | 1 | 24 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0001c0005 | 0/0 | 1464 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0001c0007 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0002c0003 | 0/0 | 1464 | 30 | 1 | 10 | 19 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0003c0004 | 0/0 | 1464 | 29 | 12 | 5 | 4 | 3 | 5 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0004c0006 | 0/0 | 1464 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0005c0009 | 0/0 | 1464 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0006c0008 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1446): Show |
chr11 | 5620001 | 5649398 | ||
| a0007c0010 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 | ||
| a0008c0011 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ATGGC others(1459): Show |
chr11 | 5620001 | 5649398 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2293 | 175 | 31 | 32 | 84 | 10 | 17 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0001c0001t0002 | 1/0 | 2293 | 29 | 20 | 4 | 0 | 2 | 2 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0001c0001t0004 | 0/0 | 2293 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0001c0002t0001 | 0/0 | 2293 | 148 | 19 | 25 | 79 | 1 | 24 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0001c0002t0005 | 0/0 | 2293 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0001c0005t0001 | 0/0 | 2293 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0001c0005t0002 | 0/0 | 2293 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0001c0007t0002 | 0/0 | 2293 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0002c0003t0001 | 0/0 | 2293 | 30 | 1 | 10 | 19 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0003c0004t0001 | 0/0 | 2293 | 28 | 12 | 5 | 3 | 3 | 5 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0003c0004t0003 | 0/0 | 2293 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0004c0006t0002 | 0/0 | 2293 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0005c0009t0001 | 0/0 | 2293 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0006c0008t0001 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2275): Show |
chr11 | 5620001 | 5649398 |
| a0007c0010t0001 | 0/0 | 2293 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| a0008c0011t0001 | 0/0 | 2293 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | ACCCA others(2288): Show |
chr11 | 5620001 | 5649398 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 0 | 0 | 20 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0004 | 0/0 | 10 | 1 | 4 | 3 | 2 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0003 | 1/0 | 11 | 7 | 2 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0002 | 0/0 | 15 | 0 | 5 | 10 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0005 | 0/0 | 8 | 0 | 0 | 1 | 0 | 7 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0009 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0027 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0002t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0005t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0005t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0005t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0005t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0001c0007t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0010 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0003c0004t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0004c0006t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0004c0006t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0004c0006t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0005c0009t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0006c0008t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0007c0010t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| a0008c0011t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | FIN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | FIN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00323 | hp2 | a0003 | c0004 | t0001 | g0034 | EUR | FIN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0169 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00438 | hp1 | a0002 | c0003 | t0001 | g0029 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00597 | hp1 | a0003 | c0004 | t0001 | g0121 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00642 | hp1 | a0005 | c0009 | t0001 | g0028 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | CHS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0112 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01069 | hp1 | a0003 | c0004 | t0001 | g0022 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0116 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0220 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01243 | hp1 | a0001 | c0005 | t0002 | g0047 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0066 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | IBS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01515 | hp2 | a0003 | c0004 | t0001 | g0012 | EUR | IBS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01517 | hp1 | a0003 | c0004 | t0001 | g0022 | EUR | IBS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01891 | hp2 | a0003 | c0004 | t0001 | g0088 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0113 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01934 | hp1 | a0003 | c0004 | t0001 | g0278 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0010 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0219 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01978 | hp1 | a0003 | c0004 | t0001 | g0109 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0115 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0111 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0030 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0117 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02074 | hp1 | a0006 | c0008 | t0001 | g0217 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02145 | hp2 | a0007 | c0010 | t0001 | g0142 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0114 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CDX | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02165 | hp1 | a0002 | c0003 | t0001 | g0119 | EAS | CDX | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02257 | hp1 | a0003 | c0004 | t0001 | g0187 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02293 | hp1 | a0003 | c0004 | t0001 | g0022 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02300 | hp1 | a0003 | c0004 | t0001 | g0167 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | PEL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02451 | hp1 | a0004 | c0006 | t0002 | g0077 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | KHV | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0286 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02622 | hp2 | a0003 | c0004 | t0001 | g0147 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02647 | hp2 | a0001 | c0002 | t0005 | g0059 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02683 | hp1 | a0003 | c0004 | t0001 | g0164 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02698 | hp1 | a0003 | c0004 | t0001 | g0012 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02717 | hp1 | a0003 | c0004 | t0001 | g0193 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0287 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0271 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02809 | hp2 | a0004 | c0006 | t0002 | g0076 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02886 | hp1 | a0003 | c0004 | t0001 | g0135 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0281 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03098 | hp1 | a0003 | c0004 | t0001 | g0127 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0134 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0272 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03195 | hp1 | a0003 | c0004 | t0001 | g0129 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03195 | hp2 | a0003 | c0004 | t0001 | g0132 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03239 | hp1 | a0003 | c0004 | t0001 | g0012 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03486 | hp1 | a0001 | c0007 | t0002 | g0060 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0189 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03516 | hp2 | a0003 | c0004 | t0001 | g0126 | AFR | ESN | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03540 | hp2 | a0008 | c0011 | t0001 | g0057 | AFR | GWD | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0282 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0232 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03942 | hp2 | a0003 | c0004 | t0001 | g0176 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04115 | hp1 | a0003 | c0004 | t0001 | g0175 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0249 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | BEB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0255 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | STU | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0118 | EAS | CHB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | CHB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | YRI | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18906 | hp2 | a0001 | c0005 | t0002 | g0273 | AFR | YRI | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0034 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18980 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18981 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18982 | hp1 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18992 | hp1 | a0002 | c0003 | t0001 | g0215 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19003 | hp2 | a0002 | c0003 | t0001 | g0153 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | LWK | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | LWK | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | LWK | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19059 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19067 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19074 | hp2 | a0003 | c0004 | t0003 | g0012 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0120 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19088 | hp2 | a0003 | c0004 | t0001 | g0182 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ASW | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ASW | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0267 | EUR | TSI | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0212 | SAS | GIH | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | GIH | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0205 | AMR | CLM | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0125 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02486 | hp1 | a0001 | c0005 | t0002 | g0223 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02486 | hp2 | a0003 | c0004 | t0001 | g0133 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG02559 | hp2 | a0001 | c0005 | t0002 | g0283 | AFR | ACB | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0010 | AFR | USA | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA20300 | hp2 | a0004 | c0006 | t0002 | g0073 | AFR | USA | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | LWK | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0188 | REF | REF | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | TRIM34_chr11_5620001_5649398 | TRIM34 | chr11 | 5620001 | 5649398 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5633796 | TCTCATAG others(13): Show |
T | 1 | a0006 | 1 | HG02074.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.424-6_437delTCATAG others(14): Show |
p.Glu142fs | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/8 | 424/1467 | 142/488 | INFO_REALIGN_3_PRIME | chr11 | 5633796 | |||
| chr11:5633806 | G | C | 1 | a0001 | 2 | HG03834.hp2 HG04184.hp1 |
missense_variant&splice_region_variant | MODERATE | c.426G>C | p.Glu142Asp | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/8 | 563/2293 | 426/1467 | 142/488 | chr11 | 5633806 | |||
| chr11:5634758 | T | C | 1 | a0005 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.647T>C | p.Phe216Ser | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/8 | 784/2293 | 647/1467 | 216/488 | chr11 | 5634758 | |||
| chr11:5642439 | G | T | 1 | a0008 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.807G>T | p.Met269Ile | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 6/8 | 944/2293 | 807/1467 | 269/488 | chr11 | 5642439 | |||
| chr11:5642458 | A | T | 1 | a0004 | 3 | HG02451.hp1 HG02809.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.826A>T | p.Thr276Ser | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 6/8 | 963/2293 | 826/1467 | 276/488 | chr11 | 5642458 | |||
| chr11:5642476 | G | C | 1 | a0002 | 30 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(27): Show |
missense_variant | MODERATE | c.844G>C | p.Asp282His | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 6/8 | 981/2293 | 844/1467 | 282/488 | chr11 | 5642476 | |||
| chr11:5643384 | G | A | 1 | a0007 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1142G>A | p.Cys381Tyr | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 8/8 | 1279/2293 | 1142/1467 | 381/488 | chr11 | 5643384 | |||
| chr11:5643454 | T | G | 1 | a0003 | 29 | HG00323.hp2 HG00597.hp1 HG01069.hp1 others(26): Show |
missense_variant | MODERATE | c.1212T>G | p.Asn404Lys | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 8/8 | 1349/2293 | 1212/1467 | 404/488 | chr11 | 5643454 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5632730 | G | A | 1 | a0001c0005 | 5 | HG01243.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.399G>A | p.Thr133Thr | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/8 | 536/2293 | 399/1467 | 133/488 | chr11 | 5632730 | |||
| chr11:5632733 | G | A | 1 | a0001c0007 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.402G>A | p.Glu134Glu | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/8 | 539/2293 | 402/1467 | 134/488 | chr11 | 5632733 | |||
| chr11:5633821 | C | T | 1 | a0006c0008 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.441C>T | p.Val147Val | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/8 | 578/2293 | 441/1467 | 147/488 | chr11 | 5633821 | |||
| chr11:5643601 | C | A | 4 | a0001c0002 a0002c0003 a0006c0008 others(1): Show |
181 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(178): Show |
synonymous_variant | LOW | c.1359C>A | p.Gly453Gly | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 8/8 | 1496/2293 | 1359/1467 | 453/488 | chr11 | 5643601 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5643739 | T | C | 1 | a0003c0004t0003 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 8/8 | 30 | chr11 | 5643739 | ||||||
| chr11:5643744 | T | C | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0002t0001 others(9): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
3_prime_UTR_variant | MODIFIER | c.*35T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 8/8 | 35 | chr11 | 5643744 | ||||||
| chr11:5643805 | C | A | 1 | a0001c0001t0004 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 8/8 | 96 | chr11 | 5643805 | ||||||
| chr11:5643832 | G | C | 1 | a0001c0002t0005 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 8/8 | 123 | chr11 | 5643832 | ||||||
| chr11:5643995 | A | G | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0002t0001 others(9): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
3_prime_UTR_variant | MODIFIER | c.*286A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 8/8 | 286 | chr11 | 5643995 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:5625079 | G | C | 1 | a0001c0005t0002g0047 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-78+19G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625079 | |||||||
| chr11:5625139 | T | A | 4 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(1): Show |
4 | HG01243.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78+79T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625139 | |||||||
| chr11:5625181 | T | C | 1 | a0001c0002t0001g0052 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-78+121T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625181 | |||||||
| chr11:5625290 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-78+230G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625290 | |||||||
| chr11:5625433 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-78+373C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625433 | |||||||
| chr11:5625625 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-78+565T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625625 | |||||||
| chr11:5625674 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(218): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(322): Show |
intron_variant | MODIFIER | c.-78+614C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625674 | |||||||
| chr11:5625696 | G | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-78+636G>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625696 | |||||||
| chr11:5625715 | G | GGTC | 134 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
198 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.-78+656_-78+658dup others(3): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5625715 | ||||||
| chr11:5625803 | C | T | 102 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0214 others(99): Show |
146 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.-78+743C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625803 | |||||||
| chr11:5625916 | T | C | 1 | a0001c0002t0001g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-78+856T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625916 | |||||||
| chr11:5625936 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(231): Show |
342 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(339): Show |
intron_variant | MODIFIER | c.-78+876G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5625936 | |||||||
| chr11:5626004 | T | C | 4 | a0001c0002t0001g0039 a0001c0002t0001g0205 a0001c0002t0001g0206 others(1): Show |
5 | HG00733.hp1 HG00738.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78+944T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626004 | |||||||
| chr11:5626158 | G | A | 6 | a0001c0001t0001g0056 a0001c0002t0001g0048 a0001c0002t0001g0049 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+1098G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626158 | |||||||
| chr11:5626185 | T | C | 6 | a0001c0001t0001g0056 a0001c0002t0001g0048 a0001c0002t0001g0049 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+1125T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626185 | |||||||
| chr11:5626195 | T | A | 1 | a0003c0004t0001g0109 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-78+1135T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626195 | |||||||
| chr11:5626261 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | HG00099.hp1 HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-78+1201T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626261 | |||||||
| chr11:5626286 | C | CT | 6 | a0001c0001t0001g0056 a0001c0002t0001g0048 a0001c0002t0001g0049 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+1226_-78+1227i others(3): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626286 | |||||||
| chr11:5626372 | G | A | 2 | a0001c0001t0001g0208 a0001c0002t0001g0209 |
2 | HG00544.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.-78+1312G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626372 | |||||||
| chr11:5626426 | A | G | 1 | a0001c0002t0001g0288 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-78+1366A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626426 | |||||||
| chr11:5626489 | A | G | 10 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(7): Show |
10 | HG00140.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.-78+1429A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626489 | |||||||
| chr11:5626574 | G | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+1514G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626574 | |||||||
| chr11:5626581 | C | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+1521C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626581 | |||||||
| chr11:5626598 | T | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+1538T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626598 | |||||||
| chr11:5626689 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-78+1629G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626689 | |||||||
| chr11:5626713 | C | G | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+1653C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626713 | |||||||
| chr11:5626717 | T | TA | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+1664dupA | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5626717 | ||||||
| chr11:5626754 | T | C | 6 | a0001c0001t0001g0056 a0001c0002t0001g0048 a0001c0002t0001g0049 others(3): Show |
6 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78+1694T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626754 | |||||||
| chr11:5626809 | G | C | 2 | a0001c0001t0001g0210 a0001c0002t0001g0211 |
2 | HG00280.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-78+1749G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626809 | |||||||
| chr11:5626882 | C | CA | 39 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(36): Show |
51 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-78+1837dupA | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5626882 | ||||||
| chr11:5626977 | C | T | 1 | a0003c0004t0001g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-78+1917C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5626977 | |||||||
| chr11:5627091 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-78+2031G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627091 | |||||||
| chr11:5627101 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-78+2041G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627101 | |||||||
| chr11:5627176 | G | A | 21 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0122 others(18): Show |
31 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.-78+2116G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627176 | |||||||
| chr11:5627237 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-78+2177G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627237 | |||||||
| chr11:5627279 | C | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0058 others(8): Show |
15 | HG00733.hp2 HG01192.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-78+2219C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627279 | |||||||
| chr11:5627329 | G | A | 104 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0214 others(101): Show |
148 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.-78+2269G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627329 | |||||||
| chr11:5627419 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-78+2359A>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627419 | |||||||
| chr11:5627476 | G | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+2416G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627476 | |||||||
| chr11:5627522 | C | T | 1 | a0001c0002t0001g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-78+2462C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627522 | |||||||
| chr11:5627526 | G | A | 5 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
5 | HG01243.hp1 HG01243.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78+2466G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627526 | |||||||
| chr11:5627584 | A | G | 1 | a0001c0002t0001g0286 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-78+2524A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627584 | |||||||
| chr11:5627631 | G | T | 2 | a0001c0002t0001g0284 a0001c0002t0001g0285 |
2 | NA18956.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-78+2571G>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627631 | |||||||
| chr11:5627633 | G | C | 1 | a0001c0002t0001g0040 | 2 | NA19011.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-78+2573G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627633 | |||||||
| chr11:5627642 | A | C | 1 | a0001c0005t0002g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-78+2582A>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627642 | |||||||
| chr11:5627770 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-78+2710A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627770 | |||||||
| chr11:5627871 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-78+2811G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627871 | |||||||
| chr11:5627944 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-78+2884A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627944 | |||||||
| chr11:5627969 | A | G | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-78+2909A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5627969 | |||||||
| chr11:5628074 | G | T | 1 | a0001c0001t0002g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-78+3014G>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628074 | |||||||
| chr11:5628118 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-78+3058C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628118 | |||||||
| chr11:5628190 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-78+3130C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628190 | |||||||
| chr11:5628199 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-78+3139C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628199 | |||||||
| chr11:5628214 | C | T | 4 | a0003c0004t0001g0132 a0003c0004t0001g0133 a0003c0004t0001g0134 others(1): Show |
4 | HG02486.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78+3154C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628214 | |||||||
| chr11:5628314 | C | G | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-78+3254C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628314 | |||||||
| chr11:5628332 | A | G | 2 | a0001c0002t0001g0038 a0001c0002t0001g0191 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-78+3272A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628332 | |||||||
| chr11:5628530 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-78+3470G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628530 | |||||||
| chr11:5628548 | A | G | 1 | a0001c0002t0001g0046 | 2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-78+3488A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628548 | |||||||
| chr11:5628626 | G | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0058 others(8): Show |
15 | HG00733.hp2 HG01192.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-78+3566G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628626 | |||||||
| chr11:5628806 | A | AT | 6 | a0001c0001t0001g0067 a0001c0001t0001g0084 a0001c0001t0001g0194 others(3): Show |
6 | HG00323.hp1 HG02145.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77-3438dupT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5628806 | ||||||
| chr11:5628806 | A | ATT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(110): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-77-3439_-77-3438d others(4): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5628806 | ||||||
| chr11:5628882 | C | A | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-77-3373C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628882 | |||||||
| chr11:5628953 | G | A | 31 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(28): Show |
43 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-77-3302G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5628953 | |||||||
| chr11:5629042 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-77-3213C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629042 | |||||||
| chr11:5629190 | T | A | 1 | a0002c0003t0001g0215 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-77-3065T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629190 | |||||||
| chr11:5629276 | C | CA | 9 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(6): Show |
9 | HG02027.hp1 HG02074.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-77-2970dupA | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr11 | 5629276 | ||||||
| chr11:5629330 | A | G | 115 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0058 others(112): Show |
163 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.-77-2925A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629330 | |||||||
| chr11:5629567 | C | G | 1 | a0001c0002t0001g0288 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-77-2688C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629567 | |||||||
| chr11:5629673 | G | A | 2 | a0001c0001t0002g0149 a0001c0002t0001g0148 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-77-2582G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629673 | |||||||
| chr11:5629705 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-77-2550T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629705 | |||||||
| chr11:5629803 | G | C | 1 | a0001c0002t0001g0212 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-77-2452G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629803 | |||||||
| chr11:5629856 | C | T | 1 | a0003c0004t0001g0129 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-77-2399C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629856 | |||||||
| chr11:5629948 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-77-2307C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629948 | |||||||
| chr11:5629975 | A | G | 1 | a0001c0002t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-77-2280A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629975 | |||||||
| chr11:5629979 | T | G | 1 | a0001c0002t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-77-2276T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629979 | |||||||
| chr11:5629980 | A | G | 1 | a0001c0002t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-77-2275A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629980 | |||||||
| chr11:5629985 | G | C | 1 | a0001c0002t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-77-2270G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629985 | |||||||
| chr11:5629991 | C | T | 1 | a0001c0002t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-77-2264C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629991 | |||||||
| chr11:5629997 | C | T | 1 | a0001c0002t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-77-2258C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5629997 | |||||||
| chr11:5630001 | C | T | 3 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 |
3 | HG01243.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-77-2254C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630001 | |||||||
| chr11:5630029 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-77-2226A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630029 | |||||||
| chr11:5630035 | C | T | 1 | a0001c0005t0002g0047 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-77-2220C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630035 | |||||||
| chr11:5630067 | C | T | 1 | a0001c0002t0001g0189 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-77-2188C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630067 | |||||||
| chr11:5630295 | T | A | 80 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(77): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-77-1960T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630295 | |||||||
| chr11:5630589 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-77-1666C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630589 | |||||||
| chr11:5630590 | A | G | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-77-1665A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630590 | |||||||
| chr11:5630661 | T | G | 35 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0002t0001g0038 others(32): Show |
48 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.-77-1594T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630661 | |||||||
| chr11:5630662 | A | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01891.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-77-1593A>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630662 | |||||||
| chr11:5630803 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-77-1452T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630803 | |||||||
| chr11:5630980 | C | A | 2 | a0001c0002t0001g0221 a0001c0002t0001g0222 |
2 | NA18747.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-77-1275C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5630980 | |||||||
| chr11:5631064 | C | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.-77-1191C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5631064 | |||||||
| chr11:5631111 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.-77-1144A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5631111 | |||||||
| chr11:5631318 | G | A | 1 | a0001c0002t0001g0224 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-77-937G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5631318 | |||||||
| chr11:5631378 | G | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(264): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.-77-877G>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5631378 | |||||||
| chr11:5631562 | G | A | 8 | a0001c0002t0001g0041 a0001c0002t0001g0225 a0001c0002t0001g0226 others(5): Show |
9 | HG01981.hp2 HG02004.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77-693G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5631562 | |||||||
| chr11:5631743 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(268): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.-77-512G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5631743 | |||||||
| chr11:5631744 | T | C | 1 | a0008c0011t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-77-511T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5631744 | |||||||
| chr11:5631917 | G | C | 100 | a0001c0001t0001g0210 a0001c0001t0001g0214 a0001c0001t0001g0236 others(97): Show |
146 | HG00280.hp2 HG00544.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.-77-338G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5631917 | |||||||
| chr11:5632107 | G | A | 1 | a0002c0003t0001g0029 | 2 | HG00438.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-77-148G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 1/7 | chr11 | 5632107 | |||||||
| chr11:5632796 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.423+42T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5632796 | |||||||
| chr11:5632822 | C | CT | 52 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0028 others(49): Show |
66 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.423+90dupT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 5632822 | ||||||
| chr11:5632822 | CT | C | 9 | a0001c0001t0001g0056 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
15 | HG01975.hp2 HG03041.hp1 HG03579.hp2 others(12): Show |
intron_variant | MODIFIER | c.423+90delT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 5632822 | ||||||
| chr11:5632865 | C | T | 1 | a0003c0004t0001g0182 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.423+111C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5632865 | |||||||
| chr11:5632960 | C | G | 7 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0005t0001g0272 others(4): Show |
7 | HG01243.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+206C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5632960 | |||||||
| chr11:5632983 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.423+229C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5632983 | |||||||
| chr11:5632993 | AT | A | 10 | a0001c0001t0001g0063 a0001c0001t0001g0124 a0001c0001t0001g0181 others(7): Show |
10 | HG01192.hp1 HG01515.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.423+257delT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 5632993 | ||||||
| chr11:5632993 | ATT | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(251): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.423+256_423+257del others(2): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 5632993 | ||||||
| chr11:5633029 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0085 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.423+275G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633029 | |||||||
| chr11:5633146 | CT | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(211): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.423+411delT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr11 | 5633146 | ||||||
| chr11:5633150 | T | C | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0208 others(24): Show |
39 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.423+396T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633150 | |||||||
| chr11:5633151 | T | C | 2 | a0001c0001t0001g0274 a0001c0002t0001g0235 |
2 | HG03209.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.423+397T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633151 | |||||||
| chr11:5633153 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0002g0180 |
7 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+399T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633153 | |||||||
| chr11:5633202 | C | T | 1 | a0003c0004t0001g0182 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.423+448C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633202 | |||||||
| chr11:5633203 | G | A | 1 | a0001c0002t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.423+449G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633203 | |||||||
| chr11:5633251 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(268): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.423+497C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633251 | |||||||
| chr11:5633306 | G | A | 5 | a0001c0005t0001g0272 a0001c0005t0002g0047 a0001c0005t0002g0223 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-498G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633306 | |||||||
| chr11:5633340 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0192 |
2 | HG02148.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.424-464T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633340 | |||||||
| chr11:5633402 | A | G | 7 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0005t0001g0272 others(4): Show |
7 | HG01243.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424-402A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633402 | |||||||
| chr11:5633413 | T | C | 1 | a0001c0002t0001g0225 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.424-391T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633413 | |||||||
| chr11:5633514 | T | C | 5 | a0001c0005t0001g0272 a0001c0005t0002g0047 a0001c0005t0002g0223 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424-290T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633514 | |||||||
| chr11:5633555 | G | A | 4 | a0001c0001t0001g0061 a0001c0001t0002g0014 a0001c0001t0002g0064 others(1): Show |
6 | HG01943.hp1 HG02109.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-249G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633555 | |||||||
| chr11:5633573 | G | C | 1 | a0008c0011t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.424-231G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633573 | |||||||
| chr11:5633781 | G | C | 7 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0005t0001g0272 others(4): Show |
7 | HG01243.hp1 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424-23G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 2/7 | chr11 | 5633781 | |||||||
| chr11:5633920 | T | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(268): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.519+21T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5633920 | |||||||
| chr11:5634003 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.519+104G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634003 | |||||||
| chr11:5634163 | G | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.519+264G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634163 | |||||||
| chr11:5634203 | C | G | 1 | a0001c0002t0001g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.519+304C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634203 | |||||||
| chr11:5634263 | A | G | 6 | a0001c0001t0001g0061 a0001c0001t0002g0014 a0001c0001t0002g0064 others(3): Show |
8 | HG01943.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+364A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634263 | |||||||
| chr11:5634329 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.520-302A>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634329 | |||||||
| chr11:5634329 | A | T | 1 | a0001c0002t0001g0218 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.520-302A>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634329 | |||||||
| chr11:5634349 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.520-282G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634349 | |||||||
| chr11:5634450 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.520-181G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634450 | |||||||
| chr11:5634467 | A | AAT | 33 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0016 others(30): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.520-154_520-153dup others(2): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634467 | ||||||
| chr11:5634492 | T | TAC | 43 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0002g0078 others(40): Show |
71 | HG00609.hp2 HG00673.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.520-101_520-100dup others(2): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634492 | T | TACAC | 13 | a0001c0001t0001g0124 a0001c0002t0001g0039 a0001c0002t0001g0216 others(10): Show |
14 | HG00738.hp2 HG01361.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.520-103_520-100dup others(4): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634492 | T | TACACAC | 22 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0208 others(19): Show |
33 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.520-105_520-100dup others(6): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634492 | T | TACACACA others(3): Show |
1 | a0002c0003t0001g0030 | 2 | HG02015.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.520-109_520-100dup others(10): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634492 | TAC | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(121): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.520-101_520-100del others(2): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634492 | TACAC | T | 16 | a0001c0001t0001g0015 a0001c0001t0001g0102 a0001c0001t0001g0199 others(13): Show |
19 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.520-103_520-100del others(4): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634492 | TACACAC | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0098 a0001c0001t0001g0150 others(3): Show |
8 | HG00733.hp2 HG01167.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-105_520-100del others(6): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634492 | TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0108 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.520-109_520-100del others(10): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634492 | TACACACA others(9): Show |
T | 1 | a0001c0002t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.520-115_520-100del others(16): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634492 | ||||||
| chr11:5634524 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0002g0014 a0001c0001t0002g0064 others(1): Show |
6 | HG01943.hp1 HG02109.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-107C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634524 | |||||||
| chr11:5634524 | CACACACA others(3): Show |
C | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.520-105_520-96delC others(9): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634524 | ||||||
| chr11:5634526 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0002g0014 a0001c0001t0002g0064 others(1): Show |
6 | HG01943.hp1 HG02109.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-105C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634526 | |||||||
| chr11:5634528 | C | CATATATA others(11): Show |
1 | a0001c0001t0001g0063 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.520-102_520-101ins others(18): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634528 | ||||||
| chr11:5634528 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0002g0014 others(2): Show |
9 | HG00733.hp2 HG01943.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.520-103C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634528 | |||||||
| chr11:5634528 | CACAT | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0152 a0001c0002t0001g0256 others(1): Show |
4 | HG02145.hp2 HG03688.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-101_520-98delC others(3): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634528 | ||||||
| chr11:5634530 | C | CACACACA others(15): Show |
1 | a0001c0007t0002g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.520-100_520-99insC others(21): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | CACACACA others(9): Show |
1 | a0001c0002t0005g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.520-100_520-99insC others(15): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | CACACACA others(13): Show |
1 | a0001c0001t0002g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.520-100_520-99insC others(19): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | CACACAT | 3 | a0001c0002t0001g0238 a0001c0002t0001g0262 a0001c0002t0001g0270 |
3 | NA18949.hp2 NA19000.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.520-100_520-99insC others(5): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | CACACATA others(17): Show |
1 | a0001c0001t0001g0137 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.520-100_520-99insC others(23): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | CACAT | 2 | a0001c0002t0001g0024 a0001c0002t0001g0243 |
4 | HG02056.hp2 NA18973.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-100_520-99insC others(3): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | CACATATA others(13): Show |
1 | a0001c0001t0001g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.520-100_520-99insC others(19): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | CACATATA others(23): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.520-100_520-99insC others(29): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | CATATATA others(15): Show |
1 | a0001c0001t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-83_520-82insAT others(20): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr11 | 5634530 | ||||||
| chr11:5634530 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0061 a0001c0001t0001g0062 others(9): Show |
17 | HG00323.hp2 HG00733.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.520-101C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634530 | |||||||
| chr11:5634532 | T | C | 7 | a0001c0001t0001g0124 a0001c0001t0002g0079 a0001c0002t0001g0242 others(4): Show |
7 | HG00609.hp2 HG01243.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.520-99T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634532 | |||||||
| chr11:5634534 | T | C | 4 | a0001c0005t0001g0272 a0001c0005t0002g0047 a0001c0005t0002g0273 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-97T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634534 | |||||||
| chr11:5634536 | T | C | 4 | a0001c0005t0001g0272 a0001c0005t0002g0047 a0001c0005t0002g0273 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-95T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634536 | |||||||
| chr11:5634538 | T | C | 4 | a0001c0005t0001g0272 a0001c0005t0002g0047 a0001c0005t0002g0273 others(1): Show |
4 | HG01243.hp1 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-93T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634538 | |||||||
| chr11:5634548 | T | TATATATA others(10): Show |
1 | a0001c0001t0001g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.520-83_520-82insAT others(15): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 3/7 | chr11 | 5634548 | |||||||
| chr11:5634874 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.750+13G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5634874 | |||||||
| chr11:5634907 | C | T | 1 | a0001c0002t0001g0287 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.750+46C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5634907 | |||||||
| chr11:5634978 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.750+117G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5634978 | |||||||
| chr11:5635020 | T | C | 8 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0137 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.750+159T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635020 | |||||||
| chr11:5635093 | A | G | 10 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0002g0014 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.750+232A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635093 | |||||||
| chr11:5635138 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.750+277T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635138 | |||||||
| chr11:5635202 | GT | G | 5 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(2): Show |
7 | HG01943.hp1 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.750+343delT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5635202 | ||||||
| chr11:5635254 | A | AT | 7 | a0001c0001t0002g0252 a0001c0002t0001g0211 a0001c0002t0001g0226 others(4): Show |
8 | HG01109.hp2 HG01358.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.750+412dupT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5635254 | ||||||
| chr11:5635254 | A | ATT | 8 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(5): Show |
10 | HG01943.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.750+411_750+412dup others(2): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5635254 | ||||||
| chr11:5635254 | AT | A | 11 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0072 others(8): Show |
11 | HG00140.hp2 HG01168.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.750+412delT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5635254 | ||||||
| chr11:5635254 | ATT | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.750+411_750+412del others(2): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5635254 | ||||||
| chr11:5635319 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0178 a0001c0001t0001g0184 |
4 | HG02083.hp2 NA18612.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+458G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635319 | |||||||
| chr11:5635375 | A | C | 1 | a0001c0005t0002g0047 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.750+514A>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635375 | |||||||
| chr11:5635379 | C | T | 4 | a0001c0002t0001g0255 a0003c0004t0001g0088 a0003c0004t0001g0147 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.750+518C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635379 | |||||||
| chr11:5635458 | G | A | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.750+597G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635458 | |||||||
| chr11:5635513 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.750+652T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635513 | |||||||
| chr11:5635710 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.750+849T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635710 | |||||||
| chr11:5635878 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0070 others(4): Show |
13 | HG00438.hp2 NA18954.hp1 NA18960.hp2 others(10): Show |
intron_variant | MODIFIER | c.750+1017G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635878 | |||||||
| chr11:5635912 | T | C | 1 | a0001c0002t0001g0166 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.750+1051T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5635912 | |||||||
| chr11:5636048 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.750+1187G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636048 | |||||||
| chr11:5636108 | A | G | 1 | a0002c0003t0001g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.750+1247A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636108 | |||||||
| chr11:5636158 | T | C | 1 | a0001c0002t0005g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.750+1297T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636158 | |||||||
| chr11:5636283 | T | C | 2 | a0001c0002t0001g0154 a0001c0002t0001g0155 |
2 | NA18947.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.750+1422T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636283 | |||||||
| chr11:5636545 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0062 |
4 | HG00733.hp2 HG01192.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+1684A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636545 | |||||||
| chr11:5636875 | G | A | 1 | a0003c0004t0001g0167 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.750+2014G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636875 | |||||||
| chr11:5636957 | T | C | 24 | a0001c0001t0001g0168 a0001c0002t0005g0059 a0002c0003t0001g0010 others(21): Show |
32 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.750+2096T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636957 | |||||||
| chr11:5636963 | A | G | 8 | a0001c0002t0001g0041 a0001c0002t0001g0225 a0001c0002t0001g0226 others(5): Show |
9 | HG01981.hp2 HG02004.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+2102A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636963 | |||||||
| chr11:5636974 | G | A | 134 | a0001c0001t0001g0013 a0001c0001t0001g0058 a0001c0001t0001g0062 others(131): Show |
191 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.750+2113G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5636974 | |||||||
| chr11:5637003 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.750+2142G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637003 | |||||||
| chr11:5637066 | A | G | 25 | a0001c0001t0001g0168 a0001c0001t0001g0179 a0001c0002t0005g0059 others(22): Show |
33 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.750+2205A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637066 | |||||||
| chr11:5637098 | A | G | 136 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0058 others(133): Show |
198 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.750+2237A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637098 | |||||||
| chr11:5637122 | A | G | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.750+2261A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637122 | |||||||
| chr11:5637128 | G | T | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.750+2267G>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637128 | |||||||
| chr11:5637154 | CAG | C | 97 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(94): Show |
146 | HG00544.hp2 HG00609.hp2 HG00639.hp1 others(143): Show |
intron_variant | MODIFIER | c.750+2296_750+2297d others(4): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5637154 | ||||||
| chr11:5637155 | A | G | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.750+2294A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637155 | |||||||
| chr11:5637207 | T | C | 11 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(8): Show |
13 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.750+2346T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637207 | |||||||
| chr11:5637264 | G | A | 1 | a0002c0003t0001g0111 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.750+2403G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637264 | |||||||
| chr11:5637336 | C | T | 131 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0168 others(128): Show |
190 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.750+2475C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637336 | |||||||
| chr11:5637399 | C | A | 1 | a0008c0011t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.750+2538C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637399 | |||||||
| chr11:5637465 | T | G | 1 | a0002c0003t0001g0220 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.750+2604T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637465 | |||||||
| chr11:5637473 | A | C | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.750+2612A>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637473 | |||||||
| chr11:5637487 | T | A | 1 | a0003c0004t0001g0187 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.750+2626T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637487 | |||||||
| chr11:5637524 | G | A | 2 | a0002c0003t0001g0112 a0002c0003t0001g0116 |
2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.750+2663G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637524 | |||||||
| chr11:5637578 | A | T | 1 | a0001c0002t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.750+2717A>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637578 | |||||||
| chr11:5637773 | A | G | 1 | a0002c0003t0001g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.750+2912A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637773 | |||||||
| chr11:5637799 | T | G | 1 | a0001c0005t0002g0273 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.750+2938T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637799 | |||||||
| chr11:5637826 | G | A | 136 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0168 others(133): Show |
195 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.750+2965G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637826 | |||||||
| chr11:5637942 | A | G | 138 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0168 others(135): Show |
197 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.750+3081A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637942 | |||||||
| chr11:5637976 | C | G | 138 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0168 others(135): Show |
197 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.750+3115C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5637976 | |||||||
| chr11:5638057 | A | G | 1 | a0001c0002t0001g0025 | 3 | HG00673.hp2 NA18971.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.751-3110A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638057 | |||||||
| chr11:5638111 | A | G | 138 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0168 others(135): Show |
197 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.751-3056A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638111 | |||||||
| chr11:5638122 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.751-3045T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638122 | |||||||
| chr11:5638298 | G | A | 1 | a0001c0005t0002g0223 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.751-2869G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638298 | |||||||
| chr11:5638325 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.751-2842A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638325 | |||||||
| chr11:5638450 | C | T | 138 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(135): Show |
197 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(194): Show |
intron_variant | MODIFIER | c.751-2717C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638450 | |||||||
| chr11:5638501 | GT | G | 137 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(134): Show |
196 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.751-2664delT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5638501 | ||||||
| chr11:5638544 | A | G | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-2623A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638544 | |||||||
| chr11:5638762 | A | C | 1 | a0001c0005t0002g0273 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.751-2405A>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638762 | |||||||
| chr11:5638776 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0151 |
4 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.751-2391G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638776 | |||||||
| chr11:5638793 | T | C | 127 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(124): Show |
184 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.751-2374T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638793 | |||||||
| chr11:5638809 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0152 |
2 | HG01167.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.751-2358A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5638809 | |||||||
| chr11:5639006 | C | G | 1 | a0001c0007t0002g0060 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.751-2161C>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639006 | |||||||
| chr11:5639136 | C | A | 2 | a0001c0001t0002g0180 a0001c0005t0002g0047 |
2 | HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.751-2031C>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639136 | |||||||
| chr11:5639138 | A | G | 1 | a0008c0011t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751-2029A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639138 | |||||||
| chr11:5639228 | G | A | 126 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(123): Show |
183 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.751-1939G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639228 | |||||||
| chr11:5639251 | G | A | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-1916G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639251 | |||||||
| chr11:5639265 | T | G | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-1902T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639265 | |||||||
| chr11:5639282 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0062 |
4 | HG00733.hp2 HG01192.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.751-1885A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639282 | |||||||
| chr11:5639403 | A | G | 137 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(134): Show |
196 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.751-1764A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639403 | |||||||
| chr11:5639449 | A | G | 137 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(134): Show |
196 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.751-1718A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639449 | |||||||
| chr11:5639451 | A | C | 137 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(134): Show |
196 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.751-1716A>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639451 | |||||||
| chr11:5639525 | T | A | 137 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(134): Show |
196 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.751-1642T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639525 | |||||||
| chr11:5639610 | G | A | 1 | a0001c0002t0001g0257 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.751-1557G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639610 | |||||||
| chr11:5639645 | A | G | 127 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(124): Show |
184 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.751-1522A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639645 | |||||||
| chr11:5639679 | C | CA | 10 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0096 others(7): Show |
10 | HG00733.hp1 HG01069.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.751-1460dupA | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | C | CAA | 27 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
51 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.751-1461_751-1460d others(4): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | C | CAAA | 7 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0106 others(4): Show |
9 | HG01069.hp1 HG01261.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.751-1462_751-1460d others(5): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | C | CAAAA | 34 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(31): Show |
62 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.751-1463_751-1460d others(6): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | C | CAAAAA | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0061 others(18): Show |
28 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.751-1464_751-1460d others(7): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | C | CAAAAAA | 9 | a0001c0001t0001g0037 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
10 | HG00099.hp2 HG01978.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.751-1465_751-1460d others(8): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | C | CAAAAAAA | 9 | a0001c0001t0001g0011 a0001c0001t0001g0136 a0001c0001t0001g0165 others(6): Show |
12 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.751-1466_751-1460d others(9): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0036 a0001c0001t0001g0170 a0001c0001t0001g0198 others(4): Show |
8 | HG00621.hp2 HG02132.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.751-1467_751-1460d others(10): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | C | CAAAAAAA others(3): Show |
3 | a0003c0004t0001g0125 a0003c0004t0001g0133 a0003c0004t0001g0147 |
3 | HG02109.hp2 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.751-1469_751-1460d others(12): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | CA | C | 50 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(47): Show |
71 | HG00438.hp1 HG00558.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.751-1460delA | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639679 | CAA | C | 6 | a0001c0002t0001g0049 a0001c0002t0001g0229 a0001c0002t0001g0259 others(3): Show |
6 | HG00639.hp1 HG01978.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.751-1461_751-1460d others(4): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639679 | ||||||
| chr11:5639696 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0002g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.751-1469_751-1458d others(14): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639696 | ||||||
| chr11:5639697 | AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0002g0014 a0001c0001t0002g0065 a0001c0001t0002g0149 |
5 | HG01943.hp1 HG02559.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-1468_751-1458d others(13): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5639697 | ||||||
| chr11:5639707 | AG | A | 5 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0005t0002g0047 others(2): Show |
5 | HG01243.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-1459delG | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639707 | |||||||
| chr11:5639708 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.751-1459G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639708 | |||||||
| chr11:5639782 | A | G | 1 | a0007c0010t0001g0142 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.751-1385A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639782 | |||||||
| chr11:5639791 | G | T | 138 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(135): Show |
197 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(194): Show |
intron_variant | MODIFIER | c.751-1376G>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639791 | |||||||
| chr11:5639816 | T | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.751-1351T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639816 | |||||||
| chr11:5639828 | T | A | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-1339T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639828 | |||||||
| chr11:5639851 | T | G | 1 | a0001c0001t0001g0100 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.751-1316T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639851 | |||||||
| chr11:5639923 | A | G | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-1244A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5639923 | |||||||
| chr11:5640005 | T | C | 1 | a0001c0001t0001g0013 | 3 | HG00733.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.751-1162T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640005 | |||||||
| chr11:5640080 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0085 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.751-1087T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640080 | |||||||
| chr11:5640145 | T | A | 1 | a0003c0004t0001g0176 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.751-1022T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640145 | |||||||
| chr11:5640190 | C | T | 127 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(124): Show |
184 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.751-977C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640190 | |||||||
| chr11:5640203 | C | T | 1 | a0001c0002t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.751-964C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640203 | |||||||
| chr11:5640204 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0085 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.751-963G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640204 | |||||||
| chr11:5640278 | C | T | 127 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(124): Show |
184 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(181): Show |
intron_variant | MODIFIER | c.751-889C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640278 | |||||||
| chr11:5640329 | G | GT | 11 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(8): Show |
13 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.751-830dupT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5640329 | ||||||
| chr11:5640331 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.751-836T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640331 | |||||||
| chr11:5640384 | G | A | 1 | a0008c0011t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751-783G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640384 | |||||||
| chr11:5640493 | GC | G | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-672delC | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5640493 | ||||||
| chr11:5640577 | G | T | 1 | a0001c0002t0005g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.751-590G>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640577 | |||||||
| chr11:5640613 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.751-554C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640613 | |||||||
| chr11:5640728 | T | C | 1 | a0001c0002t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.751-439T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640728 | |||||||
| chr11:5640778 | G | A | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-389G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640778 | |||||||
| chr11:5640839 | T | C | 1 | a0008c0011t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751-328T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640839 | |||||||
| chr11:5640863 | A | G | 1 | a0008c0011t0001g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751-304A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640863 | |||||||
| chr11:5640940 | C | CTCA | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.751-225_751-223dup others(3): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr11 | 5640940 | ||||||
| chr11:5640952 | T | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(57): Show |
97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.751-215T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5640952 | |||||||
| chr11:5641065 | A | C | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.751-102A>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5641065 | |||||||
| chr11:5641089 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.751-78C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 4/7 | chr11 | 5641089 | |||||||
| chr11:5641207 | G | C | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.773+18G>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641207 | |||||||
| chr11:5641247 | T | G | 1 | a0001c0002t0001g0043 | 2 | NA18964.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.773+58T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641247 | |||||||
| chr11:5641354 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.773+165G>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641354 | |||||||
| chr11:5641381 | T | G | 137 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(134): Show |
196 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.773+192T>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641381 | |||||||
| chr11:5641382 | T | C | 1 | a0001c0002t0005g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.773+193T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641382 | |||||||
| chr11:5641458 | C | T | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.773+269C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641458 | |||||||
| chr11:5641777 | T | C | 10 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(7): Show |
12 | HG01243.hp1 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.773+588T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641777 | |||||||
| chr11:5641811 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0178 a0001c0001t0001g0184 |
4 | HG02083.hp2 NA18612.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.774-595A>G | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641811 | |||||||
| chr11:5641814 | G | T | 3 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0005t0002g0223 |
3 | HG02486.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.774-592G>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641814 | |||||||
| chr11:5641818 | T | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(125): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.774-588T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641818 | |||||||
| chr11:5641869 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.774-537T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5641869 | |||||||
| chr11:5642005 | C | T | 128 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0214 others(125): Show |
185 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.774-401C>T | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5642005 | |||||||
| chr11:5642345 | T | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.774-61T>C | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 5/7 | chr11 | 5642345 | |||||||
| chr11:5642690 | CT | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(258): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.875-122delT | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr11 | 5642690 | ||||||
| chr11:5643114 | C | CATATAT | 31 | a0001c0002t0001g0045 a0001c0002t0001g0048 a0001c0002t0001g0049 others(28): Show |
40 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.902-23_902-18dupAT others(4): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 5643114 | ||||||
| chr11:5643125 | A | ATATAT | 17 | a0001c0002t0001g0033 a0001c0002t0001g0039 a0001c0002t0001g0042 others(14): Show |
20 | HG00544.hp2 HG00733.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.902-18_902-17insAT others(3): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 5643125 | ||||||
| chr11:5643125 | A | ATATATAT | 11 | a0001c0001t0001g0070 a0001c0001t0001g0095 a0001c0001t0001g0106 others(8): Show |
11 | HG00099.hp2 HG00408.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.902-18_902-17insAT others(5): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 5643125 | ||||||
| chr11:5643125 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0056 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.902-18_902-17insAT others(9): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 5643125 | ||||||
| chr11:5643125 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.902-18_902-17insAT others(9): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 5643125 | ||||||
| chr11:5643125 | A | ATATATT | 14 | a0001c0001t0001g0013 a0001c0001t0001g0058 a0001c0001t0001g0062 others(11): Show |
16 | HG00733.hp2 HG01109.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.902-18_902-17insAT others(4): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | 5643125 | ||||||
| chr11:5643126 | T | TA | 5 | a0001c0001t0002g0014 a0001c0001t0002g0064 a0001c0001t0002g0065 others(2): Show |
7 | HG01943.hp1 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.902-18_902-17insA | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | chr11 | 5643126 | |||||||
| chr11:5643126 | T | TATATA | 70 | a0001c0001t0001g0196 a0001c0002t0001g0002 a0001c0002t0001g0005 others(67): Show |
113 | HG00609.hp2 HG00673.hp2 HG01074.hp2 others(110): Show |
intron_variant | MODIFIER | c.902-18_902-17insAT others(3): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | chr11 | 5643126 | |||||||
| chr11:5643126 | T | TATATAGA | 24 | a0003c0004t0001g0012 a0003c0004t0001g0022 a0003c0004t0001g0034 others(21): Show |
29 | HG00323.hp2 HG00597.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.902-18_902-17insAT others(5): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | chr11 | 5643126 | |||||||
| chr11:5643126 | T | TATATATA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(79): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.902-18_902-17insAT others(5): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | chr11 | 5643126 | |||||||
| chr11:5643126 | T | TATATATA others(2): Show |
3 | a0001c0001t0001g0162 a0001c0001t0001g0170 a0001c0001t0001g0172 |
3 | HG02132.hp1 HG02165.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.902-18_902-17insAT others(7): Show |
TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | chr11 | 5643126 | |||||||
| chr11:5643127 | T | A | 7 | a0001c0001t0001g0173 a0001c0002t0001g0154 a0001c0002t0001g0155 others(4): Show |
7 | HG00735.hp1 HG01109.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.902-17T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | chr11 | 5643127 | |||||||
| chr11:5643128 | T | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0094 others(8): Show |
16 | HG00558.hp2 HG00642.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.902-16T>A | TRIM34 | ENSG00000258659.7 | transcript | ENST00000429814.3 | protein_coding | 7/7 | chr11 | 5643128 |