Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5987 |
| ensemblid | ENSG00000204713.11 |
| hgncid | 9975 |
| symbol | TRIM27 |
| name | tripartite motif containing 27 |
| refseq_nuc | NM_006510.5 |
| refseq_prot | NP_006501.1 |
| ensembl_nuc | ENST00000377199.4 |
| ensembl_prot | ENSP00000366404.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 28903002 |
| end | 28923985 |
| strand | - |
| ver | v1.2 |
| region | chr6:28903002-28923985 |
| region5000 | chr6:28898002-28928985 |
| regionname0 | TRIM27_chr6_28903002_28923985 |
| regionname5000 | TRIM27_chr6_28898002_28928985 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 513 | 408 | 95 | 70 | 182 | 16 | 44 | 140 | TRIM27_chr6_28898002_28928985 | TRIM27 | MASGS others(508): Show |
chr6 | 28898002 | 28928985 |
| a0002 | 0/0 | 513 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | MASGN others(508): Show |
chr6 | 28898002 | 28928985 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1539 | 395 | 89 | 66 | 182 | 15 | 42 | TRIM27_chr6_28898002_28928985 | TRIM27 | ATGGC others(1534): Show |
chr6 | 28898002 | 28928985 | ||
| a0001c0002 | 0/0 | 1539 | 5 | 0 | 4 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ATGGC others(1534): Show |
chr6 | 28898002 | 28928985 | ||
| a0001c0003 | 0/0 | 1539 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ATGGC others(1534): Show |
chr6 | 28898002 | 28928985 | ||
| a0001c0005 | 0/0 | 1539 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | ATGGC others(1534): Show |
chr6 | 28898002 | 28928985 | ||
| a0001c0006 | 0/0 | 1539 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | ATGGC others(1534): Show |
chr6 | 28898002 | 28928985 | ||
| a0001c0007 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ATGGC others(1534): Show |
chr6 | 28898002 | 28928985 | ||
| a0001c0008 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ATGGC others(1534): Show |
chr6 | 28898002 | 28928985 | ||
| a0002c0004 | 0/0 | 1539 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ATGGC others(1534): Show |
chr6 | 28898002 | 28928985 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2963 | 194 | 53 | 28 | 87 | 7 | 18 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0002 | 0/0 | 2963 | 128 | 15 | 28 | 60 | 6 | 19 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0003 | 0/0 | 2963 | 51 | 9 | 9 | 29 | 2 | 2 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0004 | 0/0 | 2962 | 6 | 6 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2957): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0005 | 0/0 | 2963 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0006 | 0/0 | 2963 | 4 | 0 | 0 | 2 | 0 | 2 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0007 | 0/0 | 2963 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0008 | 0/0 | 2963 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0009 | 0/0 | 2963 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0010 | 0/0 | 2963 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0001t0011 | 0/0 | 2963 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0002t0002 | 0/0 | 2963 | 5 | 0 | 4 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0003t0003 | 0/0 | 2963 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0005t0002 | 0/0 | 2963 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0006t0012 | 0/0 | 2963 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0007t0002 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0001c0008t0001 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| a0002c0004t0001 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | ACGCT others(2958): Show |
chr6 | 28898002 | 28928985 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 0 | 2 | 15 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 4 | 8 | 1 | 2 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0005 | 0/0 | 7 | 2 | 0 | 5 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0007 | 0/1 | 6 | 0 | 0 | 3 | 0 | 2 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0008 | 0/0 | 6 | 3 | 0 | 0 | 2 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0011 | 0/0 | 5 | 2 | 2 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0002 | 0/0 | 17 | 0 | 3 | 10 | 0 | 4 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0004 | 0/0 | 13 | 0 | 4 | 6 | 0 | 3 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0006 | 0/0 | 7 | 0 | 1 | 4 | 1 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0055 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0004g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0004g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0006g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0010g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0001t0011g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0003t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0005t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0006t0012g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0007t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0001c0008t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| a0002c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0135 | EUR | GBR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | GBR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | FIN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0060 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00544 | hp1 | a0001 | c0001 | t0010 | g0211 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0059 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0227 | EAS | CHS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0134 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0240 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0256 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | IBS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | IBS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | IBS | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02055 | hp2 | a0001 | c0007 | t0002 | g0112 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0201 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CDX | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02630 | hp1 | a0001 | c0003 | t0003 | g0248 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02683 | hp2 | a0001 | c0005 | t0002 | g0073 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0044 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02895 | hp1 | a0001 | c0008 | t0001 | g0217 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0246 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0245 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03239 | hp1 | a0001 | c0006 | t0012 | g0258 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0247 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0132 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04115 | hp1 | a0001 | c0001 | t0009 | g0058 | SAS | STU | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0205 | SAS | STU | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | STU | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18906 | hp2 | a0002 | c0004 | t0001 | g0139 | AFR | YRI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | LWK | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | LWK | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0255 | AFR | LWK | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | YRI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ASW | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ASW | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0237 | EUR | TSI | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | GIH | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0138 | AMR | CLM | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | USA | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | USA | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | LWK | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0257 | AFR | LWK | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0007 | REF | REF | TRIM27_chr6_28898002_28928985 | TRIM27 | chr6 | 28898002 | 28928985 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:28921912 | G | C | 1 | a0002 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.496C>G | p.Gln166Glu | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/8 | 849/2963 | 496/1542 | 166/513 | chr6 | 28921912 | |||
| chr6:28923619 | C | T | 1 | a0002 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.14G>A | p.Ser5Asn | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | 367/2963 | 14/1542 | 5/513 | chr6 | 28923619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:28904415 | G | A | 1 | a0001c0006 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.1197C>T | p.Thr399Thr | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 8/8 | 1550/2963 | 1197/1542 | 399/513 | chr6 | 28904415 | |||
| chr6:28904631 | G | C | 1 | a0001c0007 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.981C>G | p.Pro327Pro | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 8/8 | 1334/2963 | 981/1542 | 327/513 | chr6 | 28904631 | |||
| chr6:28920075 | G | A | 1 | a0001c0003 | 4 | HG02630.hp1 HG02896.hp1 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.684C>T | p.His228His | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/8 | 1037/2963 | 684/1542 | 228/513 | chr6 | 28920075 | |||
| chr6:28920234 | G | T | 1 | a0001c0005 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.525C>A | p.Thr175Thr | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/8 | 878/2963 | 525/1542 | 175/513 | chr6 | 28920234 | |||
| chr6:28923399 | T | C | 1 | a0001c0002 | 5 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
synonymous_variant | LOW | c.234A>G | p.Val78Val | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | 587/2963 | 234/1542 | 78/513 | chr6 | 28923399 | |||
| chr6:28923546 | G | A | 1 | a0001c0008 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.87C>T | p.Leu29Leu | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | 440/2963 | 87/1542 | 29/513 | chr6 | 28923546 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:28903070 | C | T | 1 | a0001c0001t0005 | 4 | HG02572.hp1 HG02723.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1000G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 8/8 | 1000 | chr6 | 28903070 | ||||||
| chr6:28903198 | C | T | 5 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(2): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*872G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 8/8 | 872 | chr6 | 28903198 | ||||||
| chr6:28903237 | A | G | 1 | a0001c0001t0010 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*833T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 8/8 | 833 | chr6 | 28903237 | ||||||
| chr6:28903271 | G | A | 1 | a0001c0001t0006 | 4 | HG02080.hp1 HG02735.hp2 HG04199.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*799C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 8/8 | 799 | chr6 | 28903271 | ||||||
| chr6:28904028 | T | A | 1 | a0001c0001t0011 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 8/8 | 42 | chr6 | 28904028 | ||||||
| chr6:28923646 | G | A | 5 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(2): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-14C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | chr6 | 28923646 | |||||||
| chr6:28923681 | T | C | 6 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(3): Show |
206 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(203): Show |
5_prime_UTR_variant | MODIFIER | c.-49A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | 49 | chr6 | 28923681 | ||||||
| chr6:28923692 | C | A | 1 | a0001c0001t0007 | 3 | HG01255.hp2 NA19043.hp1 NA21309.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60G>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | chr6 | 28923692 | |||||||
| chr6:28923736 | CG | C | 1 | a0001c0001t0004 | 6 | HG02922.hp1 HG03098.hp1 HG03453.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-105delC | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | 105 | chr6 | 28923736 | ||||||
| chr6:28923745 | G | A | 5 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0009 others(2): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-113C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | chr6 | 28923745 | |||||||
| chr6:28923755 | G | A | 1 | a0001c0006t0012 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-123C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | 123 | chr6 | 28923755 | ||||||
| chr6:28923845 | C | T | 1 | a0001c0001t0008 | 2 | HG00408.hp2 HG00544.hp2 |
5_prime_UTR_variant | MODIFIER | c.-213G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | 213 | chr6 | 28923845 | ||||||
| chr6:28923949 | A | G | 1 | a0001c0001t0009 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-317T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/8 | 317 | chr6 | 28923949 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:28904669 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(178): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
splice_region_variant&intron_variant | LOW | c.947-4A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28904669 | |||||||
| chr6:28904847 | G | C | 14 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0062 others(11): Show |
16 | HG01175.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.947-182C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28904847 | |||||||
| chr6:28904853 | T | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.947-188A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28904853 | |||||||
| chr6:28904965 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
206 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.947-300G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28904965 | |||||||
| chr6:28905198 | C | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0215 |
6 | NA18950.hp1 NA18954.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.947-533G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905198 | |||||||
| chr6:28905238 | G | A | 4 | a0001c0001t0005g0129 a0001c0001t0005g0130 a0001c0001t0005g0131 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-573C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905238 | |||||||
| chr6:28905252 | A | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
19 | HG00544.hp1 HG01192.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.947-587T>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905252 | |||||||
| chr6:28905255 | C | G | 2 | a0001c0001t0002g0085 a0001c0001t0002g0101 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.947-590G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905255 | |||||||
| chr6:28905276 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0147 a0001c0001t0001g0152 others(2): Show |
9 | HG00735.hp2 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.947-611T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905276 | |||||||
| chr6:28905283 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.947-618A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905283 | |||||||
| chr6:28905384 | A | C | 46 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(43): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.947-719T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905384 | |||||||
| chr6:28905391 | A | C | 1 | a0001c0001t0002g0095 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.947-726T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905391 | |||||||
| chr6:28905471 | A | AT | 14 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0062 others(11): Show |
16 | HG01175.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.947-807dupA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28905471 | |||||||
| chr6:28906057 | G | C | 2 | a0001c0001t0003g0220 a0001c0001t0003g0221 |
2 | HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.946+1179C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906057 | |||||||
| chr6:28906181 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.946+1055G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906181 | |||||||
| chr6:28906211 | T | C | 1 | a0001c0001t0003g0237 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.946+1025A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906211 | |||||||
| chr6:28906221 | A | T | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.946+1015T>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906221 | |||||||
| chr6:28906595 | T | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0125 |
3 | HG02109.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.946+641A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906595 | |||||||
| chr6:28906702 | C | T | 1 | a0001c0001t0003g0239 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.946+534G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906702 | |||||||
| chr6:28906751 | C | G | 1 | a0001c0001t0002g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.946+485G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906751 | |||||||
| chr6:28906761 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0156 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.946+475C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906761 | |||||||
| chr6:28906775 | G | A | 3 | a0001c0001t0007g0255 a0001c0001t0007g0256 a0001c0001t0007g0257 |
3 | HG01255.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.946+461C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906775 | |||||||
| chr6:28906968 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.946+268C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906968 | |||||||
| chr6:28906979 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.946+257C>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 7/7 | chr6 | 28906979 | |||||||
| chr6:28907417 | T | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0198 |
2 | HG02155.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.920-155A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28907417 | |||||||
| chr6:28907555 | C | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
6 | HG02896.hp2 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-293G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28907555 | |||||||
| chr6:28907724 | T | C | 5 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-462A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28907724 | |||||||
| chr6:28907725 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.920-463G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28907725 | |||||||
| chr6:28907731 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0035 others(3): Show |
13 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.920-469G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28907731 | |||||||
| chr6:28907909 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.920-647A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28907909 | |||||||
| chr6:28908182 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0197 |
6 | HG00609.hp1 HG02155.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+626C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28908182 | |||||||
| chr6:28908192 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0156 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.919+616A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28908192 | |||||||
| chr6:28908273 | T | C | 4 | a0001c0001t0002g0067 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+535A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28908273 | |||||||
| chr6:28908420 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.919+388G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28908420 | |||||||
| chr6:28908548 | GGATT | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.919+256_919+259del others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28908548 | |||||||
| chr6:28908553 | GATTA | G | 4 | a0001c0001t0002g0067 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+251_919+254del others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28908553 | |||||||
| chr6:28908732 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(75): Show |
145 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.919+76C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 6/7 | chr6 | 28908732 | |||||||
| chr6:28908869 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.887-29C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 5/7 | chr6 | 28908869 | |||||||
| chr6:28909112 | A | AT | 8 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(5): Show |
8 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.771-25dupA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909112 | |||||||
| chr6:28909188 | AC | A | 46 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(43): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.771-101delG | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909188 | |||||||
| chr6:28909211 | G | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01255.hp1 HG02602.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.771-123C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909211 | |||||||
| chr6:28909254 | T | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0180 a0001c0001t0001g0186 others(3): Show |
7 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.771-166A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909254 | |||||||
| chr6:28909296 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.771-208C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909296 | |||||||
| chr6:28909470 | T | C | 5 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.771-382A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909470 | |||||||
| chr6:28909646 | A | G | 2 | a0001c0001t0002g0085 a0001c0001t0002g0101 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.771-558T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909646 | |||||||
| chr6:28909958 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.771-870A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909958 | |||||||
| chr6:28909993 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.771-905T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909993 | |||||||
| chr6:28909996 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.771-908T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28909996 | |||||||
| chr6:28910109 | C | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.771-1021G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910109 | |||||||
| chr6:28910123 | G | GA | 30 | a0001c0001t0002g0017 a0001c0001t0002g0025 a0001c0001t0002g0027 others(27): Show |
35 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.771-1036dupT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910123 | |||||||
| chr6:28910123 | G | GAA | 34 | a0001c0001t0002g0031 a0001c0001t0002g0062 a0001c0001t0002g0067 others(31): Show |
46 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.771-1037_771-1036d others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910123 | |||||||
| chr6:28910123 | G | GAAA | 14 | a0001c0001t0002g0030 a0001c0001t0002g0069 a0001c0001t0002g0121 others(11): Show |
17 | HG00673.hp2 HG01884.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.771-1038_771-1036d others(5): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910123 | |||||||
| chr6:28910123 | GA | G | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0158 others(3): Show |
6 | HG00738.hp1 HG01167.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-1036delT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910123 | |||||||
| chr6:28910123 | GAAAAA | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0156 others(3): Show |
7 | HG02027.hp2 HG02683.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.771-1040_771-1036d others(7): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910123 | |||||||
| chr6:28910123 | GAAAAAA | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
195 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.771-1041_771-1036d others(8): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910123 | |||||||
| chr6:28910124 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.771-1036T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910124 | |||||||
| chr6:28910142 | A | C | 1 | a0001c0001t0006g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.771-1054T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910142 | |||||||
| chr6:28910143 | A | C | 1 | a0001c0001t0002g0087 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.771-1055T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910143 | |||||||
| chr6:28910269 | G | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0194 |
2 | NA18985.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.771-1181C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910269 | |||||||
| chr6:28910284 | A | G | 2 | a0001c0001t0002g0031 a0001c0001t0002g0125 |
3 | HG02109.hp1 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.771-1196T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910284 | |||||||
| chr6:28910332 | CT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
202 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.771-1245delA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910332 | |||||||
| chr6:28910335 | T | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
202 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.771-1247A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910335 | |||||||
| chr6:28910406 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0207 others(3): Show |
15 | HG01099.hp1 HG01106.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.770+1290A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910406 | |||||||
| chr6:28910415 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0171 |
2 | HG01192.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.770+1281G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910415 | |||||||
| chr6:28910437 | G | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.770+1259C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910437 | |||||||
| chr6:28910620 | G | A | 1 | a0001c0001t0003g0222 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.770+1076C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910620 | |||||||
| chr6:28910683 | C | G | 1 | a0001c0001t0002g0100 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.770+1013G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910683 | |||||||
| chr6:28910749 | G | T | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.770+947C>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910749 | |||||||
| chr6:28910789 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.770+907C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910789 | |||||||
| chr6:28910814 | A | G | 1 | a0001c0002t0002g0134 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.770+882T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910814 | |||||||
| chr6:28910864 | T | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0179 a0001c0001t0001g0182 |
4 | NA18612.hp2 NA18939.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+832A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910864 | |||||||
| chr6:28910890 | A | T | 1 | a0001c0001t0003g0223 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.770+806T>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28910890 | |||||||
| chr6:28911061 | A | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | NA18961.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.770+635T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28911061 | |||||||
| chr6:28911101 | C | A | 4 | a0001c0001t0003g0056 a0001c0001t0003g0240 a0001c0001t0003g0241 others(1): Show |
5 | HG00642.hp2 HG01081.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+595G>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28911101 | |||||||
| chr6:28911208 | C | CT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.770+487dupA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28911208 | |||||||
| chr6:28911288 | T | C | 1 | a0001c0001t0007g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.770+408A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28911288 | |||||||
| chr6:28911339 | G | GAA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
203 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.770+355_770+356dup others(2): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28911339 | |||||||
| chr6:28911351 | T | A | 1 | a0001c0001t0001g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.770+345A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 4/7 | chr6 | 28911351 | |||||||
| chr6:28911978 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.748-260G>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28911978 | |||||||
| chr6:28911997 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
9 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.748-279C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28911997 | |||||||
| chr6:28912064 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.748-346G>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912064 | |||||||
| chr6:28912106 | C | CT | 12 | a0001c0001t0001g0159 a0001c0001t0001g0187 a0001c0001t0001g0208 others(9): Show |
12 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.748-389dupA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912106 | |||||||
| chr6:28912106 | CT | C | 54 | a0001c0001t0001g0035 a0001c0001t0001g0150 a0001c0001t0001g0151 others(51): Show |
69 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.748-389delA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912106 | |||||||
| chr6:28912157 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.748-439A>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912157 | |||||||
| chr6:28912330 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0035 others(3): Show |
13 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.748-612C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912330 | |||||||
| chr6:28912362 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0071 a0001c0001t0002g0072 |
4 | HG01934.hp2 HG01978.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-644C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912362 | |||||||
| chr6:28912441 | CTT | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0181 others(5): Show |
16 | HG02080.hp1 HG02735.hp2 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.748-725_748-724del others(2): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912441 | |||||||
| chr6:28912604 | T | A | 9 | a0001c0001t0002g0030 a0001c0001t0002g0069 a0001c0001t0002g0074 others(6): Show |
10 | HG01175.hp1 HG02145.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.748-886A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912604 | |||||||
| chr6:28912641 | T | C | 1 | a0001c0001t0002g0106 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.748-923A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912641 | |||||||
| chr6:28912737 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.748-1019T>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912737 | |||||||
| chr6:28912738 | T | A | 1 | a0001c0001t0001g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.748-1020A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912738 | |||||||
| chr6:28912742 | CAAATATA others(37): Show |
C | 1 | a0001c0001t0002g0116 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.748-1068_748-1025d others(46): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912742 | |||||||
| chr6:28912793 | A | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
19 | HG00544.hp1 HG01192.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.748-1075T>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912793 | |||||||
| chr6:28912839 | C | T | 1 | a0001c0001t0002g0023 | 2 | HG00280.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.748-1121G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912839 | |||||||
| chr6:28912852 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.748-1134A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912852 | |||||||
| chr6:28912853 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
203 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.748-1135C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912853 | |||||||
| chr6:28912876 | G | C | 14 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0062 others(11): Show |
16 | HG01175.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.748-1158C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912876 | |||||||
| chr6:28912931 | G | C | 1 | a0002c0004t0001g0139 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.748-1213C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28912931 | |||||||
| chr6:28913005 | C | T | 1 | a0001c0001t0007g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.748-1287G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913005 | |||||||
| chr6:28913030 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0156 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.748-1312G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913030 | |||||||
| chr6:28913084 | C | T | 2 | a0001c0001t0003g0223 a0001c0001t0003g0224 |
2 | HG01361.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.748-1366G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913084 | |||||||
| chr6:28913085 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.748-1367C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913085 | |||||||
| chr6:28913169 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.748-1451G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913169 | |||||||
| chr6:28913255 | CA | C | 9 | a0001c0001t0001g0143 a0001c0001t0001g0177 a0001c0001t0001g0178 others(6): Show |
9 | HG03041.hp1 HG03041.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.748-1538delT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913255 | |||||||
| chr6:28913267 | A | AAT | 10 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(7): Show |
10 | HG00673.hp2 HG01255.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.748-1550_748-1549i others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913267 | |||||||
| chr6:28913267 | A | AT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0018 others(10): Show |
24 | HG00735.hp2 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.748-1550_748-1549i others(3): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913267 | |||||||
| chr6:28913267 | A | T | 8 | a0001c0001t0001g0147 a0001c0001t0002g0092 a0001c0001t0004g0219 others(5): Show |
8 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.748-1549T>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913267 | |||||||
| chr6:28913269 | A | AAT | 32 | a0001c0001t0001g0186 a0001c0001t0002g0094 a0001c0001t0002g0113 others(29): Show |
42 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.748-1553_748-1552d others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913269 | |||||||
| chr6:28913269 | A | AATAT | 10 | a0001c0001t0002g0133 a0001c0001t0003g0014 a0001c0001t0003g0057 others(7): Show |
14 | HG01981.hp1 HG02056.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.748-1555_748-1552d others(6): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913269 | |||||||
| chr6:28913269 | A | AT | 19 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0045 others(16): Show |
25 | HG01168.hp2 HG01169.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.748-1552_748-1551i others(3): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913269 | |||||||
| chr6:28913269 | A | T | 58 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
85 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.748-1551T>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913269 | |||||||
| chr6:28913271 | T | A | 7 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0016 others(4): Show |
9 | HG02451.hp2 HG02622.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.748-1553A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913271 | |||||||
| chr6:28913287 | T | A | 5 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-1569A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913287 | |||||||
| chr6:28913294 | C | T | 4 | a0001c0003t0003g0245 a0001c0003t0003g0246 a0001c0003t0003g0247 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-1576G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913294 | |||||||
| chr6:28913295 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.748-1577C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913295 | |||||||
| chr6:28913347 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0035 others(3): Show |
13 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.748-1629T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913347 | |||||||
| chr6:28913378 | C | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.748-1660G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913378 | |||||||
| chr6:28913503 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.748-1785T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913503 | |||||||
| chr6:28913578 | AGT | A | 13 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0062 others(10): Show |
15 | HG01175.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.748-1862_748-1861d others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913578 | |||||||
| chr6:28913597 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.748-1879C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913597 | |||||||
| chr6:28913681 | T | G | 8 | a0001c0001t0003g0056 a0001c0001t0003g0220 a0001c0001t0003g0221 others(5): Show |
9 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.748-1963A>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913681 | |||||||
| chr6:28913711 | C | T | 1 | a0001c0001t0002g0016 | 3 | NA18967.hp1 NA19064.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.748-1993G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913711 | |||||||
| chr6:28913795 | C | G | 1 | a0001c0001t0002g0114 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.748-2077G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913795 | |||||||
| chr6:28913883 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
206 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.748-2165A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913883 | |||||||
| chr6:28913955 | A | G | 1 | a0001c0001t0003g0229 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.748-2237T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28913955 | |||||||
| chr6:28914010 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.748-2292C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914010 | |||||||
| chr6:28914023 | G | GT | 34 | a0001c0001t0001g0185 a0001c0001t0001g0195 a0001c0001t0001g0212 others(31): Show |
47 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.748-2306dupA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914023 | |||||||
| chr6:28914075 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.748-2357C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914075 | |||||||
| chr6:28914099 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0156 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.748-2381C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914099 | |||||||
| chr6:28914137 | C | CT | 7 | a0001c0001t0001g0153 a0001c0001t0001g0184 a0001c0001t0001g0213 others(4): Show |
7 | HG02148.hp1 HG02738.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.748-2420dupA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914137 | |||||||
| chr6:28914182 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0146 |
5 | HG00741.hp2 HG01243.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-2464G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914182 | |||||||
| chr6:28914321 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
206 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.748-2603C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914321 | |||||||
| chr6:28914324 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0035 others(5): Show |
15 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.748-2606C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914324 | |||||||
| chr6:28914444 | A | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
19 | HG00544.hp1 HG01192.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.748-2726T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914444 | |||||||
| chr6:28914454 | C | T | 6 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0087 others(3): Show |
8 | HG02074.hp2 HG02165.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.748-2736G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914454 | |||||||
| chr6:28914581 | T | TC | 3 | a0001c0003t0003g0246 a0001c0003t0003g0247 a0001c0003t0003g0248 |
3 | HG02630.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.748-2864_748-2863i others(3): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914581 | |||||||
| chr6:28914581 | T | TG | 83 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0036 others(80): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.748-2864dupC | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914581 | |||||||
| chr6:28914581 | T | TGG | 31 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0182 others(28): Show |
36 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.748-2865_748-2864d others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914581 | |||||||
| chr6:28914582 | G | C | 1 | a0001c0003t0003g0245 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.748-2864C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914582 | |||||||
| chr6:28914584 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.748-2866C>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914584 | |||||||
| chr6:28914587 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.748-2869C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914587 | |||||||
| chr6:28914760 | G | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.748-3042C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914760 | |||||||
| chr6:28914891 | G | GT | 7 | a0001c0001t0001g0153 a0001c0001t0001g0212 a0001c0001t0002g0082 others(4): Show |
7 | HG00642.hp2 HG02738.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.748-3174dupA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914891 | |||||||
| chr6:28914970 | C | A | 4 | a0001c0001t0002g0067 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-3252G>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28914970 | |||||||
| chr6:28915266 | T | A | 1 | a0001c0001t0007g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.748-3548A>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915266 | |||||||
| chr6:28915293 | T | TA | 32 | a0001c0001t0002g0074 a0001c0001t0002g0110 a0001c0001t0002g0111 others(29): Show |
45 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.748-3576dupT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915293 | |||||||
| chr6:28915293 | T | TAA | 9 | a0001c0001t0002g0128 a0001c0001t0003g0237 a0001c0001t0003g0238 others(6): Show |
9 | HG00642.hp2 HG01123.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.748-3577_748-3576d others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915293 | |||||||
| chr6:28915293 | TA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(89): Show |
175 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.748-3576delT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915293 | |||||||
| chr6:28915293 | TAA | T | 24 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0040 others(21): Show |
29 | HG01255.hp1 HG01884.hp1 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.748-3577_748-3576d others(4): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915293 | |||||||
| chr6:28915299 | A | T | 4 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG01255.hp1 HG02602.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.748-3581T>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915299 | |||||||
| chr6:28915461 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.748-3743A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915461 | |||||||
| chr6:28915519 | G | A | 5 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.748-3801C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915519 | |||||||
| chr6:28915545 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.748-3827C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915545 | |||||||
| chr6:28915558 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.748-3840C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915558 | |||||||
| chr6:28915592 | G | A | 31 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(28): Show |
44 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.748-3874C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915592 | |||||||
| chr6:28915831 | C | G | 1 | a0001c0001t0011g0227 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.748-4113G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915831 | |||||||
| chr6:28915911 | T | C | 46 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(43): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.747+4101A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915911 | |||||||
| chr6:28915920 | A | G | 14 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0062 others(11): Show |
16 | HG01175.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.747+4092T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915920 | |||||||
| chr6:28915929 | T | G | 46 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(43): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.747+4083A>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915929 | |||||||
| chr6:28915958 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0035 others(3): Show |
13 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.747+4054C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28915958 | |||||||
| chr6:28916118 | T | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0037 others(4): Show |
13 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.747+3894A>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916118 | |||||||
| chr6:28916166 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.747+3846A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916166 | |||||||
| chr6:28916204 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.747+3808G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916204 | |||||||
| chr6:28916205 | G | A | 31 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(28): Show |
44 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.747+3807C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916205 | |||||||
| chr6:28916206 | C | T | 46 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(43): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.747+3806G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916206 | |||||||
| chr6:28916207 | G | A | 5 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0115 others(2): Show |
5 | HG01109.hp2 HG01261.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+3805C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916207 | |||||||
| chr6:28916373 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.747+3639C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916373 | |||||||
| chr6:28916382 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0141 others(3): Show |
11 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.747+3630C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916382 | |||||||
| chr6:28916552 | C | CA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0207 others(9): Show |
22 | HG01099.hp1 HG01106.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.747+3459dupT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916552 | |||||||
| chr6:28916652 | G | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0148 |
4 | HG02965.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+3360C>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28916652 | |||||||
| chr6:28917006 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
19 | HG00544.hp1 HG01192.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.747+3006C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917006 | |||||||
| chr6:28917111 | C | CG | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.747+2900dupC | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917111 | |||||||
| chr6:28917113 | A | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.747+2899T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917113 | |||||||
| chr6:28917170 | A | G | 5 | a0001c0001t0002g0024 a0001c0001t0002g0063 a0001c0001t0002g0082 others(2): Show |
6 | NA18956.hp2 NA18973.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.747+2842T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917170 | |||||||
| chr6:28917286 | A | G | 1 | a0001c0001t0003g0226 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.747+2726T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917286 | |||||||
| chr6:28917297 | G | A | 8 | a0001c0001t0003g0056 a0001c0001t0003g0220 a0001c0001t0003g0221 others(5): Show |
9 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.747+2715C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917297 | |||||||
| chr6:28917425 | A | G | 31 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(28): Show |
44 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.747+2587T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917425 | |||||||
| chr6:28917450 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
206 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.747+2562G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917450 | |||||||
| chr6:28917577 | T | TA | 13 | a0001c0001t0001g0049 a0001c0001t0001g0157 a0001c0001t0001g0210 others(10): Show |
14 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.747+2434dupT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917577 | |||||||
| chr6:28917577 | TA | T | 6 | a0001c0001t0001g0142 a0001c0001t0001g0147 a0001c0001t0001g0164 others(3): Show |
6 | HG01884.hp1 HG03225.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.747+2434delT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917577 | |||||||
| chr6:28917637 | G | A | 4 | a0001c0001t0002g0067 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+2375C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917637 | |||||||
| chr6:28917811 | A | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0075 |
2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.747+2201T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917811 | |||||||
| chr6:28917830 | C | CT | 7 | a0001c0001t0001g0172 a0001c0001t0002g0061 a0001c0001t0002g0062 others(4): Show |
7 | HG01175.hp1 HG02300.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.747+2181dupA | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917830 | |||||||
| chr6:28917859 | G | A | 4 | a0001c0001t0004g0051 a0001c0001t0004g0052 a0001c0001t0004g0218 others(1): Show |
6 | HG02922.hp1 HG03098.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.747+2153C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917859 | |||||||
| chr6:28917867 | C | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.747+2145G>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917867 | |||||||
| chr6:28917929 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.747+2083G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917929 | |||||||
| chr6:28917975 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.747+2037A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28917975 | |||||||
| chr6:28918066 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.747+1946A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918066 | |||||||
| chr6:28918086 | A | G | 5 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+1926T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918086 | |||||||
| chr6:28918088 | A | G | 5 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(2): Show |
5 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.747+1924T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918088 | |||||||
| chr6:28918167 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0146 |
5 | HG00741.hp2 HG01243.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+1845C>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918167 | |||||||
| chr6:28918180 | A | G | 1 | a0001c0001t0002g0023 | 2 | HG00280.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.747+1832T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918180 | |||||||
| chr6:28918197 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
206 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.747+1815A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918197 | |||||||
| chr6:28918235 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.747+1777G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918235 | |||||||
| chr6:28918320 | C | T | 1 | a0001c0001t0003g0225 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.747+1692G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918320 | |||||||
| chr6:28918538 | G | T | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.747+1474C>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918538 | |||||||
| chr6:28918613 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.747+1399G>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918613 | |||||||
| chr6:28918630 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
6 | HG02896.hp2 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.747+1382G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918630 | |||||||
| chr6:28918725 | A | C | 46 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(43): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.747+1287T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918725 | |||||||
| chr6:28918748 | C | T | 1 | a0001c0001t0005g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.747+1264G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918748 | |||||||
| chr6:28918749 | G | A | 4 | a0001c0001t0002g0067 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+1263C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918749 | |||||||
| chr6:28918944 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG02040.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.747+1068T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918944 | |||||||
| chr6:28918977 | G | C | 1 | a0001c0001t0007g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.747+1035C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918977 | |||||||
| chr6:28918988 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.747+1024A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918988 | |||||||
| chr6:28918994 | A | C | 4 | a0001c0001t0003g0220 a0001c0001t0003g0221 a0001c0001t0003g0223 others(1): Show |
4 | HG01109.hp1 HG01361.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+1018T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918994 | |||||||
| chr6:28918996 | T | G | 4 | a0001c0001t0003g0056 a0001c0001t0003g0240 a0001c0001t0003g0241 others(1): Show |
5 | HG00642.hp2 HG01081.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.747+1016A>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28918996 | |||||||
| chr6:28919036 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
19 | HG00544.hp1 HG01192.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.747+976G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919036 | |||||||
| chr6:28919077 | G | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0075 |
2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.747+935C>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919077 | |||||||
| chr6:28919139 | C | T | 1 | a0001c0001t0003g0053 | 2 | HG00408.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.747+873G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919139 | |||||||
| chr6:28919245 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0207 others(3): Show |
15 | HG01099.hp1 HG01106.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.747+767A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919245 | |||||||
| chr6:28919311 | G | A | 4 | a0001c0001t0003g0014 a0001c0001t0003g0057 a0001c0001t0003g0243 others(1): Show |
8 | HG02056.hp2 NA18968.hp2 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+701C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919311 | |||||||
| chr6:28919348 | A | G | 1 | a0001c0003t0003g0245 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.747+664T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919348 | |||||||
| chr6:28919552 | A | C | 1 | a0001c0001t0002g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.747+460T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919552 | |||||||
| chr6:28919710 | G | C | 1 | a0001c0001t0010g0211 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.747+302C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919710 | |||||||
| chr6:28919828 | T | C | 4 | a0001c0001t0002g0067 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+184A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919828 | |||||||
| chr6:28919929 | G | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
9 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.747+83C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 3/7 | chr6 | 28919929 | |||||||
| chr6:28920281 | G | A | 6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0005g0129 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-39C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920281 | |||||||
| chr6:28920398 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0071 a0001c0001t0002g0072 |
4 | HG01934.hp2 HG01978.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-156T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920398 | |||||||
| chr6:28920694 | GAGCACAT others(20): Show |
G | 1 | a0001c0001t0001g0163 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.517-479_517-453del others(27): Show |
TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920694 | |||||||
| chr6:28920740 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.517-498A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920740 | |||||||
| chr6:28920812 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.517-570T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920812 | |||||||
| chr6:28920838 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG02040.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.517-596A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920838 | |||||||
| chr6:28920910 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.517-668G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920910 | |||||||
| chr6:28920980 | T | C | 1 | a0001c0001t0002g0061 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.517-738A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920980 | |||||||
| chr6:28920981 | C | T | 1 | a0001c0001t0002g0061 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.517-739G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28920981 | |||||||
| chr6:28921109 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.516+783C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28921109 | |||||||
| chr6:28921178 | C | T | 1 | a0001c0001t0004g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.516+714G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28921178 | |||||||
| chr6:28921377 | TA | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
214 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(211): Show |
intron_variant | MODIFIER | c.516+514delT | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28921377 | |||||||
| chr6:28921420 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.516+472T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 2/7 | chr6 | 28921420 | |||||||
| chr6:28922293 | G | A | 4 | a0001c0003t0003g0245 a0001c0003t0003g0246 a0001c0003t0003g0247 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-306C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28922293 | |||||||
| chr6:28922437 | T | C | 6 | a0001c0001t0003g0249 a0001c0001t0003g0250 a0001c0001t0003g0251 others(3): Show |
6 | NA18951.hp1 NA18955.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-450A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28922437 | |||||||
| chr6:28922442 | G | A | 46 | a0001c0001t0003g0006 a0001c0001t0003g0014 a0001c0001t0003g0053 others(43): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.421-455C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28922442 | |||||||
| chr6:28922525 | C | T | 3 | a0001c0001t0007g0255 a0001c0001t0007g0256 a0001c0001t0007g0257 |
3 | HG01255.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.421-538G>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28922525 | |||||||
| chr6:28922630 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.420+583A>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28922630 | |||||||
| chr6:28922798 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.420+415C>T | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28922798 | |||||||
| chr6:28922941 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.420+272T>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28922941 | |||||||
| chr6:28923023 | G | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
144 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.420+190C>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28923023 | |||||||
| chr6:28923023 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.420+190C>A | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28923023 | |||||||
| chr6:28923040 | A | C | 1 | a0001c0001t0002g0133 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.420+173T>G | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28923040 | |||||||
| chr6:28923044 | T | G | 1 | a0001c0001t0002g0133 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.420+169A>C | TRIM27 | ENSG00000204713.11 | transcript | ENST00000377199.4 | protein_coding | 1/7 | chr6 | 28923044 |